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NCT07154264RecruitingPhase 2

A Study of DZD8586 Combination in CLL/SLL (TAI-SHAN10)

A Phase 2 Study of DZD8586 Combination Therapy in Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma (CLL/SLL)

Source: ClinicalTrials.gov · Last updated 22 Jun 2026

Brief summary (registry, in English)

This is a phase 2 study to investigate the efficacy and safety of DZD8586 in combination in participants with CLL/SLL. This study consists of two parts: Part A is the safety lead-in phase, and Part B is the dose expansion phase.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
66 (estimated)
First submitted
18 Aug 2025
Start date
22 Sept 2025
Primary completion date
31 Dec 2029
Lead sponsor
Dizal Pharmaceuticals
NCT number
NCT07154264

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 66
  • From 22 Sept 2025 to the primary completion date, 31 Dec 2029
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any of previous or current treatment prohibited by protocol.
  • Any unresolved \> grade 1 drug-related adverse events.

Other illness

  • Active infection.
  • Any of severe cardiac or pulmonary abnormalities.
  • Poorly controlled autoimmune anemia or autoimmune thrombocytopenia.
  • Poorly controlled gastrointestinal disorder, inadequate absorption of medication or other systemic diseases.
  • Prior malignancy within the past 3 years.
  • Known allergy to study drugs, any of the ingredients of the study drugs, or xanthine oxidase inhibitors or rasburicase.

Other

  • Known or suspected Richter's transformation, or prolymphocytic leukemia.
  • CNS involvement.

Who the study is looking for

  • Male and female ≥ 18 years of age.
  • ECOG performance status 0-2, and life expectancy ≥ 6 months.
  • Confirmed newly diagnosis or treatment naïve CLL/SLL with indication for treatment.
  • Patients with SLL must have at least one measurable lesion.
  • Adequate bone marrow reserve and organ functions.
  • Willing to comply with contraceptive restrictions.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University Third Hospital
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BeijingChinaRecruiting
The First Bethune Hospital of Jilin University
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ChangchunChinaRecruiting
Hunan Cancer Hospital
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ChangshaChinaRecruiting
The First People's Hospital Of Changzhou
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ChangzhouChinaRecruiting
West China Hospital of Sichuan University
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ChengduChinaRecruiting
Zhujiang Hospital of Southern Medical University
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GuangzhouChinaRecruiting
Nanfang Hospital, Southern Medical University
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GuangzhouChinaRecruiting
The First Affiliated Hospital Zhejiang University School of Medicine
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HangzhouChinaRecruiting
Anhui Provincial Cancer Hospital
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HefeiChinaRecruiting
The First Affiliated Hospital of NanChang University
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NanchangChinaRecruiting
Affiliated Hospital of Nantong University
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NantongChinaRecruiting
Shengjing Hospital Of China Medical University
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ShenyangChinaNot yet recruiting
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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WuhanChinaRecruiting
Yichang Central People's Hospital
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YichangChinaRecruiting
Henan Cancer Hospital
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ZhengzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.