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According to the company, Zevaskyn is the first and only autologous cell-based gene therapy. The FDA’s decision is supported by the outcomes from the pivotal randomised intrapatient-controlled multi-centre

This status is conferred by the European Commission following a positive opinion from the EMA Committee for orphan medicinal products and offers several benefits, including market exclusivity and

The acquisition enables Apnimed to advance the therapy through its joint venture (JV) with Japanese pharma company, Shionogi & Co. Desitin Arzneimittel will receive an upfront, future milestone

This initiative aims to harness biological and clinical insights, identify new drug targets, and create therapeutics for the oncology sector. The collaboration will leverage de-identified oncology data of

This recommendation facilitates treating the activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in patients aged 12 years and above. The oral therapy is now accessible and funded in

This allosteric pan-mutant-selective phosphatidylinositol 3-kinase alpha (PI3Kα) inhibitor and degrader is poised to enter first-in-human trials in the second quarter of this year. According to the company, mutant

Effexor, a serotonin-noradrenaline reuptake inhibitor (SNRI), has shown promise in treating GAD in adults through a recent study in Japan. The Phase III trial, Study B2411367, confirmed venlafaxine’s

This clearance is intended for treating solid tumours in adults, with a focus on head & neck cancer, breast cancer and soft tissue sarcoma. Preclinical data included in

The funding round was spearheaded by CTI Life Sciences Fund, Advent Life Sciences, and abrdn-managed funds. Current investors, including Sanofi Ventures, Novo Holdings, RiverVest Venture Partners, Sanderling Ventures,