Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HP-3180 is a transdermal patch formulation of fesoterodine, a muscarinic acetylcholine receptor antagonist, being developed by Hisamitsu Pharmaceutical for the treatment of overactive bladder (OAB). Fesoterodine is a prodrug that is rapidly hydrolyzed to its active metabolite, 5-hydroxymethyl tolterodine (5-HMT), which acts as a competitive antagonist at muscarinic receptors in the bladder detrusor muscle. By inhibiting these receptors, the active metabolite suppresses involuntary bladder contractions, thereby reducing symptoms of urgency, frequency, and urge incontinence. The transdermal delivery system is designed to provide sustained drug release, potentially improving patient compliance and tolerability by avoiding the peak plasma concentrations associated with oral administration. As of 2024, HP-3180 is in Phase 1 clinical development in Japan.
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 HP-3180.