Teva Faces Laquinimod Setback After High Dose Linked To CV Events

Teva will discontinue higher doses of laqunimod in two ongoing studies for multiple sclerosis after cardiovascular events were experienced in eight patients. Trials will continue with a lower dose.

Teva Pharmaceutical Industries Ltd.’s attempt to produce greater efficacy with the investigational multiple sclerosis drug laquinimod by testing higher doses has backfired. The company revealed Jan. 4 that it will discontinue higher doses of laquinimod in two ongoing clinical trials after eight non-fatal cardiovascular events occurred.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Clinical Trials

More from R&D