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|Articles|November 1, 2007

Oncology NEWS International

  • Oncology NEWS International Vol 16 No 11
  • Volume 16
  • Issue 11

FDA removes partial hold on Telcyta clinical development

FDA removes partial hold on Telcyta clinical development

PALO ALTO, California—Telik, Inc. has announced that the FDA has removed the partial hold on Telcyta (canfosfamide HCl) clinical trials. This action follows a complete review of Telcyta data by the agency and permits the resumption of Telcyta clinical development. Telcyta is a tumor-activated small-molecule product candidate in clinical development for the treatment of advanced ovarian cancer and non-small-cell lung cancer. FDA placed the hold on development after phase III data showed lower median survival for women with advanced ovarian cancer receiving Telcyta vs standard chemotherapy.

Articles in this issue

over 18 years ago

MT103, BiTE antibody, enters phase II testing for ALL

over 18 years ago

Sides dig in as ESA policy debate heats up

over 18 years ago

Ixempra gets ok for resistant breast cancer

over 18 years ago

ASCO adds Oncotype DX to marker guideline

over 18 years ago

Dr. Norton hopes to weed 'molecular' tumor garden

over 18 years ago

Accelerated approval for Tasigna

over 18 years ago

Oxidative stress inducer ups survival in advanced melanoma

over 18 years ago

Should all HER2+ pts receive adjuvant trastuzumab?

over 18 years ago

R-CHOP is standard of care for advanced DLBCL patients

over 18 years ago

FDA oks Velcade for patients with renal dysfunction

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