Clinical Trial

Neoadjuvant Lymph Node Targeted Immunotherapy in Cervical Cancer: a Feasibility Study (NEOLYNC)

Study acronym: NEOLYNC
Recruiting Phase 1
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Summary
We aim to determine feasibility, safety and efficacy of TDLN-targeted immune checkpoint inhibition in different doses (nivolumab) in patients with cervical cancer.
Trial Details
NCT Number NCT07653503
Lead Sponsor University Medical Center Groningen
Conditions Cervical Carcinoma
Enrollment 12 participants
Start Date 2026-01-05
Primary Completion 2027-12-01 (estimated)
Study Completion 2027-12-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-17