Study of 2LPAPI® on the Clearance of Genital HR-HPV Infections.

Recruiting Phase 4 Interventional Study
Human Papilloma Virus
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
25 – 45
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
284 (estimated)
Sponsor
Labo'Life · Industry
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About This Trial
Human papillomavirus (HPV) is a prevalent pathogen, the epidemiology of which has mostly been studied in the uterine cervix and the vagina. The KCE Report 238Cs (2015) recommends " HR-HPV-positive women should not be offered colposcopy immediately. Triage should be done using cytology for this purpose. If cytological abnormalities (ASCUS+) are found, immediate referral should follow for diagnosis…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Women 25-45 years, * Women of childbearing age under effective contraception, * Patient with last cytology less than 3 years and normal or not more than LSIL or CIN I at the histology, * Patient with current cytology presenting normal, ASC-US, AGUS, LSIL, ASC-H, AGC or LSIL+AS…
Contacts

Laura FERTE

+32499717964

laura.ferte@labolife.com

CONTACT

Charlotte BOLLE

charlotte.bolle@labolife.com

CONTACT