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Study identifier: NCT07619287 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

An Investigational Study of BG-75202 Alone and in Combination With Other Agents in Patients With Myeloid Malignancies

Condition: Myeloid Malignancy  ·  Sponsor: BeOne Medicines

PhasePhase 1
Planned participants118
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where7 locations · 3 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary efficacy of BG-75202 (KAT6A/B inhibitor) alone and in combination with other agents in patients with myeloid malignancies.

This description comes directly from the study's public registry record.

Talk to the study team

Study Director  ·  877-828-5568  ·  clinicaltrials@beonemed.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (7)

St George HospitalKogarah, New South Wales, AustraliaRecruiting
Icon Cancer Centre Kurralta ParkKurralta Park, South Australia, AustraliaRecruiting
Linear Clinical ResearchNedlands, Western Australia, AustraliaRecruiting
The Second Hospital of Hebei Medical UniversityShijiazhuang, Hebei, ChinaRecruiting
The First Affiliated Hospital of Nanchang University Branch DonghuNanchang, Jiangxi, ChinaRecruiting
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciencestuanbo BranchTianjin, Tianjin Municipality, ChinaRecruiting
Auckland City HospitalAuckland, New ZealandRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

KogarahKurralta ParkNedlandsShijiazhuang

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