Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Terclara is a topical cutaneous solution containing terbinafine hydrochloride (equivalent to 98 mg/mL terbinafine) developed for the treatment of mild to moderate fungal infections of the nails (onychomycosis) caused by dermatophytes and other terbinafine-sensitive fungi. It is indicated for adult use only and is applied once daily to affected fingernails or toenails, with typical treatment durations of about 6 months for fingernails and 9–12 months for toenails. The mechanism of action involves inhibition of fungal sterol biosynthesis at an early step, leading to ergosterol deficiency and intracellular accumulation of squalene, resulting in fungal cell death. Clinical trials have shown high efficacy rates with daily dosing regimens. Developed by Moberg Pharma, Terclara has market approval in 13 EU countries and is marketed as a leading product in Sweden and Norway[1][2][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 Terclara.