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The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

Released Monday, 4th March 2024
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The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

The Innovator's Dilemma with Lumen Bioscience's Brian Finrow, J.D.

Monday, 4th March 2024
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0:00

The business of biotech is produced by

0:02

LifeScienceConnect and its community

0:04

of learning , solving and sourcing

0:06

resources for biopharma decision

0:08

makers . If you're working on biologics

0:11

process development and manufacturing challenges

0:13

, you need to swing by bioprocessonlinecom

0:16

. If you're trying to stay ahead

0:18

of the Cell or Gene Therapy curve , visit

0:20

cellenginecom . When it's time

0:22

to map out your clinical course , let

0:25

clinicalleadercom help , and

0:27

if optimizing outsourcing decisions

0:29

is what you're after , check out OutsourcePharmacom

0:32

. We're LifeScienceConnect and we're

0:34

here to help . I'm

0:40

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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