Preliminary results from the TIMI 14 trial, the first study looking atthe role of glycoprotein IIb/IIIa receptor antagonism in combination with thrombolysis in myocardial infarction, were reported at the 70th Scientific Sessions of the American Heart Association in Orlando, Florida. The interim results show that standard doses of Centocor/Eli Lilly's ReoPro (abciximab), when combined with reduced-dose tissue plasminogen activator (Genentech's Activase; alteplase), provide equivalent arterial patency rates to full-dose tPA.
Thrombolytic drugs have been shown to improve outcome in patients suffering an MI, but their use is associated with a 1.5% incidence of stroke (including 0.7% hemorrhagic stroke). The rationale behind TIMI-14 was to investigate whether lower doses of tPA, combined with an anti-platelet drug that prevents clots from forming, might offer comparable efficacy with a lower risk of bleeding events.
Furthermore, despite thrombolysis only 54% of MI patients achieve optimal arterial patency (blood flow), and inadequate early patency is associated with increased mortality at 30-days. The TIMI 14 team were also hoping to demonstrate that the combination of abciximab and tPA can improve patency rates over tPA alone.
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 2025 | Headless Content Management with Blaze