Charles W. Bishop, PhD
President and Chief Executive Officer
E-mail: charles.bishop@cytochroma.com
Dr. Bishop has served as President and CEO
since June 2006. Dr. Bishop has over 24 years of management
experience in the pharmaceutical industry across multiple disciplines
including Research & Development, Regulatory Affairs, Operations,
and Business Development. Dr. Bishop co-founded Proventiv Therapeutics,
LLC in September 2005 where he served as President. Proventiv
Therapeutics, LLC was acquired by Cytochroma Holdings ULC in
June 2006. During the period of September 1987 to June 2005,
Dr. Bishop held various senior management positions at Bone
Care International, Inc., a public specialty pharmaceutical
company focused on developing and commercializing Vitamin D
hormone therapies. Dr. Bishop’s positions with Bone Care
included President, CEO, Director, Executive Vice President
of Research and Development, and Chief Scientific Officer.
Under Dr. Bishop's direction, Bone Care advanced a portfolio
of proprietary Vitamin D hormones and analogs to varying stages
of development for SHPT, metabolic bone disease, psoriasis
and cancers of the prostate, breast and colon. Dr. Bishop was
responsible for the successful preparation and prosecution
of three New Drug Applications (NDAs) that ultimately led to
FDA approval of a novel Vitamin D drug, named doxercalciferol,
for SHPT in dialysis patients (Hectorol® 2.5 mcg Capsules
and Hectorol® Injection) and pre-dialysis patients (Hectorol® 0.5
mcg Capsules). Prior to joining Bone Care, Dr. Bishop held
various management positions in the Health Care Division of
the Procter & Gamble Company. Dr. Bishop completed a four-year
National Institutes of Health Postdoctoral Fellowship in Vitamin
D Biochemistry at the University of Wisconsin-Madison and received
his Ph.D. degree in Nutritional Biochemistry from Virginia
Polytechnic Institute and State University, after earning an
undergraduate degree in Chemistry from the University of Virginia.
Joel
Z. Melnick, MD
Vice President, Clinical & Regulatory Affairs
E-mail: joel.melnick@cytochroma.com
Dr. Melnick joined Cytochroma in August
2007 as Vice President, Clinical & Regulatory Affairs.
Prior to joining Cytochroma, he was Senior Medical Director
in the Global Pharmaceutical Research and Development Group
at Abbott Laboratories (North Chicago, IL). While at Abbott,
Dr. Melnick managed clinical trials, regulatory submissions,
marketing approvals and post-launch support for Zemplar® (paricalcitol)
Capsules and Injection, currently one of the world’s
leading Vitamin D hormone replacement therapies for secondary
hyperparathyroidism (SHPT) in chronic kidney disease (CKD).
Prior to Abbot, Dr. Melnick served as Assistant Professor
of Pediatrics at Northwestern University, where he conducted
research in metabolism and cardio-renal disease. Dr. Melnick
completed his medical degree, internship, and residency in
internal medicine and pediatrics at Creighton University,
and completed a post-doctoral fellowship in pediatric and
adult nephrology at the University of Texas Southwestern
Medical Center.
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Eric J. Messner, MBA
Vice President, Commercial Operations
E-mail: eric.messner@cytochroma.com
Mr. Messner has served as Vice President
of Commercial Operations since June 2006. Mr. Messner has
over 18 years experience in the pharmaceutical and biotechnology
industry, in both large and small companies. In his current
role, Mr. Messner is responsible for managing the commercial
functions of business development, marketing, sales and
finance. Previously, Mr. Messner co-founded Proventiv Therapeutics
in September 2005. While at Proventiv, Mr. Messner was
the Vice President of Commercial Operations, focusing on
business development and marketing. In this role, he negotiated
terms with licensing partners and fundraising institutions
and created commercial marketing strategies and associated
financial forecasts. Prior to Proventiv, Mr. Messner held
senior positions at Bone Care International and Abbott
Laboratories. Mr. Messner earned his MBA from the J. L.
Kellogg Graduate School of Management at Northwestern University
and a BS in Management from Miami University.
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Martin Petkovich, Ph.D.
Chief Scientific Officer
E-mail: martin.petkovich@cytochroma.com
Martin is a co-founder of Cytochroma
and has provided scientific guidance as a consultant
until 2006 when he joined the Company as a full-time
Chief Scientific Officer (CSO). Dr. Petkovich served
as a Director of the Company until his appointment as
CSO. Dr. Petkovich has been involved in all of the Company’s
efforts to raise capital and played a pivotal role in
completing Cytochroma’s first license agreement
(with Allergan, Inc.) and served as Chair of the Joint
Research Management Committee established under this
agreement. Dr. Petkovich received his B.Sc. from McMaster
University in 1981 and Ph.D. in Biochemistry in 1986
from the University of Toronto. He was a post-doctoral
fellow in the laboratory of Dr. Pierre Chambon in Strasbourg,
France from 1986 to 1989. He moved to Queen's University
in 1990 to join the Departments of Biochemistry and Pathology
and was appointed Full Professor in 1998. Dr. Petkovich
is an expert in small molecule signaling, nuclear receptors
and metabolism. Dr. Petkovich discovered the fundamental
mechanism of action of vitamin A by cloning the first
receptor for the vitamin A metabolite, retinoic acid.
This discovery is cited as a major breakthrough in the
vitamin A field.
Jay White, Ph.D.
Vice President, Product Development (Nephrology)
E-mail: jay.white@cytochroma.com
Mr. White has over 10 years experience
in the biotechnology industry. He has served in his current
role of Vice President, Product Development, since June 2006
and is responsible for project management, analytical methods
development and quality control, manufacturing of drug substances
and products, formulation development and toxicology testing.
Dr. White previously held the position of Vice President,
Operations at Cytochroma from September 2003 to June 2006.
In this capacity, he was responsible for corporate finance,
project management, drug manufacturing, information technology,
facilities and infrastructure planning. Since 1997, he has
played a key role as a member of the research and development
team at Cytochroma and is named as co-inventor on 18 patent
applications and 32 issued patents. Dr. White received his
M.Sc. and Ph.D. in Pathology and Molecular Medicine from
Queen's University.
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