DEINOVE selected for a presentation at BARDA Industry Day 2019 in Washington DC
October 15, 2019 12:30 ET | Deinove
DEINOVE selected for a presentation at BARDA Industry Day 2019 in Washington DC DEINOVE will present DNV3837/DNV3681, its antibiotic candidate targeting both urgent threats to public health and...
DEINOVE retenue pour une présentation au BARDA Industry Day 2019 à Washington DC
October 15, 2019 12:30 ET | Deinove
DEINOVE retenue pour une présentation au BARDA Industry Day 2019 à Washington DC DEINOVE présentera DNV3837/DNV3681, son candidat-antibiotique qui cible des pathogènes majeurs, tant en matière de...
Summit Awarded Additional $12 Million by BARDA for Phase 3 Development Programme of Ridinilazole for the Treatment of C. difficile Infection
August 16, 2018 07:00 ET | Summit Therapeutics plc
Brings Total Committed Funding Under BARDA Contract to $44 Million OXFORD, United Kingdom and CAMBRIDGE, Mass., Aug. 16, 2018 (GLOBE NEWSWIRE) -- Summit Therapeutics plc (NASDAQ:SMMT, AIM:SUMM), a...
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Rapid Micro Biosystems Awarded a Contract by Biomedical Advanced Research and Development Authority (BARDA) for the Implementation of a Rapid Sterility Test for Vaccines
October 23, 2017 07:00 ET | Rapid Micro Biosystems
LOWELL, Mass., Oct. 23, 2017 (GLOBE NEWSWIRE) -- Rapid Micro Biosystems, a leading provider of automated, non-destructive, rapid microbial detection, is pleased to announce the receipt of a $7.3...
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Summit Awarded BARDA Contract Worth Up to $62 Million to Support the Development of Ridinilazole for the Treatment of C. difficile Infection
September 11, 2017 07:00 ET | Summit Therapeutics PLC
CAMBRIDGE, Mass. and OXFORD, United Kingdom, Sept. 11, 2017 (GLOBE NEWSWIRE) -- Summit Therapeutics (NASDAQ:SMMT) (AIM:SUMM), the drug discovery and development company advancing therapies for...
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Cempra Authorized to Receive Funds From BARDA for a Phase 2/3 Clinical Trial of Solithromycin in Pediatric Patients
March 07, 2016 07:00 ET | Melinta Therapeutics, Inc.
Phase 2/3 Pivotal Trial Will Test Intravenous, Oral Capsule and Oral Suspension Formulations of Solithromycin in Pediatric Patients From Age 2 Months to 17 Years Cempra to Receive $25.5...
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Cempra to Receive BARDA Funding for 1b and Start-Up of Phase 2/3 Solithromycin Pediatric Studies
November 19, 2014 06:00 ET | Melinta Therapeutics, Inc.
$16.0 Million Will be Provided to Cover the Cost of the Study and Other Activities Specified in the Contract Phase 1b and Phase 2/3 Studies Will Test Intravenous, Oral Capsule and Oral Suspension...
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VaxInnate Quadrivalent Seasonal Influenza Vaccine Candidate, VAX2012Q, Meets Phase 1 Seasonal Influenza Endpoints
November 11, 2014 08:00 ET | VaxInnate Corporation
Cranbury, NJ, Nov. 11, 2014 (GLOBE NEWSWIRE) -- VaxInnate Corporation, a biotechnology firm pioneering next-generation vaccine technology, announced today that enrollment has concluded in the Phase 1...
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VaxInnate Updates Plans to Advance Lead Vaccine Candidate, VAX2012Q in Elderly
October 08, 2014 09:00 ET | VaxInnate Corporation
Cranbury, NJ, Oct. 8, 2014 (GLOBE NEWSWIRE) -- VaxInnate Corporation, a biotechnology firm pioneering a breakthrough vaccine technology platform, provided an update on clinical development plans for...
Aeolus Files Investigational New Drug Application With US Food and Drug Administration to Enable Initiation of Human Safety Studies for the Development of AEOL 10150 as a Medical Countermeasure Against Lung Damage From Radiation Exposure
August 20, 2014 13:00 ET | Aeolus Pharmaceuticals
MISSION VIEJO, CA--(Marketwired - Aug 20, 2014) - Aeolus Pharmaceuticals, Inc. (OTCQB: AOLS) today announced that it has filed an Investigational New Drug Application (IND) with the Division of...