New pill for tough blood cancers enters first human tests
NCT ID NCT07619287
First seen Jun 26, 2026 · Last updated Sep 15, 2026 · Updated 13 times
Summary
This early-phase trial is testing a new oral drug called BG-75202, alone or with another medicine, in about 118 adults with myeloid blood cancers that have come back or not responded to prior treatment. The main goals are to check safety, find the right dose, and get a first look at whether the drug can shrink tumors. The study is not yet recruiting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BG-75202 (a KAT6A/B inhibitor taken orally, alone or with another drug)
- What this could lead to
- If it works, this could point toward a new treatment option for certain blood cancers that have not responded to prior therapy.
- What could go wrong
- This is a very early Phase 1 trial with only 118 participants. The main goal is safety, not proof of effectiveness. Many early-stage drugs fail to show benefit or have unexpected side effects.
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 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 118 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Sep 2028
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: * Patients must be ≥ 18 years of age (or the legal age of consent in the jurisdiction in which the study is taking place), inclusive, at the time of signing the Informed consent form (ICF). * Patients must have a confirmed diagnosis of myeloid malignancies based on 2016 World Health Organization criteria, and meet the following categories: * Relapsed/refractory; myeloid malignancies after ≥1 prior systemic therapy, per ELN; 2022 criteria; patients with actionable genetic alteration must have previously received targeted therapies unless contraindicated, unavailable/inaccessible, or declined by patient. * Patients must have a stable Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2. Exclusion Criteria: * Prior exposure to KAT6A/B inhibitors/degraders. * A diagnosis of acute promyelocytic leukemia or BCR-ABL-positive leukemia. * Known central nervous system involvement by leukemia * Use of antileukemic therapies without sufficient washout period Note: Other protocol defined Inclusion/Exclusion criteria may apply.
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Get notified about this study
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Genom att skicka in godkänner du våra Användarvillkor
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 study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
16 sites in 3 countries. 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
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Auckland City Hospital
RECRUITINGAuckland, 1023, New Zealand
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Austin Health
RECRUITINGHeidelberg, Victoria, VIC 3084, Australia
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Concord Repatriation General Hospital
RECRUITINGConcord, New South Wales, NSW 2139, Australia
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Icon Cancer Centre Kurralta Park
RECRUITINGKurralta Park, South Australia, SA 5037, Australia
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Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciencestuanbo Branch
RECRUITINGTianjin, Tianjin Municipality, 301617, China
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Linear Clinical Research
RECRUITINGNedlands, Western Australia, WA 6009, Australia
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North Shore Hospital
RECRUITINGAuckland, 0622, New Zealand
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St George Hospital
RECRUITINGKogarah, New South Wales, NSW 2217, Australia
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The First Affiliated Hospital of Nanchang University Branch Donghu
RECRUITINGNanchang, Jiangxi, 330006, China
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The First Affiliated Hospital of Nanchang University Branch Xianghu
RECRUITINGNanchang, Jiangxi, 332000, China
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The First Affiliated Hospital of Soochow University
RECRUITINGSuzhou, Jiangsu, 215006, China
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The First Affiliated Hospital of Zhengzhou Universitysouth Branch
RECRUITINGZhengzhou, Henan, 451161, China
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The First Hospital of Lanzhou University
RECRUITINGLanzhou, Gansu, 730000, China
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The Second Hospital of Hebei Medical University
RECRUITINGShijiazhuang, Hebei, 050000, China
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Tongji Hospital of Tongji Medical College Huazhong University of Science and Technology
RECRUITINGWuhan, Hubei, 430030, China
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Zhujiang Hospital of Southern Medical University
RECRUITINGGuangzhou, Guangdong, 510000, China
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Other studies related to the condition(s) this trial covers.
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