Tests a venetoclax combination against standard chemotherapy in older adults with leukemia
Tests a venetoclax drug combination in older adults with newly diagnosed acute myeloid leukemia.
Plain-language title generated from the registry record
Registry title: Venetoclax-Azacitidine in Combination With Chidamide and CAG in Fit Older Patients With Acute Myeloid Leukaemia
Key facts
- Where
- Beijing, ChinaSee the site
- Phase
- Phase 3
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for people aged 60-75 who have just been diagnosed with acute myeloid leukaemia (AML) and are fit enough for intensive treatment.
- Age
- 60 to 75 years
- Sex
- All sexes can join.
- Disease stage
- Newly diagnosed AML, diagnosed by the Chinese Medical Association 2021 standards. Performance status 0-3 (ECOG), expected survival of at least 4 months.
Main reasons for not taking part
- Allergy or contraindication to the study drugs
- Pregnant or breastfeeding women
- Active infection
- Major organ surgery within the last 6 weeks
- Abnormal liver or kidney function
Read by machine on 9 November 2026.
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 60 and 75 years old?
Source: NCT07514936, who can take part
Where in China
- Chinese PLA General HospitalBeijing, ChinaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Chinese PLA General Hospital
- Trial code
- NCT07514936
- Record updated
- 20 August 2026
- Original description
This study is a multicenter, prospective, randomized, controlled clinical trial, observing the efficacy and safety of the CACAG+Venetoclax regimen (Chidamide + Azacitidine + Aclarubicin + Cytarabine + Recombinant Human Granulocyte Colony-Stimulating Factor + Venetoclax) in elderly patients with newly diagnosed Acute Myeloid Leukemia (AML). The control group applies the standard "3+7" regimen. The aim is to improve the remission rate of AML patients, reduce the probability of adverse events, and thereby improve patient prognosis and extend patient survival.Read full original descriptionShow less
Venetoclax-Azacitidine in Combination With Chidamide and CAG Versus 3+7 Regimen in Fit Older Patients With Acute Myeloid Leukaemia：A Multicenter, Randomized, Controlled, Phase 3 Trial
This study is a multicenter, prospective, randomized, controlled clinical trial, observing the efficacy and safety of the CACAG+Venetoclax regimen (Chidamide + Azacitidine + Aclarubicin + Cytarabine + Recombinant Human Granulocyte Colony-Stimulating Factor + Venetoclax) in elderly patients with newly diagnosed Acute Myeloid Leukemia (AML). The control group applies the standard "3+7" regimen. The aim is to improve the remission rate of AML patients, reduce the probability of adverse events, and thereby improve patient prognosis and extend patient survival.
Inclusion: Voluntary participation in the clinical study; the subject or legal guardian fully understands and is informed about the study and has signed the Informed Consent Form (ICF); willing to follow and able to complete all trial procedures; Age between 60-75 years at the time of screening, with no gender restrictions; Patients are newly diagnosed with AML, and the diagnosis conforms to the standards of the Chinese Medical Association 2021 edition; No severe allergic constitution; Liver function: ALT and AST <= 2.5 times the upper limit of normal values, bilirubin <= 2 times the upper limit of normal values; Renal function: creatinine <= upper limit of normal values; No uncontrollable infections or severe mental illnesses; Performance status score is 0-3 (ECOG), with an expected survival of at least 4 months.
Exclusion: Patients who have undergone major organ surgery within the last 6 weeks; Patients whom the investigator deems unsuitable for this clinical trial (e.g., poor compliance, drug abuse, etc.); Patients who are allergic to the study medication or have contraindications to it; Patients with active infections; Patients with mental disorders or other conditions that prevent obtaining informed consent, or who are unable to cooperate with the treatment and examination procedures; Abnormal liver function, with total bilirubin > 1.5 times the upper limit of normal, ALT/AST > 2.5 times the upper limit of normal, or liver-infiltrated patients with ALT/AST > 5 times the upper limit of normal; abnormal renal function, with serum creatinine > 1.5 times the upper limit of normal; Pregnant or breastfeeding women; Patients with long-term smoking or alcohol abuse that could affect the evaluation of trial results.