Plain-English translation of NCT04411043 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research study collecting detailed information from patients with prolymphocytic leukemia T, a rare and aggressive blood cancer. Researchers will gather information about your disease, your genetic makeup, and how you respond to treatments like alemtuzumab or other therapies. The goal is to help doctors understand this disease better and find new, gentler treatment options for patients who can't tolerate intensive chemotherapy.
Prolymphocytic leukemia T is rare and serious, and patients often don't respond well to standard cancer drugs. While alemtuzumab has helped some patients, the benefits don't last long, and many people need better treatment options. This study aims to learn which patients respond best to current treatments and to identify new, kinder approaches that target the specific genetic changes driving this cancer.
You likely qualify if…
You likely don't qualify if…
In this study, you would allow researchers to collect and review your medical records, treatment history, and blood or tissue samples to extract genetic information. You would not receive a new experimental drug; instead, researchers would track your current treatment and outcomes over time. This is an observational study, meaning doctors are watching and learning from your existing care rather than testing a brand-new therapy.
AI-generated summary from trial data · Jul 12, 2026 · Not medical advice
France
Collaborators
University Hospital, Lille
Enrollment target
~50 participants
Started
July 2020
Primary completion
July 2026
This trial's estimated completion date has passed — the record may not be fully up to date.
Age range
18 Years and older
Last updated on clinicaltrials.gov in July 2026.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Charles HERBAUX, Dr
French Innovative Leukemia Organisation
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.