Promethera Biosciences Announces First-Dosing in Phase 2a Clinical Study Evaluating World’s First Liver Stem Cell Therapy in Late-Stage NASH Patients
Retrieved on:
Thursday, May 9, 2019
The multicenter, open-label PANASH study will evaluate the safety and preliminary efficacy of Prometheras investigational drug HepaStem, a novel allogenic cell-based therapy for severe liver diseases, in patients with cirrhotic and pre-cirrhotic NASH.
Key Points:
- The multicenter, open-label PANASH study will evaluate the safety and preliminary efficacy of Prometheras investigational drug HepaStem, a novel allogenic cell-based therapy for severe liver diseases, in patients with cirrhotic and pre-cirrhotic NASH.
- The study will enroll a minimum of 24 patients via centers in 8 European countries.
- Moving HepaStem into clinical studies in NASH in addition to the ongoing clinical evaluation in Acute-on-Chronic Liver Failure, represents a significant milestone for our therapeutic development activities.
- Promethera Biosciences is a global innovator in liver therapeutics whose mission is to bring life-saving treatments to reduce the need for liver transplantation.