Episode Transcript
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The business of biotech is produced by
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LifeScienceConnect and its community
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. We're LifeScienceConnect and we're
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here to help . I'm
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Matt Pillar . This is the business of biotech
0:42
, and my guest today is a repeater
0:44
. He last joined us in late 2021
0:47
, way back on episode 73
0:49
of the podcast , but he's welcome back
0:52
anytime because he's among the most thoughtful
0:54
biotech conversationalists I've had
0:56
the pleasure of sitting down with . Brian
0:58
. Finrow is a lawyer by training
1:01
and if that doesn't make him an outsider by default
1:03
, the work his company is doing surely
1:05
does . Finrow is founder
1:07
of Lumen Biosciences , a
1:09
company that's working in earnest to
1:12
democratize or improve the cost
1:14
and accessibility of biologics by
1:16
developing therapeutic molecules from
1:19
spirulina . That's a great
1:21
start , but even Finrow will admit that the safety
1:23
, replicability and availability
1:26
advantages of spirulina address
1:28
just a fraction of the democratization
1:30
effort . The bigger challenges
1:32
the cost of clinical and commercial activities
1:35
are much harder to solve , but
1:37
that didn't stop Finrow and I from addressing
1:39
them when we met in San Francisco to record
1:42
this episode . Let's give it a listen . Brian
1:44
Finrow , join me . I believe it was
1:46
episode 73 , which was a long
1:49
, long time ago . It was like , I
1:51
think , close to the end of 2021,
1:53
. It was my first exposure to Lumen Biosciences
1:56
, the company that you founded and served as CEO
1:58
. So
2:00
I don't know . Two plus years
2:02
have gone by , two and a half years . I
2:04
thought we'd start maybe just with an update . Long
2:07
time listeners may remember that episode . It was an
2:09
interesting conversation , but
2:11
maybe you could
2:13
probably go long on this right In
2:16
that in the ensuing two
2:18
and a half , close to three years
2:20
, give us an update on some recent progress
2:22
in Lumen .
2:24
Yeah , happy to just broght briefly More
2:27
of the same . Basically , if anybody
2:29
happens to remember that prior conversation
2:32
, Well , it's out there .
2:33
If you don't go , listen to that one first and then come back
2:35
. There we go yeah it's a prequel so
2:38
more of the same from us .
2:40
We've been in no great surprises
2:42
. It's all continued to work just like we expected
2:44
and if anything
2:46
, I'd say where we've learned
2:49
is that the breadth of application
2:51
for the platform is
2:53
larger , if anything , than what we were really
2:56
conceptualizing two and a half years ago . The
2:59
big dramatic thing of course that happened in the interim was
3:01
the COVID-19 pandemic came and
3:03
went and that was
3:06
important for us , particularly
3:08
because we do a lot of work funded by
3:10
the US federal government , the NIH
3:12
, the Department of Defense , barda
3:14
, and so a lot of
3:17
that pandemic defense work has been
3:19
happening at Lumen , as it has with a lot of companies
3:21
, and so that was really important , building out a lot of our infrastructure
3:24
. We built a much larger GMP manufacturing
3:26
facility , completed a couple more clinical
3:28
trials . We've got a bunch more trials teed up for this
3:30
year , added a couple of commercial programs and
3:32
several other clinic
3:35
bound but not yet in the clinic Charitable
3:37
I'm calling them charitable programs as
3:40
well . So just more growth , but more
3:42
all along the same lines of what we discussed
3:44
two and a half years ago .
3:45
Yeah , it's interesting , isn't it , how COVID
3:47
affected the business climate
3:49
in a positive way . In some cases . For
3:52
you it was more
3:54
federal engagement , probably more resources
3:56
along those lines , non-traditional support
3:58
For our business . People
4:01
weren't traveling , people weren't coming to conferences like this
4:03
. They just weren't happening . You couldn't . So podcasts
4:06
and live digital events really boosted
4:08
our business Now full transparency
4:11
. We felt that taper off a bit
4:13
, as we recovered , as the world has
4:15
gotten back to normal . Are you feeling any of the same
4:17
? Do you feel like that momentum that , perhaps
4:20
ironically , covid helped build
4:23
in biotech not just aluminum
4:25
, but biotech in general has
4:28
faded ?
4:28
Some of it has . Yeah , for sure . I mean it can discreet areas
4:31
, but there's been some real improvements , I think , to the way
4:33
the world works , something
4:35
that hasn't stuck around as well
4:38
. Basically , just to be honest , blunt about it
4:40
nobody cares about COVID anymore or pandemic
4:42
defense . It's like all these lessons we thought we
4:44
were going to learn once and for all . Yeah , we're
4:46
well within six feet , right now , that's
4:48
right , but
4:51
not just on the financial side
4:53
, of course . If you see , you're very excited about COVID-19
4:55
things for about a hot minute , but
4:58
even we see this with our federal
5:00
partners there's just a lot more challenging to
5:02
get that research funded Again
5:05
. I mean it's still happening . A lot of artists are doing a lot of work . Right
5:07
now , for example , dod continues to be very
5:09
interested for their own reasons
5:11
.
5:11
So yeah , I mean some of that came and went
5:13
, but I think there are some completely permanent
5:15
changes that have happened .
5:16
I'll just give you two examples that are relevant
5:19
to my life . Number one very
5:22
usually people used to go public and the
5:24
way you would public is you would charter a jet and you'd fly
5:26
around and do a roadshow . I don't think anybody does that
5:28
anymore .
5:29
I'll zoom .
5:29
Everybody just sit on , zoom in like 48 hours
5:31
and you're done . It's a much better way to
5:34
go . They're flying flocks of bankers
5:36
and accountants from city to city
5:38
on private jets , so I think that's here
5:40
to stay . It was forced on the industry and
5:42
I think it's a better world now without it
5:44
. The other thing that's even more directly relevant
5:47
to our work is there
5:49
was a big cultural bias against distributed
5:52
clinical trials before COVID , and
5:54
it was strange because it wasn't
5:57
like Zoom existed before COVID
5:59
. I mean , docusign didn't exist before COVID
6:01
, but it's a cultural bias against
6:03
it that people would say , well , yes
6:05
, no , of course you can use DocuSign to buy
6:07
a house , but for something important like
6:09
a consent form for a clinical trial , that
6:13
would be unethical . And then COVID happened and all of a a sudden it
6:15
became ether . A
6:17
lot of things that were technically feasible for a
6:19
long time but culturally impossible became
6:21
commonplace and I think that there's
6:24
some real potential for
6:26
product TV in our industry coming out of things
6:28
like that . Just one example . I think there's a lot of them like that
6:30
.
6:30
Yeah , looking
6:32
back on the progress that
6:35
you've made in the past two to three years
6:37
, I mean , obviously it's been a very challenging time for a
6:39
lot of biotechs . The
6:41
capital markets have been down , all
6:43
the index indices are down . What's
6:47
your reflection on that ? Like I know
6:49
, that's a big conversation , but can you point
6:51
to anything post COVID
6:54
that has maybe been
6:56
a barrier
6:58
to the pace of progress at
7:00
Lumen ? Anything in particular
7:03
? I mean , I know there are a number of things you could probably point to
7:05
.
7:06
Well , it's always raining somewhere
7:08
. During COVID
7:11
there was plenty
7:13
of money , but there's no supply . I mean
7:15
even crazy things like pipette tips . Remember
7:17
the pipette tips crisis ? It
7:19
just happened us too . Nobody could get pipette tips
7:21
of all the things in the world , but
7:23
it was everything Lab space big
7:25
companies that used CDMOs couldn't find
7:28
a CDMO space . They're about a year
7:30
or years out in the future . Cros
7:32
were overmaxxed because of all the
7:34
COVID trials and all the disruption and everything . So
7:37
pretty much every input into the drug development
7:40
process was hard to get your hands
7:42
on , except for money . There was plenty of money around . So
7:46
the economy did its thing right . So prices rise , drawing
7:48
new supply , and then
7:50
there was this look
7:53
, sort of low interest rate phenomenon happened . At
7:55
the same time . A glut of supply
7:57
came on the market and then now we
7:59
have the opposite right there's no money . I
8:02
mean , the Federal Reserve Bank took away all the money and
8:05
there's plenty of supply . It's
8:07
like lab equipment , lab space . Cros
8:10
are returning phone calls and everything , so everything's easy to
8:13
hold up . So there's
8:15
always headwinds , I guess , is the short
8:17
answer .
8:18
Yeah , cros and
8:21
CDMOs . Cmos like that's
8:23
an interesting , that's gonna be an interesting space
8:25
to watch . I think I'm interested in your perspective
8:27
on that . Like during and immediately
8:30
post COVID , I don't think a day
8:32
went by where hundreds
8:34
of thousands , if not millions , of new
8:36
manufacturing space
8:38
were being constructed Right
8:40
like I got probably says every single
8:42
day , just a giant , giant
8:45
thing . But in at
8:47
the same time , the biotechs
8:49
that I spent time with still
8:51
complained about the fact that they were
8:54
backburner and it was hard to get
8:56
time and space with those outsourcing
8:58
partners . Is that a
9:00
bubble ? Is that a bubble that's like gonna
9:02
come back and bite all the outsource
9:04
manufacturing capacity that was
9:07
built ?
9:08
I don't know man , Economists are very fond of
9:10
pointing out that
9:12
nobody knows how to call bubbles . Every time it seems
9:15
like there's a bubble , now sometimes there is some
9:17
dangerous , I don't know . But I would say from our approach , we
9:21
don't participate in a lot of these , we don't use CDMOs
9:23
, for example , so it's all kind of indirect . But it does seem
9:26
like it has a lot of characteristics of
9:28
real estate , which is famously bubble prone
9:31
. Because , why ? Because why they're very
9:33
capital intensive projects . Build , at say , a new office building
9:35
or a new apartment building . It
9:38
takes years , particularly because of the permitting , and
9:40
then you end up with this
9:42
sort of high cost capital
9:45
asset and it comes online just at the time
9:47
. All the other ones come online when
9:50
there's eventually an economic downturn . So
9:54
CDMO capacity , cro capacity , they
9:57
seem like kind of lab space capacity . Very , very direct analogy
9:59
. They seem to kind of have
10:01
some characteristics of real estate , which is a famously
10:03
bubble prone business where
10:06
people are always making and losing fortunes over and over again . So
10:08
, maybe , so maybe so I think I've
10:10
heard that .
10:13
Yeah , you're so . Remind me and our listeners you
10:16
don't use CDMOs , you're manufacturing clinical
10:19
supply and in-house .
10:20
We built our own GMP plan and then we
10:22
built the big expansion to the GMP plan which
10:24
we brought online last year . So it's also give me an illustration
10:27
of that space and what's going on
10:29
there .
10:30
It's very different from , I think , from most of your listeners
10:32
.
10:34
We use an unique bio manufacturing host . It's
10:37
a photosynthetic micro . It
10:39
doesn't require sterility . That's the key
10:41
to the scalability and safety of it . And
10:44
with this micro we
10:46
can express a variety of a very wide range
10:49
of therapeutic proteins and
10:51
therapeutic peptides . And
10:54
the easiest applications are all GI diseases , diseases
10:57
with some kind of an excess to the GI tract . Now
10:59
this has some implications for the GMP , the GMP
11:02
facility . One
11:04
of them is that well , they
11:06
are , you know , because
11:08
the roots of the company are in cell engineering
11:10
technology and so , just
11:12
like with Genentech and Amgen , and then in the 80s , they
11:15
also couldn't go to the CDMO industry . Why is it ? Because
11:17
of the brand new technology in the industry
11:19
hadn't been created yet . So , like them
11:21
then we now had really
11:24
no choice . But the
11:26
fortunate thing for us is
11:28
about two-fold . Number one , because
11:30
it doesn't require sterility for safe
11:32
GMP manufacturing . It's a way less
11:34
expensive to build out a facility like this , like
11:37
literally towards a magnitude cheaper
11:39
. And the other
11:41
second advantage we have is because of all of our
11:44
relationships with grant
11:46
funders and the US federal government and DOD in
11:48
particular , we were
11:50
able to convince them to support the
11:52
capital investment necessary to build the
11:54
facility , and so that's
11:57
how we were able to do this big expansion , and so that's a good
11:59
thing , because we're maxing
12:01
out the capacity of that
12:03
newly expanded facility already for
12:05
clinical trials this year .
12:06
Yeah , are there plans to expand or ?
12:09
We have plans to expand . We don't even
12:11
have the funding for that . So if you know someone in DC
12:13
, well , that's a good message . Any listeners
12:15
?
12:15
Yeah , beautiful segue you
12:17
mentioned . If you know anyone in DC , I
12:20
mean that's sort of been the go-to . Tell me a little
12:22
bit about that . Like , yeah , you and I have chatted about
12:24
this sort of the I
12:27
don't know the silo
12:29
I guess the lumen kind of finds itself into
12:32
in terms of its funding resources
12:34
.
12:35
Like what's what's ?
12:37
described why that is . Why is the traditional
12:39
biotech VC
12:42
community maybe isn't such a sweet spot for a lumen ? I
12:44
?
12:44
try not to take it personally . I
12:47
put a lot of them around the question . I
12:51
think you're calling me out on this , just
12:56
that that selling stock . The institutional investors
12:58
we have are all Seattle
13:00
based investors . We're based in Seattle and
13:03
we have a handful of angel investors as well , some
13:07
famous guys among the list . What they all have
13:09
in common is their , their friends of
13:11
mine and my co-founder from
13:13
the biotech world or
13:15
industry generally . So it's a very unusual capital structure . I
13:18
like to say it has more in common with the way innovation was
13:21
funded in the Renaissance . You know you
13:23
go to the Medici family rich
13:25
families and get that it's
13:27
your idea funded If you're Leonardo da Vinci
13:29
. And less in common with the modern , professionalized
13:33
biotech investor . You know
13:35
kind of model that's . That's mixed
13:37
blessings , the you know
13:39
the the modern biotech model has definitely
13:41
has a lot more capital , and
13:44
so you know you can accelerate
13:46
a lot of things with capital . On
13:50
the other hand , I've been at companies where
13:52
they had a lot of capital and
13:55
one of the things that happens
13:57
in my experience is that a lot of problems that
13:59
can't be solved with money people that's
14:01
their first tool , because it's just lying around
14:03
including a lot of problems that cannot
14:05
be solved with money People to first
14:07
go to . And so I wonder sometimes
14:10
, you know , if we were , like you
14:12
know , lavishly funded , it would be fun
14:14
to have a few hundred million dollars in the bank I'm not going
14:16
to lie but I wonder if we would
14:18
have made errors . There's a
14:20
, you know , a
14:22
necessity with breeds invention . We've been
14:24
incredibly inventive .
14:26
I mean , isn't that scenario a lot
14:29
of what's led us to
14:31
this ? I mean , let
14:33
us to the , to the brink of being overpopulated
14:36
, with biotechs and
14:39
the ensuing downturn . I mean , doesn't
14:41
that doesn't that sort of easy
14:44
access to capital and
14:47
that sort of bread , the situation that we found ourselves
14:49
in for the last two and a half years ?
14:51
Yeah , I kind of wonder , right . I
14:54
mean , drug development is expensive . It's
14:56
important to do it safely , so it's never going
14:58
to be cheap , right , like
15:00
starting starting a website . But
15:03
you know , does the ? You know there's this persistent
15:05
decline in our deep productivity
15:07
in our industry . That's been written about extensively
15:10
for you know , 10 or 15 years now by banks
15:13
and Scannel and other
15:16
researchers . And you
15:19
kind of wonder , I mean it does it sort
15:21
of tracks the growth in capital
15:24
abundance for the industry , at
15:26
least for the last 15 years ? And
15:28
is there a causal relationship between the
15:31
two ? Or is it just you know we need more capital
15:33
because it really is fundamentally harder ? I don't know
15:35
. I mean it's hard to disentangle cause and effect
15:37
. My , my scientist colleagues are always telling me
15:39
so well .
15:40
I mean it's difficult to add , is difficult to do . Yeah , it is difficult
15:42
to discern that , like we've seen a lot
15:44
of great , seemingly great
15:46
, you know , stated
15:49
great programs go by the wayside or be backburner
15:51
to Shell because of resource constraints . You
15:54
know , I guess the definition of
15:56
greatness and what gets money when
15:58
money gets thinner is up to
16:01
the , up to the investor . I don't know
16:03
. It sounds to
16:05
me like your approach is is
16:08
strategic . It sounds
16:10
to me maybe this is CEO spin . Be
16:12
honest with me . It
16:15
sounds to me like it's more strategic than
16:17
a matter of that VC
16:19
community . You know , institutional investors
16:22
just maybe shine away from
16:24
a
16:27
a different way of
16:29
developing biologics , or is there
16:31
some of ?
16:31
that too . Well , I mean , I can give you
16:33
some anti-spin , because I said it the outset . It
16:36
might just be that I'm a poor salesman of stock . I'm
16:38
trying to take it personally . I
16:41
have some theories about it , you
16:44
know .
16:45
One is one is very simple .
16:48
I was talking with the VC , I
16:51
know , and he's close guy and I'll
16:53
tell him what we're up to . You
16:55
know , it's kind of just working and it's all great
16:57
, just big markets , all this stuff . And
17:00
he says to me he says , brian , I
17:02
was like , well , why don't you join us
17:04
? And he says , well , here's the thing
17:06
, brian , I like a little bit of doing . It's amazing
17:08
, it's definitely going to work
17:10
. Love the sign , it's
17:12
all the things right . But he says look , I
17:14
got I got a department of self-therapies over
17:17
here and I got a . I got a department of oncology
17:19
. You know , oncology over
17:21
here . I don't have a department of whatever the hell you
17:23
are , because there's like literally no one
17:25
in the firm to do this , and it's
17:27
, I think of it as being a a kind
17:31
of a version of the innovator's dilemma . If
17:36
you're doing something really innovative , then
17:40
by definition there's not a market for your
17:43
product , because it's an innovative product that hasn't existed
17:45
yet , but there might not also be any investors
17:47
to invest in your thing . Before
17:51
the Netscape's IPO
17:53
, nobody ever heard of the internet
17:55
, for example . Somebody had to
17:57
be the trailblazer and then all of a sudden , a bunch of internet
17:59
VCs came into existence . The rest of
18:01
history . So
18:06
in my optimistic moments , I like
18:08
to think , wow , this is what we're
18:10
doing .
18:11
We're going to be the Netscape , but
18:13
in my pessimistic moments , I think but
18:15
how are you ?
18:17
How would you know any better ? We're just some guy
18:19
.
18:22
Do you consider Lumen in
18:25
the I guess , in the camper in
18:27
the sector of plant-based
18:29
biologics ? No , okay
18:32
, tell me what
18:34
discerns that you
18:37
guys are starting materials ? Spirulina you
18:41
don't equate that to some of these companies that
18:43
are developing antibodies from some
18:46
genus of
18:48
tobacco plant .
18:52
The reason I'm very specific about my word
18:54
choice is probably because I went to law school , practice
18:56
law for 10 years . Lawyers
18:58
are one of the few groups of people that will never say the phrase . They're
19:01
semantics , because the semantics are oftentimes
19:03
very important . In this case , they are very
19:05
important . Plants are a certain thing
19:07
and spirulina is a cyanobacterium
19:09
and cyanobacterium , even though it is photosynthetic
19:12
like a plant , it's definitely not a plant . Why
19:14
is this important ? It's important
19:16
for a regulatory reason . If you're going to make a
19:19
drug in a plant , then
19:21
the FDA more importantly the USDA
19:23
and more importantly than the USDA is the
19:25
farmer's lobby is going to care a lot about what's
19:27
going to happen with that plant , because plants
19:29
breed asexually and there's going to be a risk
19:32
that the gene for your drug is
19:34
going to go somewhere where
19:36
maybe it shouldn't . There's
19:39
a lot of technology out there . You can put protein
19:41
therapeutics in potatoes or
19:43
rice or tobacco . They
19:46
have their pros and cons . The tobacco leaf is usually
19:49
transient expression . It's almost always , I think , grown
19:51
in greenhouses . From
19:54
our perspective , we are very interested
19:56
in not being hard with the plant brush
19:58
, simply because we don't want to have
20:00
a second regulator in
20:02
the form of the USDA . More importantly
20:04
, we don't want to pick a fight with the farmer's lobby , which
20:07
is the most powerful political
20:09
force in the country .
20:12
So you don't run that risk .
20:13
No , where cyanobacterium it is definitely
20:16
. There's no mechanism
20:18
for genuscape like sexual
20:21
recalination or anything like that . It's
20:23
very important regulatory legal distinction
20:25
, I would say . The other
20:28
thing is more
20:31
conceptual . I say plant-based biotechnology
20:33
companies . When I come across them periodically
20:36
, to me it always seems like
20:38
they're just trying to do the same
20:40
thing everybody else is doing with E coli
20:42
or Cho Trying
20:45
to save a bit of money on the upstream processing side
20:47
. What we do is very different . It's a completely
20:49
different therapeutic modality . You
20:53
can actually make an
20:55
injectable monoclonal antibody
20:58
in tobacco leaves . They've done it and you're actually
21:00
got a GMP process approved a few
21:02
years back at Oxford . But
21:06
to me I don't understand the utility of it . There's
21:08
vast amounts of Cho manufacturing
21:10
capacity in the world . It's
21:14
not obvious to me that at scale , particularly
21:17
with the regulatory headwinds of a plant-based kind
21:19
of system , that you're going to be able
21:21
to compete with that enormous amount of sun
21:23
capital just because it's nothing
21:25
cheaper than the factory that's already been built and depreciated
21:28
. What we're doing is
21:30
wildly different . We're topically delivering
21:32
cocktails of protein therapeutics , to
21:34
be coastal , out of topical surfaces of the body
21:36
like the GI tract , intranasally skin . There
21:41
are almost all of the
21:43
distinctions , while they're
21:45
all unlocked by the unique scalability
21:47
and cost efficiency of our platform . All
21:50
that matters is the action
21:52
of the therapeutic proteins themselves
21:55
and how we design them . That's actually where almost all
21:57
of our time gets spent . The fact that it's just grown
21:59
and something that's photosynthetic is seven-year-old
22:02
news that is almost
22:05
irrelevant , aside from the fact that it's fundamental to
22:07
making it commercializable and scalable .
22:09
Yeah , okay , very good , I'm
22:13
glad I cleared that up . What
22:16
are you doing at an investor
22:18
conference ?
22:19
Given what you've told us about your strategic
22:21
approach to investment
22:24
.
22:25
What are you looking for here ? What's
22:27
your goal ?
22:29
Two things really . We have some pharma
22:32
partnerships and there is
22:34
almost a ritualistic meeting
22:36
of people . It happens at JPMorgan
22:39
. We're doing that and it's important to keeping
22:41
the relationship moving forward
22:43
. We have meetings here
22:46
in the city for that . Then there are some
22:48
of our government partners have
22:51
teams here as well . It's
22:53
a good opportunity to touch base with them , much in the same way
22:55
. Okay , A
22:57
lot of the rest of it is just going around and seeing old friends
22:59
and looking for serendipity . I
23:01
would say Just waiting in the
23:04
lobby of the St Francis and seeing
23:06
who wanders by A lot of times . That's the most productive
23:08
thing for me .
23:09
Yeah , you made a joke , I think , when we were
23:11
trying to get this scheduled and there was some jostling
23:13
that a lot of these meetings don't go anywhere anyway
23:15
this is going to be more fun .
23:18
Yeah , I don't know , some people do that . The
23:21
thing where it's like 30 minute time slots and
23:23
everybody's sprinting from building
23:25
to building through the ring . We
23:29
don't do that . Maybe we should , I don't
23:32
know . Am I missing out ?
23:33
I don't know . I
23:35
come here and I pull up in a room like this and do interviews with
23:37
folks like you . I don't know , until
23:40
it's reception time and the evening . I really don't know
23:42
what's going on out there , yeah , Fewer
23:44
fewer better meetings . I think that's the philosophy
23:46
I might be wrong about that . Another
23:50
thing we talked about last time we chatted was
23:52
sort of the , I guess , big
23:55
picture biologics development sort
23:57
of cost paradigm and
24:01
as a result of that and suing patient
24:03
pay or costs and just the way that business
24:05
has always been done . And I know that's
24:07
a great big , giant question
24:10
. But you had some opinions , if I
24:12
recall , on how that
24:14
changes and perhaps how Lumen
24:16
is contributing through what the work
24:18
that you're doing to drive change . Yeah
24:21
, let's talk about that a little bit Like I
24:23
guess first give me your perspective on the
24:27
sort of the status quo and
24:29
then some thoughts on where you see
24:32
yourself and Lumen affecting
24:34
that status quo .
24:35
Yeah , I think this is a fascinating topic . I
24:38
mean there's a lot of good data out there , in my opinion , the
24:42
data from Deloitte Touche . That is a big accounting
24:45
firm and every year they look at the productivity
24:47
, the R&D productivity industry , and they add up income
24:49
. What are the costs of making a new drug across
24:52
the industry ? So it's an average and there's exceptions , both
24:54
up and down . And then they
24:56
say , well , now let's do our best to estimate
24:59
what are the revenues going to be from
25:01
all the products that , all that R&D is . So you can say
25:03
calculate or return
25:05
on investment . So , very
25:07
simply , if you borrow your money
25:09
from the US Treasury , it's always , just a couple of
25:11
years ago , 2% to 1% and then you invest
25:13
it in bonds at 10% and you don't have
25:16
any defaults , then that's good because you made a 9%
25:18
margin , right , Makes sense , profitable . But
25:20
what our industry does , by Deloitte's
25:23
math , is they borrow money from shareholders
25:25
and bondholders at 11%
25:27
and their return on investment for
25:29
R&D is 1% . So
25:32
they're destroying capital , according
25:34
to Deloitte .
25:35
To my amazement , this is not a universally
25:38
held view .
25:39
I was at a perception last night talking with a
25:41
senior person , a very , very large CRO
25:44
, and she insisted that this couldn't possibly be true . So
25:47
not everybody believes that . I
25:50
think , though , it's hard to disagree with the math
25:52
. Deloitte's pretty good at running numbers
25:54
, and there's some other academics like Jack Scannnell
25:56
who's written about this extensively too . So
26:00
if it's true , it kind of puts you in a pickle if
26:02
you're running a biotech company , because
26:05
how is that appropriate , taking
26:07
money from investors and destroying it ? So
26:11
I spent a lot of time thinking about this . For
26:13
us it goes a little bit back to what we were talking about earlier . We
26:15
were fortunate . There's an awful lot of serendipity in
26:18
how lumen came to be and
26:21
sort of path dependency and random
26:23
introductions to the Gates Foundation
26:25
, the DOD with COVID and other things . A
26:28
little bit of it is that well , okay , it's much
26:30
easier to make a return on investment if
26:32
there's a public interest in the thing
26:34
, and so the federal government
26:36
helps build it out , a great example
26:38
being the COVID vaccines that Moderna made . A lot of money
26:41
went in there Fabulous deal
26:43
for the American taxpayer , even
26:46
despite the subsidies . But
26:48
mostly it's the fact that , of necessity
26:51
, we've had to be much more efficient
26:53
, and , by luck , our
26:55
biology because it doesn't require
26:57
sterility is just a lot cheaper . So
26:59
, at the end of the day , ultimately
27:02
, what it boils down to is everything up
27:04
to early clinical development
27:06
is between 10
27:08
and 100 fold cheaper on
27:11
our platform to put a single therapeutic
27:13
protein into the clinic . Where
27:15
we hit the wall , though , is in late
27:18
clinical development , where you're
27:20
on multi site trials for a lot of diseases
27:23
and there were thrown into the clutches
27:25
of the market price , and
27:28
then standing behind that is
27:30
commercialization , which I think is another
27:32
interesting and risky and
27:34
very expensive area that we haven't yet started
27:37
to unpick , but
27:39
I think there's . In my ideal world , we figure out a way
27:41
to make those two things also 10 or 100 fold
27:43
cheaper for the types of products we make
27:45
, and then we really have something on our hands
27:48
, wouldn't we ? But
27:52
how do you go about doing that in particular ? I
27:54
think it's pretty interesting . There was an article this morning
27:56
and I
27:58
think it was in either a stat or end points , and we're
28:00
talking about Beijing . Something unusual
28:02
about Beijing is they run all of their own clinical
28:04
trials and have a huge staff of people . They don't outsource
28:07
it to contract CROs
28:09
and the point of the article is their
28:11
view anyway is that this allows
28:13
them to run better trials
28:15
less expensively , basically reversing
28:18
the outsourcing trend . And
28:20
I think there's another interesting thing on the commercial side
28:22
going on right now . Did you see this news about Lilly
28:24
?
28:26
It's pretty funny actually they announced they're going to sell
28:29
Majaro basically direct to consumer .
28:32
But it was alongside an angry letter saying
28:34
look , it's scolding people that were getting
28:36
the GOP one . Analog drugs
28:38
for cosmetic weight
28:41
loss and everything .
28:42
Definitely don't do that . But
28:44
, by the way , here's our direct to consumer portal .
28:48
But definitely only use it if it's appropriate , not
28:50
for cosmetic purposes , which is sort
28:52
of an interesting example of speaking out of both sides of
28:54
your mouth . I
28:58
think it's an interesting experiment and
29:00
the GOP ones might be the perfect way to do this . If we
29:02
can figure out a way to disintermediate all
29:04
of those sort of middlemen
29:07
in the supply chain for biopharmaceuticals , could
29:09
that make a big difference in cutting
29:12
the costs potentially . Maybe that's
29:14
part of the productivity improvement
29:17
our industry needs .
29:19
What are I mean ? You're in the throes
29:21
of that CRO . You talked about the
29:24
cost of clinical development and clinical
29:26
activity . What
29:29
are you , I guess , finding or
29:31
taking away from that experience , where you think
29:33
you hinted at it ? Well , if we could address
29:35
that , how do we do that ? Would
29:37
you have any ?
29:39
thoughts on how to do that . I don't think we've
29:41
figured it out yet . I wish we had . For
29:46
an honest , I'm not a clinician . I
29:48
trained as a lawyer , so I'm a bit of an outsider
29:51
to all of this . That's an advantage and disadvantage
29:53
, because outsiders come into problems
29:56
with the fresh perspective and
29:58
you ask dumb questions and
30:00
it's acceptable . But
30:02
on the other hand , clinical development is a baffling
30:05
activity . There's a lot
30:07
of things that happen and many of these CROs
30:09
are very , very good at what they do , but
30:12
there are also a lot of crazy horror
30:14
stories about budget overruns or performance
30:17
lapses . I
30:20
think at the moment , the thing
30:22
that I'm sort of obsessing
30:24
about most right now is this fact that
30:27
legally , as a proud sponsor
30:31
, the organization , my company is
30:34
responsible for everything going right that the contractor
30:36
does . The difficult thing
30:38
is that it's hard enough to manage employees
30:41
and have transparency into what people are doing
30:43
and make sure everybody's got the resources
30:45
they need and thinking about it in an aligned
30:47
way and all of the management talent
30:50
that goes into getting an organization
30:52
to all row
30:55
the ship in the right direction . The
30:58
thing is , when you outsource it , all of those problems
31:00
become much harder . But your legal responsibility
31:02
, your ethical obligations to make sure it's all done
31:04
correctly are no different
31:07
, but it's just a much more difficult talent
31:09
management problem . I think I
31:13
don't know what the answer is . We'll
31:16
see how this unfolds . Maybe Beijing's right .
31:20
I was going to ask , not how credible , but how
31:24
realistic is that for a company
31:26
that's not Beijing ? How
31:33
realistic is it for a biotech , a clinical
31:35
stage biotech , that is
31:37
relying on outside funding to even
31:40
consider that ? I would imagine not
31:42
.
31:43
I don't know . Plenty
31:47
of people told us that it was impossible to build a
31:49
GMP plan . Then we built
31:51
not one , but two
31:54
. I don't know , it's
31:57
just something fishy about the facts
31:59
of the world which is the CRO industry . The clinical
32:01
CRO industry is pretty new , actually
32:03
. Really in its modern version , the
32:06
story I've heard is really originated
32:09
in the late 90s . How
32:13
were people running all those trials before
32:16
that existed ? It's
32:19
encouraging because new drug discovery R&D
32:21
productivity was much higher back then too
32:23
. It's a fishy coincidence . You
32:26
might say well , Brian , that's
32:28
a good news because thank God they
32:30
brought in the clinical CROs when they did in the 90s
32:33
, because imagine how much worse it would have been if
32:36
it weren't for that professionalization and
32:38
efficiencies of this
32:40
outside specialist function
32:43
coming into being . It could have been even worse . Like
32:48
I say , causation is a difficult
32:50
thing to nail down . There's
32:54
something to that , I think . I
32:57
wonder if Beijing might be in the right path .
33:01
Another thing that just occurred to me you and I talked about
33:03
the last time we chatted was
33:06
and I see it playing out so far here is
33:09
making us flash is AI . When
33:12
you and I talked about it
33:14
, you were , I'd say , decidedly
33:17
pragmatic about putting
33:19
AI at its best as a
33:21
tool . It's
33:24
just I'm exposed to a
33:27
lot of companies who are foundationally
33:30
AI , who are creating
33:32
a splash right during the pool waving
33:34
their arms around making waves . What's
33:37
your perspective on that ? Like , maybe even since you've been
33:39
here , is that a buzz that
33:41
you're catching ?
33:44
We use an AI ML
33:46
. I'm not sure exactly
33:48
where the dividing line is . We use these methods
33:50
pervasively in our business . We
33:54
publish some papers , we have a
33:57
string of collaborations with Google's
33:59
machine learning AI team
34:01
, and so
34:03
we . I don't think we're slouches
34:06
at AI or like
34:08
skeptical that it has utility
34:10
, but I think there's a lot of people interested
34:12
in how's anybody going to make any money in
34:15
that world that isn't like Microsoft
34:18
, like , for example , like you know , chat
34:20
GBT . It's very obviously
34:22
Microsoft's going to stick that in every office product
34:25
, right , and it's going to be amazing
34:27
. It's going to be great when they get that all done
34:29
, deployed and the drive to cost of
34:32
the processing down and everybody can use
34:34
it . No doubt about it . But
34:36
it's going to be the channel owners
34:39
. I think it seems to be the answer
34:41
. I know there's some questions about like
34:43
search and maybe AI is going to displace Google
34:45
. And nobody saw Google coming either , me
34:48
included . So I don't think I have
34:50
any great answers . But in our industry
34:52
I kind of vacillate back and
34:54
forth . On the one hand I
34:57
think there's so much utility
34:59
and so many things that we do , but then I step
35:02
back from it and I realized but wait a second . The problem isn't
35:04
like a shortage of new
35:06
molecules with
35:08
different attributes . The problem is that trials
35:11
are too risky and expensive and slow and that's
35:13
where all the capital gets gobbled up . And
35:16
while there are people talking
35:18
about AI is how it's going to help that
35:20
? There's precious little
35:22
evidence yet that
35:25
it's going to happen . But maybe there'll be , like the
35:27
Google thing , and it'll
35:29
happen . And I said I think
35:31
remember very clearly when the
35:33
law school librarian introduced me to Google
35:36
. It was a new website . I'm
35:38
like this is ridiculous . You know who needs a new search
35:40
engine ?
35:41
I can go to Alta Vista . There's Yalu
35:43
, you know .
35:44
If I want to ask my query
35:46
in the form of a question I can ask .
35:48
Jeeps Asked
35:50
why you may need to point some
35:53
. Put something in the show notes for reference to
35:55
our younger listeners when you bring up .
35:56
ask me I remember saying that before
35:59
there was Google and it just totally changed everything
36:01
. And maybe someone out there I hope they are there we're
36:03
going to find a thing that'll just make drugs
36:05
routine and amazing
36:07
, like Google made search routine and amazing
36:10
, and
36:13
I guess I'm not really betting in that direction . Yeah
36:15
, yeah , you would know better . You talked to all
36:17
the guys . Well , I talked to all the guys
36:19
and typically those conversations
36:22
revolve around molecular
36:24
identification and zeroing
36:27
in on targets .
36:29
It's not . I'm not in the clinical execution
36:32
around as much as I am . And
36:35
biologics , discovery , design and then process
36:38
development . So I'm
36:40
just curious about where
36:42
that's going to take . Conceivably
36:45
those
36:47
early efficiencies , like you said at
36:49
Lumen , your early molecular
36:54
creation is considerably
36:57
cheaper . Right , it's
36:59
when you get into the clinic that expenses
37:01
mount up like they do for
37:04
everyone . So
37:07
I'm as interested I guess what I'm saying is I'm as interested
37:09
as you are in and how
37:11
AI might contribute to a
37:14
change in the cost paradigm
37:16
across the spectrum , Right ?
37:19
Maybe . So I think the shortage in
37:21
early stage discoveries and molecules
37:23
. It's targets , good targets , and
37:26
you know this is true because anytime there's a good target
37:28
emerges , like PD1 , then
37:31
there's just flood of
37:34
great molecules and
37:36
GLP1 right now . Right , how many
37:38
GLP1 analogs are there out there ? Every
37:40
different flavor of ice cream is being
37:42
rapidly pushed through the clinic . So
37:45
there doesn't seem to be a shortage of
37:47
ways to go after
37:49
a target Like if only
37:52
we had a way to make a molecule like it go
37:54
after the GLP1 receptor
37:56
. It's not really the issue . It's
37:59
just that all of these companies have to spend
38:01
, depending on whose numbers you believe $2
38:04
billion risk and probability
38:06
and time adjusted
38:08
, or $7 billion
38:10
probability and time adjusted capital
38:13
to get one product through the
38:15
clinic . That's where all the money goes . Getting
38:18
a molecule to load into
38:20
that process is easy .
38:23
So , given the breadth and depth of
38:25
molecules and
38:28
targets , that perhaps
38:31
targets ? You tell me that Lumen
38:33
has . In the years since you founded
38:35
the company , you mentioned that
38:37
you've got a sort
38:40
of choose your own adventure path . How do you
38:42
like you've got a lot of opportunity there . How does
38:44
that play into your calculus around
38:46
target identification and the indications
38:48
that Lumen will pursue , is
38:50
pursuing and will down the road ?
38:53
Yeah , I'm a little talking about it . How do you kind of call
38:55
me out on this here ? Because we don't do any of that
38:57
In our business . We
39:00
have the luck of being the first
39:02
to the field , so it feels a little bit like being I
39:04
don't know genetic in the early 80s , where
39:08
they finally figured out how to make molecule antibody
39:10
and there was a list as long as you're on
39:12
, a great idea to go after , and I didn't mean
39:14
all of them worked , but
39:17
many of them were amazing products
39:19
and they prop up the
39:22
stock prices of some of these companies , and Amgen
39:24
, for example , to this day . Right Enbril
39:26
I think the first patent on Enbril was founded
39:28
in 1989 . So
39:31
the persistence of being a first
39:33
mover in a new field where you can do
39:35
anything that everybody knew would be a good idea for a long
39:37
time , but now you can actually scaleably
39:40
execute on it is huge . For
39:44
us , that means we really only
39:46
go after targets that have a
39:49
lot of not just animal data
39:51
but human clinical data , validating
39:53
the target , biology
39:55
and also in all the cases
39:58
, also the therapeutic modality , the mucosal
40:00
topical delivery , and
40:02
so for us , what
40:05
keeps ? others at bay at least at
40:07
the moment we've kind of got this base to ourself is
40:10
the scalability and cost efficiency
40:12
of our platform for this particular application
40:14
. If we could find a
40:16
way , if the AI guys
40:19
, as we're calling them , could find a way
40:21
to get the same confidence in
40:23
the target biology that
40:26
we're using these techniques , that we
40:28
get out of double-fashioned
40:30
reading papers from some
40:32
80s and 90s and then
40:35
they really have something . I mean , that would be a real gift to
40:37
humanity and I
40:39
think they've cracked that yet , but maybe
40:42
there's something there .
40:43
Yeah , so give
40:45
us an update on the
40:48
clinical activity element .
40:50
Right . So a bunch of activity
40:52
. We just wrapped up a trial
40:54
a few weeks ago in December . There's
40:58
a new area for assistance . Instead of delivering
41:00
our protein therapeutic cocktail
41:02
or antibody cocktails to GI
41:04
mucosal services , this case we were delivering into
41:06
intranasal passage and
41:09
what we're interested in that trial was
41:11
well , tolerability and safety . Obviously
41:13
we always look at that , but there's decades
41:15
of clinical trials on that therapeutic modality
41:17
so we weren't so worried about that , but still
41:20
happy to see that it's very well tolerated . The
41:23
thing we're more interested in we don't have the data on this yet
41:25
, but we did a staggered dosing . We dosed
41:27
some of these individuals who are dosing them daily , some
41:29
of them every other day and some of them every third day . What
41:32
we're really interested in is taking the mucosal
41:35
samples from the nasal passages so
41:37
we can build out a
41:39
rough measure of how long the antibody
41:42
cocktail persists in those tissues
41:44
. This is under the
41:46
COVID-19 program , the DOD funded
41:48
clinical trial , but very
41:50
obvious applications for not only for COVID-19
41:52
, which , as I mentioned earlier , nobody cares about anymore , but
41:54
there's a lot of other viral infections influenza
41:57
, rsv . This could have
41:59
great utility , for the
42:01
use case is really obvious . I
42:04
think a lot of people would be interested before
42:08
they go on an airplane , taking some kind of
42:10
antibody cocktail and just sort
42:12
of coding the mucosal membranes of your nasal
42:14
passages that were respiratory tract , to at
42:17
least reduce the odds of
42:19
getting an infection during that window
42:21
of exposure .
42:23
And so that's very exciting .
42:25
We'll have the PK data from that , I think , in
42:27
a couple of months . This
42:29
year we have a lot on deck . We're
42:32
running five trials
42:34
We've got funded , we've got three more
42:36
in various stages of getting funding committed for
42:38
. So we can pull that off . That's eight clinical
42:40
trials to initiate this year and
42:42
some of them will kind of extend out their
42:45
different lengths . So
42:47
that's where the huge growth is for us and it's
42:49
why we're hiring and thinking
42:51
so aggressively about clinical development costs
42:54
very salient and
42:56
also the manufacturing facility , because
42:58
that's a lot of clinical trial
43:00
material to manufacture in our GMP plan
43:02
. So we're hiring very aggressively . If
43:04
you're interested in a job , look out our website
43:07
. What sort of jobs are you hiring
43:09
for ? Clinical manufacturing , r&d
43:11
.
43:12
Yeah , those three areas . Lumen
43:15
, biosciencesorg , Lumenbio
43:18
All right , Lumenbio , Go
43:20
there and check out the job offers . Speaking
43:23
of jobs , so what you found ? You found the company when
43:25
2017 . 2017
43:27
. Looking back on the
43:30
years that have passed since then , what
43:34
offers some pointed advice for
43:36
companies ? I'm sorry for
43:38
folks who are in your shoes back then
43:40
for stipping a toe and founding
43:42
a biotech company .
43:44
Okay , okay , if you could walk on
43:46
this , I'm sure . No , no , I've tried the other
43:48
side , I was gonna say
43:50
. When I was selling overpriced legal services
43:52
as a lawyer at Cooley , I
43:57
used to tell people that advice
43:59
is worth roughly what you pay for it .
44:01
Okay so .
44:04
Free advice you gotta take with
44:06
extra grains of salt , sure .
44:09
So I don't know that I have any . It's like the gift horse analogy
44:11
, right .
44:12
The gift horse . The saying is you
44:14
don't look at it .
44:16
What you do like , if you're gonna take on that or
44:18
the horse that's given to you is the one you really wanna
44:20
assess . Right , you wanna take that
44:22
apart .
44:25
I think advice comes in matched
44:27
proverbs , and I think proverbs
44:30
are always matched right . There's always like look
44:32
before your leap . But it's also true
44:34
that who has the tastes is lost
44:36
. So a lot of advice comes in these
44:38
sort of mix and match things and I think of them as being more
44:40
like cones . There's just sort of
44:43
the things you wanna meditate
44:45
and think about and then you still gotta make
44:47
your own decision about what's
44:49
the right thing . So
44:53
two cones that I recommend is
44:55
thinking about that
44:57
were important to me . First of all , I
45:00
can endorse the lifestyle .
45:02
It's not for everybody .
45:03
So you gotta know yourself and make
45:05
the right choice . But
45:08
it's great fun starting a company . I
45:11
mean it's especially fun when it's winning . It's especially
45:13
agonizing when you're struggling
45:15
and you get plenty of doses of boats
45:17
. It's a very high emotional balance activity
45:19
running an early stage company
45:21
, but
45:24
it's great fun . I recommend it to anybody that
45:27
has the slightest inclination . And
45:30
then the second thing is
45:33
maybe related . Part
45:36
of what makes it fun is the unpredictability
45:38
of it . And boy
45:41
our experience is there's just been so
45:43
much serendipity driving
45:45
, so many critical events
45:48
in the company's development . There's just no way
45:50
you could have planned . I mean , just almost from the minute
45:52
we stepped out of the gates things
45:54
started happening Good
45:58
and sometimes challenging , but mostly
46:01
for the good . There's
46:03
this feeling that as you
46:05
start a new thing like this and it's not just
46:07
starting companies , it's starting new
46:09
art programs or
46:11
writing a book or something there's
46:15
a tendency of the world to just sort of it
46:17
looks like it's all closed up and impenetrable
46:19
. And then you , just you take the first step and everything
46:22
just starts opening up in front of you . That's
46:24
the kind of lived experience of it . So
46:27
I guess it translated into advice form
46:29
, it would be to keep
46:32
an eye out for the opportunities and don't get too attached
46:34
to the path you think you're gonna take
46:36
.
46:37
How do you enable that ? Like you know , serendipity
46:40
doesn't happen in a vacuum
46:42
. Like you can't have a great idea
46:44
, pull up in a space like
46:46
this , Take meanings .
46:47
You do just have an open
46:49
mind and a naive attitude
46:51
and kind of a learning mindset
46:54
and you take me . So very
46:56
short anecdote . We have time for a short anecdote
46:58
. Yeah , this is for sure . I like this one . My
47:01
co-founder , Jim . He's a scientist and we
47:03
started the company and he , with
47:05
Gates Foundation , found us . We're based
47:07
in Seattle , they're based in Seattle . I found us through a friend of
47:09
friend and they had this problem that they were interested in . So
47:13
they invited themselves to come over and they said well
47:16
, I said , Jim , this is great , the Gates Foundation
47:18
is gonna come over .
47:19
I don't know if you know this .
47:20
But they got all this money . It's great . So
47:24
he says , well , what do they want to do ? He says well . I said , well , they
47:26
want us to make antibodies in spirulina . He
47:28
said , well , that's a ridiculous idea . He
47:30
says spirulina is a prokaryote . You
47:32
know the male in the antibodies require a
47:34
glycosylation , all of this sort of complicated
47:36
stuff .
47:38
So that's a really dumb idea . You take the meeting
47:41
. I've got real work to do . That's
47:43
a little word . I've got real work to do .
47:45
And so I took the meeting , because that's kind of my attitude
47:48
, who knows . And
47:53
it was sat down and I said so what's going
47:55
on ? So we want you to help us . We got this problem we
47:57
need all these kids are dying in the developing world . We want to make
47:59
an antibody cocktail so
48:01
cheap that we can just feed it to these kids , stop
48:04
them from getting these enteric diarrheal diseases
48:06
and save their lives , and it's going to be
48:08
great . And I said , oh well , I do what I usually
48:10
do in this case , which is I kind of roll back in
48:12
my head Robotically . I try to remember exactly the
48:14
words Jim said there . You know the science
48:16
, not the words . He said
48:18
where ? I
48:21
explained well it's like a prokaryote
48:23
. I don't know this , but you can't . Glycosylation
48:26
and all these things . And I stopped and he
48:28
says no , no , no , no , no , no , no no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no
48:30
, no , no , no , no , no , no , no , no , no , no no no no , no , no , no , no , no , no no no , no , no , no
48:32
, no , no , no , no , no , no , no , no , no , no , no , no , no , no
48:34
, no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no , no
48:37
, no , no , no , no , no , no , no . And
48:40
so I was like , oh hey , I'm going to have to shift my mind
48:42
. So
48:45
I do know that somebody's saying , hey , you
48:47
got a million antibodies why
48:50
don't you make a camel antibody fragment and ? he
48:53
expressed a brain in prokaryotes , and I had dragged
48:55
one of my science colleagues with me who was
48:57
less rude than mechalophantic flowed from that meeting and
49:00
I tell you there's been 10 or 15 other
49:02
things like this , where just
49:04
random circumstances generate
49:08
the most spontaneously a path
49:10
forward , where , like I say , it just seems
49:12
impenetrable , an impenetrable triple ticket
49:14
, and it happens
49:17
so often To
49:19
answer your question , I don't know how to
49:21
create it While we're talking earlier
49:23
, when I come down here , I try to have
49:25
fewer meetings and more serendipity , and my way
49:27
of doing that is lurking in the
49:30
St Francis lobby or different places
49:32
and waiting
49:35
for things to happen and , god damn , it always
49:37
does yeah .
49:39
Well , it's always a pleasure to have you
49:41
. I'm gonna let you go make some of that serendipity
49:43
happen . I really enjoy talking with you
49:45
. Very thoughtful , excellent
49:47
conversation . I appreciate having you on and
49:49
we'll do it again . I hope so . Yes , man
49:52
, we'll keep it up . Okay , thanks , brian . I'm
49:54
Matt Pillar and you just listened to the business of
49:56
biotech , the weekly podcast dedicated
49:59
to the builders of biotech . We
50:01
drop a new episode with a new exec every
50:03
Monday morning and I'd like you to join
50:05
our community of subscribers at bioprocessonlinecom
50:09
, apple podcast , spotify , google
50:11
Play or anywhere you get your podcasts . You
50:14
can also subscribe to our Never
50:16
Spammy , always insightful monthly
50:18
newsletter at bioprocessonlinecom
50:21
backslashbob . If
50:23
you have feedback or topic and guest suggestions
50:26
, hit me up on LinkedIn and let's chat and
50:28
, as always , thanks for listening .
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