Seasoned Manufacturing Executive Joins Manufacturer of
Therapeutic Proteins
Phage Pharmaceuticals, Inc., a
clinical-stage developer and manufacturer of therapeutic proteins,
announced today that it has appointed David Jackson to the position
of Vice President, Operations Planning. In this role, Mr. Jackson is
responsible for oversight of the company’s cGMP-certified therapeutic
protein manufacturing facility in San Diego. He reports to Robert J.
Beckman, CEO of Phage Pharmaceuticals.
Prior to joining Phage
Pharmaceuticals, Mr. Jackson was the Vice President of Process
Development and Manufacturing at VaxInnate Corporation, where he was
responsible for creating Development, QA/QC, and Regulatory teams, and
as well as for building the company's infrastructure and overseeing
capital projects. He previously was VP of U.S. Operations and later VP
of Global Biologics Manufacturing at Lonza Biologics Inc., a
wholly-owned subsidiary of Lonza Group Ltd. (Switzerland), where he was
responsible for green-field site construction and other capital
projects, as well as technology transfer and GMP contract manufacturing.
He also served as VP of Manufacturing at BioReliance Corporation and VP
of Manufacturing and Pharmaceutical Support at EntreMed, Inc. Mr.
Jackson served honorably in the United States Marine Corps and received a
B.A. in Chemistry from Olivet Nazarene University.
About
Phage Pharmaceuticals
Phage Pharmaceuticals makes use of a
proprietary production method that improves upon well-established
approaches for the manufacture of targeted proteins and results in the
production of properly-folded therapeutic proteins at high yields. The
production method results in lower manufacturing costs with fewer waste
by-products and impurities compared with current conventional methods
used in the manufacture of similar therapeutics.
Phage
Pharmaceuticals has two product candidates in clinical development,
Human Growth Hormone ("hGH") and Fibroblast Growth Factor-1 ("FGF-1").
Both product candidates have open, active INDs with the FDA. Phase I
clinical trials of the company’s hGH drug candidate have been completed
successfully, and the company is positioned to begin further clinical
development of hGH as a biosimilar. FGF-1 manufactured at Phage
Pharmaceuticals' facilities has been assessed successfully in a Phase I
clinical trial for treatment of wounds and was shown to be safe and
well-tolerated. Other preparations of FGF-1 prepared in Phage
Pharmaceuticals' facilities in the same manner were assessed in Phase I
safety and Phage II efficacy trials for the treatment of severe Coronary
Heart Disease. Phage Pharmaceuticals has other therapeutic proteins in
various stages of pre-clinical development. Among the programs are those
involving Beta Interferon, G-CSF, Parathyroid Hormone, EGF, the various
forms of FGF (1 to 22), and pegylated versions of Interferon Alpha,
hGH, C-CSF, Beta Interferon, EPO, Coagulation Factor VIII, Coagulation
Factor IX, FGF-1, Interferon Gamma, Interleukin-12, and Insulin-Like
Growth Factor-1.
Contact:
Phage Pharmaceuticals, Inc.
Philip
N. Sussman, 212-330-8076
Chief Business Officer
info@phagepharma.com
Source:
Phage Pharmaceuticals Inc