Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lanoteplase is a recombinant, second-generation tissue plasminogen activator (tPA) developed as a thrombolytic agent for the treatment of acute myocardial infarction and other thrombotic disorders. It is a serine protease engineered from tPA by deletion and point mutation, resulting in increased half-life compared to alteplase. Lanoteplase binds to fibrin within blood clots and cleaves the Arg-Val bond in plasminogen, generating active plasmin that degrades fibrin clots, thereby restoring blood flow in occluded vessels. Clinical trials demonstrated its efficacy as a single bolus intravenous injection with dose-dependent reperfusion rates comparable or superior to alteplase; however, development was discontinued due to safety concerns including higher rates of intracranial hemorrhage at certain doses[1][2][3].
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 lanoteplase.