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New hope for tough blood cancers: experimental drug enters human testing

NCT ID NCT05828589

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 15, 2026 · Updated 2 times

Summary

This early-stage study is testing an experimental drug called BGB-21447 in about 112 people with certain blood cancers (like lymphoma or leukemia) that have returned or not improved after prior treatments. The main goal is to find a safe dose and check for side effects, while also seeing if the drug can shrink tumors. Participants will take the drug alone, and the study will help decide if larger trials should move forward.

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

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

51 people

The number who actually took part.

Started

Jun 2023

Finished

Jun 2026

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria 1. Confirmed diagnosis (per World Health Organization \[WHO\] guidelines, unless otherwise noted) of one of the following: Cohort A1 and Cohort A2: 1. R/R DLBCL (for Cohort A1 and Cohort A2.1) * High-grade B-cell lymphomas with translocations of MYC and Bcl-2 and/or Bcl-6 are not allowed in Cohort A1 but may be allowed in Cohort A2.1 2. R/R FL (for Cohort A1 and Cohort A2.2) 3. R/R MZL (for Cohort A1 and Cohort A2.2) 4. Transformed B-cell NHL (for Cohort A1 only) 5. Richter's transformation to DLBCL (for Cohort A1 only) 2. Measurable disease by computed tomography/magnetic resonance imaging. Exclusion Criteria: 1. Prior malignancy (other than the disease under study) within the past 2 years, except for curatively treated basal or squamous skin cancer, superficial bladder cancer, carcinoma in situ of the cervix or breast, or localized Gleason score ≤ 6 prostate cancer or lentigo maligna melanoma that has been curatively resected 2. Known central nervous system involvement by lymphoma/leukemia 3. Prior autologous stem cell transplant \< 3 months before the first dose of study drug. Or prior chimeric antigen receptor T-cell (CAR-T) therapy \< 3 months before the first dose of study drug 4. Prior allogeneic stem cell transplant. 5. Major surgery \< 4 weeks before the first dose of study treatment NOTE: Other protocol-defined Inclusion/Exclusion criteria may apply.

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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.

Contacts and locations

Locations

  • Affiliated Zhongshan Hospital of Fudan University

    Shanghai, Shanghai Municipality, 200032, China

  • Auckland City Hospital

    Auckland, 1023, New Zealand

  • Avera Cancer Institute

    Sioux Falls, South Dakota, 57105-2108, United States

  • Blacktown Cancer and Haematology Centre

    Blacktown, New South Wales, NSW 2148, Australia

  • Fujian Cancer Hospital

    Fuzhou, Fujian, 350014, China

  • Henan Cancer Hospital

    Zhengzhou, Henan, 450000, China

  • Institute of Hematology and Hospital of Blood Disease

    Tianjin, Tianjin Municipality, 300020, China

  • Jiangsu Province Hospital

    Nanjing, Jiangsu, 210029, China

  • Laura and Isaac Perlmutter Cancer Center At Nyu Langone Health

    New York, New York, 10016-2708, United States

  • Linear Clinical Research

    Nedlands, Western Australia, WA 6009, Australia

  • Linyi Peoples Hospital

    Linyi, Shandong, 276000, China

  • Mater Cancer Care Centre

    South Brisbane, Queensland, QLD 4101, Australia

  • Mission Cancer and Blood

    Waukee, Iowa, 50263, United States

  • Monash Health

    Clayton, Victoria, VIC 3168, Australia

  • Nyu Langone Health Perlmutter Cancer Center At Nyu Langone Hospital Long Island

    Mineola, New York, 11501, United States

  • Peking University Third Hospital

    Beijing, Beijing Municipality, 100000, China

  • Pindara Private Hospital

    Benowa, Queensland, QLD 4217, Australia

  • Shandong Provincial Hospital

    Jinan, Shandong, 250021, China

  • Shengjing Hospital of China Medical University

    Shenyang, Liaoning, 110004, China

  • Sibley Memorial Hospital Johns Hopkins Medicine

    Washington D.C., District of Columbia, 20016, United States

  • Sidney Kimmel Comprehensive Cancer At Johns Hopkins

    Baltimore, Maryland, 21287, United States

  • The First Affiliated Hospital of Nanchang University Branch Donghu

    Nanchang, Jiangxi, 330006, China

  • The First Affiliated Hospital of Nanchang University Branch Xianghu

    Nanchang, Jiangxi, 332000, China

  • The First Affiliated Hospital of Soochow University

    Suzhou, Jiangsu, 215006, China

  • The First Peoples Hospital of Changzhou

    Changzhou, Jiangsu, 213000, China

  • Tongji Hospital of Tongji Medical College Huazhong University of Science and Technology

    Wuhan, Hubei, 430030, China

  • University of Iowa Hospitals and Clinics

    Iowa City, Iowa, 52242-1009, United States

  • Yichang Central Peoples Hospitaljiangnan Branch

    Yichang, Hubei, 443001, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.