Dilanubicel is under clinical development by Coeptis Therapeutics and currently in Phase II for Acute Lymphocytic Leukemia (ALL, Acute Lymphoblastic Leukemia). According to GlobalData, Phase II drugs for Acute Lymphocytic Leukemia (ALL, Acute Lymphoblastic Leukemia) have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Dilanubicel’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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.
Dilanubicel is under development for the reduction of morbidity and mortality associated with hematopoietic stem cell transplantation, acute myeloid leukemia, acute lymphoblastic leukemia, chronic myeloid leukemia and myelodysplastic syndrome. The therapeutic candidate constitutes universal donor ex-vivo expanded cord blood progenitor and hematopoietic stem cells. It is based on ex vivo expanded umbilical cord blood platform. It is administered intravenously as an infusion. It was also under development for the treatment of chemotherapy-induced neutropenia in pediatrics and adults, rejection of solid organ transplant and acute radiation toxicity.
Coeptis Therapeutics overview
Coeptis Therapeutics is a biopharmaceutical company that involved in the development, and commercialization of branded and generic pharmaceutical products and cell therapy platforms for patients with cancer. The company is headquartered in Wexford, Pennsylvania, the US.
For a complete picture of Dilanubicel’s drug-specific PTSR and LoA scores, buy the report here.