Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This entry refers to the comparative study of unfractionated heparin (UFH) and certoparin (a low-molecular-weight heparin) within the HIT-TRAP clinical trial. Conducted by University Medicine Greifswald, the Phase 4 trial evaluated the incidence of heparin-induced thrombocytopenia (HIT) antibodies and thromboembolic complications in trauma patients requiring thrombosis prophylaxis. Both agents are anticoagulants that function by activating antithrombin III, which subsequently inhibits clotting factors such as thrombin (Factor IIa) and activated Factor X (Xa). Certoparin, being an LMWH, typically exhibits a more predictable pharmacokinetic profile and a higher anti-Xa to anti-IIa ratio compared to UFH. The study specifically highlighted that certoparin was associated with a significantly lower rate of HIT-antibody seroconversion (1.7%) than UFH (6.6%) in the trauma patient population.
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 heparin + certoparin (Universitätsklinikum Greifswald).