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BridgeBio and Origin's Nulibry (fosdenopterin) Receives the US FDA's Approval as the First Therapy to Reduce the Risk of Mortality...
March 1, 2021
NightWare Receives the US FDA's Approval for the First Medical Device to Stop NightMAres Related to PTSD
November 11, 2020
Merck and Bayer Receive the US FDA's Priority Review for Vericiguat to Reduce the Risk of CV Death in Patients with Symptomatic Ch...
July 16, 2020
Baysient to Release iDose Software Technology Platform 1.0 to Reduce the Biosimilar Cost in Market
February 28, 2020
Eli Lilly's Trulicity (dulaglutide) Receives the US FDA's Approval to Reduce MACE in T2D Adults
February 24, 2020
Astellas Reports Results of Mirabegron in P-IV PLUS Study to Reduce Overactive Bladder Symptoms in Men
May 6, 2019
Amarin Reports (REDUCE-IT) Trial Results of Vascepa/Vazkepa (icosapent ethyl) for Cardiovascular Diseases
August 29, 2022
PharmaShots Interview: Dr. R. Preston Mason, Consultant at Amarin, Corp. Shares Insights from its in vitro Study Results
August 3, 2022
Corvia Medical Reports Results of Corvia Atrial Shunt in P-III (REDUCE LAP-HF II) Trial for the Treatment of Heart Failure
April 1, 2022
Amarin Publishes Results of Vascepa (icosapent ethyl) in (REDUCE-IT) Study for the Treatment of Cardiovascular Diseases in JAHA 20...
March 11, 2022
Cytokinetics Presents Results of Omecamtiv Mecarbil in P-III (METEORIC-HF) Trial for Heart Failure with Reduced Ejection Fraction...
February 16, 2022
Cytokinetics Receives the US FDA Acceptance of NDA for Omecamtiv Mecarbil to Treat Heart Failure with Reduced Ejection Fraction
February 7, 2022
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