Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Duteplase is a two-chain recombinant tissue-type plasminogen activator (rt-PA) that was developed by Burroughs Wellcome as a thrombolytic agent. It is chemically distinguished from alteplase, which is a predominantly single-chain form of rt-PA. Duteplase works by catalyzing the conversion of plasminogen to plasmin, an enzyme that dissolves fibrin clots, thereby restoring blood flow in occluded vessels. It was extensively evaluated in the early 1990s for the treatment of acute myocardial infarction (AMI) and acute ischemic stroke. Most notably, it was one of the thrombolytic agents compared in the large-scale ISIS-3 trial. Despite showing efficacy in achieving coronary artery patency and improving neurological outcomes, duteplase was associated with a risk of intracranial hemorrhage, and its development was eventually discontinued as other thrombolytics like alteplase and tenecteplase became the clinical standards.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on duteplase.