Asieris Receives NMPA’s IND Approval to Evaluate APL-1202 + Tislelizumab as Neoadjuvant Therapy for MIBC Patients
Shots:
- NMPA’s CDE has approved the IND application of oral APL-1202 in combination with BeiGene’s tislelizumab as neoadjuvant therapy in patients with muscle invasive bladder cancer. The US FDA has cleared the IND of the therapy in Jun’2021
- The P-I/II study will evaluate the safety in MIBC patients, to determine RP2D and to assess efficacy as neoadjuvant therapy for MIBC
- APL-1202 is an orally available reversible MetAP2 Inhibitor with anti-angiogenic, anti-tumor activities and can also modulate tumor immune microenvironment
Click here to read full press release/ article | Ref: PR Newswire | Image: Asieris