Clin2
NCT06878196Possibly a fitNot yet recruiting

ctDNA-Guided Immunotherapy De-escalation for Advanced Cervical Cancer

Uterine Cervical Neoplasm

Part of Cancer, Women’s health & pregnancy clinical trials.

This trial tests if a ctDNA blood test can help guide treatment to use less immunotherapy in patients with advanced or recurrent cervical cancer. It's looking at which patients might safely reduce treatment based on their cancer's genetic signals in the blood.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
20 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are a woman aged 18 to 75 with cervical cancer that is either stage IVB and hasn't been treated, or a recurrence that hasn't been treated.
  • Your cancer type must be squamous cell, adenocarcinoma, or adenosquamous (the most common types).
  • You must have at least one tumor that can be measured on scans and be in fairly good health (ECOG score 0 or 1, meaning you can do daily activities).
  • Your blood counts, kidney function, and liver function must be within certain limits (your doctor will check this).
  • You cannot have had immunotherapy before, active autoimmune disease, or active infections like HIV or hepatitis that are not well controlled.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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