New hope for Tough-to-Treat blood cancers: phase 3 trial launches
NCT ID NCT07139873
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new drug called DZD8586 against standard treatments in 250 adults whose chronic lymphocytic leukemia or small lymphocytic lymphoma has come back or stopped responding to prior therapy. The main goal is to see if DZD8586 can delay cancer growth longer than the doctor's choice of current treatments. Participants are randomly assigned to receive either DZD8586 or another approved therapy.
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.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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: 1. Male and female participants ≥ 18 years of age. 2. ECOG performance status 0-2. 3. Confirmed diagnosis of relapsed or refractory CLL/SLL with indication for treatment. 4. Adequate bone marrow reserve and organ system functions. 5. Participants willing to comply with contraceptive restrictions. Exclusion Criteria: 1. Any unresolved \> Grade 1 adverse event at the time of starting study treatment. 2. Known or suspected Richter transformation. 3. Known or suspected CNS involvement. 4. Previous or current therapy and comedications meet exclusion criteria. 5. Participants with major cardiovascular disease, active infection, malignancy or uncontrolled systemic disease. 6. Nausea and vomiting not controlled or chronic gastrointestinal diseases, unable to swallow the formulated product or previous bowel resection that would preclude adequate absorption. 7. Women who are breast feeding. 8. History of hypersensitivity to active or inactive excipients of DZD8586 or drugs with a similar chemical structure or class.
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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 places running it
2 sites. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital
RECRUITINGNanjing, Jiangsu, China
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National Clinical Research Center for Blood Diseases, Blood Disease Hospital & Institute of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College
RECRUITINGTianjin, Tianjin Municipality, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New BTK blocker aims to outsmart drug resistance in elderly CLL patients
- New combo aims to shorten CLL treatment
- New pill shows promise against Hard-to-Treat blood cancers
- New cocktail aims to tame Slow-Growing blood cancers
- Could a cancer drug tame a blood disorder?
- Triple threat: new drug cocktail aims to wipe out CLL/SLL