Leuprolide mesylate SR is under clinical development by Foresee Pharmaceuticals and currently in Phase III for Central Precocious Puberty. According to GlobalData, Phase III drugs for Central Precocious Puberty does not have sufficient historical data to build an indication benchmark PTSR for Phase III. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Leuprolide mesylate SR LoA Report. Buy the report here.
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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.
Leuprolide mesylate SR overview
Leuprolide mesylate (Camcevi) is a synthetic peptide analogue of gonadotropin-releasing hormone (GnRH). It is formulated as sustained release emulsion and suspension for subcutaneous route of administration. Camcevi is indicated for the treatment of adult patients with advanced prostate cancer. Camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.
FP-001 (Leuprolide mesylate) is under development for the treatment of prostate cancer and central precocious puberty. The therapeutic candidate is a synthetic peptide administered through subcutaneous and parenteral route. It is a sustained release formulation delivered through a depot system. It acts by targeting gonadotropin-releasing hormone receptor. It developed based on stabilized injectable formulation (SIF) platform technology.
Foresee Pharmaceuticals overview
Foresee Pharmaceuticals (FP) is a clinical-stage pharmaceutical company. It focuses on developing drugs for unmet medical needs. The company’s product portfolio comprises FP-001, for prostate cancer, FP-002, for acromegaly and carcinoid tumors, FP-025, for asthma and chronic obstructive pulmonary disease, FP-020, for Alport syndrome and FP-008, for diabetic retinopathy. It harnesses the stabilized injectable formulation (SIF) platform technology to develop controlled release drug delivery systems for peptides, small molecules and proteins. The company works in collaboration with ScinoPharm and Pierre Fabre to research and develop its product portfolio. It has operational presence in Taiwan and the US. FP is headquartered in Taipei, Taiwan.
For a complete picture of Leuprolide mesylate SR’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
