Endgame with Gita Wirjawan - Dr. Raymond Tjandrawinata: Pandemic, Maintaining the Innovation Momentum
Episode Date: August 6, 2021Dr. Raymond Tjandrawinata, executive director at Dexa Laboratories of Biomolecular Sciences (DLBS), talks about collective conscience, co-evolving with pathogens, and the first monoclonal antibody the...rapy in Indonesia—a breakthrough treatment for patients with preexisting comorbidities and elderlies. In collaboration with PT Dexa Medica.
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Is the other than the more than the other than the more than the more than the more than that?
In the past 20, President Trump, it's kind of,
because of SARS-CoV-2, when he got to get COVID,
and then he's just out, why he's out, it's like, it's like,
it's like, it, even what's what happened,
maybe there's cosmetic changes and and other,
But at least he can't even to helicopter,
he can't go back to White House,
in a helicopter in a three-four days.
That's not a man.
And, it's not that he's given monocular antibody.
And one other, with 1,350 patients,
it's,
that's the patients that made up to runoffing,
and end upensiveness,
and the passivocal.
And the pernournation from progressivitias,
not mind, man,
72%.
Artin patients who had made upon monotron
body body,
not be more
not in the hospital,
not in the room,
as a hospital,
not in the room,
and that's not,
and that's been taken
$7.00.
This is NG.
Hi,
this,
we're coming
Professor Raymond Jandra Winata,
Ilmuan, or Molecular
Pharmacologists, from Dexar Group.
Format Wauwancara
I'm a bit of the other thaning the same thing we've got to be herenation.
Hello, Mr. Raymond, what's about?
Welcome to you.
Thank you, Mr. Okay, thank you.
I'm here, is here at-hara endgame.
I want to go brook-progel, I'm going to be able to be able to be able to be able to be able to.
Mr. Raymond, you're
you're in December,
in 2004.
And the life of your life of Bapa,
in the 257 years' last year this.
Silacan, decedicaan,
from, from, from, from, from, after,
and, through, school,
and, profesies,
and, then, at the end of the
I'm going to go about
about about
about the
of the future in 2015.
Willa.
Oh, sir, sir, paquita.
Yeah, so I was in Gembert,
in 1964.
My dad's that,
then,
he was pension in the U.S.
but he was still
making time of the interment of the United
so, and then
after the U.S.
Then, after the discharge
of the U.S.
He had a certain
and I wasa I wasa in Jember,
with my sister SMP.
Then, SMP, I had hijacked to Jakarta.
When I took to SMA Canisius in 1983.
I was a bitulant, I was as a guyra from Jember,
can get to MASSAD in Jakarta.
I was I'm soo'n't really.
After from Canius, I was from America.
When I was going to learn about science.
If you can't know,
why Canisius in Jakarta?
Yeah.
From Cembourg, we also know that Canisius
is one of one school that's most
who's known in Jakarta,
while Fungu de Lourg, Ursula, and the other.
So, that, it, really, one of the same time I'ma
in the S&P, if I was, I'm going to be
to go to a school in Jakarta
that way, Kanishis, one
that's one of the time.
Mugot, please.
Then,
I'm even, at the time I'm sorry, I'm sorry
like in the science and physical, and also,
biology.
So, I think, I'm going to be,
there's two of the way that,
I want to be a scientist, or I want to be a doctor.
And, at the time I,
I was a certain to be a scientist just.
Because I like to work in a laboratory,
I'm trying things.
I'm always curis from the little,
So if I have
I've always bonkare-in one-per-one
to every other,
I'm having some of the things I've used, I've been trying to make
the way of my parents, it's a protot.
Because I've always made something
from the catamata, this is bonkart.
And it's, that's curiosity that's what made me
for me, very curious,
so I'm going to be a scientist just.
So, I'm going to be a scientist just.
Now, area that I liked in that
research I was in the field of biology molecular,
like that self-physiology of molecular.
Now, in the 80s-an,
that's about the biology molecular
to, we must have made,
I'm not so that's
so that's going to get to get up,
but if I'm going to get back
all the time of all the other,
so I'm doing all of the same way,
so I'm from the basican,
make chemiawing,
make sure,
make sure,
and to keep it,
I'm doing it,
and then,
it's more,
because I know
from science,
from the first
where it was
being developed,
that's DNA,
RNA and that's 20083
in the 183, just only one company in the molecular biology,
the name is Genet.
Then, the second, the second, that's just around.
That's in the 80s, it was exciting period.
Because I justeruptuant many times insight
from the budding elmewan,
when it was still still known.
Herbert Boyer, all that,
that's all right, to,
to do that's what I'm making, what I mean, what's the
DNA, RNA, made insulin, that,
when I was in genetic, I'm going to do history.
Because it's almost same, yeah, regenerations and that and other.
So, more than I'm more, more than I'm, more than,
I'm more than, more than that.
Because, many times I'm doing their
and to make paper their.
And, at the time that, I was very interested
and cancer.
One of the compound
that was the one of the same thing
was the gulomines.
I'm trying
professor who worked
in the building polyamins
that, in all the America
in some of the time, in several times,
the most of the one of the doctor great by is in the U.C. Riverside.
So, I'm going to gojure him.
So I'm going to get a master and PhD
in the case bias,
then I'm at UCSF
after that.
Post-doctoral, yeah?
Post-doctoral, in UCSF,
molecular pharmacology,
work with Dr. Milihyushilovac.
Now, now, I'm notherom,
now, because why I also
like with this
because, after poli-amine,
when I was lulled,
then, it, was lulled,
I was relapse,
I'm going to prostaglandin.
That's Milingus Warfurt, the plightioning in UCSF, to Prostaglandin.
And, in the bestrothalian,
million million years ago,
so that STS-4-6, it was sent to
Ankasa for two weeks.
Then, well, I'm notunging that I also
made up project from NASA
that was that I'm making keep Canaveral and other
and other, to make up to make uproaic,
because the astronauts,
who came to the world in the 80s,
and then, and then,
but then in the state of graphics,
it's only one week.
Now, this we researched,
that, and Milly, PI,
I said, because this is important
because many people that,
to be boponged out of STS, that,
because he's illang the same amount of the lunging.
Because of the condition of serogativity that.
So we've done many times,
penitian about cancer,
and prostate cancer.
At the same thing, NASA also,
also, bedatangerness.
So I remember,
at that, project, is not apis-abish-upes-n't,
and we spend in lab,
to be hours, ma'am, ma'am,
to make sure that.
Basically, we have two projects,
one can't one that's about NASA
that.
After,
after I've got approached doctoral science,
I worked for Smithline-Bicham.
Because what I'm going to choose Smycline-Clems,
because at that I've got to know
that target my,
after basic science,
I want to do clinical science.
Now, in Smith-Cline-Bichm,
now, Gluckus Smith-Kline,
yeah, at the work I was in there,
he merged with Glaxis,
to be called to Clive Klein.
I've been given a lot of work
to do with a work,
so I've learned,
how new,
the clinic,
to be clinical scientist.
So, that,
I'm not that I'm from,
is,
well, basic science,
in vitro,
but also clinical science,
that's for,
in my own own
in this,
what I'm going to
achieve,
that's been able to
science,
and clinical science.
If you can't back to the conclusion of the study that
did with the same asapeutic, how about?
Yeah, so,
we've got to make sure how osteoporosis for the astronauts that.
Not need to be lullough with other, but also with the
and other.
We've given recommendations, formulations of the
that can't
autochoplast,
we're also making osteoplast,
and thenimulase,
and then can't bring
transgramming growth factors
three, two, three, and that and all
and that,
and,
they're not corposed.
Tullang they don't
have a destruction
in the
of their
in the state of gravity
that.
And that we recommend
recommendacation
that,
that's got to
now,
the standard
for the astronauts
The other than the astronaut,
that's one day,
out of the world of the world of the pasting that
has not been done in the way
what's done in the pastoralists
the other generation that's before.
Because now,
now, it's already in the
time,
that's in the time
we,
when we're doing
test with osteoporosis.
There's other
other than
with the astronauts
the surrogeneat
in the surrogeney,
zero-gravity, so that's the human being more
more than more than that.
For the result of the other than what?
For example of the planet
this, what is it is what is it from the gaii-idupe?
Or whatever?
Yeah, it's like a life, exercise, it's important,
because of the lung is, if we're not only
the muscle, but the muscle, but the muscle,
the body also, also,
yeah, that's important.
If we're also, what we're going to
if we're doing, what, the way,
because ofoporosis, that's going to exercise,
the kind of life that is very modest,
that, man, everyone has to do that,
especially the people who are in the people who are
people who are pre-monopausal and and other,
that they're doing that.
Okay.
Okay, sir.
Yes.
Yes.
There's a supplement in the way what name, vitamin D, vitamin calcium, and other,
that's, so we can't not be able to do it,
so, so...
So, after that,
at Glouaccio, yeah?
Yeah, in Glacosmith,
I'm going to do many of the clinic,
and I'm going to learn about how to design
of a lot of about some ofabot-a-obotan.
From there, because I networked,
I also, I'm also in Stanford University,
and I used in Bay Area.
Because when I was,
I was trying to work in Genentech,
but I'm not going to come to Indonesia.
Then I'm going to make
a clinic at Stanford, at UCSF,
UC Davis,
then UCLA,
some projects, and
I've got to get down
how to design a drug,
making a newie proclinous,
and a case of a clinic as a certain ofabat.
Now, the other that's what I've learned in America.
Then I came to Indonesia in 2000,
the time that was given by Daxa Medica
and had gotten to do what I've done
what I've done,
design opat ofabat and so farcein
of the obatowns.
Now, since the year 2005,
we've madeirited a laboratory
name's Dexas Laboratouris of Biomolecure Sciences,
it's actually, from Roodie Sutigno,
the director of dexamedica,
that's really,
he's been citas, expertise of production of health
that at the DECA, it,
but one day,
we can, we can, we can,
we can't,
because,
because from him,
if from,
if from,
but we're from
many of the resources
that in Indonesia,
and it's not even
that it's not even without
the abat ofabat that's been able to standard
from chemiwi, that's been made from tumbu-tumbuant.
And he said, so in that, he said, okay,
we're going to make,
we're going to beaubsteadicitsa of Alam Indonesia.
Now, in that, then I'm going to
use all the knowledge that I've learned from bachelor
to PCHMB postdoc,
to the time I've got to design
opatine, abatting,
and now we've got to get around,
we've got 12 opad that new biological entity,
new chemical entity,
but from from the tumbu-tumbuant,
that's called phytopharmacca,
now it's as well as much,
yeah, Obabod Modern Asly, Indonesia.
Now, we automatically have,
that,
to do not many of Indonesia,
because in Indonesia, there's not many
the other than we're doing that
we can't from half-singhamah,
and we have to look at technology what
that's in Indonesia.
If from the part of my own,
that's many of biodiversity that's still
in exploitation,
and potency's,
yeah, potency that's still
back,
so, but,
why, we must have more import of the world
if it's from Indonesia,
but I'm sure that now,
now, there's already,
there's many of the roots that come up,
that we can do, that we can do,
even though, even when we can't makele of things
in the other, we can't do that in Indonesia,
If you can't say,
that's the Pemerdayamai,
that's what percent,
is from total consumption of opatobat
Obat Obat Ombudsian in Indonesia,
yeah, if you're saying OMA,
OAT, and FITO-FARMA,
still not many,
so,
20%, 1, 2%,
maybe,
maybe,
maybe,
5%,
because,
because number 1,
doctor that merseptan
still not yet.
The other than the government also
still doesn't even be able to serve as well as well as well
from OMAI, until this is one of one PR that we have
how the METERAL that's in the
Immuneration of Indonesia to in the formularium national.
That is one PR, so that's the innovation
that is in Indonesia,
this is also by the government,
because if not it's not going to be mainstream
with a new about that's not that.
For that, if we don't do that,
then, about, abat,
and the abacca,
of the other than the other than
indusia,
the industry of pharmacies,
not much,
refusely,
import of the baku.
Now,
like,
like, with the
COVID,
we,
importation,
because what?
Because the
country that's export
the backu,
he's also
For the country that's already, because of the
we're from where we're bansan bachewa.
For that, we in Indonesia,
we have to make making make make make up a bhawned.
But what most is, what's the fact that is very
being very much-denjanked.
So, if we look,
we're making potential potentials is much
the development in Indonesia.
And we, from Deksa,
we're trying to reset,
not only in the bidang herbal,
because that's a technology that we have
but now, but again,
it's going to biological,
like, biological,
example of what,
bacteria in the same of our own
our body,
that's also,
potentially, so bad,
then, bacteria that are in the
land, also potency,
so it's, and then if we talk about biologicals,
yeah, to Indonesia,
don't have structure
from the
research,
bi-reliability and biologous,
By similar, we still import.
Now, the time we have to be able to make it
self, until, next one day,
we have to be able to be able to be able to make
bioligic from from
other, but from scientists
of Indonesia, but it's been
making, that's now
this, and with the
COVID this, we can
make, to,
make technology technology
that's a potential
intensions of the same.
Yeah.
Yeah.
Mr. Raymond,
as a bit of the
as a molecular pharmacologist,
what is,
what is,
in the other DECSA that is that
did not.
Yeah.
As a scientist,
I, I,
have to be contributed
many of the
other one of the
one of the
I'm doing
I'm going to do some universities
atmajaya, university of Admajaya,
in the Bidongatology,
because that's my kind of myrile of pharmacologists.
Because that's my own local pharmacologists.
I have also educated
from scientists,
muddhist,
budding scientists,
so,
and how they also have to have
what is science,
and how can I apply?
And how can I dedicate myself as a scientist
for the commoing in Indonesia?
So I'm in the technology,
I'm also in business in the biotechnology,
Nutrigyomics, biotechnology,
pharma along those lines.
At the same thing, I've always made school,
give you a class in the university,
in many,
Panasal, UNR, and all of it.
That is my own work in here.
other than publishing. I also, I'm also
I'm also, that's a good, that's a good,
that's a good, for as a person scientist,
and to be itchara, and bicarer.
So, how I'm going to teach atma Jaya?
Oh.
A week's a little, or?
Yeah, just the SKS' just about SKS, yeah,
20 SKS, sorry, 18 SKS I'm going to
So it's a lot of the study that I've done.
Yeah.
Yeah.
Mr. Paul, before we'll continue,
Mr. Bapaguer,
Bapa, you know,
hobby, playing piano, right?
Yeah, right.
Tell us a little,
sir, before we dive about science.
Yeah, yeah, okay.
So, it's,
I'm, maybe,
I was, I was, I'm, and I'm just,
yeah, I was like with music, yeah?
I was like music, so in the S&A, I've learned in
different different, organ and piano, but I more
like piano.
At the time I first, I also, I'm going to make music composition and the
other, because that's one of the one that makes me play piano,
and, and, I was more than I more than I'd more than to.
And, I think I, there's a contribution to piano, because it's the
the other than the other, so that
makes me more creative in the way of it,
and then like, now,
I'm saying, I'm trying to play piano,
but principles and other, I'm still, I think of all.
But I'm actually, I'm still like to
and I'm going to analyze the chord
from music, dynamics, and that,
although I'm not even though,
but I like, because
my education, too,
in the big of music, I got into music.
Lebe more than music classic, pop, dungdut, rock,
yeah.
Yes, I'm just like jazz and popular,
okay, okay, okay, okay, okay,
like, okay, like, okay, like,
okay, like, okay, like,
this is, ma'amacus,
ha, uptta, one, yeah, yeah?
Yeah, okay,
I've got to do that,
I'm going to talk about
about the
perkemean the last month this,
the last month this,
the world has been very 200,
200 people have been there are
in Asia, Tengara,
it's more than 6 jute,
in Indonesia,
more than 3,000,
the number of the death
not, not,
If I'm not quite
DECSA, this can make suret of
if I'm notherned-of, or,
or, it's not-d-d-degenerate,
especially to be monoclonal antibody therapy.
It's about,
this is how
how the peran-an-an-an-chlonal antibody
antinoclonal antibody therapy
to be with the development COVID-19
the last year.
Yeah.
So if we look, we're going to
to go to COVID-in-necuitan
about COVID,
about COVID,
it's actually
not more and not
not quite from collective intelligence
from the scientists in the world.
That's what I'm saying that's why I'm saying that's why we're not
not that we're not being a lot, but we're
having a lot of we're in one or something,
and we're directly in one or another.
Contonion just, that's why I've got to collective intelligence?
Because, for the Pfizer,
They're not going to vaccine.
Then in AsaSahedka, it's also,
while other than vaccines.
But, actually, there are many vaccines
other vaccines that can also be out
. Now, the same again,
with monoclon antibodies.
So, there's about 70 monocon antibodies
to the SARS-Kog2.
Although they're not
not even though,
somehow, it's been able to be
and this I'm saying,
we are collective intelligence
scientists in the world. And in the
out of the world, automatically, because collective intelligence,
not only we, we're, we have the law,
where we're putting up, we're doing, that's
other, that they're also, they're not in the way,
that in the way that, that's in the way that we're
that we're giving to the, what we're
bacteria and the virus and other,
with drug, and other, they're also mad,
They also because they have law
itself, natural law.
So, so that's called as SARS-CoV-2
in 2009.
Now, if we talk about
WUH, Pasar in Wuhan,
people who are
being animals, and other, that's
only technists just.
But if we talk,
why that's that's
that can be a virus
that's from from
human, that's actually
unheard-of, it's
interspecies jumping.
Gene pool that's in
being in in in in-stained.
human human human but it's because of the human human being
but that's because selective pressure too.
We've got used many of the other than,
we're using many of chemicals, chemical,
that they're making up and they're going to
them to make a generation that new.
Now, the way not be the other.
As a virus, they also think,
I'm going to have evulation and I have to survive.
Now, the other one is the way jumping to medium
to mediums, which is from thean to human
because, because of the theory of conspiracies and other
but in the evolutionary biology, it's even
just, the virus is jumping from the human to manusia.
Not impossible, that.
So because it, we're adaptation, we adaptatopatization.
In our evolutionary history, we adapt to be better human beings.
The virus, too, don't do.
Don't think that's bad
that's a bit more smart.
So, until now we can't defeat them at least.
They become smarter and smarter,
and apalachy, and they can be able to revolutions
and get more smarter again.
What we're, what's the strategic pressure
we give to them, they're taking to them,
they're more defiant in behavior.
So, so, since there's now,
there's variant delta,
it's alpha,
wall type,
Then alpha, beta, gamma, delta,
now come up again, Kappa, Lambda,
so when clarene.
Now, for example, like, selective pressure.
In India,
many people who are milded
already have given corticosteroid.
Dexhametason, doses,
dorsesis tingy,
bodhis, d'osyndal,
what's what did is.
It's out of the black fungus.
That's fungal that there
in the down tubu-manusia
and then to get back again.
That's come back again.
That's a concept of collective intelligence
that they have because they've been pressured by us and we've got to be
people who got to goopat, antibiotics, antipongal.
Ruffalo.
And corticot.
Yeah, that's more.
It's just very.
It's just being used to be milked and then.
And then, same with us in here.
If we don't, what we're not doing,
we don't, we don't make upbate this with right.
If we're from our case,
then it's not much and not to
not make sure that there are variants of
other in Indonesia, too.
Now, with that we've got,
how did we're coming from the monocleantibody this?
Monoclonty body is one of one of the other one
viral that's not drug repurposing.
Because, this is drug repurposing,
with indication that long,
we've indicated for SARS-Co2,
SARS-Co-2.
But that's actually not the
opat that's designed for SARS-CoV-2.
So, affinity, constant, that's not
choccurts not with SARS-CoV-2.
The last thing we've got to be initialed
that, that's people who are people.
Now, now, the antivirus,
for the first SARS-CoV-2 is what?
It's actually, there's monoclonal antipodity.
Now, there's monoclonal this,
can be procuracy from from 80-an,
80s, right?
Yeah, right.
So, sir Milstein is the pioneer
from monocle antibody.
The permulaan it, but they
they're using system that's
called the hybridoma cell,
and when the system
melancholytembert, that's
used to research just
actually,
but then,
people,
more than more smart,
and not only reset,
but also as therapy,
but we're also
for other kinds of therapy, for cancer,
there are many of the cancer,
even for cancer monoclon antibody,
also, and that's other.
Now, the last year, monocleone antibody
since 80 to 80, from 40 years,
then, it's also,
maybe think, how we can do-feed the virus
with using antibody.
Because if we're going to go back in the time,
that is still long.
So they have to have a good
to make up the virus,
we're going to end up the virus
we're using anti-virus
without making chemi-chimiawi.
So, not small molecules,
not antiviral, antipolarit,
we're using small molecules.
We're using molecules
macromoleverative of protein,
the number of antimicode.
Now, what did you do you
because monocoonotone antibody is very specific
specific, specific, from the spike region,
from the place he's connected with receptor that is in the cell baru-paru.
So, the attack is precisely,
the spike region from the protein that's in the body
of the virus,
so on the surface area, in the lower-tuburned,
from the virus.
And because specific,
he has the data antiviral is very high,
and, really,
to get-in-habilize it from the virus to
neutralistic from the virus that's
that's true
that's not only in
the other places
but also in America,
in Europe, in
some of the other
one of the other
from Asia is that from Korea
Southan,
Namediname
Named.
Yeah.
Rekirona.
Rekirona, that's the name,
Pelagana.
That's,
That's just, it's just to be restuil,
like, in international,
termasue, through FDA, right?
Yeah.
Maybe it's about how it can be comparasic can
with some other,
but not only monoclonal, the other,
but I want to try to take a bit
with, or to the
the predetatants that's
by the company for vaccines,
if we can
Pfizer-Biontech moderna
that's using the predateatea,
while the other than AstraZeneca,
more than DNA.
Now,
why,
there are some of the
and in the other than what's more than
more than we're in Indonesia,
maybe in a way that's the other than
monoclonal antibody therapy is more than
for the importance of mitigating risk of hospitalization
or even than that,
dabbling can,
what's there in the past.
Okay.
Munga, sir, sir, sir.
So, if we're going to be,
We've got to look at the
SARS-CoV-COVID, that we're from hydroxychloroquine.
Trenata, the effect is not good.
Then, people who are trying to make an antiviral, but anti-HIV,
Lopinavir, Rito-navir, it's not good.
Trenupt, it's also out of Rambesifil,
the last is Favi-Virapirapir.
That's the really repurposed drug,
They're not for SARS-CoV-2, but for Ebola, for
the other, like, hydroxychloroquine, it's like,
the indication for malaria.
The last we've heard, many, the WAWA group Ivermectin,
it's actually a drug in the manusia, and, and that.
So that's the name is repurposed drug,
so it's not indication aslady, but it's,
It's maybe it's about to have the effectivity.
But if monocontidibati-body,
come back again,
they're even effectiveness that's
directly to start-cagifted-to,
because the result-asal from convalesance plasma
from the patients that's been in-jankyth.
So the penitaphs SARS-CoV-2,
who's-comit-in-tac-a-oh-and-bid,
that's-ehan-gallis-a-bondy-boddiness.
Now, Tadayorna, there's two kinds.
There's MMRNA.
There's three of many.
One, MRNA-based vaccine.
The second, adenovirus DNA-based vaccine.
The third is inactivated virus.
What we know, Xenovacs, xenophic,
synopharm, and other than the three.
But in the two, MRNA and DNA,
the platform technology,
it's already,
but, but before SARS-CoVito,
to make a molecule or a vaccine,
it's a lot of because of regulations that's long as well.
But with the platform that's already,
then, de-adaptisiccate to,
they've got to Pfizer and,
actually, biotech, that's getting,
that's made for MRNA.
Because, it's really, it's quick,
it's made.
If, if, we made from the...
If we were from the...
...inactivated vaccine,
it's been for boulde for a month to make.
But if we talk about the laboratory that's small,
the lawympathorum of the first, as well as we need the
parloria, and propagations it with a big way,
as fast as fast as much as well as it,
just the last year not there, but the study plightiniscsia,
there's just the clinis.
But if the mulchulna, it's just thereinorana,
because MRNA is there, that's in many-mana, that.
Now, we also mentioned about dinovirus and DNA vaccine.
So actually, technology is
together together.
And then I was at school,
DNA is more important than MRNA.
But now, this is,
maybe 10, one decade ago,
10 years ago,
10 years ago,
the MRNA is more,
more important for interference,
to make make transcription,
and other.
Now,
now,
the more important,
this,
I'm going to
is a new technology that's more than one day, not only vaccine,
but therapeutic MRNA.
And this, the dampact not a big amount of course.
Now, if DNA with adenovirus, as a factor to make it to draw
it to the heart, to end up to the target tissue,
which, if in this, is pulmonary lung tissue.
That technology also, did delivery in adenovirus.
Now, if DNA is also similar than MRNA,
DNA that's already from the world,
so that technology is not sooo-susas
and there's in many,
the delivery of the time that was hard to do it,
but with adenovirus that,
for the asser of the Nekal.
If you're not for Indonesia or in the world,
it's based on the result of the clinic,
which is zero-conversion
from the patients to be.
We can, now,
can't even if we can't get lab,
using RPD, SRBD just,
used machines of various machines,
yeah, system of Rosh or systems of the other,
can't come out of the amount of the amount of the amount of the
antibody, neutralizing,
or binding antibody,
from the result of the vaccine that's before.
If you're from the case of the way of the way,
R&A is more simple, because it's,
because it's right, it's in the time,
and it's still inotovirus, it,
it's, it, is given to nucleus it,
before he's going to put into stuplasmany,
it's more multi-stage,
than the legatting arena.
Yeah, I know, I thinkeran,
maybe, it's the good with AstraZeneca,
is this, can, be it's more open source,
more democratization, because he's not
not even though
because of the intellectual property and
all right.
But, is,
but is it more
more than perennation
RNA,
than DNA?
Yeah,
so, but really,
technology R&A is,
can be better from DNA.
But if you look
with cost,
people, and the,
and the things,
the, and the,
Because MRNA is a
because of DNA,
if DNA is double helix,
if R&A is single helix.
So, so the transcripts,
the transcripts for the same,
and it's actually,
it's just a good,
so it's a synthesizer
from the nucleotite that's just,
so it's more,
less a little.
The last, what we talked,
delivery is also important.
MRNA, vaccine we have now technology,
and if you're the DNA that's the Pakenorovirus.
But, the two-two-two-dust, if we're going to be made,
the two-two-neciccicciccic, in the Bidant-N-A or R&A.
But...
Not simple, sir, sir, for D&A,
is because d'nobble-stranded,
he's more stable, he's more good to the front.
Not asbestiness, right, yeah?
Not the samestin-of-ne-a-be-d-you, yeah.
Okay, I'm-hmm.
Because because of mRNA is still
vaccine MRNA,
the first in the world molecule
that can be applications to human beings,
so that's the fact that hypothesisa is also.
So I don't know that the possibility
to the more than more than more than vaccines
in the vaccines in Bermal.
If you're being monoclonal,
how, if, if, or the people of the people
that's a while they can
learn to them banding, banding.
Okay.
So if monoclonal antibodies, it's
that's the therapy that we propose this,
not as vaccine.
Because, if we're in vaccine, it's going to
be out antibody, but it's just long.
And responsivitize from the
other people, that, and if we're going to
so if we're in one of one laboratory,
maybe the RPDs, just if you're using the Eclipse,
it's just a reactive.
But there's no.
Kama 8, there's one, two, three, six,
there's one, there that's two hundred and fifty.
That's a high, right?
If you're going to be on the 250.
Now, how we can't know,
stratification from the people who are responsive,
if I'm like, I'm afraid to get COVID-lady,
What else is a high-risk patient?
Mopuited,
has diabetes,
perna asma,
have a problem because I've got
been rocked to beppocke,
and then, and then,
this is high-risk patient,
at the up of 50, and other than that.
Automatist, if that,
antiviral that's the most
that we have in the world
is anti-body monoclonal.
Because he's targeted
and very specific
to the SARS-Govieto.
Why is that?
because it's not in the laboratory,
so if we're talking about opetopat
of chemical, it's, can still,
if it's actually more natural.
It's from plasma,
from convalescence,
from the penitase co-2,
SARS-CoV2.
So it's really,
very natural and specific
to rederaping
due to such COVID-2,
especially despite protein.
And this is not repurpose drug,
What's the idea?
Not, the idea is called back.
So, recycle not recycle drug, basically.
This is really,
that's really,
designed, and be taken from the penitask such-gocto.
So that's the efficacy is
far more than than the other
therapy that are at this.
But it's how we just
We just look at the number of the
from the people from the disease
in the world.
Now, it's going to be it up.
We're going to be able to be able to be able to
but with the mutations,
we're still not even to bellowing
the pressure to be able to bring in burden
from morbidity, or mortality,
over the SARS-COVID,
even though, even have had
or other than repurpose drug, that even with the
with the other than we still can't.
And then, that's the molecule molecule,
more that we can also make up to be able to be able to be in the parotic
from sarcovito, this, that's the most
best, is the most of the body.
If you can't, sir,
to the case of the case with Rekirona this,
where the result, whatever, what we need to know.
Okay, thank you, so, so we have done.
So, the Ujic Clinic, from Rikirona, this,
did do you do a lot,
including in Europe,
because many people are people who are in Europe,
that's people that need from the drug drug drug addictiveadi.
Now, phase three, the second one
is the publication,
the month last, June, in 21,
with 1,350 patients,
it's, it's turned,
patients who made up against reggerona,
it's getting,
and, it's not getting passivot.
And the penuronement from the progressivitness,
it's not mind, man, 22%.
Artion patients who got to get monotone antibody
to be more than more than more than in the hospital,
also not in the world,
and that's not even though,
and that's the number of, that's been called as a primary endpoint.
So, it's actually, that can't be that regina this is working not only patients,
high-risk, but all patients who are people who are still mild-puner,
also has to get up to 50%.
If you're high-risk, 72% and all-comer,
all-comer, all-comer,
that's all-comer, that's much,
that's many of the number.
Now,
then, secondary end-point is that is called
as a,
for a for a new-embuburn.
So, if we just, I'm just
I'm getting symptoms,
like, batuk,
or, if,
not so that's, what I'm nother,
or pyrre, or tengorokan,
and all the other.
Now, that's, it's all right,
and it's all right now, although it's not
PCR-Sace, but,
I'm, my well-being is better,
my well-being is better,
that means up, that means up to be 5-hary,
compared to, without using recirona this.
So, in fact, statistic, it's very significant.
P-1-1, if it's if it's a lot of 0.001.
So, it's very significant,
so much significant-exic-trial the clinic that did
and that's done, not only in the United States,
but in Europe also, yeah.
So, so it's the implication of, if we're making,
if we're making, as far as how recirunate did be indicis
actually, many people in the
people who are, because
comorbidity and the
contabstion, why
complexities and percussive
and the person is
that always there's
on patients.
Yeah, there's a
but how can't
know that it will be
able to be able or
to be more.
Now, this can't be
not can't be
not any of any other,
there's one of the
one is, to
try to
use that,
is to use
Rackierona
this,
as an insurance that I'm not going to be
or I'm not being matty.
I'm going to be sure that's an assurancy that I'm going to buy
to make sure that I'm not in a car,
because if you're still in ICU, you can't think,
you can't be able to napas,
and not have HP, not have entertainment,
that's looking right-kirre,
is people who, right, right,
the contum of the contum of the rest,
tut, what's not there, and it's stress,
and, it's psychologous,
has made up against the other people who are
who's out of ICU, that can be able to make
making re-kirona.
If this is a problem from plasma
who's been able, from the virus non-delta,
apaca, can't get-hannan or immunities
to the delta variant?
Yeah, that's a very good question.
It's a very good question.
that we design that will
be a bit of the spike protein that's,
there are areas that are as well as conservation,
unconservidion, and all the other.
But if he design it's a good
to where there's a lot of mutations,
then variants of other
other variants of the other than
monocon antibody this.
That's a beautiful, the beauty of the molecular antibody,
because they're not synthetic.
If synthetic, synthetic, it's where, but if this is specific,
because it's like a key and anac-cunci,
anac-cunci certain, only can't be able
a key to cut a certain.
Now, this is also the monocompatide is very specific,
so he only can't make up to SARS-Govintu.
He's not to where,
If you can't, this if you're
if you're being
with plasma that we're
often with,
I'mguptain with, what's
proposed by Parasin, how, ma,
comparasiness?
Now,
Paterawan, it's,
the novel concept,
in myroth, I, yeah.
I, as scientist, I like
concept dendritic cell
to be applied as vaccine.
It's very, very much.
So, I'm not talking about, what I mean?
But, but in fact, if we're saying,
if we talk about dentistic cells
to make sure the antibody,
where he'd be injected, one of the virus,
that's very very because it's very specific,
also as monochololidic cells, because it's not very good.
So, it's very good.
And it's also, it's also very good.
And it's also, using dendritic cell.
It's already in America.
They can't make make sure the case of cancer,
with preventive, with using prostate cancer vaccine
this is a specific with the genetic cell.
Now, if you're going to dox-COVID-2,
then you cannot doubt about that.
Because it will give them protection
that's a good.
Now, the practicality with the easiest of to get the genetic cell,
to make back the genetic cell,
that's questions,
it's about, infrastructure,
chiroc, and things.
Now, if therapy monoconatibody,
this is very much shock. So,
I'm just a high risk.
I'm still high risk.
The second, I'm still mild. I still
don't need to be able to oxygen therapy, but I'm high risk.
Now, this is people who are noty-hatty because
he progressivitiveness to be in,
ICU, hypoxia, cytokine-stom, and all right, that's
this is a high-risk because of morbidity.
Now, this is a target from monoconantibody.
In the 20, President Trump, it was,
kind of, suddenly, starts COVID-2,
and got to get COVID.
Tibba-dibati, he'd come out,
like, like, secure, like,
even what's what happened,
maybe there's cosmetic changes, and and other.
But at least, he can show up,
he can't get to helicopter,
he can't go back to the White House
lewate helicopter in a 3, 4 days.
That's not mine, and it's not been given monocleanderon.
It's that powerful.
Because what?
It's that powerful.
Because what's specific to the virus that we have to SARS-CoV-2
with affinity and the power neutralization
that's high.
So, it's quick so much the sameuania.
Now, like President Trump,
Donald Trump, can't, IRIS, is it,
It's like the most of 50.
If you have, if you have some of the body
there's some of the disease,
there's got to be a caribuscular,
we don't know what's actually.
But this, this, people,
or patients who are potential
do you give can monocle antibody?
If that's...
If you're from the same demographic,
that's the most of the therapy monoclonal
antibody, this?
Is it, ma'amia?
in Indonesia.
The most is that's most is mild.
But anyone who has a high risk for COVID is to
be very much more than the hospitalization risk.
Okay.
So this is really
minimalization risk.
Yeah, exactly.
If this regardless of age, if you're,
Yeah, it's regardless of age.
Anyone who has,
now just as people who have,
just who are people who are in rock,
you know,
eat, not,
not,
not,
not,
not,
not a little,
in Indonesia,
even,
even though,
even if there's
even though,
there's been
there's been
because,
like,
life,
and,
and, and,
and,
and,
and then,
and then,
and then,
and,
all of the people
who are
high-res,
this is,
potential to
,
to be a patient monoconty body.
So we don't know,
if I'm, what I'm going to be?
What I'm going to be?
If I'm not?
If hospitalization, it's going to
if you're going to be ventilator or not?
Now, cost that's been
many of the ICU,
give you, give you,
give you,
the AL6 inhibitor,
yeah,
the same,
T.C.
Then, it's the cost of
many times.
With the cost of money,
only one shot,
one shot, Mark.
This is,
right man,
this,
in the
in the
front of our
right
right
this,
and if we
see the
that's
from the
population,
maybe 12%
and
if we
can use
people
people
people
who can
be vaccinated
per-h-h-a-a-d-a-d-a-d-a-d-a-d-lety
can,
Right, right-hundred-hundred-a-burd,
100-a-per-tour-a-tour-a-tour-tenth.
Population we have,
280-gutte.
...belom-lom-lacquick than variations or variants
variant of the new.
At the end of the day, it's a game of scale,
and speed.
Yeah, right.
Now, this, I'm looking,
Rekirona, this,
It's very potency,
for be able to be able to be able to speak.
Yeah, right?
This is not zero-sum game with vaccination,
but this is very complimentary, if I'm in myruthsay,
yeah,
so, as far as a small as possible,
as fast as possible,
be able to ratasy.
And, suor-suckur,
can't
the other,
in the other,
in the other,
that's what,
how do you,
that's about,
yeah,
so,
don't think that
that's COVID-2 virus
at this moment in Indonesia
will not stay they are.
Because,
they're going to
be mutation and
can come out many
many times
variant variant of
that,
the game of skill
because it's more than more than
more than we can look,
if we're still high in Indonesia,
positive rate's also still
still.
Sedgant, many people
people who are not active,
in the art,
in and other,
or risk the riskiness,
now this is the potential
from the patients can
receive from Rekinvap or Rekirona
because we don't know,
if we're going to come to the hospital,
what's a chance of me,
getting into the hospital, even where that's one question.
But if we talk about,
you know,
how can we can't survive or not?
That's, it's going to be able to survive or not.
We'll make sure that the drug.
That's not a drug,
but it's targeted to have
the SARS-COVID-2 virus.
I'm sure that many patients who are menning
criteria that's there are many times.
We don't want gamble.
We don't want to gamble.
We're not going to gas for COVID-2.
This is a virus that's very bad.
We're not going to get,
and we're going to be used,
progression that's not being passed.
He's invisible.
And people that's people that,
that's the people, who, who?
Yeah, the one, man, right, the time, we're going to be.
Now, that's one, sir, man, back.
Now, that's the first degree of freedom.
already.
Not at the school, not the manned Koleha,
not a ghanotta of the otherga,
this is, here I want to ask,
if I'm going to get a treatment
or therapy, this,
how much, ma'am.
Yeah, nanty they have to go-mong
with the doctor's,
the doctor's,
have a few area to make an IV infusion.
Okay, this is in the room, yeah?
Not, sobeenna, so much it's in the clinic, ma.
There's a doctor who
who will be administratersation from the
from the abutantarant to be.
Because, pa, yeah,
how can't even up-upon,
can be able to create effect that we not
we're not evened but it's not much
mean it's a lot of people who are in sotik,
there who's sick in the place in the area sotik,
there's that he's having fever,
same with vaccine, you know,
but he's check 30 to 1,
1,000 before he can be be able to get back.
That's the same with the way.
From the side of the biosephemy,
how we?
Yeah, if we look at pharmacoeconomics,
that's from the same of the payersers
people who are high-res, because they're
going to go to the hospital, they're giving up,
and not just one doctor,
basically, two or three doctors, specialization.
Blum, must go to ICU,
the opad the other, and other than that.
So if we look, cost of therapy,
it's a fraction of the cost if he must be
to come to the hospital.
That's.
I'm.
Let's start discussing the future.
This is where and when do you see the end of COVID-19?
Number one, we never know.
And COVID-19 will always be with us.
It will be another flu, basically.
It's like a flu virus, which you follow in us.
Abadi, yeah, it's about it.
Yeah, it's about it.
That's what we're making,
that we must be careful and we're taking
from the progress,
and other than that.
So,
how much more than,
it's about how much,
it's about how much
the episode that's
not as dramatic as what we've
seen what we're
If you're
Spanish flu, yeah?
The early 1900s,
it's,
it's about three,
four-t-town,
but that
three-four-town,
there not many ofabat-obot-o-o-battan
At that, penicillin, it was not much.
So at that time, they were making natural,
herbal,
minimum, and, and, and, and, and, and,
it's needed three, four years
so that flu can be in our body,
and co-evolution with our body.
Now, if SARS-COV-2,
you know, maybe two, three years,
yeah, maybe from the time,
maybe, it's not, maybe,
maybe, it's just as we speak.
Nobody knows.
Because at the same thing I said that we've got to
let's pressure that we've got to make suredic
to, what, name, he's, he's, he's going to, he's not,
the idea that's not.
It's the human that, like virus, like, virus,
can be said, mhaloomati, also not, and the other than not.
He's smart, he has DNA.
But he also, he also,
he's got to be able to be curing mutation,
dechlorine, what, and that's...
We have to co-evolvement with them in our body, basically.
If not, yeah, not,
they're not going to die,
they're not in the body,
or in the other,
one day, they can infect us again,
like virus,
like with dengue,
like also with mumps,
mizoles,
same, too,
demigian.
Now, this,
if I'm going to
take to the
little, if you know, if in 2002, when SARS,
it's out of October, that's in October,
it's actually mysterious,
in November 2003.
And if I was going to talk with
with the people in CDC and the
it's about it,
it's, to now, it's not to know what it's going to be
Now, is that
episode that can't
be with episode COVID-19?
It's, because of the
mutation or evolution
from SARS in 2002-200-2003.
Yeah.
Same, coronavirus.
So, so one lineage, yeah.
But what we have
remember, if, you know,
if we're from Spanish flu
the language is that's
the people that's
because the behavior
human behavior that's
also, it's also,
it's underlisks,
with the probleming,
the blockade,
tracing, and that and other,
it's made,
Spanish flu, it, really,
can't be able to be able to
be gone.
Now, SARS-COV-1 at that time,
SARS, only,
only SARS,
that's not been up, at least in the world
at least in Indonesia, only the areas of the certain
even Merva, Middle Eastern,
respiratory virus,
that's also just
just a few different
and in the country that's just that's
what?
If we're really vigilant
and can localize
the people who are infected
then,
then one day,
he can be genocan
He can't be taken
so that can't be raja-lela.
Now, this is the problem that's actually
in the world where globalization
to move to be able to go back to here,
so that's kind of how,
you know, to handle it in this,
and not just the beno that we're just in Indonesia
or the case in India or in where,
that they can't come in other like
we can't, what we can't,
we can't, you can't,
we're just as much to get up,
we're socialization, we're
one-one-one-lux-virus,
there's one of the other people of our population
this.
Now, one's the only way,
from the history,
from the Spanish flu, yeah, we must be able to,
this is a behavioral disease,
sir, so, actually.
This is a behavior.
If you change your behavior,
if you do not change the behavior,
it will go with us all the time.
If we change the behavior, then it will go away.
If we can't go away, it will always be with us.
Maybe three years, not clear, because now,
more than than than the time,
the number of manusia, it's more than in the 2009
than in 2021.
Explosion of the human population growth
made this, wow, this, my man, my can't.
I'm going to be having yourself.
because I'm what I'm, what my generation my species
and I'm more than more than I'm more than I'm really believe in this theory
collective consciousness because they have their conscious too.
They're very conscious of what we're doing.
This is like this, this is a example that I've got to.
Gibraltar is one of one
the world that's in the world,
where the population is almost pervasinati.
Now in India, there's explosive delta-variant.
Now in Indonesia, and maybe in Europe,
in now, at the time of the Olympics in Japan,
there are also in there.
Then, Malaysia, the other, Malaysia, Thailand, and all.
Europe also, too, in Gibraltar,
and then, Israel also might be there,
people are there are vaccinated,
and because the country's small,
the people are not going to get to come out,
like the country and the country that's kind of
can't even be able to be able to be it.
Why still there are variant delta
in the country of the country that's up,
but all, it's been vaccinated.
Now, this, collective consciousness,
they're all,
appeared at the same time,
within this period of weeks.
Why?
But why there's not even though there's very, very interesting.
That's why I believe that we have to co-evolve with them.
But the evolution can only be broken down if we can manage our own behavior.
This is why we have to take care of our lives.
If we look, if we look at,
it took billions of years
to get to 1 million first, that's in 1,800.
2 million that's to be in 1920.
It's only in period 120 years,
1 million the next year that's to be it's up.
And ever since then, it has accelerated.
So it's increments 1 million population
that's in 13-15-15-town.
That's not just like,
or long-longsumens can perilacu manusia
to the nature.
And I, I suppose with a pepatah or purgathe
or purgatant baffa,
that's more provocative
to the world,
the more of the world will back to us.
Yeah, right?
So we have to learn how to co-inhabit.
and everything
and harmonis.
Now, this not gampang,
if I'm being I'm bunged in the
keypentingan
the world that's
more capitalist, right?
Because
the hausan our and
the peningan we to
keep on to
keep on-emisive fossil,
emissy carbon,
it's not
going to be
We're not in the time we're
doing that's more friendly
than we're more friendly,
than we're more friendly,
more friendly,
to be around,
that's kind of
that's very
to be a confuguration
virus,
configuration,
and so if I'm
if I'm
if I'm
that's to talk to
arguably,
one one that's
in a very different in fact,
this is actually we can be a per-perman,
to make up our own
to keep our lives
to get-earedes.
Jolase.
Not just for the
impottingan
and to consume
omai just,
but for we can
also can
make up to
get a way of
and we can
be able to
work,
the world in the
Yeah, exactly.
So, yeah,
partumbuant,
then we must be really,
learn about ecology.
Because,
want, not want,
we're living,
the human who's more perplex,
and more,
more, more,
more practice,
everything.
In a side,
the technology,
it's,
it's,
make,
but, on the other hand,
we must be thinking
that,
that,
that must be revolutions
with evolution
manusia,
so if we're
we can't live co-exist. If we can live co-exist,
then we don't even if we're not much of many people,
look just the banquoise effect, that we've talked about, and all right,
that's all right, allah, we don't take care of them.
So, it's just like this. There's a lot.
Now, but it's the other than pandemic,
and epidemic that we don't know what,
because what, because of our caravanic and we want to practice
to do.
But, but that, I'm sure with the SARS-CoV-2 and the other
that, it's, we as a human being,
we will emerge stronger and smarter.
I believe in that.
Why?
we have we have a bad, we're
very smart being. We're
we're looking, we can't make up,
if we're pepette can, there's been a lot of people,
and innovations, innovation, innovation,
and it's also in Indonesia, I see that
that it's not-enag-enaghan, now we're getting,
oh, yeah, we're now, we're now, we do something.
Why don't we do, as a collective human being,
we do something?
As a big as well as to do something,
so that's just to be able to be better.
Now, I think that we're being smarter,
and we'll be stronger.
Not only in the alat of the health,
but in all of the other than SARS-COVID,
electronic is already,
artificial intelligence,
barang of which are using telemedicine,
and that it was still still,
now we've got used every day,
So that's positive aspect
from the case of COVID.
But like you said, I really believe,
if we don't take care of our environment,
they will get back to us,
and we have to pay at a hefty sum
to to to be a hefty sum
to to
and, you know,
but temptation to
be put-picta
that's a pandemic
that's catastrophic,
this cyclos,
100 years, this I'm
I'm more
accelerated to the time.
We're not going to
not going to look for
seeing the pandemic
the next
catastrophic.
But I believe human ingenuity
that is also
in the
purouan
and this
we can't
see how,
in what,
in a few
people can
to be able to the monoclonal anti-body therapy
that's been a men, or even if you're going to be able to,
but it's not that we're going to have to take it for granted
that we're not really to make making the environment,
we're not putting to make sure about our diversities our and
and all the other.
Now, I want to go about Indonesia to the next,
but you're not
has been inspired
to,
not only only
the time
but in Jember,
but, but,
but,
this is how to
can clone
Professor Raymond
so that
many in Indonesia?
Because this,
if I try to
come with
with
prestation we
in the
science or scientific,
it's,
yeah,
Well, Scalance, ma'amac,
what we can look at
in Thailand, in India,
in the agamacarer
in big, or inhagra
major, or, you know,
and the country of our
people, they can
make make sure
more than we more than we
than we're going to be
before, for, so, in the
year, in 20145,
that Indonesia, is
great, really.
Yeah,
for students,
that's science, technology, engineering, mathematics.
This country will not develop if we don't have enough engineers,
we don't have enough scientists, we don't have enough innovators,
because we will be on the other
which they, possibly,
actually, economy, will manage us with
doing to sell product that's always to us.
And one of the only way is
is that is in elementary level,
or secondary high school.
Plageantan STEM is very interesting,
not going to use system that's new,
mathematics is making very boring.
Chemia, it's very boring.
Then, the study of physical, biology, and other than that.
We're making them really,
we're really,
with more experimentation,
more than more that more that more
that more that more that make of thinking,
If that's that can't have
can't have a way of the way that's not always
because the students'adic learning that we've got to be
from the time we're small, we're doing,
we're together, from the generation that.
So, now, I think I,
even though it's a competency level,
but didactic learning is,
where the road learning memorization,
and then, and then, and then,
it's actually,
that's how much more than that's
to help you.
And the other, how we can also
to give them to understand to people too,
so if they're,
if they're going to make up to make up,
don't think of what,
want to work what,
want to be it in where,
the barraigny of what,
and all right.
Like that must be it's
to be it.
We'll look,
Now we look at the
if I'm going to campus in India,
everyone wants to be engineers,
everyone's being mathematicians,
being biologists,
and being chemists,
and that's not enough to
that,
so,
they're going to make
mobile,
they can make a bushel
plane,
if in the world of pharmacy,
they're not only
can make pill,
but it's making the machine,
people,
and that and the other
even biological.
Now, this is not.
There's not there, but there
but not many, because in Indonesia,
it's the only engineering,
but if science and technology,
the term of science and science,
the knowledge, the world,
biology, physics, and mathematics,
it's,
it's not getting better
and, he's not giving
the layak of the life in the future.
And that's very,
it's very,
When I was in the other than,
people who are, oh, yeah,
why not engineering, why not to doctorate,
why not to not to the area business,
but if we have conviction,
what we're doing will develop,
will be good for human beings,
then what we're doing will make up and
we have positive thinking,
it's just, but I'm going to be able to
be able to becky.
And I'm just can't
I'm like that's like that.
My friends who are people who are like
people who are still doing,
they're still doing that,
and they're doing good,
back back.
Now, this is what we have
in Indonesia
that's the time that's really
really,
so in that in the
time in 2004,
we're not the
number of scientists,
engineers,
mathematicians,
scientists, and other
if we're
if we're just
technology,
we import,
In fact that's in 100-year of the United.
This is I try to
take the experience
Tyeongk, where,
since Deng Shopping in the
in 2008-79,
that's,
they're to have more
to more to be
medepanking technology.
Burdue-dun-dun,
they're giving him
the people,
to all the world,
to Europe,
even in America, America,
to America, the people.
Now, now, in America, the people who are
people who are in there,
to 400,000 to 500,000.
Yeah, right.
Even in our time we,
back in 2000, that was
far more than than
now.
This is not
even in a different
only one of the
country just, but
if we're
to learn technology,
we have to learn
from the other
and our own people, and our own
I think that's like,
Hongk, German, Japan, Japan, Korea, America, Australia.
That's something to offer, right?
Now, this at the end of the day,
back back to what we've had been about as,
it's a game of scale.
For the country that's perpopulation 280,000,
that we have towaughan that,
more than the world to the world,
the number of the world
to be the world
the world, the Americas of the world,
the Americas of the world, the
Germany's of the world.
Now, if we're just
about 8,500,
the most banter, 9,000
who are in America,
how many of the
people, in Europe or in Europe,
that's,
it's,
than what is what
what did by the
India just in America, now
150,000 who've been learned in the campus,
the whole campus.
And we can't passpacred from
ideas new that out of Silicon Valley
that's from people, people,
from India, immigrant.
Now, no, ma, for we,
not to we can't do things that same, right?
Yeah, right.
Right, right.
Yeah, we must move from our comfort zone,
because no change without the change itself.
If we don't move out from our comfort zone,
change will not happen to our society, basically.
So what we're saying,
if people, they want, they're going to,
they're going to be able to beaer again
to Europe, to America, to anywhere
they are, to Japan, to Australia,
a country that really,
that's really been metacetack record in the
technology.
The South Korea, in the
In fact of 40s, in the 20s,
he's just a lot of people,
while he's a dictator
who's named Kim Il-zung,
who's what's in the
time in the 70s.
Yeah, Park Jung-he,
right.
Parkung-he,
Seoul is,
more,
more,
back.
Oh,
that's in the
Korean,
used for the name of
malice and bego and
Jorok.
Now that,
There's like that's the way.
Intingia, right?
So we have to move from our comfort zone.
And they're going to be in our comfortsome.
And it's actually cultural,
it's only a nuclear family.
They must realize that to build a
bank of this has to have
nationalism that
to want with any other
So if we're only one tool to do that,
so if we're going to talk,
we know knowledge that can't be able to beware,
but if it's an experience,
and what's important,
we have to go where we can, basically.
And that, if we're, if we're saying,
school in Indonesia, actually,
not california, but if we're going to bechara S-2,
S-3, in the other than that's even better.
Because of the nationality,
it's in the banked in the world,
we're still in the same, A, SMA, S.M.A.S.2, and that's like,
So if...
Nankar, exactly.
...monger, exactly.
...monger, because if we're not to,
if we're going to come from,
since we're not, it's notherstim-a-samping.
BASA-Indonisiness just, it's allan,
so it's just to go-mongue.
So, this is important,
If they're already,
Indonesia is more than
more than investations in the
research and development,
which is more, less than 1%
or even more, maybe or 2%.
Oh, no, no, way less than 1%
for R&D.
For GDP, right now,
yeah.
Yeah, yeah.
If the country,
Magu, it's 4-5%
from,
Israel, Singapore,
to 4-5% from the
PDB's,
to get gulotorking for research and development.
Wow.
And that's not only the government, but also the company
swastah.
This is we're going to galacted.
Where the country that's not
not having innovation in the technology
not going to bea from the country's satan,
the first time he made a mobile,
Hyundai or the first,
who used to make,
even though you like to mock.
Then I remember,
when we had,
when we had a recording tape for telephone, what name is that,
that's, yeah, right, recording machine to telephone, that,
it's the first one, life is good, and LG, that's actually.
And I think it's like to die, so that's up,
and they're export that when in Korea,
it must be used to use.
Even AC, Merex Samsung, the brand LJ,
it's just, yeah, it's just it,
but they're just being tried in in the population
that's more than we can't have yet in this country,
where the company,
where the company is self-sustra is in the business and development.
How can we move?
So, so far as far as far as far as far as far as from the education,
and other than people,
still have to make up to investation.
And, uh, and I'm doing I'm working in one of the company,
DECSA, who wants to make a commitment
to make a research and development investment,
So we get amy and mulco-mucco
new, too, ma'am.
Maybe there's a person that you're
about the diaspora we're,
but, but,
maybe if I can't take from the
this is as well as I'm as well as
with what I think about
that we're from
people,
who are in the
who are
school in the world
and making
research in the
that's the way to go ahead, right?
Yeah, right?
So they're galley as much as much,
the world.
Because I'm saying,
nationalism is not illang.
And, as much more they galley
the more than more,
then, in the next day,
they can makeapplication for the
importance of the world in Indonesia.
Like what you've done
You've done,
Lama in America,
in Ghali, in post-doctoral,
in some of the other companies,
but, actually, it's back.
And, Bapak, and Bapacchartic right,
right.
Absolutely, I agree with you,
but, don't pull-d-dul-d-lul-dural.
Because, here, we,
in the bidecine science, it's,
but on the other hand,
remember, that in the binaxan,
infrastructure is just as well.
The other than the network.
Now, in Indonesia,
for the science,
the technology that's just,
we've got to say,
scientists in Indonesia,
so,
what?
What is the collective mindset that we have
collective consciousness
from scientific
is,
compared to people
in the world
like we
like,
we've said,
in China,
in Tokyo,
in India, in Taiwan,
in where even,
Now, this is that we have
built structure,
where infrastructure this will
answer what we have in Indonesia.
Because they're still in the world
have automatically accessibility
to have, gampal it, for example,
that we're just to get in Indonesia,
it's in there, there,
more than brain,
which, where, in there,
the people of the people think of minker,
people of mongue,
is the
with the collective mindset that we have in Indonesia,
the number of people, if we're looking,
if there's a lot, yeah,
yeah, so with that I'm just too.
If they're not back,
don't pull down,
don't go out of many,
get infrastructure so many,
get connection and network
so many of the same.
Because that will be
the government,
bantan,
I have one other,
I want to ask.
this time I'm about about
people about biological intelligence.
This is a
molecular biologist.
This is the
not-noticant,
for,
for biologous,
IQ,
manusia,
or tatanan of our
human body, it's
in re-caiasa, so that we can
be much
more than more
more than the
IQ-in-law
more that
that's a kind of
that's how,
how,
I'm going to come
come back in context
in the context
in which
innovation technology
this is kind of
exponentiality,
and the kind of
of the position,
or posture of the biggilderate
that's kind of
with linearity.
Now, gap
of the exponentiality that's
in non-pemirintas
or the government
with linearity
that's very
in the
Pembertah.
It can
can beaughan
some risk,
can,
that,
Where is how much, I want to try contextualize this in
in the future future in 2005?
Yeah, it's going to be it back again.
Science is a blessing or can be it not blessing for us.
If there are a man like Hitler, that's the example of it.
He extermination one of the
bank of the Japanese and other.
But he's made man who's being able to be able to be able to be able to be able to
alert, that's life,
much more than to do logical,
that we have now, we have.
All equipment we have and
it's used it's just and morehous,
now, sir,
that's what we're getting,
if we're going to get,
if we're slow,
for transistors,
because we can look very
like electronics,
it's quick-uporkempanity
just one-one,
one-one,
now, biology is like that
because we're
and we have technology that's bigotica
that's very strong-involuntic by computer,
apolloing of industry 4.0,
where there convergence,
and electronics and biological.
It's very much as well as we've said,
we're making superhuman.
Very simple.
With using stem cell,
with using MRNE,
we can't bring up problems, problem,
with the health and with the beauty
we can reprogram.
We have a crisset.
Chris, yes.
Chrisper, yeah.
Crispor, yeah.
Crisper, if we can, if there's a problem with transcription gene,
that we can give one day,
maybe in the Guardian, in Central Week,
out there, that, there's,
we can't buy in Center, Guardian,
better than our genes our own.
If we want to be able to becantycan.
That's not that.
So, from that,
exploitation from the biological system
this is very key-attie.
Because number one that we talked about,
natural law,
that always co-evolve with us.
The other, we must have
seen see see at least
where if we're going
out of many of many
innovation that's not a natural human being, we become superhuman, and that
and that's where, that's, where we have to have to be the batas-batus, we can call
ourself human. Because, to be right now, with robots that's more
we have to coexist with them, and we're making humanitas our own, this is
the philosophy, how are we going to be as a human?
For example, 500 years from now, are we become part of the robot, part human,
or are we still human being? And if you're still human being, are we still abiding to the natural law?
Which is in every single religion, always there, this is we have to be asked.
So, ethical principle, to must be done, in all the biological, in it.
So there's the other to
to be able to be able to be it.
Now, if you're non-linear and linearity is that,
it's like non-linear.
Explosy from the elmoboanetawan,
because it's more than
more,
the dominion effect.
With domino that we can trigger
domino that's great to curing.
Demigian,
even if we're not
even to change our own
we're on status quo
with linearity and we're
we're very happy and
we're not able to make sure as a
country.
How can't we can make up to make up to
linear, we're making linear.
In order to change, we have to change,
if we have to change.
The other generation of the next
the next yearnation and the other than
the other is more
more than more than
competition with other,
who's more competition more.
Because of that, that's not-linear,
and that's what we need to be able
to put people who are willing to build a putusans,
and all of all of things that have been puttaparte in
any or in any, anywhere even if we're doing,
we're not going to be able to beaute as a country
Indonesia, apalady in 2004-linger 100-11-11-11
of the unlawful government.
Platform this, is, is it's just a matter of what?
not just to educations
but also provocation
provocation percabotation.
Because I'm not sure that
this has been more
being done by
the whole component
or element of the community
and the way of the same.
And penikaping that
is puttuked to the purpose
that we've talked to beacarcan.
This, if I think I,
have inclusive.
have not only only about
not only about
but about
people from bureaucracy
and got from
community
spiritual, community
cultural, community
cultural and
all the
unnered
the panatown
to
kreemned
so not to
pleset,
but but
the first and foremost
is we have
to have to be more than
actuality this is
really and it's not yet
in the negatian
in the country that's
much more than
we're more than we're
not just
but we're discursus
on topics like this
topic,
topic like this.
There,
there,
there,
some of
Pesan from
about,
about what,
Pekirona,
about monoclonal antibody therapy,
or umay, or, um, or, what's what,
that's, that's, that, that,
that, that, that,
with the importance of our,
we, that's in our course,
in our course, in the in the
COVID-19,
It's even when we have a
that virus that will live with us with us all over.
And for that, we're aty-haty.
And as a patient, and as a person,
we, we know when we,
we'll get a virus if we're going to get a virus
if we're doing, if we're going to dock,
but if it's been able,
this is PPPM,
we're going to be able,
we're going to be able to bea-brient,
variants, that's made vigilant.
It's always remain vigilant.
I mean, we must be careful,
with that we need to be able to be able to
other, to be able to more,
more than more than more than more than more,
because let's face it,
it, it's a behavioral disease.
Although it's the thingal act that we're
the thing that we need to make,
it's the more that's more
even giless.
With the other,
opat opat of the new,
like monotomyth, Rekyrona,
it's very much more than help help in hospitalities
and even the number of people who have risk of big.
That's number one.
Number two, we're in Indonesia also
in many of different universities.
And Omahe, this is really,
has to be paid.
If we're going to move on to now,
investations and research that's already
to be out of the OMA that's before it,
have to get up,
and get up to get reinvestation in research
the next.
And, it's not even to the other,
Indonesia, too,
monoconal antibody from Convalesan spasma in
time for the time to come back.
But, come back again,
the more than,
to make-gunnaker product in the
country, it's really,
because this is the result
of the collective mind
from the scientists that are in Indonesia.
If we don't make
our mainstream,
because we usually
use the import-import,
now when the country is going to
make up to be
we can't even in the country
and for that product in the country
it's like it's used to be used
because it's been doing
research,
it's just more
more than,
it's more than
it, it's more
so it's a lot
in this is
what name,
futile cycle in a way.
the power of the world, it's very much.
That's about it.
Wow.
Wow.
Wow.
Thank you, thank you.
Thank you.
Thank you, thank you, thank you, Pat, sir.
It's been,
had been,
ha, ha,
you know.
That's,
Professor Raymond Chandra Winata,
Ilmuan, or Molecular Pharmacologist,
from Dexagosur.
Thank you.
Endgame is a podcast by the School of Government and Public Policy
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