Inaugural members of the Zavante Scientific Advisory Board:
- Paul G. Ambrose, Pharm. D., F.I.D.S.A.
- John S. Bradley, M.D., F.A.A.P., F.I.D.S.A.
- George L. Drusano, M.D.
- Ronald N. Jones, M.D.
- Keith Rodvold, Pharm.D.
- Albert T. Sheldon Jr., Ph.D.
- Andrew Shorr, M.D., M.P.H.
- Robert K. Flamm, Ph.D.
For a full biography of each advisory board member, please visit www.zavante.com/sab.
Zavante's ZTI-01, is a first-in-class injectable antibiotic that has demonstrated a broad spectrum of bactericidal Gram-negative and Gram-positive activity in vitro, including activity against most contemporary multi-drug resistant (MDR) strains.
FDA granted Fast Track designation and Qualified Infectious Disease Product (QIDP) designation for the investigation of ZTI-01 for the following indications:
- Hospital-Acquired Bacterial Pneumonia (HABP)
- Ventilator-Associated Bacterial Pneumonia (VABP)
- Acute Bacterial Skin and Skin Structure Infections (ABSSSI)
- Complicated Intra-Abdominal Infections (cIAI)
In July 2016, the first patient was randomized in the ZEUS (ZTI-01 Efficacy and Safety) study. ZEUS is the pivotal study intended to support a New Drug Application for ZTI-01 in the U.S. The study is titled "Multi-center, randomized, double-blind, comparative study to evaluate the safety and efficacy of ZTI-01 vs. piperacillin/tazobactam in the treatment of complicated urinary tract infections, including acute pyelonephritis, in hospitalized adults." More clinical trial information is available at www.clinicaltrials.gov.
The Company expects to complete enrollment in the ZEUS study in the first half of 2017.
About Zavante Therapeutics, Inc.
Zavante Therapeutics, Inc. is a privately-held, late clinical-stage biopharmaceutical company focused on developing novel therapies to improve the outcomes of hospitalized patients.
Additional information is available at www.zavante.com
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SOURCE Zavante Therapeutics, Inc.