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Telik Says FDA Removes Partial Hold On TELCYTA Clinical Trials - Quick Facts

By RTTNews Staff Writer   ✉  | Published:  | Google News Follow Us  | Join Us
rttnewslogo20mar2024

Telik, Inc. (TELK) announced that the U.S. Food and Drug Administration or FDA has removed the partial hold on TELCYTA (canfosfamide HCl, TLK286) clinical trials. The company said that this action follows a complete review of TELCYTA data by the agency and permits the resumption of TELCYTA clinical development.

The company noted that its most advanced drug development candidates are TELCYTA, a tumor-activated small molecule product candidate in clinical development for the treatment of advanced ovarian cancer and non- small cell lung cancer; and TELINTRA, which is in clinical development for the treatment of myelodysplastic syndrome.

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