Dr. John Charles Martin (born 1951)

John Martin in San Mateo, CA (2019) Image (Figure 1 from 2022 AntiViral Therapy journal memorial): [HP00DR][GDrive

ASSOCIATIONS

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John Charles Martin (May 7, 1951 – March 30, 2021) was an American billionaire businessman, and the former executive chairman (2016–2018) and  CEO (1996–2016) of the American biotechnology company [Gilead Sciences].[3][4] He joined Gilead Sciences in 1990 as vice president for research and development.[5][1] Gilead is known for developing drugs such as Atripla (for HIV/AIDS) and commercializing Sovaldi (sofosbuvir) for the treatment of the liver virus hepatitis C. Martin is the recipient of a number of awards, including the Biotechnology Heritage Award (2017).

Education

Martin earned a bachelor's degree in chemical engineering from Purdue University,[3] an MBA in marketing from Golden Gate University and a PhD in organic chemistry from the University of Chicago.[6] He served on the board of trustees of the latter two universities.[6]

Career

Syntex Corporation

Martin worked at Syntex Corporation from 1978 to 1984.[7]

Bristol-Myers Squibb

Martin was director of antiviral chemistry at Bristol-Myers Squibb from 1984 to 1990.[1]

Gilead Sciences Inc

External audio :   “Pandemic Perspectives with John C. Martin”, interview, Science History Institute, May 5, 2020.

Martin joined the American biotechnology company [Gilead Sciences] in 1990 as its vice president for research and development.[7] He was Gilead's CEO from 1996 to 2016.[6][3] He became chairman in May 2008, and executive chairman in 2016.[3][7]

At Gilead, Martin helped to develop Atripla, a single pill combining Gilead's drug Truvada (a combination of tenofovir and emtricitabine) with Bristol-Myers Squibb's Sustiva (efavirenz). Truvada and Sustiva were already "the most widely prescribed antiretroviral treatment regimen in the U.S."[8] for the treatment of HIV and AIDS.[9] One of the benefits of a combined pill was that patients would be more likely to consistently comply with treatment by taking a full dose of the prescribed drugs, which in turn would lessen the chance that drug-resistant HIV strains would develop.[8] The two companies announced that they would collaborate on the drug in 2004. An initial formulation of once-a-day single-dose Atripla was approved by the FDA on July 12, 2006.[10] Purchase of Atripla was included in the President's Emergency Plan for AIDS Relief (PEPFAR) program.[11]

In 2014, Martin led the commercialization of Sovaldi (sofosbuvir) — "a treatment for the liver virus hepatitis C that can cure 90% of patients and generated $12 billion in revenue in its first year on the market."[1] Martin is credited with taking Sovaldi from "zero-to-blockbuster in a couple of months" with profits topping $10 billion for 2014.[12] However, in April 2014, U.S. House Democrats  Henry Waxman, Frank Pallone Jr., and Diana DeGette wrote Martin questioning the $84,000 price for Sovaldi. They specifically asked Martin to "explain how the drug was priced, what discounts are being made available to low-income patients and government health programs, and the potential impact to public health by insurers blocking or delaying access to the medicine because of its cost."[13]

Sofosbuvir is cited as an example of how specialty drugs present both benefits and challenges.[14][13][15]

Sofosbuvir also is an excellent example of both the benefit and the challenge of specialty medications. On one hand, this agent offers up to a 95% response rate as part of an interferon-free treatment regimen for hepatitis C.6Generally speaking, it is more effective and better tolerated than alternative treatments.6 Unfortunately, the current per pill cost—$1,000—results in an $84,000 treatment course, creating barriers to therapy for many.6 Patients, providers, and payors alike have expressed outrage, and the debate has even drawn the attention of the US Congress.7 Despite these concerns, sofosbuvir rapidly has become a top seller in the United States. ...[14]

Appointments

Martin was president of the International Society for Antiviral Research (1998-2000); chairman of the California Healthcare Institute (2005-2006, 2009); and chairman of BayBio (1999-2001).[7]

Martin has worked with the Federal government of the United States in a number of capacities. Martin served on the council of the National Institute of Allergy and Infectious Diseases (2000-2003). He was part of the Centers for Disease Control and Prevention/Health Resources and Services Administration's Advisory Committee on HIV and STD Prevention and Treatment (2004-2007). He was on the Presidential Advisory Council on HIV/AIDS (2006-2009).[7]

In May 2018, Martin joined the board of directors at The Scripps Research Institute.[16]

Awards

Personal life

Martin was married, and lived in Hillsborough, California.[2] He died on March 30, 2021 at a hospital in Palo Alto, California from head injuries sustained after a fall.[21]

References

2021 (April 21) - NYTimes : "John C. Martin, 69, Dies; Led Drugmaker in Breakthroughs ; A chemist by training, he turned Gilead Sciences into a leading, and lucrative, innovator with single-pill treatments for H.I.V. and hepatitis C."

By Sam Roberts  /  April 27, 2021  /  Saved as PDF : [HN02AG][GDrive

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John C. Martin, who became a billionaire by developing and marketing a daily single-dose pill that transformed H.I.V. into a manageable disease and who popularized another drug that cures hepatitis C, died on March 30 in Palo Alto, Calif. He was 69.

His death, in a hospital, was confirmed by [Gilead Sciences], based in Foster City, Calif., where he was chief executive from 1996 to 2016 and executive chairman from 2016 until he retired two years later. The cause was head injuries suffered the day before, when he fell on a sidewalk while walking home in Old Palo Alto, according to the Santa Clara County medical examiner.

A chemist who rocketed from research director to chief executive of Gilead in six years, Dr. Martin turned a struggling pharmaceutical firm with a staff of 35 into a $100 billion company based in Foster City, Calif., with some 12,000 employees.

Gilead jolted the industry with several major scientific breakthroughs, beginning with the development of the first anti-influenza pill, Tamiflu, which the company licensed to the Swiss drugmaker Hoffman-La Roche in 1996. Its advance against hepatitis C came in 2014, with the marketing of Sovaldi, which has been said to cure 90 percent of patients with that liver virus.

Gilead’s work on H.I.V. began to bear fruit in 2004, when its Truvada was approved to treat the virus; the drug went on to gain approval as a means to prevent H.I.V. infection in 2012.

The company’s biggest advance on the H.I.V. front came in 2006, with Atripla, which combined Truvada with Bristol-Myers Squibb’s Sustiva in a single pill, replacing as many as 32 separate medications that some patients were taking daily to treat the virus, which can lead to AIDS.

The single-pill treatment was meant to be more than a convenience. By making it easier for patients to self-medicate, they were more likely to take the full doses that were prescribed, reducing the risk that they could become breeding grounds for drug-resistant strains of the disease.

During Dr. Martin’s tenure, Gilead also created remdesivir in 2009, which proved ineffective in its original mission, to treat hepatitis C and other viruses, but which turned out to be a therapeutic weapon during the Covid-19 pandemic.

A truck circled Gilead’s headquarters in Foster City, Calif., in 2012 to protest the high cost of the company’s anti-H.I.V. drugs. Credit...  Noah Berger/Associated Press, via AIDS Healthcare Foundation Saved image : [HN02AI][GDrive

While the company’s annual revenue soared past $20 billion and its products were hailed as medical miracles, the federal Department of Health and Human Services claimed that Gilead had infringed government patents in making Truvada. (That case is still pending.) The company also drew fire from state and federal regulators over the prices it charged — $1,000 a month for Sustiva and $1,000 for each hepatitis pill.

Dr. Martin defended Gilead in an opinion article in The Wall Street Journal in 2017. He argued, among other things, that high prices for successful products were needed to subsidize future research.

The company’s defenders also pointed out that Gilead had donated drugs in some cases and that it had partnered with local manufacturers in developing countries to produce discounted generic versions of some treatments for H.I.V. and hepatitis C.

“John’s legacy,” Daniel O’Day, the company’s chief executive, said in a statement, “will be felt for generations to come, living on through the scientific progress made under his leadership and the programs he championed that expanded access to medications for people around the world.”

John Charles Martin was born on May 7, 1951, in Easton, Pa., the son of Tellis Alexander Martin, a chemist for Bristol-Myers, and Janet (Sacks) Martin, who taught chemistry, physics and computer literacy at a prep school in Indiana.

Mr. Martin earned a bachelor’s degree in chemical engineering from Purdue University, where he met Rosemary Carella at a party; they married in 1977 and each earned a master’s degree (his in business administration and marketing) from Golden Gate University in San Francisco. He later received a doctorate in organic chemistry from the University of Chicago.

After working at Syntex Corporation, another drugmaker, from 1978 to 1984, Mr. Martin was director of antiviral chemistry at Bristol-Myers Squibb until 1990, when he joined Gilead.

As chief executive, he and John Milligan, who would become his successor, engineered the $11 billion takeover of Pharmasset, a developer of antiviral drugs, in 2012. In addition to running Gilead, Dr. Martin was president of the International Society for Antiviral Research from 1998 to 2000.

His marriage to Ms. Martin ended in divorce. Among his survivors are their son and daughter, his three siblings and his partner, Lillian Lien-Li Lou, who was listed in a recent filing as the secretary-treasury of the John C. Martin Foundation, whose stated mission is to improve health care for medically-underserved populations.

Commentary/Memorial for John C. Martin (1951–2021) in May 2, 2022, Antiviral Therapy

Show all authors :   Lillian L Lou, Amy Flood, Taiyin Yang, 

First Published May 2, 2022 Article Commentary  

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https://doi.org/10.1177/13596535211067895 

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John Charles Martin, a chemist, longtime chief executive officer of the biopharmaceutical company Gilead Sciences, and more recently, a philanthropist and global health advocate dedicated to addressing health disparities in communities around the world passed away on 30 March 2021.

John was born in Easton, Pennsylvania, on 7 May 1951 to Dr Tellis Alexander Martin and Janet Sacks Martin, both chemists by training. Growing up as the eldest of four children in Evansville, Indiana, John’s first of many subsequent jobs was picking strawberries. Seemingly unrelated to the career path he would take, his work ethic, humility, and perseverance were evident even at a very young age.

College took John to Purdue University, where he graduated with honors in Chemical Engineering (1973). Continuing on to University of Chicago and joining the laboratory of Professor Josef (Gus) Fried, John worked on the synthesis of prostaglandins, where he solved many unique synthetic chemistry challenges [1]. After receiving his PhD in organic chemistry (1977), John joined Syntex in Palo Alto and quickly advanced to section leader in drug discovery. During this time, John attended evening classes and earned an MBA from Golden Gate University in San Francisco (1984), an experience that years later led him to design and implement an onsite and subsidized MBA program for employees of Gilead Sciences, many of whom would neither have had the time nor resources to advance their education. This program was one of many examples of John’s unwavering focus on supporting the development of his employees, in all roles and at all levels.

A creative and prolific synthetic chemist, John, had an extraordinary ability to mentally visualize the orientation and symmetry of atoms and molecules in 3 dimensions. At Syntex, he continued to invent new chemistries to allow efficient synthesis of complex molecules [2,3]. He synthesized ganciclovir, thus co-inventing the first acyclic nucleoside antiviral drug to treat and prevent infections caused by cytomegalovirus [46]. This drug and its prodrug remain cornerstones in the management of cytomegalovirus infections today [7]. John joined Bristol Myers in 1984 to lead its antiviral and anti-infective research programs in Syracuse, New York, where he directed the development and eventual licensure of two dideoxynucleoside antivirals to treat HIV/AIDS—didanosine and stavudine [811]. While at Bristol Myers, John initiated collaborations with Professors Antonín (Tony) Holý in Prague and Erik De Clercq in Leuven, and together they forged the new field of nucleotide antivirals [12].

Innovative science to fulfill unmet medical needs

In 1990, John joined the then early-stage biotechnology company Gilead Sciences in California and led the evolution of its research. John’s first accomplishment was negotiating rights from Tony and Erik to a library of nucleotide analogs. After sustained research and development of these compounds [13,14], Gilead was transformed to become the world’s powerhouse of antiviral drug manufacturing and commercialization [1521]. Gilead’s continuous success drove the productivity level of an entire industry and, most importantly, reduced life-threatening viral infections to manageable chronic diseases.

In 1996, John was appointed Gilead’s chief executive officer, a role he would hold for the next 20 years. During that timeframe, John launched 20 innovative medicines, made Gilead drugs accessible to millions of patients in developing countries, and ncreased the company value 140-fold to 120 billion USD. He was appointed Chairman of Gilead’s Board of Directors in 2008 and would remain in that role until 2019. His tenure and leadership at Gilead was—and will continue to be—nothing short of legendary. Under his leadership, the company developed multiple breakthrough medicines, perhaps most notably for people with HIV, hepatitis B and hepatitis C. These inventions changed the treatment paradigm; John’s leadership reshaped the foundation of global access to life-saving therapies.

To simplify HIV treatment, John directed Gilead in forming an unprecedented partnership between three companies, that led to the creation of the first single tablet regimen of three best-in-class anti-HIV medicines formulated into one pill dosed once daily [22]. This single tablet regimen, approved by the FDA in 2006, transformed the care of people living with HIV by avoiding regimens of multiple pills that made compliance challenging and led to the potential for drug-resisting treatment failures [19]. A few years later, following John’s vision, the company gained regulatory approval for the first HIV medication indicated to prevent the transmission of the infection, an approach known as pre-exposure prophylaxis, or PrEP, for people at risk for HIV infection [16,18,23]. To continually advance patient care, John’s directive was that “we must continue to innovate to make our own products obsolete,” such that each innovation improved on the prior advance. Meanwhile, John turned his focus to curing hepatitis C with an unwavering conviction and put Gilead in the lead to bring to patients several ground-breaking, safe and curative regimens, essentially eliminating the need for liver transplantation caused by hepatitis C [20].

Figure 2. John Martin, Lillian Lou, Laura Lehman, and Richard Whitley on Little Cumberland Island, GA (2007) Image (Figure 2): [HP00DS][GDrive

Providing medicines to fulfill unmet access needs

John’s pursuit of innovative science expanded into pioneering solutions for global health. In 2003, when John traveled to Africa with Tommy Thompson (then the U.S. Secretary of Health and Human Services) he was struck by the immense devastation HIV/AIDS was having across the continent. He recognized that this devastation extended beyond human lives, impacting economies and societies as a whole. There was no precedent or blueprint for how a company could enable equitable access, but Gilead forged the path under John’s leadership. He directed the design of a revolutionary access program that would deliver the company’s HIV treatments to more than 130 resource-limited countries. This access program provides licenses and technology transfers to generic manufacturers in India and other countries, thus enabling the licensees to rapidly produce quality drug products in high volume and at low cost [24]. The program later extended beyond HIV to include Gilead’s medicines for viral hepatitis B and C [25]. Today, more than 18 million people in low-income countries around the world receive these life-saving medicines each day, owing to John’s business ingenuity, engineering excellence and kind-heartedness.

John’s commitment to addressing health disparities was fueled by a deep understanding that can only come from first-hand experience. He met with healthcare providers, public policy experts, and community workers, whether in low-income countries or devastated neighborhoods in the United States, to develop a better understanding of the barriers individuals faced daily. John stimulated the formation of the Gilead Foundation in 1995 for improving health and well-being in underserved communities around the world. Separately, in 2014, John established his private foundation, the John C. Martin Foundation, with the goal of facilitating the establishment of sustainable improvement of health care for populations in socially and economically disadvantaged settings (https://thejcmfoundation.org) [26,27].

Recognitions and services

John was widely recognized for his scientific and global health contributions to humanity. He received many awards, including the Horace S. Isbell Award from the Carbohydrate Division of the American Chemical Society (1990), the Gertrude Elion Memorial Lecture Award from the International Society for Antiviral Research (2003), the Lifetime Achievement Award for Public Service from the Institute of Human Virology at the University of Maryland School of Medicine (2014), the Biotechnology Heritage Award from the Biotechnology Industry Organization (2017), the Stanford Medicine Lifetime Achievement Award for contributions to science benefitting humanity (2019), and the National Academy of Sciences Award for Chemistry in Service to Society (2019). He was elected to the National Academy of Engineering in 2008.

In addition, John was honored by Belgium’s Order of the Crown (2017), Senegal’s Order of the Lion (2017), and the Republic of Georgia’s Golden Fleece (2017). He accepted Honorary Doctoral Degrees from Katholieke University Leuven (2017) and The Scripps Research Institute (2019).

John’s expertise was widely sought after through many private and public sector appointments. John was president of the International Society for Antiviral Research (1998–2000) and chaired two leading industry organizations (California Healthcare Institute, 2005–2006 and 2009 and BayBio, 1999–2001). He served on the boards of Golden Gate University, University of Southern California, University of Chicago, University of California School of Global Health, The Scripps Research Institute, [Sarepta Therapeutics (AVI BioPharma)], Leyden Labs, and Kronos Bio. He was a member of the National Academy of Engineering’s COVID-19 Call to Action Committee (2020–2021), and National Academies of Sciences, Engineering, and Medicine’s Board on Global Health (2020–2021), and Committee on Advancing Pandemic and Seasonal Influenza Vaccine Preparedness and Response—Vaccine Research and Development (2021). John’s public service included the National institute of Allergy and Infectious Diseases Council and AIDS Research Advisory Committee (2000–2003), the U.S. Centers for Disease Control and Prevention Health Resources and Services Administration’s Advisory Committee on HIV and STD Prevention and Treatment (2004–2007), and the Presidential Advisory Council on HIV/AIDS (2006–2009).

A quiet, unassuming force, John was a visionary leader, an admired mentor, a trusted friend, a loving father, and an endearing partner (Figure 2). His overwhelming generosity and humility remained notable characteristics. Never one to seek the spotlight, he took great joy in celebrating others’ accomplishments, even when those accomplishments were achieved through his steady guidance and support. His brilliance changed forever what a diagnosis of HIV or viral hepatitis mean, and his commitment to helping people around the world never faltered.

Summary

We celebrate the life and contributions of John C. Martin. His impact on the treatment of life-threatening viral infections will endure forever. Let all who read this Commentary continue the outstanding global work he initiated.

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iDs

References

  1. Ghosh, SS, Martin, JC, Fried, J. A total synthesis of the methyl ester of the 9,11-dithia analogue of l3,14-dehydro-PGH2. J Org Chem 1987; 52:862–876.  (   Google Scholar | Crossref   )
  2. Martin, JC . A heterocylic diels-alder approach to the synthesis of the pyridine C ring of streptonigrin. J Org Chem 1982; 47:3761–3763.   ( Google Scholar | Crossref   )
  3. Madhavan, GVB, Martin, JC. A novel and stereospecific synthesis of (±)- and (-)-aristeromycin. J Org Chem 1986; 51:1287–1293.   (  Google Scholar | Crossref   )
  4. Martin, JC, Dvorak, GA, Smee, DF, Matthews, TR, Verheyden, JP. 9-[(1,3-Dihydroxy-2-propoxy)methyl]guanine: a new potent and selective antiherpes agent. J Med Chem 1983; 26:759–761.   (  Google Scholar | Crossref | Medline   )
  5. Smee, DF, Martin, JC, Verheyden, JP, Matthews, TR. Anti-herpesvirus activity of the acyclic nucleoside 9-(1,3-dihydroxy-2-propoxymethyl)guanine. Antimicrob. Agents Chemother 1983; 23:676–682.   ( Google Scholar | Crossref | Medline )
  6. Prisbe, EJ, Martin, JC, McGee, DP, et al. Synthesis and antiherpes virus activity of phosphate and phosphonate derivatives of 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine. J Med Chem 1986; 29:671–675.   ( Google Scholar | Crossref | Medline )
  7. Whitley, RJ . Development of Therapeutics for Congenital Cytomegalovirus Infection. NewYork, NY: Springer.   ( Google Scholar )
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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357487/


Curr Res Pharmacol Drug Discov. 2021; 2: 100045.

Published online 2021 Aug 12. doi: 10.1016/j.crphar.2021.100045

PMCID: PMC8357487

PMID: 34870151

Comparison of anti-SARS-CoV-2 activity and intracellular metabolism of remdesivir and its parent nucleoside

Sijia Tao, Keivan Zandi, Leda Bassit, Yee Tsuey Ong, Kiran Verma, Peng Liu, Jessica A. Downs-Bowen, Tamara McBrayer, Julia C. LeCher, James J. Kohler, Philip R. Tedbury, Baek Kim, Franck Amblard, Stefan G. Sarafianos, and Raymond F. Schinazi

Author information Article notes Copyright and License information Disclaimer

This article has been cited by other articles in PMC.

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Abstract

Remdesivir, a monophosphate prodrug of nucleoside analog GS-441524, is widely used for the treatment of moderate to severe COVID-19. It has been suggested to use GS-441524 instead of remdesivir in the clinic and in new inhalation formulations. Thus, we compared the anti-SARS-CoV-2 activity of remdesivir and GS-441524 in Vero E6, Vero CCL-81, Calu-3, Caco-2 ​cells, and anti-HCoV-OC43 activity in Huh-7 ​cells. We also compared the cellular pharmacology of these two compounds in Vero E6, Vero CCL-81, Calu-3, Caco-2, Huh-7, 293T, BHK-21, 3T3 and human airway epithelial (HAE) cells. Overall, remdesivir exhibited greater potency and superior intracellular metabolism than GS-441524 except in Vero E6 and Vero CCL-81 ​cells.

Keywords: COVID-19, Antiviral agents, Coronavirus, Anti-SARS-CoV-2, Remdesivir, GS-441524, HCoV-OC43, Pharmacology

Abbreviations: COVID-19, coronavirus disease 2019; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; HAE, human airway epithelial; WHO, World Health Organization; CES1, carboxylesterase 1; CatA, cathepsin A; HINT1, histidine triad nucleotide-binding protein 1; MP, monophosphate; DP, diphosphate; TP, triphosphate; NTP, nucleoside triphosphate; icSARS-CoV-2-mNG, SARS-CoV-2 infectious clone virus containing mNeonGreen reporter; ACE2, angiotensin-converting enzyme 2

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Acknowledgements

This work was supported by NIH grants R01-AI-141327 (BK and RFS), and in part by the Emory Center for AIDS Research P30-AI-050409 (RFS) and R01-AI-121315 (SGS) grants. The Nahmias-Schinazi Chair fund is also acknowledged (SGS). We thank World Reference Center for Emerging Viruses and Arboviruses (WRCEVA) and Dr. Pei-Yong Shi from the University of Texas Medical Branch for providing icSARS-CoV-2-mNG. This paper is dedicated to the memory of our friend and colleague Dr. John C. Martin whose leadership in the field of antiviral agents led to the development of remdesivir for Ebola and more recently for COVID-19.

https://www.sciencehistory.org/distillations/podcast/interview-with-john-c-martin

2020-05-05-sciencehistory-org-distillations-podcast-john-c-martin-transcript.pdf

2020-05-05-sciencehistory-org-distillations-podcast-john-c-martin-transcript-img-1.jpg

Interview with John C. MartinThe former CEO of Gilead Sciences tells us about remdesivir, an older drug showing promise in the fight against COVID-19.
Episode 247 | May 5, 2020

gilead-johnmartin-ap_crop.jpgFormer Gilead CEO John C. Martin holds bottle of TruvadaFormer Gilead CEO John C. Martin holds a bottle of Truvada.Over the next several weeks Distillationswill be talking to people with special insight into the coronavirus crisis—biomedical researchers, physicians, public health experts, and historians.
In this episode we speak with John C. Martin, a biomedical researcher and former CEO of Gilead Sciences. Gilead is a pharmaceutical giant best known for its antiviral therapies for HIV/AIDS and hepatitis, but it’s also the company behind remdesivir, an antiviral drug that has recently made headlines as a possible treatment for COVID-19.
Martin talked to senior producer Mariel Carr about remdesivir, antiviral treatments for HIV and other illnesses, and working with Anthony “Tony” Fauci.
For more information about John C. Martin, see the Science History Institute’s oral history interview.
Credits  |  Research Notes  |  Transcript
CreditsHosts: Alexis Pedrick and Elisabeth Berry DragoSenior Producer: Mariel CarrProducer: Rigoberto HernandezResearcher: Jessica WadeMusic: "Balti," "Tuck and Point," and "Slimheart" by Blue Dot Sessions.Image: Former Gilead CEO John C. Martin holds bottle of Truvada (Paul Sakuma/Associated Press)
Research Notes"Fauci: New Drug Remdesivir Cuts Down Coronavirus Recovery Time," NBC Nightly News. April 29, 2020.

TranscriptAlexis: Hello and welcome to Distillations. I’m Alexis Pedrick.
Lisa: And I’m Lisa Berry Drago. In our former lives, you know, way back years and years ago in the before times …
Alexis: Actually, Lisa, I think it’s really only been like six or seven weeks.
Lisa: Ah, if you say so. Well, anyway, what I’m trying to say is that usually here at Distillations, we dive into stories that while relevant to our lives now, either happened in the past or are just around us all the time.
Alexis: Like migraines or rare earth elements.
Lisa: We aren’t used to talking about anything close to breaking news. But since we’re a podcast that talks about the role of science in our lives, we couldn’t ignore the elephant in the self-isolated room, COVID-19.
Alexis: So we’ve been working on a brand-new series focused entirely on the coronavirus. Over the next several weeks we’ll be bringing you interviews with people working at the heart of the crisis, including biomedical researchers, physicians, public health experts, and yes, historians too.
Lisa: This first episode is with John C. Martin, a biomedical researcher and the former CEO of Gilead Sciences. Gilead is a pharmaceutical giant that focuses on antiviral therapies, namely, for HIV and AIDS, but they’re also the company behind remdesivir, an antiviral drug that has recently made headlines for being a hopeful treatment for COVID-19.
Alexis: John Martin talked to our senior producer, Mariel Carr, about remdesivir antiviral treatments for HIV and working with Anthony Fauci.
Mariel: Thank you so much for joining us. Please introduce yourself for us.
John Martin: Yeah. My name’s John Martin. I’m a scientist trained in organic chemistry that worked the last four decades in medicinal chemistry for a variety of companies. Most prominently, I started 30 years ago when Gilead was a very small company. I’d led the development of that to be an antiviral powerhouse that has really changed medicine, in HIV, viral hepatitis, influenza, and other diseases.
Mariel: So I have to tell you that I just 10 minutes ago said, let me just check the news and see if there’s anything relevant that has recently happened. And I saw the news about remdesivir. I’m not pronouncing that correctly.
John Martin: Yeah, that’s close, remdesivir.
NBC Archival: For doctors and nurses on the front lines a new weapon in the fight against COVID-19: an antiviral medication proven effective in clinical trials. Dr. Fauci announced a breakthrough at the White House.
Mariel: So I thought that was a funny coincidence to sort of hit the news right before we were talking.
John Martin: Perfect.
Mariel: I wish I could say I planned it this way.
John Martin: Tony Fauci is just now in the White House with the Louisiana governor talking about it.
NBC Archival: (Dr. Fauci) The data shows that remdesivir has a clear-cut, significant positive effect in diminishing the time to recovery. This is really quite important.
(Newscaster) The drug is remdesivir made by Gilead Sciences. It comes in IV form administered to the sickest COVID patients. The drug trials involved nearly 1,100 people worldwide. The preliminary NIH data showed remdesivir cut the recovery time in the hospital from 15 to 11 days.
John Martin: The news this week is apparently the news we’ve been waiting for, and I look forward to hearing the scientific details, which presumably will come out over the course of today and this week. You know, publications are coming out very rapidly. With electronic publication we see data analysis almost published in real time, and it’s important for scientists to actually see the published data to be able to analyze and interpret what these results mean.
Mariel: So Gilead is best known for antivirals to treat and prevent HIV, hepatitis. It’s actually—I only recently learned—also behind Tamiflu. Where does remdesivir fit into its history?
John Martin: Tamiflu came along a couple of years before big pandemic flu, but less than 20 years ago it led to stockpiling all around the world.
Most of my colleagues, we still travel with Tamiflu when we go internationally because it works for treatment and prevention. Hopefully there’ll be a solution like that eventually to coronavirus in addition to the vaccine.
Mariel: Right.
John Martin: Most people get a flu vaccine every year, but there’s still a disease that we need treatment and pill prevention for.
So remdesivir came out of a respiratory program at Gilead quite a few years ago that was looking for activity against one of the common respiratory viruses, respiratory syncytial virus. But in that program, specifically remdesivir was discovered as a broad-spectrum antiviral against many of the pandemic viruses that are emerging.
And so a good example is, of course, SARS, which happened about 15 years ago, 17 years ago. It’s active against MERS. And importantly, there were studies for Ebola when we were concerned Ebola could spread to the United States. And it was at that time that Gilead made a substantial stockpile  of remdesivir to prepare for potential Ebola outbreaks and also awareness of coronaviruses, for instance, for when MERS became a problem in the Middle East and Korea. So that stockpile being on hand is what allowed Gilead to respond quite rapidly to this current pandemic. And as you know, there’ve been a lot of studies, some of them in ill patients, very ill patients where you wouldn’t necessarily expect to see a benefit.
And I can give the example of Tamiflu. Influenza is a very rapid infection, and Tamiflu to be efficacious against influenza needs to be given within the first 48 hours of symptoms.
Mariel: Yeah, this winter both my husband, well, first my husband got the flu, and then as soon as I felt like the first sniffle, I was able to get Tamiflu.
He was unfortunately not able to do that. But you know, I just talked to my doctor, and she was like, yup, here you go.
John Martin: Yup. Well that’s perfect because if, you know, if you take it right away, if you take it within two days, you reduce symptoms, but if you take it right away or take it before you have symptoms, you have a much better outcome of course.
So you had that personal experience.
Mariel: So just back to remdesivir for a minute, and just to clarify. It’s a drug that’s been around for a while, and it’s been investigated. But it’s never actually, it hasn’t really been used anywhere yet.
John Martin: Yup. Only studied. It’s not approved anywhere in the world. It was originally being investigated for a very common respiratory pathogen called respiratory syncytial virus, but it didn’t move forward for that indication.
And then it was studied for emerging viruses like coronaviruses, like Ebola, but it hadn’t found its place in those infections either. And part of it, uh, the diseases in the past have been self-limiting. As you know, SARS was contained and went away. MERS was also contained. It started in the Middle East, and there was a serious outbreak in Korea, but it didn’t really get beyond that.
So this is unique in the time that remdesivir has been studied that there’s such a serious outbreak that’s affecting society so dramatically.
Mariel: So is it too soon to say, like, does it seem like this will be effective for coronavirus?
John Martin: Well, we haven’t seen the data yet, but it was announced today that it was effective in the NIH study.
And I’d just like to point out your experience with Tamiflu versus your husband’s, how you need to take it early. And most of the studies with remdesivir have been people who were quite ill, and we don’t know a lot about how the coronavirus progresses, but we do know influenza, by the time people are in the hospital, it’s for inflammation in the lungs due to the virus, secondary infections. If you want to head that off, you want to treat a virus early in the course of the disease before the disease gets bad. Your immune system is causing a lot of the problems in your body because it fights the virus. If you stop the virus replication early, you reduce, you can prevent the development of serious symptoms with influenza.
Mariel: So, um, I’m going to back up a little bit. So, you know, the average person is sort of living through this pandemic right now, and it feels like, to people that are not, you know, in the field of medicine or in science, that this kind of came out of nowhere. But talk to me about what it’s like for someone like you.
Is this out of nowhere, or is this sort of, you knew this was coming or something like this?
John Martin: Well, there’ve been a number of these pandemics, and they always seem acute when they happen and we all get, uh, fairly scared. This particular coronavirus, it caught everyone by surprise because it is so contagious.
And what wasn’t realized at first is people without symptoms can still transmit the virus. So there’ve been a number of scholarly papers now that half the people who get infected by the virus are infected by someone without symptoms yet. And the vast majority of people, you know, recover very well from infections, including maybe half who never even developed symptoms.
So for most people it’s not that dangerous. But again, what is unique—for a small number of people it’s highly fatal. And the medical system has struggled and worried about being overwhelmed across the country. And of course that did happen in some hospitals in New York, but broadly that hasn’t happened because of all the shelter-in-place rules that have been put out by states. There’s also, you know, examples of other countries that have controlled it in different ways. So this is a pandemic that we’re learning more about every day, and it’s the uncertainty and unknowns that make us all worried very much about our personal safety.
Mariel: Yeah. So I noticed that you called Anthony Fauci, Tony Fauci. So this is someone who’s been a government scientist for decades, and all of a sudden …
John Martin: I’ve worked with him since the 1980s. He’s always been there.
Mariel: Right. And he’s sort of a celebrity now to the average person. Tell me a little bit about him and working with him and …
John Martin: Well, he’s not different than what everyone sees on TV.
He’s a dedicated public servant. He’s been involved in every activity that has been in infectious diseases for decades. When I started working on HIV and other viruses in the 1980s, I got to know him back then. So for nearly 40 years we’ve lived in a similar world. He, he’s been famous over and over as we’ve had these things happen.
I’m pretty sure he’s testified in front of Congress hundreds of times. I gave a talk in 2007 to several thousand infectious disease doctors, and one of my slides was a quote from Fauci on HIV. “We won’t be judged on our last 25 years of success but our next 25 years of success.” So he’s always been that type of visionary person that, uh, it’s very important for the nation.
Mariel: How do you think the world is going to be different after this? Will science be different? Will the way that we do basic research or even just the way that people think about it, do you think that’ll change?
John Martin: What I feel is that science progresses so rapidly, that this will only fuel that rapid change of scientific innovation.
Who would have thought five years ago, we’d have so much going on on gene therapy as we do today. The vaccine technology, a lot of the vaccine technology that’s being done now. There’s technology that’s novel that didn’t exist five years ago that allows for these very rapid vaccines to be developed. But I’m always an optimist.
But the attention and advances in science are coming at such a phenomenal rate now that I believe that will continue. My concern of course is sort of the people I work with; we’re all very busy. We’re figuring out ways to be efficient and with, you know, embracing different types of technology, but to, you know, how to open up the economy, get people back to work.
What is going to be the standard of how we work together? All that’s evolving in real time. My concern is not necessarily scientific; it’s more just one we face as a society—how do we get organized to get on with our lives?
Mariel: Thank you so much for taking the time to talk with us.
Lisa: Thanks for listening to the first installment of our special new series Pandemic Perspectives.
Alexis: We’ll be bringing you more interviews from all sides of this crisis. So stay tuned and watch your feeds.
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