LifeCycle Pharma Submits Phase 3 Protocol For LCP-Tacro To FDA
LifeCycle Pharma (LCP) has submitted the phase 3 protocol for LCP-Tacro in de novo kidney transplant recipients, to the FDA. LCP is expected to review the protocol with
Teva Pharmaceuticals International and Polpharma Biologics have signed a global licensing agreement for a proposed biosimilar to Ocrevus (ocrelizumab) to treat multiple sclerosis (MS).