GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Clascoterone overview

Clascoterone (Winlevi) is a cortexolone 17alpha-propionate derivative acts as anti-acne agent. It is formulated as cream for topical application. Winlevi is indicated for treatment of acne vulgaris in patients with 12 years of age and older.

Clascoterone (CB-0301, Winlevi) is under development for the treatment of acne vulgaris, solid tumors including androgen-independent prostate adenocarcinoma, relapsed/refractory pancreatic adenocarcinoma, androgenetic alopecia and relapsed/refractory triple negative breast cancer (TNBC). The drug candidate is a new chemical entity. It is administered through cutaneous (topical) route. The drug candidate is derived from 11-deoxycortisone that acts by targeting androgen receptor and glucagon receptor. It is developed based on Matrix MMX technology. It was also under development for the treatment of hirsutism.

Cosmo Pharmaceuticals overview

Cosmo Pharmaceuticals (Cosmo) develops drugs for the treatment of gastrointestinal diseases and dermatology. It develops pharmaceutical products based on its multi-matrix technology. The company offers products such as Lialda, Mezavant, Mesavancol and Uceris for the treatment of ulcerative colitis. It also offers Eleview which is a submucosal injectable composition for use in gastrointestinal endoscopic procedures. The company’s manufacturing facility is located in Lainate, Milan. Cosmo is headquartered in Dublin, Ireland.

For a complete picture of Clascoterone’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.