Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Paremyd is a sterile ophthalmic solution used as a topical mydriatic combination product for ophthalmic use. It contains two active ingredients: hydroxyamphetamine hydrobromide (1%) and tropicamide (0.25%). Hydroxyamphetamine hydrobromide is an indirectly-acting sympathomimetic agent that causes the release of endogenous norepinephrine from adrenergic nerve terminals in the eye, resulting in pupil dilation (mydriasis). Tropicamide is an anticholinergic (parasympatholytic) agent that blocks cholinergic stimulation of the iris sphincter muscle and ciliary muscle, leading to further pupil dilation and partial paralysis of accommodation (cycloplegia). The combination provides rapid onset mydriasis within 15 minutes, with maximum effect at 60 minutes; effects typically last 3 hours with recovery beginning at about 90 minutes and complete recovery usually within 6–8 hours. Paremyd is primarily indicated for use in routine diagnostic procedures requiring short-term pupil dilation[1][2][4][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 Paremyd.