Mocravimod is under clinical development by Priothera and currently in Phase II for Ulcerative Colitis. According to GlobalData, Phase II drugs for Ulcerative Colitis have a 44% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Mocravimod’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.
KRP-203 is under development for the treatment of the autoimmune diseases like ulcerative colitis, subacute cutaneous lupus erythematosus, Acute Myeloid Leukemia (AML), secondary acute myeloid leukemia, primary mediastinal large b-cell lymphoma and Crohn’s disease and hematopoietic stem cell transplantation. The drug candidate is an orally administered immunosuppressant that acts by targeting S1P receptor. It was also under development for the treatment of the subacute cutaneous lupus erythematosus and ulcerative colitis and also for inflammatory bowel disease in Japan.
It was under development for the treatment of autoimmune diseases, inflammatory bowel disease, graft versus host disease (transplantation) and Crohn's disease.
Priothera is a clinical stage company developing orally applied sphingosine 1 phosphate (S1P) receptor modulators for haematological malignancies. Priothera is headquartered in Dublin, Ireland.
For a complete picture of Mocravimod’s drug-specific PTSR and LoA scores, buy the report here.