Threshold Pharmaceuticals announces results on TH-302 prodrug for cancers at EORTC-NCI-AACR Symposium

Nov 19 2010

Threshold Pharmaceuticals, Inc. (Nasdaq:THLD) today announced clinical trial results related to Threshold's clinical stage hypoxia-activated prodrug, TH-302. The results were presented at the 22^nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics taking place in Berlin, Germany from November 16 to19, 2010.

Today's presentation focused on two clinical trials, the 402 trial and the 403 trial. The 402 trial is a Phase 1/2, three arm, multicenter, dose escalation and dose expansion trial to determine the safety, efficacy and pharmacokinetics of TH-302 in combination with gemcitabine (Gem) or docetaxel (Doc) or pemetrexed (Pem) in patients with various advanced solid tumors including, but not limited to, advanced or metastatic pancreatic cancer, castrate-resistant prostate cancer (CRPC) and relapsed or refractory non-small cell lung cancer (NSCLC). The 403 trial is investigating TH-302 in combination with doxorubicin (Dox) in patients with advanced soft tissue sarcoma. Today's presentation primarily discussed the results for those patients with pancreatic cancer, CRPC, recurrent NSCLC, and soft tissue sarcoma.

Results, as measured by RECIST (Response Evaluation Criteria In Solid Tumors), from the selected tumor types are summarized as follows:

Additionally, in the gemcitabine treatment arm, median progression free survival (PFS) was 6.4 months (95% CI: 4.7 to 7.7 months). Among the patients with relapsed or refractory NSCLC, median PFS was 4.2 months (95% CI: 2.8 months to not reached). Among the 15 patients with CRPC, 11 (73%) had a PSA decline of at least 50%. Among the patients with soft tissue sarcoma, median PFS was 6.4 months (95% CI: 5.6 to 6.9 months). Overall, hematologic toxicity was acceptable and skin and mucosal toxicities were well managed at current dose levels.

"We designed TH-302 to specifically address a significant unmet need in the treatment of cancer and, in so doing, complement those other approaches that comprise the mainstay of cancer therapy. These results suggest that TH-302 is behaving as designed with broad activity against multiple tumor types and in all combinations with which it has been evaluated. TH-302 is well-tolerated and the activity seen in all combinations is greater than what would be expected from any of the individual chemotherapy agents alone," said Charles Hart, Ph.D., Threshold's vice president of biology. "A definitive randomized comparison of the combination versus the chemotherapy alone has been initiated in pancreatic cancer with results expected in 2011 and we look forward to continuing our investigations in additional indications."

A copy of the poster may be obtained by calling the Company.