Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Lotiglipron + dabigatran** is a combination of two drugs studied together to assess pharmacokinetic interactions. Lotiglipron (PF-07081532) is an investigational, orally administered small-molecule glucagon-like peptide 1 receptor agonist designed for overweight and obesity management; it acts by increasing insulin secretion, slowing gastric emptying, and promoting satiety. Dabigatran is an approved oral direct thrombin inhibitor, indicated for reducing risk of stroke and thromboembolism, as well as for treatment and prevention of venous thromboembolism. In clinical research on overweight or obese adults, lotiglipron was shown to reduce plasma dabigatran concentrations by approximately 20% when co-administered; development of lotiglipron has been terminated due to safety concerns, primarily elevation in liver transaminases. No branded combination of these agents is marketed; this combination was studied only in clinical research settings for drug–drug interaction purposes[1][2][3][4].
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 lotiglipron + dabigatran.