🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT07458542
Active, not recruiting Observational

Effectiveness and Safety of ONUREG (Oral Azacitidine) in Chinese Patients With Acute Myeloid Leukemia

NCT07458542 · tracked via the Priya Life Science China tracker
Sponsor
Bristol-Myers Squibb
Phase
Observational
Started
2025-12-09
Last updated
2026-03-09

Condition(s) studied

Acute Myeloid Leukemia (AML)

Investigational drug(s) / intervention(s)

Azacitidine →

Azacitidine: According to the product label

Study summary

The purpose of this study is to assess real-world effectiveness and safety of oral azacitidine in adults diagnosed with acute myeloid leukemia (AML) in Hong Kong

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Documented diagnosis of Acute Myeloid Leukemia (AML). * Achieved first complete response (CR) or complete response with incomplete blood recovery (CRi) following intensive induction chemotherapy. * Not able or unwilling to undergo Hematopoietic Stem Cell Transplantation (HSCT). * Received oral azacitidine as maintenance therapy after first CR or CRi following intensive induction chemotherapy in real-world settings (Note: CR/CRi status at oral azacitidine treatment initiation is left to the judgment of the local clinicians depending on the treatment response and the condition of the patient in routine clinical practices). * Age ≥ 18 years at the index date (oral azacitidine initiation date). Exclusion Criteria: • Evidence of relapse prior to oral azacitidine initiation recorded in electronic health record (EHR).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The University of Hong Kong Hong Kong China

More Bristol-Myers Squibb trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07458542 on ClinicalTrials.gov ↗ ← All trials in China