Actively Recruiting
Effect of Anti-Psoriatic Biologics on Risk of Anogenital Warts (CONDYPSO)
Led by Jonathan Krygier · Updated on 2026-03-18
600
Participants Needed
3
Research Sites
130 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to assess the impact of anti-TNF-α, anti-IL-17, and anti-IL-23 biologic therapies on the risk of development or recurrence of anogenital warts (AGW) in patients with moderate to severe psoriasis. By modulating systemic and mucosal immunity, these treatments may alter host defenses against human papillomavirus (HPV) infections, which are responsible for AGW. In particular, inhibition of Th1 pathways (by anti-TNF-α) and Th17 pathways (by anti-IL-17 and anti-IL-23), both central to the antiviral response, may reduce local production of pro-inflammatory cytokines (such as IFN-γ, IL-17, and IL-22), decrease the activity of CD8+ cytotoxic T lymphocytes, and impair dendritic cell function, thereby compromising viral clearance at the genital mucosa. AGW are a frequent and recurrent manifestation of HPV infection, and their incidence may be influenced by these immunomodulatory treatments. The retrospective component will review cases already documented in medical records and analyze, to the extent permitted by available data, the same risk factors as in the prospective component, including history of sexually transmitted infections (STIs), risk behaviors, treatments used (systemic or topical), and time to onset or recurrence of AGW. This analysis will be conducted as a retrospective case-control study, matching each patient who developed AGW with one or more controls receiving biologics who did not develop AGW, in order to identify factors associated with their occurrence. The prospective follow-up will assess, over 24 months, risk factors for occurrence or recurrence of AGW in patients with moderate to severe psoriasis, according to the treatment received: no treatment, topical treatment, systemic non-immunomodulatory treatment, or immunomodulatory treatment, including biologics. Acceptability of HPV vaccination will also be evaluated, at enrollment, in a subset of prospectively included adult patients without a known history or current clinical lesion of condyloma, HSIL, or HPV-induced carcinoma.
CONDITIONS
Official Title
Effect of Anti-Psoriatic Biologics on Risk of Anogenital Warts (CONDYPSO)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age ≥ 18 years
- Moderate to severe psoriasis (BSA > 10% or PASI > 10) prior to current therapy at inclusion
- Planned dermatological follow-up for approximately 24 months with no additional study visits
- Signed informed consent
You will not qualify if you...
- Severe immunosuppression not related to psoriasis or its therapy, including major immunosuppressant treatments or uncontrolled HIV infection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
CHU Saint-Pierre
Brussels, Brussels Capital, Belgium, 1000
Actively Recruiting
2
CHU Brugmann
Brussels, Brussels Capital, Belgium, 1020
Actively Recruiting
3
Hôpital Erasme
Brussels, Brussels Capital, Belgium, 1070
Actively Recruiting
Research Team
J
Jonathan Krygier, MD
CONTACT
P
Pauline Lecerf, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here