Sanofi Pasteur Feb 2011 - Mar 2013
Corporate Development Advisor
Jbbda Feb 2011 - Mar 2013
President
Sanofi Pasteur 2003 - 2011
Senior Vice President, Corporate Development
Pfizer 1995 - 2003
Vice President, Business Development
Repligen Corporation Jan 1, 1992 - Dec 31, 1995
Vice President, Business Planning
Education:
University of California, Davis 1974 - 1976
Doctorates, Doctor of Philosophy, Genetics, Molecular Biology
Northeastern University 1972 - 1974
Master of Science, Masters, Molecular Biology
Bowdoin College 1966 - 1970
Bachelors, Bachelor of Arts, Biology, Music, Chemistry, Composition, Studio Art
Pentucket Regional High School
Bowdoin College
Skills:
Biopharmaceuticals Biotechnology Technology Transfer Vaccines Pharmaceutical Industry Clinical Development Drug Development Lifesciences Drug Discovery Infectious Diseases Immunology Biologics Fda Cro Business Development Monoclonal Antibodies Strategic Planning Virology Regulatory Affairs Clinical Trials Antibodies R&D Oncology Gmp Pharmaceutics Assay Development In Vitro Microbiology Medical Devices Protein Chemistry Molecular Biology Glp Regulatory Submissions Ind Gcp Pharmacology Biochemistry Cancer Translational Medicine Strategic Alliances Biomarkers Purification Genomics Drug Delivery Cell Immunoassays Licensing Negotiations Business Transactions Alliance Management International Business
Allan P. Jarvis - Newburyport MA Franklin Lim - Richmond VA
Assignee:
Damon Biotech, Inc. - Needham Heights MA
International Classification:
C12N 500 C12N 502 C12N 1100 C12N 1104
US Classification:
435241
Abstract:
Disclosed is a method of growing anchorage-dependent cells: cells of the type which normally undergo mitosis only when anchored on a substrate, e. g. , fibroblasts or epithelial cells. The method comprises the steps of encapsulating a seed culture of the cells within a semipermeable membrane and suspending the capsules in a growth medium. The interior surfaces of the capsule membrane and/or collagen enclosed within the capsules serve as a substrate for the cells. The ratio of the available substrate surface area to the volume of the culture may be large, thereby allowing the cells to be grown substantially throughout the volume of the culture medium.
Allan P. Jarvis - Newburyport MA David I. Kosowsky - Newton MA
Assignee:
Damon Biotech, Inc. - Needham Heights MA
International Classification:
A61K 4502 C12P 2100
US Classification:
424 85
Abstract:
Disclosed is a new material having antiviral activity designated interferon epsilon. The material may be produced, for example, by exposing primary, diploid human epithelial cells to a virus and then incubating the cells under conditions in which the new interferon is produced and is secreted into the culture medium. The material is antigenically distinct from interferon alpha, interferon beta, and interferon gamma, and displays marked antiviral activity in human epithelial cells but no detectable activity in other cell types.
Induction Of Immune Response By Immunization With Encapsulated Antigen-Producing Cells
Allan P. Jarvis - Newburyport MA George A. Koch - Medfield MA Paul G. Abrams - Washington DC
Assignee:
Damon Biotech, Inc. - Needham Heights MA
International Classification:
A61K 39395 C12N 1500 C12P 2100
US Classification:
424 85
Abstract:
Cells such as genetically modified cells, e. g. , hybridoma, which secrete an antigenic substance are encapsulated within capsule membranes having pores of dimensions sufficient to permit efflux of the antigens secreted by the cells but insufficient to permit traverse of the cells. The capsules are injected into an experimental animal where antigen passing through the pores of the capsule membrane induces lymphocytes to produce antibodies complementary to the antigen. The antibody may be harvested from the circulatory system of the animal. Preferably, lymphocytes are sampled from, e. g. , the spleen of the animal, fused with a malignant cell line to produce a hybridoma which synthesizes the antibody in vivo, and the hybridoma is cultured to produce large quantities of monoclonal antibody.
Disclosed is a process for damage-free encapsulation of a variety of core materials including viable cells. The core material is suspended in an aqueous solution of a polymeric material containing cationic groups such as an aminated glucopolysaccharide, e. g. chitosan. A temporary matrix is formed by gelling droplets of the suspension with a divalent or multivalent anion. The temporary matrix is permanently cross-linked with a polymeric material containing plural anionic groups, e. g. , polyaspartic or polyglutamic acid, to form a semipermeable membrane. The interior of the microcapsule may be resolublized by subjecting the capsule to a solution of low molecular weight cations. The process produces microcapsules which are not sticky, do not clump and allow viable cell growth and proliferation.
Process For Recovering Nonsecreted Substances Produced By Cells
Disclosed is a process for recovering nonsecreted substances produced by cells. The process eliminates some of the high molecular weight contaminants thereby simplifying the purification process. The cells are encapsulated within a semipermeable membrane having properties which permit rapid passage of the relatively low molecular weight substances of interest but retard or prevent passage of higher molecular weight contaminants. The encapsulated cells are suspended in a culture medium and undergo normal cell growth and mitosis. The encapsulated cell culture grows to substantially fill the capsules but not rupture them. The cell membrane is then lysed without disrupting the capsule membrane. The permeability of the capsule membrane is such that the substances of interest diffuse rapidly through the capsule membrane into the extracapsular fluid while the higher molecular weight contaminants and cell fragments are retained within the capsule. The process is particularly useful for obtaining low to moderate molecular weight substances produced by pyrogen-producing prokaryotic, genetically modified organisms because the crude product can be collected relatively free of high molecular weight pyrogenic contaminants.
Allan Jarvis (1980-1984), Gordon Gallenger (1974-1978), Janet Vella (1977-1981), M McKay (1985-1989), Susan Rogers (1983-1987), Gareth Hall (1987-1990)