Trial · NCT07132684
Comparison of VA and D/IA Induction Regimens in Elderly Fit Acute Myeloid Leukemia Patients
NCT07132684, Phase 3, Recruiting, Institute of Hematology & Blood Diseases Hospital, China
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of VA and D/IA Induction Regimens in Elderly Fit Acute Myeloid Leukemia Patients. Trials, record NCT07132684. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07132684
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of VA and D/IA Induction Regimens in Elderly Fit Acute Myeloid Leukemia Patients
- NCT number
- NCT07132684
- Status
- Recruiting
- Phases
- Phase 3
- Enrollment
- 228 participants, estimated
- Lead sponsor
- Institute of Hematology & Blood Diseases Hospital, China
- Conditions
- AML, Adult
- Interventions
- Daunorubicin/Idarubicin, Cytarabine, Azacitidine, Venetoclax
- First posted
- 2025-08-20
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Overall Survival (OS) | up to 1 years after completion of enrollment | Time from randomization to death from any cause. |
| Secondary | Composite Complete Remission Rate (CR/CRh/CRi) | Six weeks after induction therapy | Proportion of patients achieving CR, CRh, or CRi after induction. |
| Secondary | MRD Negativity Rate | up to 1 years after completion of enrollment | Proportion of patients achieving MRD negativity after induction and overall treatment. |
| Secondary | Relapse-Free Survival (RFS) | up to 1 years after completion of enrollment | Time from achieving CR/CRh/CRi to relapse or death. |
| Secondary | Event-Free Survival (EFS) | up to 1 years after completion of enrollment | Time from randomization to treatment failure, relapse, or death. |
| Secondary | 30-Day and 60-Day Mortality Rates | within 30 and 60 days of starting treatment. | Proportion of patients who die within 30 and 60 days of starting treatment. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07132684
GET https://conductscience.org/api/trials/v1/NCT07132684/registered