Telomir Pharmaceuticals (TELO) announced that the U.S. Food and Drug Administration, FDA, has cleared the Company’s Investigational New Drug, IND, application for its lead candidate, Telomir-Zn, for the treatment of patients with advanced or metastatic triple-negative breast cancer, TNBC.
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Read More on TELO:
- Telomir Pharmaceuticals Completes TELI Acquisition, Expands Telomir-1 Rights
- Telomir Pharmaceuticals completes acquisition of TELI Pharmaceuticals
- Telomir Pharmaceuticals Regains Nasdaq Listing Rule Compliance
- Telomir Pharmaceuticals submits IND to FDA for Telomir-1 in TNBC
- Telomir Shareholders Approve Equity Plan and Bylaw Changes
