DZD8586 in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma (TAI-SHAN9)

Last updated: August 16, 2024
Sponsor: Dizal Pharmaceuticals
Overall Status: Active - Recruiting

Phase

2

Condition

Lymphoma, B-cell

Lymphoma

Treatment

DZD8586

Clinical Study ID

NCT06539195
DZ2023B0003
  • Ages > 18
  • All Genders

Study Summary

This study will treat patients with DLBCL whose disease comes back or is not responding to prior therapy. 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Participants who meet all the following criteria:

  1. Male and female ≥ 18 years of age.

  2. ECOG performance status 0-2.

  3. Histologically confirmed recurrent or refractory DLBCL.

  4. Adequate bone marrow reserve and organ system functions.

  5. Willing to comply with contraceptive restrictions

Exclusion

Exclusion Criteria:

Participants who meet any of the following criteria:

  1. CNS involvement

  2. Stem cell transplantation, cell therapy, or gene therapy within 90 days. Approvedsmall molecule therapy within 5 half-lives. Monoclonal antibodies and antibody-drugconjugates within 28 days.

  3. Major surgery or significant traumatic injury within 4 weeks. Live attenuatedvaccines or viral vector vaccines within 4 weeks.

  4. Take vitamin K antagonists or take more than 2 anticoagulants or antiplatelet drugsat the same time. Take proton pump inhibitors or strong CYP3A inhibitors orinducers.

  5. Active infection.

  6. Clinically significant cardiac disorders. History of thrombotic diseases, stroke orintracranial hemorrhage within 6 months.

  7. Nausea and vomiting not controlled or chronic gastrointestinal diseases, unable toswallow the formulated product or previous bowel resection that would precludeadequate absorption.

  8. Another malignancy within 2 years prior to enrollment with the exception ofadequately treated in-situ carcinoma of the cervix, uterus, basal or squamous cellcarcinoma or non-melanomatous skin cancer.

  9. Women who are breast feeding.

  10. History of hypersensitivity to active or inactive excipients of DZD8586 or drugswith a similar chemical structure or class.

Study Design

Total Participants: 180
Treatment Group(s): 1
Primary Treatment: DZD8586
Phase: 2
Study Start date:
March 13, 2024
Estimated Completion Date:
April 30, 2028

Connect with a study center

  • Research Site

    Hefei, Anhui 230031
    China

    Active - Recruiting

  • Research Site

    Beijing, Beijing 100083
    China

    Active - Recruiting

  • Research Site

    Guangzhou, Guangdong 510060
    China

    Active - Recruiting

  • Research Site

    Nanning, Guangxi 530016
    China

    Active - Recruiting

  • Research Site

    Zhengzhou, Henan 450003
    China

    Active - Recruiting

  • Research Site

    Wuhan, Hubei 430023
    China

    Active - Recruiting

  • Research Site

    Changsha, Hunan 410031
    China

    Active - Recruiting

  • Research Site

    Nanjing, Jiangsu 210009
    China

    Site Not Available

  • Research Site

    Dalian, Liaoning 116021
    China

    Site Not Available

  • Research Site

    Jinan, Shandong 250117
    China

    Active - Recruiting

  • Research Site

    Linyi, Shandong 276002
    China

    Site Not Available

  • Research Site

    Xi'an, Shanxi 710061
    China

    Active - Recruiting

  • Research Site

    Chengdu, Sichuan 610041
    China

    Active - Recruiting

  • National Clinical Research Center for Blood Diseases, Blood Disease Hospital & Institute of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College

    Tianjin, Tianjin 300020
    China

    Active - Recruiting

  • Research Site

    Tianjin, Tianjin 300181
    China

    Active - Recruiting

  • Research Site

    Hangzhou, Zhejiang 310009
    China

    Active - Recruiting

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