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CLL study aims to link genes to treatment success
NCT ID NCT07162532
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study will follow 45 adults newly diagnosed with chronic lymphocytic leukemia (CLL) for at least one year. Researchers will collect blood samples and genetic information to see how certain markers, like IGHV mutations and chromosome changes, relate to how well patients respond to treatment. The goal is to better understand which factors lead to better or worse outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better predict which CLL treatments work best based on a patient's genetic profile.
- What could go wrong
- This is a small, early-stage observational study with only 45 people. It is not testing a new treatment, so it will not directly improve outcomes for participants.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 45 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
1. Age ≥ 18 years newly diagnosed with CLL. 2. Adequate diagnostics (flowcytometry and cytogenetics) and follow-up data (at least 1 year). 3. Patients giving informed consent.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years newly diagnosed with CLL. * Adequate diagnostics (flowcytometry and cytogenetics) and follow-up data (at least 1 year). * Patients giving informed consent. Exclusion Criteria: * Incomplete diagnostics (e.g. flowcytometry of cytogenetics) * Lost to follow-up within 12 months of diagnosis. * Refused to give informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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