DZD8586 in Patients With Relapsed or Refractory CLL/SLL (TAI-SHAN8)

Recruiting Phase 2 Interventional Study
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
155 (estimated)
Sponsor
Dizal Pharmaceuticals · Industry
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About This Trial

This study will treat patients with CLL/SLL whose disease comes back or is not responding to prior therapy, or if they can not bear side effects of the prior treatment. This study will assess the anti-tumor activity of DZD8586 as monotherapy. It will help to understand what type of side effects may occur with the drug treatment. It will also measure the levels of drug in the body.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: Participants who meet all the following criteria: 1. Male and female ≥ 18 years of age. 2. ECOG performance status 0-2. 3. Confirmed diagnosis of CLL/SLL with indication for treatment. 4. Adequate bone marrow reserve and organ system functions. 5. Willing to comply with contrac…
Contacts

Tianmo Sun

0086-21-61097800

Tianmo.Sun@dizalpharma.com

CONTACT