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Developing
World Cures Management Peter Farina, Ph.D. Before joining
Developing World Cures, Dr. Farina was Senior Vice President of
Development at Boehringer Ingelheim Pharmaceuticals, Inc. In this
capacity he was responsible for an interdisciplinary organization of
scientists and staff with oversight for pre-clinical development of
drugs in the therapeutic areas of immunology/inflammation,
cardiovascular diseases, and virology.Most recently, Dr. Farina’s team
was responsible for the development of Aptivus â
(tipranavir), an HIV protease inhibitor. Prior to his development
position, he was Vice President of Research for Boehringer Ingelheim
Pharmaceuticals, Inc. Dr. Farina’s
research interest has been generally at the interface of chemistry and
biology. He has worked over his career in inflammatory and immunological
mechanisms, particularly cytokines and arachidonic acid mediators. In
addition, he was engaged in HIV virology research that led to discovery
and successful registration of one of the first non-nucleoside reverse
transcriptase inhibitors, Viramuneâ
(nevirapine). He is the author of over fifty publications and patents Dr. Farina’s
undergraduate education was at New College at Hofstra University, where
he received a B.S. in chemistry. He was an Allied Chemical Corporation
Fellow at The State University of New York at Buffalo, where he
completed a Ph.D. in organic chemistry. Dr. Farina went on to do
postdoctoral work as an NIH Fellow in bio-organic chemistry with Stephen
Benkovic at the Pennsylvania State University. Dr. Farina currently
serves as the Co-Chair and as a Board Member of Connecticut United for
Research Excellence (CURE); He also serves on the Advisory Board of the
University of Connecticut School of Pharmacy, NYAS President’s
Council, as an advisor for The Center for Biological Innovation (CBI) at
MIT, as senior advisor to Canaan Partners and PureTech Ventures, and as
an advisor to other biotech companies.
As the President of
Developing World Cures Dr. Spero brings executive leadership in the
areas of pharmaceutical research and development. Before joining
Developing World Cures, Dr. Spero spent 18 years in research and
development at Boehringer Ingelheim Pharmaceuticals, Inc. Most recently,
as Vice President of drug discovery support, she was responsible for
establishing and leading the discovery organization’s science in drug
metabolism, pharmacokinetics, pharmaceutics, and general pharmacology
for the therapeutic areas immunology and inflammation and cardiovascular
diseases. Dr. Spero has been highly active in the Diversity and Inclusion
initiative at Boehringer Ingelheim and was a women’s leadership mentor
and diversity spokesperson to R&D. Dr. Spero is
currently a consultant to Boehringer Ingelheim. She holds over 60
publications and patents and has given numerous invited lectures in the
fields of synthetic chemistry, medicinal chemistry and drug metabolism
and pharmacokinetics. Dr. Spero holds a
B.A. in chemistry and biology, Summa Cum Laude and Phi Beta Kappa, from
Wheaton College, an M.S. in organic chemistry from the Massachusetts
Institute of Technology, and a Ph.D. in organic chemistry from Brown
University. She did post-doctoral research at Harvard University in the
laboratory of Professor Y. Kishi working on the total synthesis of the
anti cancer drug Halichondrin B.
Dr. Gerald Miwa
is President of Nextcea, Inc., a company devoted to the identification
and utilization of biomarkers for drug efficacy and toxicity.
Prior to his appointment at Nextcea he was Vice President of Drug
Metabolism and Pharmacokinetics (DMPK) at Millennium Pharmaceuticals in
Cambridge, MA where he was responsible for ensuring that drug
development candidates had adequate exposure to be effective in
patients, minimizing drug-drug interactions, and anticipating toxicities
arising from drug metabolites. During his
career, Dr. Miwa directly contributed to the pharmaceutical development
and registration of a number of drugs including: Ivermectins, Zofran,
Ultiva, Zocor, Sustiva and Velcade. Dr. Miwa also led numerous
research programs to develop new methods for evaluating the metabolism
and pharmacokinetics of drugs and the biochemical basis for their
toxicities. More recently, he has been engaged in research to
discover biomarkers to predict and monitor drug efficacy and safety in
humans. He is past chairman of the Drug Metabolism Steering
Committee for the Pharmaceutical Research and Manufacturers Association
(PhRMA) and chairman of the Gordon Conference on Drug Metabolism.
He is a member of multiple societies related to DMPK and toxicology, a
Fellow of the American Association for the Advancement of Science and
author of more than 90 publications and book chapters in the DMPK field. Dr. Miwa completed his undergraduate degree in Chemistry at the University of California, San Diego, his Ph.D. in Pharmacology from the University of California, Los Angeles, and a postdoctoral fellowship at Hoffmann La Roche. Dr. Miwa was the head of DMPK at Millennium, DuPont, and Glaxo Pharmaceutical companies and a research scientist at Merck and Hoffmann La Roche companies.
DWC has assembled
an outstanding team of volunteer pharmaceutical experienced executives
and scientific specialists. Members are: Lou Capalbo,
Retired Director of Investigational Supplies, Pharmaceutics Department,
Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT. Mr. Capalbo has
extensive experience in GMP manufacture of drugs for first in man
studies through registration. He has also worked at Pfizer and GSK. Valerie Ceva,
MBA, The Strategic Choice LLC, Life Sciences Management Consulting, has
over 20 years of experience in operational and leadership roles with
major pharmaceutical firms and healthcare start-ups, as well as in
consulting and private equity/venture capital. Richard
Chizzonite, Ph.D., former Executive Director of R&D Global
Licensing Group, Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT,
has over 26 years of experience in the pharmaceutical industry having
held leadership positions in R&D and licensing and business
development. Most recently, Dr. Chizzonite was responsible for global
licensing for cardiovascular disease and chronic inflammatory diseases,
as well as enabling technologies. Dr. Chizzonite also held the position
of research leader at Hoffman LaRoche and in that capacity was
responsible for drug discovery in the area of inflammation and
immunological diseases. Jayne Douglas,
M.D., Vice President, Development at Pfizer Global R&D. Dr. Douglas
has 23 years of experience in medical device and pharmaceutical research
and development, primarily in the areas of global clinical trials and
outcomes research. Dr. Douglas has also held the positions of VP,
Development Site Head and VP, Clinical R&D site head at Pfizer
Global R&D. Diana Galer,
Ph.D., D.A.B.T., Vice President, Strategic Management Group, Pfizer,
Inc. Dr. Galer brings extensive experience in toxicology,
pharmacokinetics/metabolism and regulatory affairs in both the human and
animal pharmaceutical industry. Dr. Galer has also held the positions of
VP, Operations, Drug Safety Research Development and VP, Worldwide Head,
Safety Sciences Global Operations at Pfizer Global R&D. Susan Levinson,
Ph.D., The Strategic Choice LLC, Life Sciences Management Consulting.
Dr. Levinson has over thirty years of experience in the pharmaceutical
industry where she held leadership positions in project management,
licensing, business development and marketing. Most recently, Dr.
Levinson held executive positions in business strategy and marketing at
Novartis Pharmaceuticals. Paul Pescatello,
J.D., Ph.D., CEO and President of CURE. CURE is a CT statewide coalition
of over 100 educational and research institutions, biotechnology and
pharmaceutical companies. Mr. Pescatello is an attorney and lobbyist
with over 20 years of technology, public affairs and public policy
experience. Mr. Pescatello serves on numerous boards including
Connecticut Innovations, Inc., a quasi-public seed and venture capital
firm, and the United Way of Connecticut. He also serves on the
Connecticut Stem Cell Research Advisory Committee. Michael
Rosenberg, M.D., MPH, President and CEO of Health Decisions, Inc., a
private clinical research company. In studies conducted throughout the
world, the company has established itself as a leader in the application
of technology to improve the efficiency and speed of clinical trials.
Dr. Rosenberg has been involved with the strategic design and execution
of pharmaceutical development programs for more than 25 years. Dr.
Rosenberg is the author of more than a hundred and fifty scientific
articles and serves on numerous advisory groups in business, technology
and medicine. He currently serves as Clinical Professor o Obstetrics and
Gynecology at the School of Medicine and Adjunct Professor of
Epidemiology at the University of North Carolina. Dr. Rosenberg has
worked with the CDC and has run clinical trials in numerous developing
world countries. James
Stevenson, Ph.D., former Director, Chemistry Information
Technologies at Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT.
Dr. Stevenson also headed structural research/computational chemistry as
well as the biophysics and protein structure determination groups. Scientific
Specialists Yuhpyng Chen,
Ph.D., retired research fellow from Pfizer, Inc. Groton, CT. Dr. Chen
has 20 years of experience as a medicinal chemist with expertise in
organic synthesis and drug design. Karl Grozinger, retired organic chemist from Boehringer Ingelheim. Mr. Grozinger has over 30 years of experience in process chemistry and has expertise in purchasing and sourcing chemical precursors.
The company is in
the process of recruiting a board of directors. The board will be
responsible for overseeing financial controls, intellectual property,
and company policies. The board will also act as ambassadors for DWC to
gain support for the company’s mission. The board members will be
chosen from among the following: CEO(s) from the pharmaceutical or
biotech industry, noted Professors of Science or Medicine who are
recognized as international scholars, a diplomat and international
policy advisor, a legal expert in pharmaceuticals and international
trade relations, an expert in business administration and finance, a
noted goodwill ambassador and highly recognized former government
leader. A scientific
advisory board (SAB) will also be established. The SAB will assist in
identifying critical medical needs in developing countries and provide
scientific and clinical expertise for DWC’s assessment of IP and
R&D strategic planning. Therapeutic area and targets for research
will be identified with input from the SAB. In addition, the SAB will
critique research programs and DWC’s scientific efforts.
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