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Home » Newsletters » BioWorld

BioWorld

Oct. 13, 2022

View Archived Issues
Brain maze

Relmada stock flounders after phase III study fail in MDD

Relmada Therapeutics Inc. is scratching its collective chin as it sifts through data from the failed phase III Reliance III study of REL-1017 (esmethadone) in treating major depressive disorder (MDD). A higher-than-expected placebo response, however, prompted the company to label the study’s results as “paradoxical.” Read More

‘SOFA’ so good: Inotrem’s nangibotide improves organ function in phase IIb septic shock study

A phase IIb trial of nangibotide in septic shock has demonstrated preliminary signs of efficacy in a subset of biomarker-defined patients and provided its developer, Inotrem SA, with a dataset that will inform the design of a registration program for the drug. Subject to agreement from regulatory agencies, the company aims to move the triggering receptor on myeloid cells 1 inhibitor into a first phase III trial in early 2024. “We should have a clearer picture by the beginning of the second next year,” CEO Sven Zimmermann told BioWorld. Read More
Gary Glick, founder and CEO, Odyssey Therapeutics

Odyssey opens second chapter with $168M series B

Odyssey Therapeutics Inc. closed a hefty $168 million series B round to progress multiple small-molecule and protein-based drug discovery and development programs in autoimmune disease and cancer. Read More
deal-handshake2

Slowing deals in Q3 drop 2022 behind last two years

Biopharma deals lost speed in the third quarter and are now falling behind each of the last two years, while merger and acquisition values doubled the amount from the first half of 2022. The industry completed a total of 283 deals, including licensings, collaborations and joint ventures, in Q3. They were worth a combined value of $40.98 billion, a rise of 8.3% over the second quarter but down by 28.7% from the first quarter. Read More
Elderly person receiving shot

GSK posts strong results for RSV shot, as Pfizer prepares to file rival shot

GSK plc has announced results from its respiratory syncytial virus (RSV) vaccine in older people that look stronger than those from its rival, Pfizer Inc., as the race to develop a first ever vaccine against the common respiratory disease heats up. Read More

Cabaletta acquires global rights to CD19 binder from Iaso Bio in $162M deal

Nanjing Iaso Biotherapeutics Co. Ltd. has out-licensed a fully human anti-CD19 binder to Cabaletta Bio Inc. in a deal worth up to $162 million. Read More

What’s in a name? Inquiring minds at the FDA want to know

Prescription drug names are generally invented words that are often easier to spell than they are to pronounce. And, for the most part, they’re meaningless until they’ve been associated with a drug. Read More

Appointments and advancements for Oct. 13, 2022

New hires and promotions in the biopharma industry, including: Acadia, Kyverna, Maze. Read More

Financings for Oct. 13, 2022

Biopharmas raising money in public or private financings, including: Axcella, Bone, Carmine, Dice, Vectivbio. Read More

In the clinic for Oct. 13, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abivax, Amolyt, Atai, Avidity, Beigene, Cognition, Corcept, Eupraxia, Evgen, Evofem, Frequency, Fulcrum, Genentech, Janux, Junshi, Kinnate, Leap, Novavax, Sangamo. Read More

Other news to note for Oct. 13, 2022

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Adept, Aytu, Enterin, Genuv, GPCR, Jacobio, Merck KGaA. Read More

Regulatory actions for Oct. 13, 2022

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aim, Biomind, Eagle, Elevar, Galectin, Merck & Co., Moerna, Pfizer, Regeneron, Sisaf. Read More

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