About Us
Mission, Vision & Values
Rocket’s unique set of core values – “Trust,” “Curiosity,” ”Generosity” and “Elevate” – is a true beacon of hope within and outside the company. Trust is the bedrock, the ground upon which everything is built. Generosity and curiosity, derived from the same root words as “gene” and “cure,” describe a spirit of giving, aspiring for something greater than oneself, and humility in the search for excellence. Ultimately, the company’s associates and partners seek to elevate themselves, one another and the lives of patients and families around the world through gene therapy.
Trust
Generosity
Curiosity
Elevate
“For the first time in the history of our species, we are discussing not just effective treatments but potentially total cures at the genetic level, which is the deepest essence of who we are as physical living beings.”
— Gaurav Shah, MD
History
Rocket becomes incorporated with initial idea and funding from RTW Investments
Gaurav Shah, MD becomes CEO of Rocket
Rocket closes Series A financing
Jonathan Schwartz, MD and Kinnari Patel, PharmD, MBA join Rocket team
Rocket licenses Pyruvate Kinase Deficiency (PKD) program
The growing team moves to the Alexandria Center of Life Sciences in NYC
Rocket licenses Fanconi Anemia (FA) program
Rocket licenses Danon Disease program
Rocket licenses Leukocyte Adhesion Deficiency-I (LAD-I) program
Rocket closes Series B financing
Rocket goes public with only 12 employees
Rocket announces first clinical data for Fanconi Anemia (FA) program at American Society of Gene and Cell Therapy (ASGCT) annual meeting
Rocket licenses Infantile Malignant Osteopetrosis (IMO) program
Rocket headquarters moves to Empire State Building
IND for Fanconi Anemia accepted by U.S. Food and Drug Administration
Rocket announces the Danon Disease program
IND for Leukocyte Adhesion Deficiency-I (LAD-I) accepted by U.S. Food and Drug Administration
IND for Danon Disease accepted by U.S. Food and Drug Administration
Rocket hosts inaugural Rare Disease Day
IND for Pyruvate Kinase Deficiency (PKD) accepted by U.S. Food and Drug Administration
Rocket announces first clinical data for Leukocyte Adhesion Deficiency – I (LAD-I) program at American Society of Hematology (ASH) Annual Meeting
Rocket opens state-of-the-art manufacturing facility in Cranbury, New Jersey
Rocket Celebrates 5 Years
Rocket presents updated, positive data in PKD, FA and LAD-1 at ASH and in Danon disease, representing possibly the first viable gene therapy approach for cardiac diseases.
Rocket again celebrates Rare Disease Day by lighting up iconic buildings and hosting webinar featuring rare disease community advocates, including Abbey Meyers.
Rocket hosts its more than 130 employees for a summer townhall and team building event at its state-of-the-art manufacturing facility in Cranbury, NJ.
Rocket holds spring townhall featuring inspirational LAD-I patient family and professional development workshops.
Rocket presents top-line pivotal data from FA and LAD-I programs at the American Society of Gene and Cell Therapy (ASGCT) Annual Meeting.
Rocket achieves Current Good Manufacturing Practice (cGMP) readiness milestone for state-of-the-art AAV manufacturing facility in Cranbury, N.J.
Rocket presents positive updated data from the Phase 2 pivotal study for Fanconi Anemia and longer-term follow-up from the Phase 2 study for PKD at the 64th American Society of Hematology (ASH) Annual Meeting.
Rocket celebrates Rare Disease Day by hosting inspiring event at Make A Wish New Jersey and advancing Light Up for Rare initiative.
Rocket presented data from PKD, FA, LAD-I, Danon Disease and PKP2-ACM programs at the American Society of Gene and Cell Therapy (ASGCT) Annual Meeting.
Leadership
Gaurav Shah, MD
Chief Executive Officer
Gaurav Shah, MD
Chief Executive Officer
Gaurav Shah, a co-founder of Rocket Pharma, serves as Chief Executive Officer and Corporate Board Member. Prior to this role Gaurav was a Global Program Head in the Cell & Gene Therapies Unit at Novartis, where he had strategic oversight of 12 functions and helped spearhead pivotal trials with CART-19 for patients with leukemia and lymphoma. Earlier roles at Novartis included Global Clinical Program Head for CART-19 and for Biosimilars, and lead physician for Afinitor in several global oncology submissions. Gaurav started his career in industry at ImClone/Eli Lilly as a Medical Director overseeing oncology trials focused on monoclonal antibodies.
Gaurav graduated from Harvard College (summa cum laude, Phi Beta Kappa) with a degree in Behavioral Neuroscience. He received his MD from Columbia (AOA), completed his internal medicine residency at Brigham and Women’s Hospital, and hematology/oncology fellowship training at Memorial-Sloan Kettering. After receiving board certification in medical oncology, he served as an Adjunct Assistant Professor of Oncology at Columbia.
To find balance, Gaurav also has a passion for Indian classical music and has toured extensively including performances at Carnegie Hall and on National Geographic TV, a feature in the Smithsonian, and a 2019 Grammy nomination (Falu’s Bazaar) and 2022 Grammy win (A Colorful World).
Kinnari Patel, PharmD, MBA
Head of R&D and Chief Operating Officer
Kinnari Patel, PharmD, MBA
President, Head of R&D and Chief Operating Officer
Dr. Kinnari Patel is President, Head of R&D and Chief Operating Officer for Rocket Pharma, overseeing the global R&D and Technical Operations leadership team with oversight spanning discovery through late-stage development and manufacturing. This includes regulatory, clinical, global program teams, CMC, quality and the development organization. Dr. Patel’s prior responsibilities at Rocket included IR, IT, HR, finance and corporate compliance. Dr. Patel has more than 20 years of R&D experience in rare diseases and across several therapeutic areas including immuno-oncology, oncology, respiratory, virology, transplantation, cardiology and metabolism.
Dr. Patel has played a pivotal role in raising approximately $1 billion in financing, overseeing the transition of Rocket to a publicly traded company and facilitating the acquisition of Renovacor. She has helped grow Rocket from a three to about 300-person company with a diverse and inclusive culture. She maintains a strong focus on nurturing talent, leading the creation of Rocket University and the Gene Therapy Drug Development Certificate Program. Dr. Patel also spearheaded the development of the Rocket manufacturing site headquartered in Cranbury, NJ from its inception to a fully operational facility. In addition to her current role, Dr. Patel serves as the Rocket board observer and member of the Audit & Compensation Committee.
Before joining Rocket, Dr. Patel gained deep industry experience at leading pharmaceutical companies, including AstraZeneca, Bristol-Myers Squibb, Novartis and Hoffmann La-Roche. She has led both small molecule and biologic development programs from Phase I through Phase IV. Most notably, Dr. Patel has worked on eight drugs that have been submitted for review and approvals across the U.S. and EU, including Opdivo® (nivolumab) for metastatic melanoma, RCC and NSCLC and Myalept® (metreleptin) for ultra-rare lipodystrophy disease.
Dr. Patel received the dual degrees of B.S. in Biology and Doctorate of Pharmacy from the USciences in Philadelphia, PA. She also completed a two-year Post-Doctoral Regulatory Affairs Fellowship through Rutgers University with Johnson & Johnson and Pfizer. Additionally, she received her Executive MBA from NYU Stern School of Business with specialization in Corporate Finance, Leadership and Strategy. Most recently, she graduated from the C-Suite Harvard Business School Advanced Management Program.
Beyond her dedication to Rocket, Dr. Patel is a member of the Alliance for Regenerative Medicine’s (ARM) Board of Directors and serves on the Healthcare Businesswomen’s Association (HBA) Global Advisory Board. She has devoted her life to helping others through fostering a diverse, equitable and inclusive culture and advocating for female business leaders. In addition, Dr. Patel is deeply committed to making a positive impact in advancing science for rare diseases and has been widely recognized as a fearless advocate for patients and their loved ones impacted by these devastating conditions across the globe.
Isabel Carmona, JD
Chief People Officer
Isabel Carmona, JD
Chief People Officer
Isabel Carmona is the Chief People Officer for Rocket Pharma, overseeing all aspects of the company’s People strategy and operations through a period of rapid growth as the company plans its transition to commercial stage. Before joining Rocket, Isabel was Chief Human Resources Officer of Ichnos Sciences. There, she led the spin-off and set up of Ichnos Sciences as an independent oncology biotechnology company headquartered in New York City with research centers in Switzerland and India. Prior to that, she served as a member of the global operations and human resources leadership teams at Teva Pharmaceuticals and Shire Pharmaceuticals.
Isabel has developed her career across the United States and Europe, where she has held leadership positions in legal, compliance, operational excellence, and human resources in multiple industries including life sciences, information technology and financial services.
Isabel earned her JD degree with a specialty in business and international law from the Universidad de Sevilla and is also an avid listener of classical music and operas particularly of those set in her hometown of Sevilla, Spain.
Carlos Martin
Chief Commercial Operations and Revenue Officer
Carlos Martin
Chief Commercial Operations and Revenue Officer
Carlos Martin is the Chief Commercial Operations and Revenue Officer of Rocket Pharma He joined Rocket in April 2021 and established the company’s early commercial strategy and infrastructure as Chief Commercial Officer.
Prior to joining RocketCarlos was the U.S. Commercial Head of Advanced Accelerator Applications (AAA), a Novartis Oncology Company. His responsibilities included leading commercial strategy and new product launches as well as transforming their go-to-market model.
Before joining AAA, Carlos held roles of increasing responsibility at Novartis, where he developed his career across the U.S., Europe, Latin America and Asia. He brings in-depth background and experience globally and locally in commercial strategy and operations across a wide range of modalities and disease areas, including oncology, cardiovascular, metabolism and complex therapeutics.
Carlos earned a Bachelor’s degree in Economics from ESADE & the Polytechnic University of Barcelona, Spain and an MBA from the Thunderbird School of Global Management at Arizona State University. He is passionate about extending and improving patients’ lives through scientific and technological advancements.
Aaron Ondrey
Chief Financial Officer
Aaron Ondrey,
Chief Financial Officer
Aaron Ondrey is Chief Financial Officer for Rocket Pharma, leading the company’s Finance, Investor Relations, and Corporate Communications functions. Aaron is a seasoned finance executive with more than 20 years of experience in financial management, strategic planning, commercial finance, capital allocation and mergers and acquisitions across multiple therapeutic areas.
Previously, Aaron served as CFO of Mirati Therapeutics, overseeing all aspects of Finance, IT, and Facilities through the launch of KRAZATI® and the company’s acquisition by Bristol Myers Squibb in January 2024. Prior to joining Mirati as Senior Vice President, FP&A in July of 2022, Aaron was the Vice President, Finance, at Arena Pharmaceuticals and oversaw FP&A, Corporate Planning and Strategic sourcing.
Prior to Arena, Aaron served as the Head of U.S. and Global Commercial Finance at Alexion Pharmaceuticals with responsibility for financial management of approximately $5 billion in revenue across more than 50 countries. He previously held leadership positions of increasing responsibility supporting multiple product launches at Regeneron Pharmaceuticals, most recently as Head of Commercial Finance, Business Planning. Aaron received a BS in Finance from Case Western Reserve University.
In his spare time, Aaron enjoys spending time with his family, including his wife, three kids and three dogs. He is an avid soccer fan and loves to cook. Sunday morning pancakes and midnight noodles are family favorites. Aaron balances his time between the countryside of Connecticut and the coast of Maine.
Mayo Pujols
Chief Technical Officer
Mayo Pujols
Chief Technical Officer
Mayo Pujols is Chief Technical Officer for Rocket Pharma, leading Rocket’s state-of-the-art in-house Good Manufacturing Practice (cGMP) facility and Technical Operations function that includes Manufacturing, Validation Engineering, MS&T, Process Development, Analytical Development, Cell Therapy Development, Supply Chain, Project Management, Facilities Engineering and Environmental Health and Safety.
Mayo has nearly three decades of experience, working in leadership roles across technical operations, quality operations, validation, process development and cGMP. Prior to joining Rocket in July 2022, Mayo was Chief Executive Officer of Andelyn Biosciences, where he led their expansion to a full-service gene therapy CDMO. Over the course of his career, he has also held key roles at Novartis, Celgene, Merck, Advaxis, MedImmune and Schering-Plough.
Mayo earned his bachelor’s degree in Chemical Engineering from Stevens Institute of Technology and his master’s in Chemical Engineering and Applied Chemistry from Columbia University’s The Fu Foundation School of Engineering and Applied Science.
Raj Prabhakar, MBA
Chief Business Officer
Raj Prabhakar, MBA
Chief Business Officer
Raj Prabhakar is the Chief Business Officer for Rocket Pharma. Raj has over twenty years of broad experience, including the last 19 years at clinical development-stage biotechnology companies. Raj most recently comes to Rocket from Caladrius Biosciences, which through the subsidiary PCT as well as proprietary Regulatory T-cell and CD34 cell therapy programs, had direct hand-on business, manufacturing and operating experience in clinical-stage autologous ex-vivo cell and cell-based gene therapy programs. Prior to Caladrius Raj spent nearly ten years at Celsion Corporation leading multiple oncology candidates from Phase I through Phase III pivotal programs, spanning platforms including small and large molecules, including oligonucleotides and in-vivo non-viral gene therapy approaches to cancer. Prior to holding strategic planning and business development roles, Raj has also worked in clinical program management, manufacturing and operations. Raj has also worked at non-profit organizations such as PATH Vaccine Development Program, and private-staged companies such as Osiris Therapeutics and Protiveris.
Raj holds dual bachelor of sciences degrees in Biology and Mechanical Engineering from MIT and an MBA from the Harvard Business School.
Gayatri R. Rao, MD, JD
Chief Regulatory Officer & SVP, Clinical Safety
Gayatri R. Rao, MD, JD
Chief Regulatory Officer & SVP, Clinical Safety
Gayatri Rao is the Chief Regulatory Officer & SVP, Clinical Safety at Rocket Pharma, overseeing the Regulatory, Pharmacovigilance, Real World Evidence and Medical Writing functions across the pipeline of LV hematology and AAV cardiovascular programs. Previously, Gayatri served as Rocket’s Chief Development Officer, LV, and Vice President, Regulatory Policy and Patient Advocacy. Since joining the company, Gayatri has played an instrumental role in advancing the LAD-I, Fanconi Anemia, and PKD programs through clinical development.
Prior to Rocket, Gayatri served as Director of the Office of Orphan Products Development (OOPD) within the US Food and Drug Administration (FDA), where she was responsible for implementing statutory programs focused on promoting the development of medical products for rare diseases including the orphan drug and rare pediatric disease designation programs and overseeing more than $20M in grants to support natural history and clinical trial development. At the FDA, Gayatri served as the agency’s rare disease lead for interactions with Congress, international regulatory organizations, industry and patient advocacy groups.
Prior to heading FDA’s OOPD, Gayatri was an Associate Chief Counsel in the FDA’s Office of Chief Counsel with a focus on combination products, clinical trials, and medical devices, and began her career at an international law firm in Washington, D.C., specializing in healthcare and food and drug law related matters. She holds a JD from the University of Pennsylvania Law School, a Master of Bioethics from the University of Pennsylvania School of Medicine, and an MD from Rutgers New Jersey Medical School.
Jonathan Schwartz, MD
Chief Medical & Gene Therapy Officer
Jonathan Schwartz, MD
Chief Medical & Gene Therapy Officer
Jonathan Schwartz is Chief Medical & Gene Therapy Officer for Rocket Pharma, responsible for advancing Rocket’s gene therapies through critical stages in development and enhancing the Company’s dedicated focus on strategic application of gene therapy technologies to current and future therapeutic areas. In this position, he oversees Medical Directors, Clinical Operations, Clinical Scientists, Biometrics, Translational Science and Pre-clinical Research and Development. Jonathan joined Rocket as founding Chief Medical Officer in 2016 and has been instrumental in crafting and advancing an industry-leading pipeline of gene therapy programs across AAV cardiology and LV hematology portfolios.
Prior to Rocket, Jonathan was Vice President for Clinical Development at Stemline Therapeutics where he oversaw early development efforts for anticancer immunoconjugate, vaccine and small-molecule platforms. Before his role at Stemline, Jonathan had a seven-year tenure at ImClone/Eli Lilly, where he oversaw the development of the antiangiogenic monoclonal antibody Ramucirumab (CYRAMZA) from end-of-Phase-1 through a Phase 3 program resulting in stomach, liver, lung and colorectal cancer approvals by the FDA and international health authorities. Jonathan has also participated in multistage development of several additional monoclonal antibodies.
Prior to joining the industry, Jonathan was Associate Professor of Medicine at the Mount Sinai Medical Center in New York, specializing in the treatment and translational research of hepatobiliary malignancies; he was also Director for the Hematology-Oncology Fellowship training program. Jonathan received a BA in American Civilization from Brown University and an MD from Washington University in St. Louis. He completed post-graduate Internal Medicine and Hematology-Oncology training at the Mount Sinai and New York Presbyterian Hospitals.
Jonathan enjoys running, cooking and gardening and is a foremost authority on 1970s soul and funk music.
Mark White, MB.ChB
General Manager, Commercial Affairs
Mark White, MB.ChB
General Manager, Commercial Affairs
Mark White, MB.ChB, is General Manager, Commercial Affairs for Rocket Pharma, overseeing the Medical Affairs, Marketing, Commercial Operations, and Value & Access functions. He previously served as Chief Medical Officer, guiding the Medical, Clinical, Pharmacovigilance, and Biometrics organizations through the company’s first product filing and period of rapid growth as the company plans its transition to commercial stage.
Mark is a passionate and seasoned drug developer with more than 25 years of industry experience and rich expertise in late-stage drug development, global regulatory submissions and commercial strategy and launches. Prior to joining Rocket, Mark was Global Franchise Head for Fasenra (benralizumab) at AstraZeneca, where he led a large, multidisciplinary team through Phase 3 delivery, including global regulatory approvals. Additionally, he led the team through approvals and launches to achieve mega-brand status in severe eosinophilic asthma, as well as in the design and delivery of a large evidence generation program in severe asthma and in lifecycle management across multiple conditions including rare diseases, with the granting of five Orphan Drug Designations (ODDs) and one Breakthrough Therapy Designation (BTD).
At AstraZeneca, Mark was previously the program lead for Myalept (metreleptin) at the time of U.S. approval and launch for the ultra-rare condition of generalized lipodystrophy, the program lead for Saphnelo (anifrolumab) in systemic lupus erythematosus (SLE), and at MedImmune was the program lead for the influenza vaccine portfolio. In his earlier career, Mark spent time in global marketing, portfolio strategy, clinical development including as a late-stage clinical lead for multiple Phase 3 trials and regulatory submissions.
Mark joined the industry from clinical practice in the United Kingdom with post-graduate qualifications in acute medicine (MRCP), anesthesiology and intensive care (FRCA), as well as in pharmaceutical medicine (MFPM). He obtained his Bachelor of Medicine and Bachelor of Surgery (MB.ChB) at the University of Manchester School of Medicine.
Outside of work, Mark’s natural habitat is high in the mountains, but he also enjoys road and mountain biking, skiing, running and traveling with his family.
Martin Wilson, JD
General Counsel & Chief Corporate Officer
Martin Wilson, JD
General Counsel & Chief Corporate Officer
Martin Wilson is the General Counsel & Chief Corporate Officer for Rocket Pharma. Martin joined the company in December 2021 as its founding General Counsel & Chief Compliance Officer. In his current position, Martin leads the integrated Legal, Compliance and Business Operations functions as the company plans its expected transition to commercial stage.
Prior to joining Rocket, Martin was General Counsel and Chief Corporate Officer at Ichnos Sciences, where he oversaw Legal, Compliance, Business Development, Human Resources and IT. He helped establish Ichnos as an independent entity and set up its corporate structure.
Before Ichnos, Martin served as General Counsel, Chief Compliance Officer, Corporate Secretary and Head of Human Resources at Teligent, Inc. Prior to Teligent, he was Vice President and Assistant General Counsel at Endo Pharmaceuticals following the acquisition of Par Pharmaceuticals. Martin held multiple roles of increasing responsibility at Par over the course of 11 years, including Chief Compliance Officer.
Earlier in his career, Martin worked in the Licensing group at Schering-Plough. He earned his Juris Doctorate from Villanova University Charles Widger School of Law. In his spare time, Martin is an avid skier and basketball player and is involved in youth sports with his two young children.
Board of Directors
Roderick Wong, MD, MBA
Chairman of the Board
Roderick Wong, MD, MBA
Chairman of the Board
Dr. Wong founded and serves as Managing Partner of RTW Investments. Rod has more than a dozen years of experience as a life sciences fund manager. Prior to RTW, he founded and served as a Managing Director and Portfolio Manager for the Davidson Kempner Healthcare Funds. Dr. Wong started his career in investment research, first as a Biotechnology Research Associate at Cowen & Company and then as a Healthcare Analyst at Sigma Capital. He graduated from the University of Pennsylvania Medical School, received an M.B.A. from Harvard Business School, and graduated Phi Beta Kappa with a B.S. in Economics from Duke University. Rod regularly serves on a variety of corporate boards, and has a keen interest in educating the next generation of life science entrepreneurs. He serves as an Adjunct Associate Professor of Finance at NYU Stern, and as an Advisor to the University of Pennsylvania Medical School’s HealthX program.
Elisabeth Bjork, MD, PhD
Independent Director
Elisabeth Bjork, MD, PhD
Independent Director
Dr. Bjӧrk is the Senior Vice President, Head of Late-stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D at AstraZeneca leading the global development of medicines within this area. Throughout her career at AstraZeneca, she has gained broad drug development experience covering clinical development phase I-IV, large outcomes programs, major global filings and health authority interactions (FDA, EMA, Japan) and commercial strategy/implementation. Dr Bjӧrk is an endocrinologist by training and an associate professor of medicine at Uppsala University, Sweden. She is also a board member of Chalmers University of Technology, Chalmers Ventures AB, Bjӧrks Matematik o Mera AB and rfidcompare europe AB.
Carsten Boess, MBA
Independent Director
Carsten Boess, MBA
Independent Director
Mr. Boess has served as a director of Inotek / Rocket Pharmaceuticals since January 2016. His most recent role has been EVP Corporate Affairs at Kiniksa Pharmaceuticals, a publicly traded biotechnology company. He previously served as Senior Vice President and Chief Financial Officer at Synageva Biopharma Corporation from 2011 until the company’s acquisition by Alexion Pharmaceuticals in 2015. Prior to his role at Synageva, Mr. Boess served in multiple roles with increasing responsibility with Insulet Corporation, including Chief Financial Officer from 2006 to 2009 and Vice President of International Operations from 2009 to 2011. Prior to that, Mr. Boess served as Executive Vice President of Finance for Serono, Inc., from 2005 to 2006. In addition, he was a member of the Geneva-based World Wide Executive Finance Management Team. Mr. Boess was also Chief Financial Officer at Alexion Pharmaceuticals, and was a finance executive at Novozymes of North America and Novo Nordisk in France, Switzerland and China. Mr. Boess received a Bachelor’s degree and Master’s degree in Economics and Finance, specializing in Accounting and Finance from the University of Odense, Denmark.
Pedro Granadillo, BS
Independent Director
Pedro Granadillo, BS
Independent Director
Pedro is a highly-respected pharmaceutical business leader with more than 40 years of experience in the industry, primarily at Eli Lilly and Company, with a proven track record in human resources, manufacturing, quality and corporate governance. As a member of Lilly’s Executive Committee and as Lilly’s head of human resources, manufacturing and quality, he was responsible for policies affecting a global workforce of more than 45,000 employees, as well as a broad network of manufacturing facilities for its extensive line of products. He also oversaw more than 20 sites and 13,000 employees involved in the manufacturing of Lilly’s conventional “small-molecule” pharmaceuticals and “large-molecule” biotech therapies. Pedro has served on the Board of Directors of Haemonetics Corporation, Dendreon Corporation, Noven Pharmaceuticals, First Indiana Bank and most recently on the Board of Directors of NPS Pharmaceuticals, which sold to Shire for $5.2 Billion in 2015. Pedro earned his B.S. degree in Industrial Engineering from Purdue University.
Gotham Makker, MD
Independent Director
Gotham Makker, MD
Independent Director
Dr. Makker has more than 17 years of healthcare industry experience. Since 2005, he has served as CEO of Simran Investment Group, LLC, a closely held equity investment fund. Prior to Simran, Dr. Makker was a healthcare portfolio manager and principal at Citadel Investment Group LLC, a position he held from 2002 to 2005. Prior to joining Citadel, Dr. Makker served as an analyst at Oracle Partners LP covering biotechnology and medical device sectors from 2000 to 2001. From 1999 to 2000, Dr. Makker was a senior analyst on the life sciences investment banking team at Hambrecht & Quist. Dr. Makker received an M.D. from the University of Nebraska Medical School and he completed the Sarnoff cardiovascular research fellowship at Columbia University, College of Physicians & Surgeons and at Harvard Medical School, Brigham & Women’s Hospital.
Gaurav Shah, MD
Chief Executive Officer
Gaurav Shah, MD
Chief Executive Officer
Dr. Shah was appointed Chief Executive Officer of Rocket in September 2015. Prior to joining Rocket, from 2011-2015, Dr. Shah held various leadership positions at Novartis including Global Program Head for CART-19, Global Clinical Program Head for CTL-019 and Biosimilars, and Global Clinical Leader for Afinitor. Prior to Novartis, he spent three years at Eli Lilly and Company as Medical Director overseeing clinical development of numerous programs including olaratumab. During his industry tenure, Dr. Shah has participated in several drug development programs resulting in successful regulatory approvals, such as CTL-019 in pediatric ALL, the first cell and gene therapy approved in the U.S., and successful commercial launches. Prior to joining industry, Dr. Shah was Assistant Professor of Medicine/Oncology at Columbia University. He holds a B.A. in Behavioral Neuroscience from Harvard University and an MD from Columbia University. Dr. Shah completed his internal medicine residency at Brigham and Women’s Hospital/Harvard Medical School and completed his hematology/oncology fellowship training at the Memorial-Sloan Kettering Cancer Center.
David Southwell, MBA
Director
David Southwell, MBA
Director
Mr. Southwell is the President, Chief Executive Officer and Board member of TScan Therapeutics, an immuno-oncology company focused on T-cell receptors, a position he has held since 2018. Previously, he served as President, Chief Executive Officer, Board member of Inotek Pharmaceuticals from July 2014 until Inotek merged with Rocket in January 2018. From March 2010 to October 2012, Mr. Southwell served as Executive Vice President, Chief Financial Officer of Human Genome Sciences, Inc. until its merger with GlaxoSmithKline plc. Previously, Mr. Southwell served as Executive Vice President and Chief Financial Officer of Sepracor Inc. from July 1994 to July 2008, and as an investment banker at Lehman Brothers from 1984-1986 and 1988-1994. Mr. Southwell has served on the Board of Directors of PTC Therapeutics, Inc., since 2005, and has served on the Boards of Directors of Biosphere Medical (1998-2010), Human Genome Sciences Inc. (2008-2010), THL Credit Inc. (2007-2016), Inventiv Health (2016), and Spero Therapeutics (2017-2019). Mr. Southwell received a B.A. from Rice University and an M.B.A. from the Tuck School at Dartmouth College, where he has served as head of the MBA Advisory Board and currently serves on the Board of Advisers.
Naveen Yalamanchi, MD
Independent Director
Naveen Yalamanchi, MD
Independent Director
Dr. Yalamanchi has over 15 years of healthcare investment and research experience. Since 2015, He has served as Partner and Portfolio Manager at RTW Investments, a healthcare-centered investment firm. Prior to RTW, Dr. Yalamanchi was Vice-President and co-portfolio manager at Calamos Arista Partners, a subsidiary of Calamos Investments, a position he held from 2012-2015. Prior to joining to Calamos Arista Partners, Dr. Yalamanchi held various healthcare investment roles at Millennium Management and Davidson Kempner Capital Management. Dr. Yalamanchi holds a B.S. in Biology from MIT and an M.D. from Stanford University. He completed his orthopedic surgery internship at UCLA medical center.
Fady Malik, M.D., Ph.D.
Independent Director
Fady Malik, M.D., Ph.D.
Independent Director
Dr. Malik is Executive Vice President of Research and Development at Cytokinetics, a late-stage biopharmaceutical company, where he has worked in a variety of positions since he joined the founders to launch the company. At Cytokinetics, Dr. Malik has led R&D efforts resulting in multiple Investigational New Drug submissions, advancement of four programs to Phase 3, and the submission of the company’s first New Drug Application. Dr. Malik is also a Clinical Professor of Medicine in the Cardiology Division of the University of California, San Francisco, where he has held an appointment since 2000. Until 2019, he was a practicing Interventional Cardiologist at the San Francisco Veterans Administration Medical Center for over 18 years.
R. Keith Woods
Independent Director
R. Keith Woods
Independent Director
Mr. Woods is a seasoned executive with more than 30 years of industry experience who most recently served as Chief Operating Officer of argenx, where he led its global commercial organization, including marketing, market access, medical affairs, program management, and supply chain, during the company’s successful transition to commercial stage. He helped launch Vyvgart, a treatment for a rare autoimmune condition that causes muscle weakness, generating more than $1 billion in sales. Prior to argenx, Mr. Woods was the Senior Vice President of North America Business Operations at Alexion Pharmaceuticals, where he oversaw the U.S. and Canada business and was responsible for more than $1 billion in annual sales. He previously served as Vice President and Managing Director of Alexion UK, Vice President of U.S. Commercial Operations and Executive Director of Sales, leading the launch of Soliris in atypical hemolytic uremic syndrome.
Scientific Advisors
Juan Bueren, PhD
Fanconi & LAD Advisory Board
CIEMAT Gene Therapy Head
Hans-Peter Kiem, MD
Fanconi Advisory Board
Fred Hutchinson Cell & Gene Therapy Director
Donald Kohn, MD, UUC, BS, MS
LAD Advisory Board
UCLA Human Gene Medicine Program Director
Maria Grazia Roncarolo, MD
George D. Smith Professor in Stem Cell and Regenerative Medicine, Professor of Pediatrics and of Medicine, Director of the Center for Definitive and Curative Medicine, and Co-director of the Institute for Stem Cell Biology and Regenerative Medicine, Stanford University
Axel Schambach, PhD
Lecturer on Pediatrics, Boston Children’s Hospital
Jose Carlos Segovia, PhD
PKD Advisory Board
CIEMAT Investigator
Julian Sevilla, MD, PhD
Clinical Investigator, Hospital Infantil Universitario Niño Jesús
Matthew Taylor, MD, PhD
Danon Advisory Board Director, Adult Clinical Genetics, University of Colorado Anschutz
Adrian Thrasher, MD, PhD
Fanconi and LAD Advisory Board UCL Institute of Child Health, Great Ormond Street Hospital (GOSH), NHS Trust
John Wagner, MD
Director of the Institute of Cell, Gene and Immunotherapeutics, University of Minnesota
Partners
Children’s Hospital of Philadelphia (CHOP)
1 of 13Temple University
2 of 13REGENXBIO
3 of 13Memorial Sloan Kettering Cancer Center
4 of 13NYU
5 of 13CIRM
6 of 13University of Minnesota
7 of 13Stanford Medical School
8 of 13Forty Seven, a Gilead company
9 of 13University of Colorado
10 of 13University of California, Los Angeles
11 of 13University of California, San Diego
12 of 13Fred Hutchinson Cancer Research Center
13 of 13CIBER
CIBERER
CIEMAT
1 of 5University College London Great Ormond Street Hospital for Children
2 of 5Lund University
3 of 5MolMed
4 of 5University of Hannover
5 of 5