Highlights
BioCryst begins proof of concept trial in PNH patients with oral Factor D inhibitor, BCX99
BCX9930 is an oral Factor D inhibitor discovered and developed by BioCryst for the treatment of complement-mediated d
Urovant Sciences announces US FDA acceptance of NDA for Vibegron to treat overactive bladd
The NDA has been assigned a Prescription Drug User Fee Act (PDUFA) goal date of December 26, 2020. In addition, the F
Zydus secures DCGI approval for Saroglitazar to treat liver disease
NASH, a progressive disease of the liver, commences with fat accumulation in the liver and may lead to cirrhosis and
Amunix raises $73m in Series A financing led by Omega Funds
Boston-based Omega Funds led the financing, with participation from existing investor Frazier Healthcare Partners and
Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research discover
Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are es
Bristol Myers Squibb gets FDA nod for Opdivo + Yervoy to treat liver cancer
The FDA accelerated approval was based on Opdivo + Yervoy’s overall response rate and duration of response in
TOURMALINE-MM2 study on NINLARO fails to deliver desired results
The late-stage TOURMALINE-MM2 trial featured 705 adult patients who are newly diagnosed with multiple myeloma and are
InMed Pharmaceuticals announces completed enrollment in phase 1 clinical trial of INM-755
INM-755 is a CBN cream intended as a topical therapy to treat epidermolysis bullosa (EB) and potentially other dermat
Kuur Therapeutics launches to develop and commercialise off-the-shelf CAR-NKT cell therapi
IP Group, Baylor College of Medicine and Schroeder Adveq are investing to support two phase 1 studies: GINAKIT 2 (aut
Imfinzi delivers sustained OS benefit in final analysis of CASPIAN trial
Imfinzi gave the desired result for the company through its combination with a choice of standard-of-care (SoC) chemo
RIBOMIC enters license agreement with AJU Pharma for RBM-007 in age-related macular degene
Upon execution of this Agreement, AJU will obtain the exclusive license to develop and sell the Product containing RB
Merck announces top-line results from phase 3 trials evaluating Gefapixant
In these studies, the primary efficacy endpoints were met for the gefapixant 45 mg twice daily treatment arms â€