Episode Transcript
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0:05
Welcome to startuprad.io your podcast and youtube blog covering the german startup
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scene with news interviews and live events.
0:13
Music.
0:19
Hello and welcome everybody this is joe from startuprad.io your startup podcast
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and youtube blog from Germany. Today, I bring you another interesting interview.
0:31
Imagine starting your career under the supervision of a Nobel laureate,
0:35
diving deep into groundbreaking research and then making the bold leap into
0:39
entrepreneurship, only to build a company that will become a global biotech powerhouse.
0:45
Today, we're talking to Professor Detlef Reisner, a scientist turned entrepreneur
0:49
who started his academic journey at Heinrich Heine University and Technical University Darmstadt,
0:56
spent time at Princeton's Institute for Advanced Studies, and then took an even
1:00
bigger leap, trying to turn cutting-edge science into a business.
1:05
But it wasn't easy. Imagine hurdles of launching a biotech startup in Germany
1:09
in the 1980s, before venture capital was even a thing there,
1:13
against all odds, co-founding Kia Gehen, which became the first ever German
1:18
company to list on Nasdaq in 1996.
1:21
And as if that wasn't enough, he later led the company as chair of the supervisory
1:26
board, bringing into DAX 40 Germany's elite stock index.
1:32
What does it take to bridge science and business, to push through failures and
1:36
to build a global biotech leader? That's what we'll find out today. Stay tuned.
1:42
Professor Riesner, welcome to StartupRaid.io.
1:46
Thank you. I'm happy to answer your questions.
1:52
Yes, and I do have a lot here for you.
1:55
At first, would you consider yourself to be an example other entrepreneurs could
2:06
follow in what you've learned? To a particular extent, yes.
2:15
If I speak to younger people, then I say the main point is that you have a good idea.
2:25
You have not to do the market to estimate the market situation.
2:33
If you can estimate the market situation then your idea is not innovative,
2:39
when your idea is innovative then there is no market you have to build a new
2:44
market that is an innovation that is the first point whether I have seen that
2:50
at that time I don't know I do not remember but that is from the retrospective what I would say,
2:58
and so today I would say yeah, it's important you have a good idea.
3:04
People will sometimes use it.
3:08
Mostly if you are working in academia, other academicians will use it.
3:14
And that is already okay. If other academicians will use it to the normal market, it goes later anyway.
3:23
Therefore, that's the point. And the second is, yeah, If you have an academic
3:30
position, you have to agree that it is a lot of additional work.
3:38
And as a professor alone, you cannot do that. That is clear.
3:44
So you have either to good students or to good co-operators or to very good
3:52
colleagues so that you can work in a team.
3:57
From the beginning on, we worked always in a team.
4:03
And I fulfilled also in future always my academic position,
4:09
but I was, so to speak, the link to the science, which I could always then bring to the company,
4:20
and, but the link to the science, where as the younger people had to do the
4:25
link to the market, to build on the link to the market, that was not my job.
4:30
And so, what you need is a lot of endurance.
4:36
And what I see and those things sometimes I saw that later,
4:42
you have to have the capability, the mental capability, particularly the capability
4:50
of your mindset, of your character,
4:53
that you can divide success.
4:56
Some people I met, they said, oh, the main point is that I have more than 50%, so I can say what to do.
5:04
Nonsense. Bullshit, I would say.
5:08
What to do is always the opinion of the people who give the money,
5:16
and whether you have over 50 or less than 50, doesn't matter anyway.
5:22
The people who give the money they have an extremely important
5:27
word for the company and we had
5:30
to see that too yeah so that's the point i think and then if you have in the
5:37
next seeding round you have to give up shares it's completely clear but i remember
5:45
the word of mosher alafi who was one of our investors.
5:50
Moshe Alaafi was a very successful Silicon Valley investor and he told us.
5:58
He said as boys, he normally called us boys, if you have 50% of a company which doesn't work well,
6:09
all you have are sleepless nights.
6:14
If you have 2% of a well-running company,
6:19
you are rich people that is the difference between 50 and two percent okay so
6:24
that is probably the first what i have to say i don't know it did answer your question,
6:31
to some extent at least yes and we may also add that is still today you are
6:38
pretty active and involved i i've seen you at the larger business angel talk
6:43
in november in minds we didn't get the opportunity to talk there,
6:47
but they've been kind enough to help me organize this interview here.
6:52
Big thank to the organization team there. Could you share the key experiences during your time at Princeton and University
7:01
of California, San Francisco that influenced the trajectory of your research?
7:10
Yes, in Princeton, I worked mainly on nucleic acids and nucleic acid protein interactions.
7:19
And that was important for the research when I was back.
7:23
But when I have to say in Princeton, I was a postdoc and I were interested in my academic career.
7:31
I wrote already a patent, but this patent never brought any money,
7:36
so it was too theoretical.
7:40
So the Princeton experience was a very good personal experience and scientific experience.
7:48
The impact to the company was probably not so big.
7:54
And the UCSF experience, that was at the time when I had to say,
8:00
oh, I set up a company, I was involved in setting up the company as a professor.
8:05
I have to start now new things, yeah.
8:08
The company is running, but as a professor, I have to start new things,
8:13
new scientific things, yeah. And that was the reason why I went to Stanley Prusiner for postdocs before I
8:20
worked on infectious nucleic acids.
8:23
And then I heard, I had a lot of contact with Stanley Prusiner,
8:27
he said, there are infectious proteins.
8:29
Oh, I said, how interesting. Let me go into that field now.
8:34
The nucleic acids are well taken by the company already.
8:40
So the company was already working when I had my sabbatical in San Francisco. I see.
8:49
Your work on virals and prions has been pioneering.
8:55
What initially drew you to study these infectious agents and what were some
9:01
of the challenges you faced in this research.
9:04
Yeah, this question comes to the point of the company, yeah.
9:11
Viroids were infectious nucleic acids.
9:15
And I heard from a German colleague there that those things exist.
9:20
A lot of people thought it doesn't exist at all, yeah.
9:24
A small nucleic acid cannot be worked like a complete virus.
9:28
But viroids, which is probably 1% in the size,
9:34
1% of a complete virus, and viruses were thought to be the smallest infectious entities,
9:45
but viroids, only a nucleic acid, 350 nucleotides, has the same phenomenology.
9:52
That means it's infectious and it's pathological.
9:57
And I said oh that is extremely interesting for a physical researcher like me
10:03
I have now a molecule in hand which I can handle and I can study it is simple enough,
10:11
to study with physical methods if the biological system is too big at that time
10:21
it was in the 70s you could not really study
10:24
with physical methods,
10:27
you could study with X-ray proteins.
10:32
But these steroids were a complete biological system. That was so interesting. And then we said, but…,
10:40
First, we had a few micrograms from the viroid and that is very cumbersome to work with that.
10:48
And we thought, okay, we have to purify. We have to develop methods to purify
10:55
the viroids for our research.
10:58
And then I had a very good student who was a chemist who said,
11:02
okay, I will do that in my PhD work that was made in Kolpan.
11:06
I developed a chromatographer. So, we discussed a lot how this chromatography
11:12
should be, and then, one or two years later.
11:18
He could present really a chromatographic column which purified virals,
11:28
and now we had probably suddenly milligrams of virals in our hands.
11:34
And I reported that on conferences and the people said, oh, how nice,
11:40
but who is interested in viroids?
11:42
This is such an esoteric effect.
11:45
We don't know whether it even exists. Yeah.
11:48
But for example, what people are interested, can you purify plasmids?
11:55
That would be interesting. And we put plasmids on the column and it came out pure.
12:01
Pure. and that was the reason why we started to work on plasmids.
12:06
And then really I think that was about the time when we started about the company,
12:12
what we could do with the company, purification of nucleic acid and diagnosis of nucleic acid.
12:18
For example, at that time, PCR was not developed, so one had all these hybridization
12:25
methods to find mutations and those things.
12:28
But then we heard back, yeah, if you have an infectious agent and plasmid is
12:34
in particular cases also an infectious agent, but only in a particular sense.
12:39
And you put one plasmid on a column and then the next plasmid,
12:43
the columns have a memory effect.
12:47
And therefore, we said, OK, the column is not the right instrument.
12:54
We have to use small kits, use it once and throw it away. And then you have
12:59
no cross-contamination. And that was really the main invention of Chiagen.
13:07
At that point, Diagen first and then Chiagen, that's not interesting right now.
13:12
When Chiagen could sell a kit for a plasmid and the user takes the kit.
13:20
He purifies his plasmid, and next day another one, or next hour another one,
13:27
and there never cause contamination because he uses everything in U-column.
13:31
And that was when Kyagen started to sell worldwide the kits.
13:40
And I was still involved in the company and we discussed a lot,
13:45
but at that time I was already
13:48
looking for the infectious protein which
13:52
is a new phenomenon yeah so
13:55
now you have a little bit the idea how i came to the purification to the kids
14:02
together with my co-operators i i never was alone the company colpania and carsten
14:09
hank and jĂĽrgen schumacher we were together four of us.
14:17
We had several ideas, but the idea of the plasmid kit, use it once and throw it away.
14:26
That is a good idea for microbiology.
14:29
And suddenly, and then I have to say, medical doctors could suddenly work in
14:35
molecular biology because they could purify their plasmids before you have to
14:41
use plasmids to do microbiology.
14:45
And before, purify the plasmid took nearly two days.
14:52
And the medical doctor has no time, he has patients.
14:55
And he does science in the evening with students.
14:59
And therefore, with plasmid purification, there was no time left for that.
15:04
And suddenly we gave him the tool at hand, so now you can work with plasmids. It fits your time scale.
15:11
And then I think to describe the success of Chiragin is Chiragin brought the
15:19
molecular biology to medicine. Before it was only in specialized laboratories, but then it could be done worldwide.
15:27
We'll definitely get into the
15:29
key again story but before that i have one more
15:32
question because you have been the share of biophysics
15:35
at heinrich heine university in dĂĽsseldorf from 1980 to 2007 that's 27 years
15:42
that's quite a long time and an achievement but how could you just basically
15:47
balance the the responsibilities you had from all the positions your research
15:53
key again and so on and so forth. Did you develop special methodologies? At first, it was an outcome of our university research.
16:03
So we did not research on the sideline. It was our main research.
16:12
Viroids and to purify viroids. So nothing to do next to it, or we didn't, other things.
16:19
And suddenly, and when this worked, Then we went out into the company,
16:25
and then I could say, okay, I have all my lectures, everything in my institute,
16:33
but this part is now taken over by the company.
16:37
We had a lot of discussions, but we had it well separated.
16:42
So the economic part was well separated from the university part.
16:47
And I kept this up to the day of my retirement.
16:54
In my head, of course, it was always combined.
16:58
But the money and what was spent and the co-workers and so on,
17:05
they were working either there or there. And if there was a combination, then it was declared and everything went fine, yeah.
17:13
And you have to say in Germany, when we started the company,
17:18
we had no Arbeitnehmer-Erfinder-Gesetz. Yes.
17:21
Yeah. And that was very good. I told my chancellor, you see,
17:27
I have to, I will set up a company next, is there any problem?
17:33
He said, a company, you can do that on Saturday, and professor,
17:37
you have from Monday to Friday. So I don't see any problem.
17:41
And as long as you don't want to have money from me, anything is fine.
17:46
But today, the universities would like to have a lot of money when you said
17:51
have a company that is an enormous hurdle for small startups, I have to say.
17:57
I'm working on that, that this situation has to improve.
18:04
That's the law you're referring to is basically a law that regulates if one
18:10
of your employees develops an invention during work, how do you process with it?
18:15
What's the legal process to assign all the benefits.
18:21
Before we get, and by the way,
18:23
what you've been talking about, like having certain times for your research,
18:29
for your institute, and certain times for your entrepreneurial work,
18:32
I think that is a technique called today time boxing.
18:36
You have certain times allocated to special duties, and you use them to the best of your abilities.
18:42
Before we dive into the KIAGEN story,
18:46
I'd love to hear from our audience if you could ask a biotech pioneer like Professor
18:55
Riesner one question. What would it be?
18:58
Drop your thoughts down here in the comments.
19:02
In 1984, you co-founded KIAGEN with the doctoral students.
19:07
What motivated you to the transitions from academia to entrepreneurship and
19:13
how did your academic background influence the company's direction?
19:17
I mean, we already know it is a application of your research,
19:23
but I do believe you applied a few more things from your academic background
19:28
into the company, right? Okay, I have to say that is a little bit in my personal mindset.
19:34
I never, I studied physics, atomic physics and biophysics, yeah?
19:40
And then later on in my PhD work, I went more to biophysics or to pure biophysics.
19:47
But I had always in mind, oh.
19:51
Academic career is only one possibility for me.
19:54
I can work with a company and anything else.
19:58
I would always like to work scientifically, not only to sell things.
20:04
This is only a good profession to sell things. But I think I have to work in science, in research.
20:11
But whether I will do that my life in academia or in a company, I was not fixed.
20:20
That means I worked already on a patent before KayaGen, this patent was not
20:28
very successful, that doesn't matter, but therefore I had always a look into that direction.
20:35
And then there were these three students coming with me from Darmstadt Institute of Technology.
20:43
We went together to Dusseldorf, and we discussed a lot, what could we do?
20:48
And these younger people, they were, of course, not fixed to academia.
20:52
I was at that time already a little bit more fixed to academia,
20:56
but we discussed what can we do else? And where is our research good for? And so these ideas were generated.
21:08
And there were no particular time boxes or so.
21:13
You cannot box your brain into different sections.
21:19
But you have to control that the obligations to the university have to be fulfilled, 100%.
21:29
And I never skipped a lecture for a discussion with the company, also not later, never.
21:37
The company had to take care of my time box, not the other way around,
21:42
which always worked pretty well, I have to say.
21:46
And okay, what was next?
21:50
Yeah, how I could separate that pretty well, yeah.
21:54
And I think this came from the beginning, I say, for the company,
22:00
I'm advisor, but I never went to the management.
22:03
And that was the main point. My three students, they established the management.
22:12
I was on the advisory board, advisory job, yeah. And therefore,
22:18
we had a clear separation. And I would tell all the younger people, do this separation as soon as you can do it.
22:31
Otherwise, you have only trouble.
22:35
And therefore, I never had trouble with the university because everything was fulfilled.
22:42
And the other point is, there were not only the three students.
22:48
As a university professor if you like to do research you never can do it alone
22:54
you can do it only with the best of the students,
22:58
and therefore I had to give very good lectures I feel maybe I'm a little bit
23:05
superstitious but I think I gave good lectures to attract good students and
23:11
then you can do good research at the university if you say I do research
23:16
and lectures are a little bit, take a lot, too much time,
23:20
wrong, completely wrong, yeah? The other way around. Good lectures bring you the best students and with them
23:26
you can do good research.
23:30
And this went through my whole 26 years on the University of DĂĽsseldorf, yeah?
23:36
It started in Darmstadt, it started in Darmstadt, I have to say.
23:40
And for everybody who doesn't have an academic biotech background,
23:46
I'll link a lot of Wikipedia articles, prions, plasmid, virons, and so on and so forth.
23:53
Of course, TU Darmstadt as well as the Heinrich Heine University,
23:57
of course, so everybody can learn a little bit more there.
24:01
We already talked about Kiagen.
24:03
There was like a different name in the beginning. That's why you're talking
24:07
about Kiagen and Kiagen. But the entity, that was a spin-off, one of the first biotech spin-offs from a German university.
24:17
As you said, there was not the law that regulates what happens if one of your
24:23
employees invent something. But I'm sure you also encountered different hurdles.
24:30
Plus, there was a very interesting story you have in your book.
24:34
By the way, you wrote a book about your experiences. unfortunately it's already sold out but I do have,
24:41
one physical example here from you thank you very much for that for people who
24:46
are really interested in the book I have a lot of issues at home if they write to me I send them an issue.
24:56
Ok and my question would be what hurdles did you face there because I remember
25:02
from the book you came to Dusseldorf they said ok what are you going to bring
25:05
to us And then you said, OK, we do already have an idea for a company.
25:10
And I do remember that the Sparkasse, the thrift organization of DĂĽsseldorf,
25:16
was quite helpful there. Can you talk about a few other hurdles and, of course, the story of DĂĽsseldorf?
25:22
Because when I remember this correctly, there was a great investment for the local organization.
25:27
Yeah, they were not alone. First, we had another, the owner of another company who was interested in the technology.
25:36
Later on, we had a lot of problems with him.
25:39
And the Sparkasse, there was a particular opinion in the Sparkasse.
25:47
What can we do with the university together to improve the economy in DĂĽsseldorf?
25:54
And there we had a discussion. And the discussion was in that way, it's okay, we have to talk,
26:04
but not much will come out.
26:07
And then suddenly I said to the president of the Sparkasse, yeah,
26:13
we have the plans for a company in the desk.
26:18
And he said, what do you need? We said, 10 million. And he said, right away, I work on that to get the money.
26:26
That we will get the money. So that was in a minute, this decision.
26:31
And that, okay, if we have that support, then we can start.
26:35
And then with the Sparkasse, when you have such an inventor,
26:40
investor, he did not give 10 millions.
26:43
Over the time, he gave 6 millions over the time.
26:47
But he got back 240 millions later, to tell you the relationship.
26:54
But then there was another venture capitalist,
27:00
TVN in Munich, they got involved and I think then the government,
27:10
the North Rhein-Westphalian government said, okay,
27:13
we can support that. Let's see what's coming out.
27:17
It's new that we support the start-up from the university. And then by recommendation
27:26
of Charles Weisman from ZĂĽrich, there was Moshe Alafi got interested.
27:31
In California, he had, for example, started Applied Biosystems,
27:37
a very successful company.
27:40
And we met with him and we told him what we are doing and so on.
27:45
And he took a sheet of paper and wrote down one million investment.
27:51
So this was really decisions on the point, I have to say. Yeah.
27:59
And he and Moshalafi, I have to say, he looked to the young people in the company,
28:07
not to me, to the young people. What do they do? Is there fire in these people?
28:14
And he had the right judgment and therefore he gave the money.
28:18
And so these hurdles were so then we had the money to start.
28:22
And then the problem was a laboratory.
28:26
I have to say in there is always an intermediate time where the laboratory is
28:33
still in the university, but as soon as possible out of the university.
28:38
Have your own laboratories, yeah. Then it's a clear cut.
28:42
And this took some time. And later on there was a company, Henkel in DĂĽsseldorf, who had.
28:54
A level in a building with empty laboratories, which we could rebuild for our work, yeah.
29:02
And so we started there, and later on, of course, it was too small,
29:05
and we had to build our own, and so on, and so on, yeah.
29:09
But these were the hurdles a little bit. The money first, one has to have good
29:14
connections to get the money, yeah. And then the laboratory space So what was no hurdle, what was our starting capital,
29:27
so the idea and the people and the mood of the people, yeah.
29:31
That was our capital and the money and the laboratory space we had to acquire, to say that.
29:41
As we said, with KIA again, the kickoff, as you already mentioned,
29:46
was a two-part single-use plastic system for nucleate acid extraction.
29:52
That was a game changer, obviously. You already talked about the innovation process behind this product,
30:01
and you said normal doctors became part or could do biological research with that.
30:08
I also remember that you have been hired in terms of the woods in Germany,
30:16
Dyeing, Waldstäben, to also do some research there where you apply to your research.
30:23
Yeah, the Waldsterben, that was the funny thing, I have to say,
30:29
even people thought, oh, in two years there is no single tree in Germany.
30:33
If you listen to the press, yeah, then there was meaning in two years there
30:39
is no single tree in Germany. We never thought that it was so serious, but we developed tests and we used
30:46
again our methodological and our knowledge on RNA aid technology.
30:53
And then we developed those tests and we published it.
30:58
And of course, it was interesting even for investors, but this was not really part of the business.
31:06
It was besides the business.
31:09
It was good for our technology training, I have to say.
31:13
And for example, it was very good at that time, one could get good grants for Waldsterben.
31:25
And that was good for my laboratory, I could buy new instruments,
31:29
and these instruments were of course used for other experiments,
31:36
not only for Waldsterben. Yeah. And therefore, and you know, Waldsterben in Germany stopped at a particular date.
31:45
And on one day, Waldsterben stopped. Do you know that?
31:49
No no but but i vividly remember when i was a small kid i remembered coverage
31:54
everywhere in the press in the news bald stem the woods are dying in germany due to um um,
32:03
and then there probably came the catastrophe of the atomic mile in chernobyl
32:10
and on the day of the press moved to Chernobyl and Waldsterben was forgotten it was,
32:20
funny I say that was the end of the Waldsterben in Germany,
32:25
the catastrophe of Chernobyl but naja so we have not to discuss further Waldsterben
32:33
Waldsterben was an episode it was a scientific interesting episode when I later
32:39
met somebody from the minister who gave us money.
32:44
And I asked him what is the outcome of the
32:47
Waldsterben and he said there is a lot of outcome because
32:51
the Waldsterben gave the money and
32:54
now we have forest science before we
32:58
had in universities only forest economy and since the time of Waldsterben we
33:03
have a forest science in good universities so I did not look at that because
33:09
we did not believe then forest science But that was an outcome which one should not estimate too small,
33:17
that we have in Germany now a good forest science. Yeah.
33:21
Okay. So far to Waldstern.
33:26
Jumping forward a few years in 1996, you were the first company to be listed on Nasdaq.
33:33
As we've already discussed, you were co-founder, you were advisor.
33:37
Have you been at this time on the supervisory board of Kia Gin?
33:42
Yeah, but I was not the chairman of the supervisory board.
33:47
The chairman was at that time a very well-known banker, Carsten Peter Clausen.
33:57
And he was with the beginning. He helped us a lot with financial difficulty
34:04
situation, yeah, situations. And then we were happy.
34:08
He really guided the tour to the NASDAQ.
34:12
Together with Goldman Sachs.
34:23
Anyway I think the best underwriter you could get at that time.
34:28
And later on, when Professor Clausen reached his age of 72,
34:36
he had to leave the board and i
34:39
followed him as a chairman yeah i would
34:43
be interested you've been there the first company
34:46
before we get to that
34:49
how because i do understand there
34:53
are two people that helped you to get listed on nasdaq but i was i was wondering
34:59
what went through your mind when you met at the company and at the first time
35:03
somebody said oh guys uh you're here in germany but let's go over to new york
35:07
city and list your nasdaq what were your first thought about that,
35:11
now yeah we had a good people who were good consultants yeah the and our our investors,
35:21
they knew how to do those things and nasdaq they said the nasdaq is america
35:27
and there's the most money which they will buy shares and the share price can then increase.
35:34
In Germany, we had only the normal Börse, but we were too small to go to the
35:43
German Börse and the small Börse came later in Germany.
35:50
And therefore, we had to set over the company of KayaGen in holding,
35:59
in Namen Lose Vernotschap, that was a Dutch holding of the company,
36:06
and we went to the Nasdaq with the Namen Lose Vernotschap.
36:13
And they knew how to work with Nasdaq. In German, the German companies,
36:17
they could not go to Nasdaq at that time, yeah?
36:21
Whether there were fiscal improvements, that was not my business in the company, yeah?
36:29
But we knew with the Namenloser Vernotchapp and with it being public,
36:36
we could collect more money.
36:39
That is, yeah. And we could grow in Hilden,
36:44
near DĂĽsseldorf, because we had no money, more money, and then we started the
36:50
whole diagnostic part of the company.
36:55
Before, we were really the purification company, and then we had the purification
37:00
technology and the nucleic ethic diagnostic part.
37:05
And that was only with the money of the IPO.
37:10
I see. And the Namlose Vermotrapp is basically the key again N.V.
37:17
Many people would have come by a Dutch company called N.V.
37:21
Also there that is just a legal form.
37:24
So basically you moved your entity to the Netherlands and there you could so
37:28
you could list on Nasdaq. Yeah, but entity, the whole thing, that means in later time,
37:37
we were 50 people in the Netherlands, but 1,500 in DĂĽsseldorf, yeah.
37:43
That is the ratio about. I see.
37:48
Have you any story about being the first company to be listed on Nasdaq?
37:54
How were you perceived in Germany and in the US?
37:58
I could imagine in the US it was no news. But how did people react here in Germany about your listing?
38:05
Oh, this is hard to remember how they react.
38:09
You see, during the first years when we had the company, my colleagues were
38:14
always friendly, I have to say that. Sometimes they were friendly to me, but in the backyard of their brain,
38:22
they thought that it will not take long and he will come down again.
38:28
But they never said to me. They were only friendly to me. And then,
38:38
of course, there was really, I have to say, then probably there was admiration.
38:44
When we said we could develop the company, now we are on IPO and the company
38:51
is very close to several hundred million value.
38:57
Yeah, then there was a say, then a lot of people said, okay,
39:02
that is really a success. And some colleagues told me, you know, for molecular biology,
39:08
I know much more than you, Detlef Riesner, but you did it. And I was afraid to do it.
39:15
So there was this open admiration. They said, you did it. And therefore you were successful.
39:24
And then after IPO, the stock went up and then went down and went up and down. That is normal.
39:32
And then the biotechnology bubble was bursting in the beginning of 2000.
39:41
But the company, of course, the company went on and they earned money already.
39:48
These are two independent things. The revenues of the company and the value as a stock market.
39:55
Sometimes they are completely decoupled.
39:59
Thanks, Scott. They are decoupled. And Kia again went on and,
40:04
of course, recovered from the low stock price.
40:06
Hey, guys. This is Joe from startup.io. At the time when I'm reviewing my interview
40:11
with Professor Reisner, I have noticed that's almost 1 hour and 20 minutes since we try to keep our
40:19
content to a certain length. This is now the point where we'll cut this a little bit and go into episode
40:27
number two published tomorrow. That's all, folks. Find more news, streams, events, and interviews at www.startuprad.io.
40:43
Remember, sharing is caring.
40:46
Music.
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