TargeGen plans to initiate TG101348 trials early next year

17 December 2007

Privately-held US biopharmaceutical company TargeGen says that it plans to initiate a trial of its developmental JAK2 inhibitor TG101348 in the treatment of myeloproliferative diseases early next year. Data from preclinical studies of the drug, which was recently filed with the Food and Drug Administration, is due to be presented at the American Society of Hematology conference in Atlanta later this month.

Mutations in the gene encoding JAK2, and specifically the V617F polymorphism, are implicated in the pathogeneisis of certain myeloproliferative diseases, including polycythemia vera, essential thrombocytopenia and primary myelofibrosis. Such conditions are thought to affect around 400,000 patients worldwide.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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







Today's issue

Company Spotlight