Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tafluprost is a synthetic prostaglandin F2α analog used as an ophthalmic solution to lower intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. It acts as a selective agonist of the prostaglandin F receptor (FP receptor), increasing uveoscleral outflow of aqueous humor and thereby reducing IOP. Tafluprost is notable for its high affinity for the FP receptor—approximately 12 times that of latanoprost—and minimal activity at other receptors. The drug was jointly developed by Santen Pharmaceutical and Merck and is available in preservative-free formulations to improve tolerability. Common side effects include conjunctival hyperemia and possible irreversible changes such as iris pigmentation and eyelash growth[2][4][5].
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 tafluprost.