Condition: CIN - Cervical Intraepithelial Neoplasia · CIN 1 · CIN 2 · Sponsor: Papillex Inc.
The goal of this clinical trial is to investigate the safety and efficacy of Papillex® on the regression of abnormal cervical cells caused by HPV in women with a cervical intraepithelial neoplasia (CIN) 1 or 2 diagnosis. The main question it aims to answer is: Is there a difference in the proportion of participants with a regression in CIN based on histology or cytology from baseline at day 180 between Papillex® and placebo? Participants will be asked to consume Papillex® or placebo for 180 days, complete questionnaires, a PAP smear, HPV test, and colonoscopy (where applicable).
This description comes directly from the study's public registry record.
Erin Lewis, PhD · 1-226-242-4551 · elewis@kgkscience.com
Always discuss trial participation with your own doctor first.
| KGK Science Inc. | London, Ontario, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06979180