• Yingli Pharma has received FDA clearance to initiate a global Phase III registration trial of linperlisib for relapsed/refractory peripheral T-cell lymphoma (PTCL) following a successful End-of-Phase II meeting.
• The pivotal study, set to begin in Q2 2025, will compare linperlisib against physician's choice of standard care in patients who have undergone previous systemic therapies, with enrollment across multiple countries.
• Linperlisib, a selective PI3Kδ inhibitor, has demonstrated promising efficacy in over 165 PTCL patients across China, US, and Europe, with high response rates and a well-tolerated safety profile in over 6,000 treated patients.