Roger M. Echols
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Profil
Roger M.
Echols served as Chief Medical Officer of Replidyne, Inc. from January 2005 to May 1, 2008.
From 1997 to 2004, he was Vice President of Infectious Disease Clinical Research and Development for Bristol Myers Squibb and Medical Director of Immunex Corporation from 1996 to 1997 and Bayer Corporation from 1989 to 1996.
Dr. Echols was the Head of the Division of Infectious Diseases at Albany Medical College.
He received a BA degree from Yale University and an MD from the Tufts University School of Medicine.
Ehemalige bekannte Positionen von Roger M. Echols
Unternehmen | Position | Ende |
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Replidyne, Inc.
Replidyne, Inc. BiotechnologyHealth Technology Replidyne, Inc. is a biopharmaceutical company focused on developing and commercializing innovative anti-infective products. The company's new drug application (NDA) for its lead product, faropenem medoxomil, has been accepted for standard review by the FDA. Faropenem medoxomil is an orally available antibiotic for the treatment of community acquired infections, such as respiratory tract infections. Other development programs include higher dose/shorter course therapy, additional ndications for adults and a pediatric formulation of faropenem medoxomil. The ompany’s pipeline also includes a topical anti-bacterial product, REP8839, hich has a novel mechanism of action for addressing the major challenge of ethicillin-resistant Staphylococcus aureus (MRSA). The company also has iscovery programs directed to the inhibition of bacterial DNA replication, which could result in therapies to treat a wide range of antibiotic-resistant bacteria. The company is headquartered in Louisville, CO | Technik-/Wissenschafts-/F&E-Leiter | 01.05.2008 |
Ausbildung von Roger M. Echols
Tufts University | Doctorate Degree |
Yale University | Undergraduate Degree |
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Private Unternehmen | 1 |
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Replidyne, Inc.
Replidyne, Inc. BiotechnologyHealth Technology Replidyne, Inc. is a biopharmaceutical company focused on developing and commercializing innovative anti-infective products. The company's new drug application (NDA) for its lead product, faropenem medoxomil, has been accepted for standard review by the FDA. Faropenem medoxomil is an orally available antibiotic for the treatment of community acquired infections, such as respiratory tract infections. Other development programs include higher dose/shorter course therapy, additional ndications for adults and a pediatric formulation of faropenem medoxomil. The ompany’s pipeline also includes a topical anti-bacterial product, REP8839, hich has a novel mechanism of action for addressing the major challenge of ethicillin-resistant Staphylococcus aureus (MRSA). The company also has iscovery programs directed to the inhibition of bacterial DNA replication, which could result in therapies to treat a wide range of antibiotic-resistant bacteria. The company is headquartered in Louisville, CO | Health Technology |