Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DeflaGyn is a vaginal gel classified as a Class IIa medical device used for the treatment of cervical lesions, unclear cervical smears, and HPV-induced cervical abnormalities, including cervical intraepithelial neoplasia (CIN 1 and CIN 2). Developed by DEFLAMED International, the formulation contains highly dispersed silicon dioxide, citric acid, and sodium selenite. Its primary mechanism of action involves the adsorptive binding of pathogens, such as viruses and bacteria, and the provision of antioxidant effects through its patented DEFLAMIN combination (sodium selenite and citric acid). It is typically used during the 'watchful waiting' period to promote the regression of lesions and clear high-risk HPV infections, with clinical studies demonstrating significant efficacy in lesion regression compared to controls.
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 DeflaGyn.