The Future of Medicine
Welcome to The Future of Medicine, a podcast from Stanford's Department of Medicine.
We bring you into conversation with the thought leaders who are reshaping how we understand disease, deliver care, and imagine what's possible in human health. This show is built around the extraordinary speakers who join us for Medicine Grand Rounds – one of the longest-running and most respected forums in academic medicine.
Our guests include world-renowned physicians, scientists, innovators, and policy leaders from across the globe, as well as the remarkable faculty at Stanford. Together, they represent the full spectrum of modern biomedical discovery: from breakthrough therapeutics and cutting-edge genomics, to health equity, digital health, global health, neuroscience, AI, and the re-design of care systems.
This is The Future of Medicine.
The Future of Medicine
Jennifer Doudna on CRISPR, One-Time Cures, and Science Communication
In this special episode of The Future of Medicine, host Euan Ashley sits down with Jennifer Doudna, Nobel laureate and co-discoverer of CRISPR-Cas9, to explore the dramatic ascent of genome editing and what it means for the future of medicine. From the promise of precision therapy that could be “one-and-done” to the challenges of translating groundbreaking science into scalable treatments, this conversation dives deep into science, ethics, policy, and the art of communicating complex ideas to the public.
What you’ll hear:
- A primer on the CRISPR revolution: how a discovery two decades ago has evolved into a potential deluge of targeted therapies.
- Precision therapy that’s more than a symptom fix: the idea of genome editing as a “precision surgery” that could cure diseases rather than require lifelong treatment.
- From one patient to many: the path from an N-of-1 success to scalable, population-wide strategies, including the role of the microbiome in health and disease.
- Real-world regulatory perspectives: how agencies are thinking about repeatable, off-the-shelf genome-editing tools and what it takes to translate a breakthrough into a therapy.
- The regulatory and scientific roadmaps: the steps scientists and clinicians must navigate to bring CRISPR-based therapies to patients rapidly and safely.
- The power and responsibility of storytelling: why scientists must improve public communication and how clear, non-jargony narratives can build trust.
- Combating misinformation: reflections on the moment when science is under scrutiny and how researchers can connect with diverse audiences.
Guest bio: Jennifer Doudna is a pioneering biochemist and a leading figure in the CRISPR gene-editing revolution. As a founder of the Innovative Genomics Institute, her work has opened new frontiers in biology and medicine. Her research continues to shape how we think about disease mechanisms, therapy development, and the ethics of powerful new technologies.
Why this episode matters: CRISPR technology is at a pivotal moment — one that could redefine what’s possible in medicine within a generation. This episode offers an insider’s view of where the science stands, what’s required to move from amazing results to real-world therapies, and how we, as a society, can navigate the opportunities and responsibilities that come with transformative science.
Notes for listeners:
- Not a distant dream: the conversation highlights tangible progress toward therapies that could be delivered in months rather than years, with the potential to affect thousands of patients.
- A balanced view: along with the excitement, the episode addresses safety, ethics, and the essential role of clear communication in building public trust.
- Public-facing science: practical thoughts on how researchers can explain their work to non-scientists — helping to bridge the gap between the lab and everyday life.
Call to action: If you enjoy The Future of Medicine, subscribe for more conversations with leading scientists shaping the next era of healthcare. Please rate and review the podcast to help others discover these important discussions. Share with friends and colleagues who are curious about how science becomes medicine.
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What am I most excited about? Bespoke CRISPR
therapies. Dr. Jennifer Doudna is a Nobel
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Prize laureate and CRISPR pioneer turning gene
editing into real cures. A child treated with
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a therapy that was created for him. We talk
about her efforts to help treat a child with
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a devastating genetic disease. This is probably
not a one-off case and new ways to help improve
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health by working with the microbes that
live in and around us. We're in a moment
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where science is really under attack. Science
communication is more important than ever.
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What do we do? Welcome to Stanford Department of
Medicine's inside look at the future of medicine.
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Well, Jennifer, welcome to Stanford. Thank
you. Real pleasure to be here. Yeah. Thanks so
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much for coming. Coming down down the coast
to visit us. Easy ride. Yes. Pretty good.
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I was preparing for the conversation with
you today and I realized that it was only
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about 10 years ago, just a little bit
over 10 years that your paper in 2012 in
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Science that really kicked off the CRISPR
revolution. For some reason in my head,
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so much has happened. It seemed like it must
be much longer, but 2012 — in that decade,
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I mean, so much has happened. Your life
has changed a little bit in a few ways.
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What has surprised or delighted you the most
in the last kind of 10 years or so since that?
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So many things have happened as you said and
some of it has been on the science front and
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some of it's been on the frankly larger scale
of public policy and where medicine is headed,
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where agriculture is headed but with
these kinds of tools now that we have
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for manipulating DNA. It's really been very
interesting to see all of that unfolding.
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What am I most excited about? I guess certainly
top of mind today is the opportunity to create
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bespoke CRISPR therapies for patients in real
time. I think this is such an interesting moment
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we're in right now. We've seen the example with
baby KJ. We talk about that right here today.
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And there are so many things going on here at
Stanford and in the Bay Area and of course much
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more broadly across the country and elsewhere
that make us think that, you know, there really
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is an opportunity right now to seize the moment,
figure out how we can find those patients that
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can benefit from CRISPR and create the pathway
to helping them in real time and doing it in
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a cost-effective way. That's what I'm scaling
— the thing really interested in doing. Yeah.
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Well, we'll get to a little bit more
detail on the baby KJ story shortly,
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but you lead an institute with I think one of the
coolest names of any institute, the Innovative
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Genomics Institute. As a genomics nerd, that
sounds like the perfect place for me to visit
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or work. I think who wouldn't want to work there?
But tell me a little bit about the institute first
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and the work that you're doing there. And then
we'd love to dive into some specific examples.
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Well, this institute started just over 10 years
ago in Berkeley and in San Francisco. We were a
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joint institute from the very beginning linking
UCSF and UC Berkeley and UC San Francisco with
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the idea that we could bring genome editing
to bear on health and climate challenges in
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ways that would have real world impact.
How do we do that? You know, it sounds
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like a broad grand goal, but you know, how do
you actually get there? And what I'm excited
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about is that over the 10 years of our existence,
we've raised a lot of money. We've also invited a
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lot of partners in. We've just recently signed an
agreement with our third campus partner, UC Davis,
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has become a formal partner of the IGI.
And we love the idea that we can leverage
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expertise that exists on different campuses
to focus on big projects and problems that
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none of us individually would be able to
work on or really tackle meaningfully.
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And what's amazing is that we're really focused
now on building collaborative teams, especially
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with younger scientists who are just starting
their careers and with companies that can bring
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their expertise to bear on these projects and
problems and inviting people that are very excited
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about science but maybe are not scientists.
Philanthropy comes to mind. Yeah. That can
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meaningfully gather their different capabilities.
Yeah. To do things that otherwise wouldn't happen.
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So, you view the institute partly as a sort
of gathering place. Bring the smartest people,
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the most energetic people, the most innovative
people together and help them do cool — I mean,
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that's what we do here in California, right?
That's what we do. The new frontier. Yeah. I
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think that's right. Perfect place
to do it. And we're excited to be
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able to collaborate on a few of these things.
Absolutely. I love many things, but what I love
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about it most is these ambitions are not small.
Human health and disease and planetary health are
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pretty big topics. I don't think anyone would
doubt that you could make an impact in those.
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Why don't we start maybe with this amazing story
that hit the headlines in this last year with the
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collaboration that you helped put together and the
teams that came together for baby KJ. How did that
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come about? And tell us how things are going.
It's an incredible story, isn't it? It's so
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inspiring to see the example of a child who
was affected by a metabolic disease diagnosed
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in real time and treated with a therapy that
was created for him, for his disease. Yeah. And
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tested first in animals and in collaboration with
appropriate regulatory guidelines and his clinical
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team at the Children's Hospital of Philadelphia
figuring out how to actually treat this patient
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and ensure that he would have a safe path to what
we hope will be a permanent cure for the disease.
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It's really really exciting. You know, it's worth
pointing out that this is probably not a one-off
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case. This is an example of what is now possible
to do and it's partly inspiring to see a patient
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and his family of course treated effectively but
what's even bigger and inspiring to all of us is
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the opportunity to do that for so many more.
And the key features of that — this was CPS1
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deficiency, so this was a metabolic disease that
causes hyperammonemia and that can cause severe
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brain damage and would even be associated
with a 30 to 50% risk of death. So this
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is not a trivial condition and one that was
diagnosed pretty early in life — like two or
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three months when he was first diagnosed.
Yeah. I think even earlier. Yeah. Yeah.
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And then so many remarkable things about it. I
mean maybe in your world the least remarkable
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thing is that you can edit the genome to the
better copy. But being able to take that case
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and with the joint work with the group at CHOP
and at Penn to be able to develop this, test it,
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go through the regulatory agencies and within
— I think was it 7 months? — and then have
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an N-of-one therapy that was essentially
curative. I understand there were two or
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three doses that were given.
That's right, three. Yeah.
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But this is the ultimate in many ways. I
think that's one of the reasons it caught
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people's imagination in precision medicine.
Here is a precision surgery for the genome
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that is essentially curative of a disease
that would otherwise be fatal. I mean,
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that's incredible. It's incredible.
Yeah, it's really very exciting. And
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as you're saying, I think the inspiration
is part the effect on this individual,
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but it's also the idea that we could do this
for many others and we now have a pathway. We
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can see all of the steps that can happen and how
to do them in a period of time that's meaningful
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for the patient. It doesn't take years and
years — this was done in a matter of months.
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Right. Right.
And wouldn't that be great to do for more? I mean,
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there are thousands of these babies born every
day. And I think being able then to scale — and
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so you can see a path toward not N-of-one
just but N-of-10, N-of-100, N-of-1000. Yeah.
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And I think one of the challenges has been that
technology often moves so much faster than our
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regulatory agencies are able to. I mean, they
have a very important job — safety is incredibly
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important. It's hard when there's so few people
in the world who truly understand new technology,
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but it seems like there was a very collaborative
relationship with the FDA over this and that they
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are very open to the idea of scaling.
That's what we're seeing. It's really
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interesting to see this and I think it's partly
again that you know the FDA after all is human
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beings and they can see the potential,
they can see the opportunity. I think
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Fyodor Urnov at the IGI deserves a lot of
credit for his role in helping to educate
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regulators about the science. As you said, it's
often hard for them to keep up. There's so many
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things happening. How do they become experts in
every new technology? They really can't. Yeah.
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And so it does require scientists to go in and
say, “Look, you know, we'd like you to understand
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what we're doing. We want to work with you. We
want to partner with you. We want to do this
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in a way that makes sense for everybody.
And of course, safety has to come first.”
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Yeah, it's great that it's a conversation
because I think once you're conversing,
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it's possible to have those explanatory moments.
And I think so there was an industry partner as
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well. I think this was in this
large group that were involved.
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Yeah, it's very interesting because that
partnership existed already — you know,
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was kind of pre-existing to the diagnosis of
KJ. This is a partnership with a company called
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Danaher that makes molecules among other
things. And they are very good at it. They
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know how to make molecules that are prepared
in a way that can be delivered clinically.
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And so when the baby KJ case came along, they
stepped up and said, “Yes, we're willing to
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provide the molecules needed for this treatment
and we'll do it at our expense.” Yeah. Amazing.
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And then this was a base editor
delivered in a lipid nanoparticle.
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Right.
So it
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goes to the liver pretty naturally
which is exactly where you need the—
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Well you're touching on an important point that
I think is really good to just state here very
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clearly and that is that one of the reasons that
the baby KJ case could proceed the way it did
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was that the affected tissue — the liver — is one
that we know how to deliver molecules to. We used
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existing technologies with both CRISPR and
the delivery vehicle, the lipid nanoparticle,
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that were also pre-existing, that had been
clearly validated clinically. And so there
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was no new technology that needed to be
created. We simply had to refashion it
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for this particular case, but we know how to
do that after 10 years plus of doing this.
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And so I think that, you know, right there tells
you that when you have technology that's reached a
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place where you have off-the-shelf capabilities,
we need to get better at quickly pointing that
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to the problems where it can really be used in
real time. And that's what was so exciting here.
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Yeah.
And it sounds
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like there's openness on behalf of the regulatory
bodies to see that many of those elements can be
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repeated and maybe just the guide RNA can be
changed and you have a new therapy for a new
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creation — and this is game-changing, isn't it?
I mean, you know better than any of us — thinking
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about when you have rare genetic diseases, this
is something that you know in the past we would
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have said, well, you know, we can diagnose
it. Okay, we can maybe give palliative care,
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but we really don't have anything that's going to
provide a long-term or even potentially a cure.
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If the best outcome is a liver transplant,
then hopefully we can do better than that.
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Exactly. And this is what CRISPR has offered from
the very beginning, right? — this opportunity to
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create a targeted approach for each individual
mutation. It's just that, you know, if you have a
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rare disease where for each disease that you're
treating, you have to go through a full-blown
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three-phase clinical trial, it's not realistic,
right? I mean you don't even have the patients
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to do it even if you wanted to, and the expense
would be prohibitive. But here, I think the FDA
0:12:37.760,0:12:43.680
is saying, “Look, let's take a new lens to this.
Let's recognize that this is really a different
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kind of technology. And we're really talking
about a different kind of therapy, aren't we?”
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This is not something that you're going to be
injecting someone with every day or a month.
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Hopefully, it's a one-and-done.
One and done. Yeah.
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Remarkable. Really it's the sort of ultimate
for precision therapy and amazing that we're
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able to talk about that now. We move science to
cure. Now we just need to think about scaling.
0:13:08.160,0:13:10.560
Exactly.
So yeah, well talking about scaling — you know,
0:13:10.560,0:13:15.680
that's talking about an N-of-one therapy, but you
also have these ideas to potentially impact the
0:13:15.680,0:13:22.480
entire population or thinking about the planet
by editing the microbiome. And I realize that
0:13:22.480,0:13:27.760
you recently got a big grant with Jill Banfield
to think about microbiome editing. I spent a lot
0:13:27.760,0:13:33.200
of time thinking about genetics, genomics, and
also gene editing. I hadn't spent a lot of time
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today thinking about microbiome editing. So tell
me what's in scope for that. Essentially exciting.
0:13:38.800,0:13:43.280
Well, what's fun about microbiome editing
is it takes CRISPR back to its source.
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Yeah. Right. So maybe a lot of people know
this, but maybe they don't. CRISPR comes from
0:13:48.960,0:13:54.320
bacteria. It comes from an immune system
that bacteria evolved to fight viruses.
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So we think it's very interesting to now take that
technology and turn it back to those very microbes
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and use it in a way that allows targeted changes
to be made to particular microbes in the context
0:14:08.560,0:14:16.160
of a multi-species community — which is what a
microbiome really is — right? And doing that in
0:14:16.160,0:14:22.720
a way that could impact health and could impact —
well let's say just health writ large — you know,
0:14:22.720,0:14:28.240
health of humans, health of the planet, right?
And so that was the vision for the program that
0:14:28.240,0:14:34.480
we call BIOM, which is our TED Audacious
Fund project with Jill Banfield. And the
0:14:34.480,0:14:40.080
idea there was to create the kinds of
targeted tools that will allow CRISPR to
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work in the microbiome whether we're talking
about the human microbiome or the cow rumen.
0:14:45.600,0:14:47.600
Yeah.
What sort of
0:14:47.600,0:14:53.600
examples when you were working could you get? So
potential climate change is on the agenda here.
0:14:53.600,0:15:00.640
It's on the agenda because — and this involves
our wonderful colleagues up at UC Davis who have
0:15:00.640,0:15:06.720
for a long time been aware that the microbiome in
the cow rumen — which is where, you know, they're
0:15:06.720,0:15:12.880
digesting grass in multiple stomachs and got a
lot of microbes that are busily doing that kind
0:15:12.880,0:15:18.160
of metabolism — the problem is that some of those
bugs are also making a lot of methane. Yeah. And
0:15:18.160,0:15:23.040
that's one of the most powerful greenhouse gases
and it's like a third or something human-produced.
0:15:23.040,0:15:29.920
Shocking, right? I was astounded to learn that
agriculture and in particular cattle farming
0:15:29.920,0:15:36.320
accounts for almost a third of the methane
emitted annually that's human-caused. So,
0:15:36.320,0:15:41.680
what can we do about that? I don't think it's
realistic to ask everybody to stop cattle farming.
0:15:41.680,0:15:47.920
Yeah. Right. That's just not going to happen.
And so better would be to find a way to actually
0:15:47.920,0:15:53.600
just reduce the methane emissions at the source.
And so this is where we think CRISPR comes in
0:15:53.600,0:16:00.000
because we know we can manipulate genes in these
microbes. Increasingly, we know the genetics of
0:16:00.000,0:16:05.360
methane production in the cow rumen. And so
again, it's sort of an analogy to the baby KJ
0:16:05.360,0:16:09.600
case where we've got all the pieces, right?
We've just got to put them together to make
0:16:09.600,0:16:13.120
something that's going to have real impact.
And that's what we're doing with our BIOM
0:16:13.120,0:16:18.960
program. So we have a whole team of young
investigators. Jill Banfield is the leader,
0:16:18.960,0:16:25.200
but we've got a lot of scientists now who are
really focused on this kind of challenge working
0:16:25.200,0:16:30.480
both at the Berkeley site of IGI, but also
working up at UC Davis where they actually
0:16:30.480,0:16:36.720
are birthing calves and starting to test.
So it's great. The idea is that we would treat
0:16:36.720,0:16:43.920
individual cows. And again, the idea would be a
one-and-done kind of treatment that would then be
0:16:43.920,0:16:51.680
maintained through adjustments that wouldn't be
prohibitively expensive in the diet and would be
0:16:51.680,0:16:56.160
possible to distribute around the world.
I see. Really interesting. And then I'm
0:16:56.160,0:16:59.040
guessing — I'm just thinking this through
now as you're explaining it — but I suppose
0:16:59.040,0:17:04.640
offspring often don't inherit the microbiome,
but they are gifted much of their microbiome
0:17:04.640,0:17:09.520
from their parents at the time they're born —
mother predominantly at the time they're born.
0:17:09.520,0:17:16.000
But then the — I assume in an animal population
that there may be some chance that some treatment
0:17:16.000,0:17:20.160
of the mother might even impact…
It's an interesting question,
0:17:20.160,0:17:23.280
right? I mean that's one of the things we're
researching right now is to what extent you
0:17:23.840,0:17:30.960
get that kind of population change.
Yeah, that's really fascinating and
0:17:30.960,0:17:36.640
really CRISPR writ large indeed. This
is literally a climate-level question.
0:17:36.640,0:17:40.880
There's some human health elements to that
too. Did I see asthma maybe as one disease—
0:17:41.520,0:17:48.000
Sorry — Susan Lynch up at UCSF, you may know her
— she has had a longstanding clinical research
0:17:48.000,0:17:53.760
program on the connection between the human
microbiome and asthma. Yeah. And so we would
0:17:53.760,0:18:00.000
love to be able to also manipulate the human
microbiome to reduce asthma susceptibility.
0:18:00.000,0:18:05.600
Sounds a bit wild. I thought it was kind of a —
it sounded a bit like a long shot when we first
0:18:05.600,0:18:12.320
discussed it, but I think again the pieces are
coming together. We understand the genetics of
0:18:12.320,0:18:19.120
production of molecules in the human gut that
can induce asthma susceptibility. And now again
0:18:19.120,0:18:23.520
we have the tools to manipulate it. So you
can start to see the pieces coming together.
0:18:23.520,0:18:31.280
I think in many ways the microbiome has been
really ignored by human physicians and by the
0:18:31.280,0:18:36.000
health care system to date partly because we
haven't been able to manipulate it very well.
0:18:36.000,0:18:41.600
Obviously C. diff diarrhea has been one area of
great success. But overall, I think we've found
0:18:41.600,0:18:45.680
it fascinating from a scientific standpoint as
we learn more and more ways that the microbiome
0:18:45.680,0:18:53.040
interacts with the human part of the dual organism
and vice versa. Obviously a lot of diet-nutrition
0:18:53.040,0:18:58.960
work and our GI colleagues have been to the fore.
But some of the remarkable impacts that are seen
0:18:58.960,0:19:05.280
even on psychological conditions and psychiatric
conditions, on anxiety from the microbiome — it's
0:19:05.280,0:19:09.920
just remarkable. And I do think that we're
ready for another revolution there where we
0:19:09.920,0:19:14.080
understand that we can actually manipulate
the microbiome in a much more precise way to
0:19:14.080,0:19:18.480
help with these diseases where it's clearly
fundamental. Even responses to chemotherapy
0:19:18.480,0:19:22.320
and other trials that we've seen — the
microbiome could make a significant...
0:19:22.320,0:19:26.960
I think this science looks so interesting.
It's not my area of expertise at all,
0:19:26.960,0:19:31.440
but I'm fascinated by the increasing,
as you said, connections with different
0:19:31.440,0:19:35.200
human disease conditions. There's a lot
of fundamental science still to be done.
0:19:35.200,0:19:39.520
Yeah. But now we have the tools to do it.
We have a lot of people — you're here talking
0:19:39.520,0:19:45.840
to our trainees and many others here at Stanford
— and we have many who have thought, including
0:19:45.840,0:19:52.640
in our faculty, about moving into industry. Some
actually — this being West Coast — come back from
0:19:52.640,0:19:57.760
industry back to academia. We have pretty free
flow and we have many who start companies as well.
0:19:57.760,0:20:02.560
But I wondered since we have you here — you're
both somebody who spent a short time, I believe,
0:20:02.560,0:20:08.960
in industry — but also very important. And maybe
not everyone knows that story; if you want to
0:20:08.960,0:20:13.440
share, I'd love to hear that. But also you've
started companies obviously and moved technology
0:20:13.440,0:20:17.360
really into the real world. Do you have advice
for people that are thinking about that or who
0:20:17.360,0:20:25.440
are struggling with that element of what the next…
Well, it's a great question because I consider
0:20:25.440,0:20:34.880
myself the most naive person probably out there
when it comes to thinking about how to sort of
0:20:34.880,0:20:41.520
commercialize scientific discoveries. I certainly
didn't — that was not on my radar when I started
0:20:41.520,0:20:47.840
my career and even when we started working on
CRISPR it wasn't the thing that was on my mind
0:20:47.840,0:20:55.040
at all. And I had to learn about it because
I realized fairly quickly once we had done
0:20:55.040,0:21:01.520
the initial work on CRISPR that when you have
a technology that's cross-cutting like this
0:21:01.520,0:21:07.920
and you see opportunities for it to have real
impact, some of that can get done in academia.
0:21:07.920,0:21:12.800
But frankly, you're probably going
to need the teams and the financing
0:21:12.800,0:21:17.280
to do it much more broadly than would be
possible in a typical academic laboratory.
0:21:17.280,0:21:23.760
And so how to do that became top of mind for me at
that point. And I was fortunate to have a lot of
0:21:23.760,0:21:29.680
people, including a number of folks at Stanford
— I consider, by the way, I've long considered
0:21:29.680,0:21:35.120
Stanford a real leader in this. Stanford has
had a culture for a long time about how to make
0:21:35.120,0:21:41.040
that smooth transition between fundamental
discoveries and scaling that happens with
0:21:41.040,0:21:46.320
commercialization and how to do that effectively.
It's been a great journey. I can just give a
0:21:46.320,0:21:54.080
30-second summary because you alluded to my little
foray into the business world and this happened in
0:21:54.080,0:22:01.120
2009. So I had a really exciting opportunity to
move to Genentech and I decided to do it because
0:22:01.120,0:22:08.240
I felt that I was sort of mid-career at that point
and I'd been at Yale for several years before I
0:22:08.240,0:22:13.920
moved to UC Berkeley. So I'd been at two wonderful
universities. I was starting to worry a little bit
0:22:13.920,0:22:23.520
that my work although exciting on one hand was
not going to have the kind of impact — especially
0:22:23.520,0:22:27.200
in health — that I would always write about
in my NIH grants, you know? And I thought,
0:22:27.200,0:22:35.440
you know, am I really talking about that? But
yes — well — this is part of the story, right?
0:22:35.440,0:22:40.480
Because I went — I accepted the position at
Genentech and it was a bit of a tumultuous
0:22:40.480,0:22:44.560
time there. They were being purchased by Roche
at the time. And so there were lots of changes
0:22:44.560,0:22:52.240
happening. And I just realized within a few weeks
that it was, you know, a little bit like putting a
0:22:52.240,0:22:56.560
square peg in a round hole or something. You
know, I do love the academic setting in the
0:22:56.560,0:23:03.280
sense that I love the lab. I love working with
my students. I really enjoy that interchange.
0:23:03.280,0:23:08.880
So I ended up going back to Berkeley. I had taken
a leave — thankfully they took me back. Okay.
0:23:09.600,0:23:13.440
But you know an interesting thing happened
because when I went back, I had cleared my
0:23:13.440,0:23:17.600
calendar completely as you can imagine. I didn't
have any travel. I wasn't going to be there and I
0:23:17.600,0:23:21.280
didn't have any teaching, you know. And so I had —
I suddenly had — you know, I looked at my calendar
0:23:21.280,0:23:25.680
and I had like these blank days of just being
able to hang out in my lab, talk to my students,
0:23:25.680,0:23:30.400
think about things, work on things that I just
found interesting. One of them was CRISPR.
0:23:30.400,0:23:32.080
Yeah.
Because this was something
0:23:32.080,0:23:38.800
we were playing around with due to Jill Banfield
— right? Her ideas around what it might be doing.
0:23:38.800,0:23:44.720
And because of that, in part, you know, I think it
really gave us the freedom to explore some ideas
0:23:44.720,0:23:51.920
that might or might not have happened otherwise.
And so I really taught myself something
0:23:51.920,0:23:55.840
interesting in that whole process. And that
is that, you know, I think it is important
0:23:55.840,0:24:02.960
to pursue your scientific interests. I think
it's good to keep an eye toward applications
0:24:02.960,0:24:09.760
and thinking about where could this discovery
have impact. But I do think it's important to
0:24:09.760,0:24:14.640
be true to what you really love to do. And that's
kind of what I taught myself in that experience.
0:24:14.640,0:24:21.440
That's remarkable actually — the journey, the
path not traveled, you know. Yeah. But I think
0:24:21.440,0:24:26.480
this idea that you need space to be able to
think and explore and how important it is to
0:24:26.480,0:24:32.080
explore without understanding exactly where the
destination will be is really valuable. And it's
0:24:32.080,0:24:36.560
something we all love in our academic lives.
Maybe I should clear my calendar
0:24:36.560,0:24:42.720
for the next weeks. You've inspired me.
Well, talking about inspiration, I know that some
0:24:42.720,0:24:49.200
of your early inspiration toward science came from
reading books and that was certainly true for me.
0:24:49.200,0:24:55.120
Many people I think have very inspiring teachers
in school. That probably wasn't the case for me
0:24:55.120,0:24:59.520
in science, but one of my teachers did give me a
book, The Selfish Gene by Richard Dawkins, that
0:24:59.520,0:25:05.440
really — I mean — just his writing was so clear
and it just — the passion for the subject just
0:25:05.440,0:25:11.520
came across and it really lit the flame for me.
But you're really, I think, viewed of course as
0:25:11.520,0:25:16.720
one of the leading science communicators in the
world. And we're in a moment — kind of interesting
0:25:16.720,0:25:22.000
moment — where science is really under attack in
many ways and certainly science communication is
0:25:22.000,0:25:28.240
more important than ever. And I just wondered if
you had some thoughts to share about this moment
0:25:28.240,0:25:34.560
we're in, how important it is for scientists
like ourselves to be out there talking to the
0:25:34.560,0:25:39.040
real people in the world, not just the folks
in our lab but the folks at our conferences.
0:25:39.600,0:25:45.760
As scientists somewhat under attack — and it is a
fascinating moment because on the one hand we've
0:25:45.760,0:25:51.840
got more tools than ever for communication, right?
We got all kinds of social media. We've got many
0:25:51.840,0:25:58.240
people who have stepped forward as spokespeople
for science which is great. And a lot of those
0:25:58.240,0:26:04.480
folks have many followers, right? And they've
attracted a lot of attention and a big audience
0:26:04.480,0:26:10.480
on the one hand. And then on the other hand
there's a lot of frankly just false information
0:26:10.480,0:26:17.440
and disinformation that goes around. Vaccines come
to mind for example where unfortunately it does
0:26:17.440,0:26:23.040
a tremendous disservice to the science and also
to people that could otherwise benefit from it.
0:26:23.040,0:26:29.280
So what do we do? You know, and I think that it's
a tough challenge that I'm not sure there's an
0:26:29.280,0:26:36.320
easy answer to. I do think that scientists need
to be better about communicating about their
0:26:36.320,0:26:42.480
work. I don't mean that all of us need to become
national or international lecturers on the topic.
0:26:42.480,0:26:50.720
It's just that I think all of us need to figure
out where can we have an impact. It's as simple
0:26:50.720,0:26:57.200
as having a one or two sentence non-jargony
explanation of what we're doing so that when
0:26:57.200,0:27:02.480
you sit down on a plane and you're chatting with
your seatmate about what you do, you can roll that
0:27:02.480,0:27:08.000
out. Get in an elevator — you can tell somebody
quickly what you're doing and why it matters.
0:27:08.000,0:27:15.440
Unfortunately, because scientists haven't been
effectively doing that over the last few decades,
0:27:15.440,0:27:20.720
there's been a bit of an erosion of
the appreciation of science across our
0:27:20.720,0:27:27.520
country. And I think some taxpayers at least
wonder, “Yeah, why are we shelling out money
0:27:27.520,0:27:32.720
for projects on things like bacterial immune
systems? And why does that matter?” Right? And
0:27:32.720,0:27:38.240
so I think it is very important to do this.
So this is what I tell my students. I say,
0:27:38.240,0:27:44.400
“You know, figure out where you're comfortable.
You don’t have to be an author. You don’t have to
0:27:44.400,0:27:51.280
be a lecturer necessarily if you want to do that.
But just being able to tell your grandmother what
0:27:51.280,0:27:56.480
you're doing and why it matters is really key.”
I think that's something we talk about a lot
0:27:56.480,0:28:00.320
here actually. And I think an example we
often use is like your Uber driver when
0:28:00.320,0:28:04.000
you're around the country giving a talk or
something and you're often talking to your—
0:28:04.560,0:28:09.600
Exactly. It's those conversations I think can
really have an impact on people. And like you say,
0:28:09.600,0:28:13.760
just being able to understand — I often say this
to my students and trainees when they're giving
0:28:13.760,0:28:18.160
a scientific presentation — you actually want to
think about it as if you're explaining it to your
0:28:18.160,0:28:22.880
grandmother or explaining it to a family member
because that will force you into a narrative
0:28:22.880,0:28:25.920
format to sort of tell a story.
Exactly. Yeah.
0:28:25.920,0:28:29.280
And even scientists like to hear
stories. They do. They want to see
0:28:29.280,0:28:33.600
your data but they love to hear stories.
That's right. And I think that we could
0:28:33.600,0:28:38.560
all be better at that. And I think that in order
to gain a little bit of the public's trust — and
0:28:38.560,0:28:45.120
we have collectively lost some of that, whether
it's because of folks who are treating science
0:28:45.120,0:28:50.640
as something other than the rigorous approach
to truth that we know it to be or whether it's
0:28:50.640,0:28:54.720
because we're less good at communication — we
definitely have lost a step. And so either way,
0:28:54.720,0:28:58.720
I think we all do need to step up a little bit.
Agreed. Yeah.
0:28:59.280,0:29:03.200
I wanted — while I had you captive here —
to ask a specific question that there aren't
0:29:03.200,0:29:09.360
many people I could ask this to, but I was at
this — just in — some listeners may not know,
0:29:09.360,0:29:16.640
but you did your PhD with Jack Szostak at Harvard
focused on ribozymes, catalytic RNAs and studying
0:29:16.640,0:29:22.080
essentially the origins of life. And I happened
to be at a conference recently and Dante Lauretta
0:29:22.080,0:29:25.440
from Arizona was there and he had run this
mission — the OSIRIS-REx mission — where
0:29:25.440,0:29:32.400
they sent a capsule to Bennu, which is this
4½-billion-year-old asteroid, in order to capture
0:29:32.400,0:29:40.640
essentially space dust that was unimpacted,
non-contaminated by humans. It just kind of blew
0:29:40.640,0:29:48.320
my mind that they found on this asteroid that's
4½ billion years old all the nucleases and 14 of
0:29:48.320,0:29:56.560
the prebiotic amino acids and many of the things
that would be required for the origin of life. And
0:29:56.560,0:30:02.480
this is something that — where you started your
career. And I sort of have a hobby interest in
0:30:02.480,0:30:09.840
it just to read about that. But the RNA world idea
is one of the ones I think in many ways what drew
0:30:09.840,0:30:15.280
you into RNA. I wonder what you thought to that.
They just have been publishing in the last few
0:30:15.280,0:30:23.520
months these papers with this incredible prebiotic
chemistry analysis. And you must be an RNA world
0:30:23.520,0:30:29.680
person, right? Do you believe that?
Right. Yes.
0:30:29.680,0:30:33.680
It just seems like — I mean, that's one of —
I mean, we've talked about individual humans,
0:30:33.680,0:30:39.920
we've talked about planets. This is almost like,
you know, planetary-scale ideas — like thinking
0:30:39.920,0:30:44.960
about how life could actually have started.
It's such a fascinating question. Yeah. Right.
0:30:44.960,0:30:49.040
I mean it's just so interesting. When I got to
graduate school, I really didn't know what I
0:30:49.040,0:30:57.040
wanted to work on. And my adviser Jack Szostak
was brilliant at taking a huge question like
0:30:57.040,0:31:03.440
that and boiling it down to experiments that we
students could actually do in the lab. You know,
0:31:03.440,0:31:08.320
it was really interesting to me to see how you
do that, how you think about — and we try to
0:31:08.320,0:31:12.720
do this of course in our own research, right?
— as we have big questions we want to answer,
0:31:12.720,0:31:17.920
but you've got to somehow figure out how to
turn it into, you know, an experiment that
0:31:17.920,0:31:25.520
somebody can actually do in a two… you know.
And so that was my first real exposure to that
0:31:25.520,0:31:33.920
type of science. And I've never lost that
sense of wonder at, you know, the kinds of
0:31:33.920,0:31:39.360
capabilities that scientists have when they
really put themselves to a task like that.
0:31:39.360,0:31:45.360
And, you know, in the case of the RNA world —
yeah, I think it's still a really interesting
0:31:45.360,0:31:52.960
question that's not fully answered. I think we
have a good sense of the kinds of molecules that
0:31:52.960,0:32:00.000
clearly had to be around in the prebiotic Earth.
Where they came from is a question. I think this
0:32:00.000,0:32:06.240
asteroid data is fascinating, right? Because it
does kind of support the idea that Francis Crick,
0:32:06.240,0:32:12.560
I think, first proposed, which is that life
probably came from elsewhere — or at least the
0:32:12.560,0:32:17.520
components came from elsewhere — because maybe
there wasn't actually time for those molecules
0:32:17.520,0:32:25.040
to evolve here on the planet. Or to emerge, you
know, on the planet — not really known. But I
0:32:25.040,0:32:33.760
think this new evidence is certainly interesting
in terms of thinking about the origins of life.
0:32:34.720,0:32:41.680
Maybe the components arrived here and were
easy fodder for evolution to begin working on.
0:32:41.680,0:32:44.880
Maybe. Yeah. Yeah.
Just remarkable. And this idea — and
0:32:44.880,0:32:48.640
then thinking about your own journey there,
like from the prebiotic sort of chemical chaos
0:32:48.640,0:32:55.840
that was your PhD to this highly precision-based
editing and curing of individual diseases — just,
0:32:55.840,0:33:00.880
you know, it's been a remarkable journey.
It's been fun. I mean I can't imagine
0:33:00.880,0:33:07.360
having done anything else, in a way, because
it's been just such a wonderful career to be
0:33:07.360,0:33:12.080
involved in the process of discovery.
The next five or 10 years — what do you
0:33:12.080,0:33:16.400
think? Will we have — we'll have a toolbox
to use? We'll go recurrently to those?
0:33:17.440,0:33:23.120
Yeah. No, the toolbox will continue to expand.
That's for sure. You know, the capabilities will
0:33:23.120,0:33:31.520
continue to evolve. That's also for sure. I think
it's really a question of how to turn this kind of
0:33:31.520,0:33:39.120
technology now into a turnkey approach to disease.
Yeah. You know, whether we're talking about
0:33:39.120,0:33:46.080
planetary disease or human disease, it's really
about doing that in a way that becomes scalable.
0:33:46.080,0:33:52.800
And I still think there's a really important role
for academics and for nonprofits here because I
0:33:52.800,0:33:59.280
think it's pretty clear that — again, I defer to
your expertise here on the clinical side — but
0:33:59.280,0:34:02.480
humans are complicated.
Yeah, definitely agreed.
0:34:02.480,0:34:06.160
Right. And, you know, this is why — you know,
people always wonder why do so many drugs fail
0:34:06.160,0:34:12.640
in clinical trials? It's just — it's brutally
hard. And I admire people that have devoted their
0:34:12.640,0:34:18.000
careers to drug discovery because it's a really
hard problem. It's harder than anything I do,
0:34:18.000,0:34:23.200
I think. You know, right? It's — you know — our
work is the first step, but then you've got to
0:34:23.200,0:34:28.240
actually show that it works in an actual disease
situation and is safe for people to use. And,
0:34:28.240,0:34:33.200
you know, that's a whole different ballgame.
So I do think it's going to require continued
0:34:34.880,0:34:41.280
technological and scientific discovery to get
us at least closer to that goal of being able
0:34:41.280,0:34:45.920
to quickly come up with therapies that are
effective for different types of disease.
0:34:45.920,0:34:50.880
I know for you drug discoverers, you might argue
that what you do is like easier than what they do.
0:34:50.880,0:34:53.680
We're so happy to have you here. Thank
you so much for spending some time with
0:34:53.680,0:34:57.280
us. I can't think of few people who
have impacted the world currently and
0:34:57.280,0:35:00.400
more than you have in this room. It's
a pleasure to have the chance to chat.
0:35:00.400,0:35:04.800
Great to be here. Thanks again so much.
The preceding program is copyrighted by
0:35:04.800,0:35:13.200
the Board of Trustees of the Leland Stanford Jr.
University. Please visit us at med.stanford.edu.