Report workspace

Add to folder
NCT06649227RECRUITINGanonymous

Prospective Non-randomized Phase I Study Investigating the Safety of CD19 CAR-T Cells in Patients With Refractory/Relapsed AML Expressing CD19.

Sponsor

Source record

University Hospital, Lille

Phase

Source record

Phase 1

Modality

AI-normalized

gene therapy

Target

AI-normalized

CD19 B-cell antigen

Indication / condition

AI-normalized

Relapsed Adult AML

Intervention

Source record

CAR-T cell therapy

Source & freshness

Source record

NCT ID

NCT06649227

Original source

ClinicalTrials.gov

Source last updated

Dec 05, 2025

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT06649227

Title

Prospective Non-randomized Phase I Study Investigating the Safety of CD19 CAR-T Cells in Patients With Refractory/Relapsed AML Expressing CD19.

Sponsor

University Hospital, Lille

Status

RECRUITING

Phase

Phase 1

Condition raw

Relapsed Adult AML

Condition normalized

Relapsed Adult AML

Modality raw

gene therapy

Modality normalized

gene therapy

Target raw

CD19 B-cell antigen

Target normalized

CD19 B-cell antigen

Interventions

CAR-T cell therapy

Public preview

Source record

The ongoing Phase I study at University Hospital, Lille, aims to evaluate the safety and efficacy of CD19 CAR-T cell therapy in patients with refractory/relapsed acute myeloid leukemia (AML) expressing CD19. Given the high unmet medical need in this patient population, particularly for those with the t(8;21) translocation, successful outcomes could position this therapy as a viable treatment option, potentially capturing a significant share of the AML market. The competitive landscape includes existing therapies such as bispecific monoclonal antibodies targeting CD19, but CAR-T therapies may offer a more durable response. The study's results could influence future investment and partnership opportunities, particularly with stakeholders interested in advanced cellular therapies.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

Report access

Create an account to unlock this report

Choose the access model that matches the job: one urgent report, reusable credits for project work, or unlimited monthly access with AI and folders.

Early access offer

Subscribe with code FOUNDERS5 for a 5-day premium trial.

Full protocol, outcomes, eligibility, contacts and results sections
Patent/IP landscape with verified records when available
Board-ready PDF export with source provenance
Save to folders and synthesize multiple assets in premium workspace
Create account

Create a free account first, then unlock a single report, buy credits or subscribe.