Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Breviprost is a preservative-free ophthalmic formulation of travoprost, a synthetic prostaglandin F2α analogue, developed and manufactured by Liqvor. It is approved for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. As a selective agonist of the prostaglandin F receptor (PTGFR), travoprost lowers intraocular pressure by increasing the outflow of aqueous humor, primarily via the uveoscleral pathway. The preservative-free formulation of Breviprost is designed to minimize corneal toxicity, ocular irritation, and the development of dry eye syndrome, which are common with long-term use of preserved eye drops.
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 Breviprost.