Tenalisib is under clinical development by Rhizen Pharmaceuticals and currently in Phase II for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma). According to GlobalData, Phase II drugs for Hodgkin Lymphoma (B-Cell Hodgkin Lymphoma) have a 17% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Tenalisib’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.
Tenalisib overview
Tenalisib (RP-6530) is under development for the treatment of relapsed or refractory hematologic malignancies including relapsed and chronic lymphocytic leukemia, diffuse large B-cell lymphoma, Hodgkin Lymphoma, refractory cutaneous T-cell lymphoma, peripheral T-cell lymphomas (PTCL), follicular lymphoma, marginal zone lymphoma, Waldenstrom macroglobulinemia, small lymphocytic lymphoma, triple negative breast cancer, solid tumors and ovarian cancer. It is administered through oral route, topical and inhalational route. The drug candidate is a dual phosphoinositide-3 kinase (PI3K) delta/gamma inhibitor and Salt-Inducible Kinase 3 (SIK3) inhibitor.
Rhizen Pharmaceuticals overview
RhizenPharmaceuticals (RhizenPharma), a subsidiary of Alembic Pharmaceuticals Ltd, is a biopharmaceutical company that discovers and develops small molecule drugs. The company’s research products include c-Met inhibitors, selective P13K inhibitors, CRAC channel inhibitors and GPR 119 agonist. It conducts research in the therapeutic areas of oncology, immune inflammation and metabolic disorders such as diabetes and obesity. RhizenPharma’s products find application in the treatment of diseases such as solid tumors, B cell lymphomas, hematological malignancies, asthma, diabetes and chronic obstructive pulmonary disease, among others. It collaborates with other pharmaceutical companies. Rhizenis headquartered in La Chaux-de-Fonds, Switzerland.
For a complete picture of Tenalisib’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.
