Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Natamycin + lactulose is a fixed-dose combination pharmaceutical product consisting of **natamycin**, a polyene macrolide antifungal, and **lactulose**, a non-absorbable disaccharide prebiotic. It is formulated as vaginal suppositories containing 100 mg natamycin and 300 mg lactulose and is indicated for the treatment of **vulvovaginal candidiasis** in adult females[1][2][4]. **Natamycin** binds to ergosterol in the fungal plasma membrane, inhibiting ergosterol-dependent vacuolar fusion and membrane integrity, leading to fungicidal activity. **Lactulose** acts as a prebiotic, increasing vaginal lactobacilli content, which may help restore and maintain healthy vaginal flora during antifungal therapy[1]. The combination has demonstrated superior efficacy in clinical trials versus natamycin and lactulose monotherapy[1].
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 natamycin + lactulose.