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Trial · NCT06860269

A 3-cohort Randomized Study Evaluating the Role of New Immunotherapeutic Agents and of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) in Frontline Therapy of Adults With Acute Lymphoblastic Leukemia

NCT06860269, Phase 2, Phase 3, Recruiting, Assistance Publique - Hôpitaux de Paris

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A 3-cohort Randomized Study Evaluating the Role of New Immunotherapeutic Agents and of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) in Frontline Therapy of Adults With Acute Lymphoblastic Leukemia. Trials, record NCT06860269. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06860269

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A 3-cohort Randomized Study Evaluating the Role of New Immunotherapeutic Agents and of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) in Frontline Therapy of Adults With Acute Lymphoblastic Leukemia
NCT number
NCT06860269
Status
Recruiting
Phases
Phase 2, Phase 3
Enrollment
1,200 participants, estimated
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Conditions
Acute Lymphoblastic Leukemia
Interventions
Randomization + Blinatumomab + chemotherapy, Randomization + Standard frontline T-ALL chemotherapy backbone, Randomization + Isatuximab + Standard frontline T-ALL chemotherapy backbone, Randomization + Blinatumomab + Ponatinib + chemotherapy, Randomization 1 + Allo HSCT, Randomization 2 + Allo HSCT
First posted
2025-03-06
Last updated
2026-02-10

Source ClinicalTrials.gov

Registered outcomes24

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryOverall survivalAt 5 yearsFor GRAAL-2024/B HR patients (phase 3)
PrimaryOverall survivalAt 5 yearsFor GRAAL-2024/B SR patients (phase 2)
PrimaryEvent-Free SurvivalAt 5 yearsFor GRAAL-2024/T patients (phase 3)
PrimaryOverall survivalAt 5 yearsFor GRAAPH-2024 patients (phase 3) - Phpos ALL
SecondaryOverall survivalAt 5 yearsin the T-ALL/LL cohorts
SecondaryEvent Free SurvivalAt 5 years
SecondaryRelapse Free SurvivalAt 5 years
SecondaryHematological complete response rateAt 45 daysAfter induction
SecondaryHematological complete response rateAt 4 monthsAfter consolidation
SecondaryMeasurable residual disease (MRD) response levelAt inclusion(IG/TR and BCR::ABL1 markers) at diagnosis

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT06860269

GET https://conductscience.org/api/trials/v1/NCT06860269/registered?page=2