Business

Actimed regains full control of S-oxprenolol after five-year partnership with Faraday

UK-based Actimed Therapeutics has reacquired full global rights to S-oxprenolol (ACM-002), an anabolic-catabolic transforming agent (ACTA) small molecule,...

Actimed regains full control of S-oxprenolol after five-year partnership with Faraday

UK-based Actimed Therapeutics has regained full global rights to S-oxprenolol (ACM-002) from Faraday Pharmaceuticals, unwinding a 2021 licensing agreement worth up to USD 123.5 million in milestones and restoring control of the muscle-wasting therapy across all indications.

The original 2021 license granted Faraday global rights to develop and commercialize S-oxprenolol in cancer cachexia and all indications except ALS, in exchange for a combined cash and equity upfront of USD 550,000, a near-term milestone of USD 2.7 million, and up to USD 123.5 million in total potential milestones plus royalties.

No public development milestones or clinical updates relating to S-oxprenolol have been disclosed since the agreement was signed. During that period, Faraday advanced its own cachexia candidate, FDY-8801, into Phase II, suggesting its internal program became the company's principal focus.

The AllSci BriefSystematic R&D and deal news. Daily.

Actimed describes S-oxprenolol as exhibiting multi-modal pharmacology targeting the underlying pathophysiology of muscle-wasting disorders. The company said the asset demonstrated beneficial effects on survival, body mass, and functional parameters in a preclinical model of ALS, and the company plans to initiate a clinical program once chemistry, manufacturing and controls work is complete. The US FDA granted the molecule Orphan Drug Designation for ALS in September 2024.


Access the AllSci platform to explore the science behind the news.


Spot something wrong? Report an issue with this article