- | F2G
4 issues infectious disease experts are focused on as fewer enter their profession
John Rex, MD, chief medical officer at drug discovery company F2G, told Becker’s he also feels the solution is two-part: legislative and research-driven.
- | CytoReason
Sanofi and CytoReason Target IBD in Expanded Collaboration (Updated)
If data is the new oil, CytoReason is one of its barons. Combining all available information about a disease – literature, data sets, all data types – the company builds computational disease models utilized by its pharma partners to help them determine which drug avenues to pursue next.
- | Elicio Therapeutics
Cancer vaccine developer jumps to Nasdaq via reverse merger
Elicio is merging with Angion Biomedica, a Uniondale, NY-based biotech that began searching for strategic alternatives last July after Phase II setbacks forced it to shutter all R&D work.
- | PepGen
Reporter’s Notebook: Opening Day at the J.P. Morgan Healthcare Conference
In 2021, PepGen raised $113 million to challenge Sarepta in DMD and build its neuromuscular and neurologic pipeline.
- | Immunome
Betting on cell memory, AbbVie pays Immunome $30M upfront to further antibody research
AbbVie has tapped Immunome’s discovery platform in a heavily backended partnership and option agreement in a bid to discover 10 antibody-target pairs from three as-yet-unnamed tumor types.
- | Amolyt Pharma
Amolyt hauls in €130M round to fund PhIII trial of hypoparathyroidism drug
French-American biotech Amolyt Pharma has raised a €130 million ($138 million) Series C round, planning to use the cash to take its hypoparathyroidism drug into final-stage testing and move another experimental drug into the clinic.
- | Portage Biotech
Executives Reunite at JPM as Biotech Kicks Off 2023
Brian Wiley, chief business officer at Portage Biotech, spoke of striking a balance between in-person and virtual meetings.
- | F2G
F2G Announces FDA Filing Acceptance of NDA for the Treatment of Invasive Fungal Infections
Biotech company F2G announced today the FDA has accepted its NDA filing for its antifungal therapy, Olorofim. The FDA has set the Prescription Drug User Fee Act (PDUFA) date for June 17, 2023.