US biotech firm Threshold Pharmaceuticals (Nasdaq: THLD) said yesterday that data from a Phase IIb trial of TH-302 in patients with advanced pancreatic cancer will be presented at the European Society for Medical Oncology, Austria, September 28 to October 2, 2012. New finding on overall survival indicate that patients treated with gemcitabine alone had a median overall survival of 6.9 months versus 9.2 months with TH-302 340 mg/m2 + gemcitabine (HR: 0.955, 95% CI: 0.67-1.37, p=0.800) and 8.7 months with TH-302 240 mg/m2 + gemcitabine (HR: 0.960, 95% CI: 0.67-1.38, p=0.827).
However, adding TH-302 to gemcitabine only reduced the relative risk of death by 4.5% over gemcitabine alone - a small benefit that was far from statistical significance, with this news sending Threshold’s shares tumbling over 19% to $7.05 in Monday trading. The drug is being developed with Germany’s Merck KGaA (MRK: DE), which earlier this year, entered a deal worth up to $550 million to Threshold - including $25 million upfront - to gain global rights to develop and commercializeTH-302 (The Pharma Letter February 6).
Merck withdraws European filing for Erbitux in NSCLC
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze