Citius Positive Prelim Phase I in Recurrent Solid Tumors

 Study, in patients with solid tumors focusing on gynecological malignant tumors such as ovarian, endometrial, and cervical, nearing completion with three remaining subjects to be enrolled

27% Objective Response Rate (ORR)

33% Clinical Benefit Rate (CBR) with a median Progression Free Survival (PFS) of 57 weeks

Chemotherapy-free immunomodulatory regimen well-tolerated with no documented serious immune-related adverse events

https://www.prnewswire.com/news-releases/citius-pharmaceuticals-inc-and-citius-oncology-inc-announce-promising-preliminary-results-of-an-investigator-initiated-phase-i-clinical-trial-of-pembrolizumab-keytruda-and-lymphir-in-cancer-patients-with-recurrent-solid-tu-302300516.html