MAIA Biotechnology announced treatment updates from its Phase 2 clinical trial, THIO-101, evaluating THIO sequenced with the immune checkpoint inhibitor, or CPI, cemiplimab in patients with advanced non-small cell lung cancer, or NSCLC, who failed two or more standard-of-care therapy regimens. The trial’s therapeutic regimen is cycled every three weeks, with THIO 180mg administered in 60mg incremental doses on days 1, 2 and 3, followed by immune activation on day 4, and cemiplimab 350mg administered on day 5. As of the latest clinical cutoff date, June 12: six patients remain on treatment following at least 12 months of therapy. Treatment with THIO followed by cemiplimab has been well tolerated throughout the trial, with much lower toxicity compared to standard-of care treatments. Continuing treatment past 12 months demonstrates safety, efficacy and ongoing benefit from MAIA‘s novel telomere targeting NSCLC therapy.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on MAIA:
- MAIA Biotechnology Reports Progress in Cancer Drug Development
- MAIA reports THIO-101 data from third-line treatment shows ORR of 38%
- MAIA Biotechnology Highlights Clinical Progress and Investor Insights
- MAIA Biotechnology announces new efficacy data from THIO-101 clinical trial
- MAIA Biotechnology Unveils Promising THIO-101 Trial Results