This round of financing was led by SV Health Investors’ Dementia Discovery Fund (DDF), with contributions from existing investors including Newpath Partners, OrbiMed, Euclidean Capital, Chugai Venture Fund,
This change eliminates the previous requirement for a cardiovascular disease diagnosis prior to treatment. Amgen global commercial operations executive vice president Murdo Gordon said: “Far too many adults
The investment equips NewAmsterdam Pharma with the commercial capability to produce a fixed dose combination (FDC) of obicetrapib and ezetimibe, thereby addressing potential market demand. Piramal Pharma Solutions
Brukinsa’s recommended dose remains 320mg a day. The new tablets, each 160mg, allow patients to halve their intake of daily pill from four to two. Moreover, these tablets
Additionally, this combination is approved for the treatment of unresectable or advanced hepatocellular carcinoma (HCC). The approval introduces a dual immunotherapy option for two difficult-to-treat gastrointestinal cancers. Evidence
The therapy is intended for the treatment of Duchenne muscular dystrophy (DMD) in patients aged four years and above. Sales are projected to begin on a named patient
This designation comes after the FDA Office of Orphan Products Development reviewed recent Phase IIa clinical trial results, which showed both biological efficacy and safety in patients with
The FDA’s designation is designed to expedite the review of treatments. It offers opportunities for more frequent discussions with the FDA regarding the clinical development plan of a
This move is a significant step in the company’s global expansion strategy, focusing on enhancing the availability of essential cancer therapies. Bevacizumab is a targeted therapy designed to
This designation is granted for treatments that could significantly improve upon existing options. The FDA’s decision is expected by the fourth quarter of 2025, in line with the
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