Rilparencel is under clinical development by Prokidney and currently in Phase II for Type 1 Diabetes (Juvenile Diabetes). According to GlobalData, Phase II drugs for Type 1 Diabetes (Juvenile Diabetes) have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Rilparencel’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.

Rilparencel overview

Rilparencel (REACT) is under development for the treatment of chronic kidney disease, congenital anomalies of the kidney and urinary tract (CAKUT), type I diabetes and type II diabetic patients. It is administered through intra-renal injection. The therapy is composed of autologous renal cells (neo-kidney augment) formulated in a gelatin-based hydrogel. The therapeutic candidate is developed based on organ regeneration technology.

Prokidney overview

Prokidney is a clinical research and biotechnology company. The company focuses on developing a transformative proprietary cell therapy platform with the potential for treating chronic kidney disease (CKD) using a patient’s own cells. Its product portfolio includes REACT (renal autologous cell therapy). The company service offerings include preclinical research, clinical trials, research and development, drug development, and drug discovery programs. Prokidney technology restores the kidney function by using the patient’s own kidney cells to delay and prevent renal replacement therapy and kidney transplant. Prokidney is headquartered in Winston-Salem, North Carolina, the US.

For a complete picture of Rilparencel’s drug-specific PTSR and LoA scores, buy the report here.

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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.