Enrollment of Ph 1 TRE-515 Dose Escalation Trial for Patients with Solid Tumors Completed
“This milestone brings us significantly closer to advancing TRE-515 as the first-to-market dCK inhibitor,” said Dr. Ken Schultz, Trethera’s Chief Executive Officer and Chief Medical Officer. “We remain on track to expand our clinical research in 2026, building on our recent FDA Fast Track designation in prostate cancer.”
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“The designation reinforces the significant unmet need for effective treatment options for patients with advanced breast cancer,” said Charles Baum, M.D., Ph.D., Chief Executive Officer of Terremoto Biosciences. “We are committed to advancing highly selective therapies designed to expand treatment options for patients with difficult to treat cancers.”
“Up to five U.S. clinical sites are planned for THIO-101 Parts C and D this year, and we expect to activate a second U.S. site in the coming weeks,” said Vlad Vitoc, M.D., Founder and Chief Executive Officer of MAIA. “To date, data has shown overall survival (OS) beyond two
Dr. Jason Zhu, Executive Director and Chief Executive Officer of Henlius, said: “The positive CHMP opinion for the sqNSCLC indication marks another important milestone in serplulimab’s regulatory journey in Europe and brings the product one step closer to achieving comprehensive coverage of first-line lung cancer treatment indications in the EU.