CRD-100 is under clinical development by Curadev Pharma and currently in Phase I for Merkel Cell Carcinoma. According to GlobalData, Phase I drugs for Merkel Cell Carcinoma have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CRD-100’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
CRD-100 overview
CRD-100 is under development for the treatment of sarcomas like undifferentiated pleomorphic sarcoma or myxofibrosarcoma, angiosarcoma, bone sarcoma or merkel cell carcinoma. The drug candidate is a small molecule that act by targeting STING adaptor protein. It is administered through intravenous route.
Curadev Pharma overview
Curadev Pharma (Curadev) discovers and develops small molecule drug candidates to treat cancers and hematological disorders. Its immuno-oncology research programs include stimulator of interferon genes (STING) agonist and antagonist, antibody drug conjugate and small molecule inhibitors for treating liquid and solid tumors and inflammation disorders. The company developed potent small molecules inhibitors that reduce kynurenine levels in experimental paradigms. Curadev conducts research in the areas of immune oncology, metabolism, lymphoma treatment and autoimmune diseases. The company works in collaboration with University of Texas Southwestern Medical Centre, INSERM, All India Institute of Medical Sciences and Indian Institute of Technology to advance the development of its pipeline products. Curadev is headquartered in Noida, Uttar Pradesh, India.
For a complete picture of CRD-100’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.
