Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Omidenepag isopropyl is a small molecule prodrug used as an ophthalmic solution to lower intraocular pressure in patients with open-angle glaucoma or ocular hypertension. After corneal penetration, it is hydrolyzed to its active metabolite, omidenepag, which acts as a selective agonist of the prostaglandin E2 (EP2) receptor. Activation of this receptor increases intracellular cAMP levels in the ciliary body and trabecular meshwork, promoting aqueous humor outflow through both trabecular and uveoscleral pathways. This mechanism provides an alternative for patients who do not respond adequately to FP receptor agonists like latanoprost. Omidenepag isopropyl was first approved in Japan in 2018 and received FDA approval in September 2022 for the reduction of elevated intraocular pressure[1][3][5][6].
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 omidenepag isopropyl.