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NCT07148180RECRUITINGanonymous

A Multi-Site Break Through Cancer Trial: Targeting Measurable Residual Disease in Patients With Acute Myeloid Leukemia: A Phase 1/2 Study of Tagraxofusp, Azacitidine, and Venetoclax

Sponsor

Source record

Jacqueline Garcia, MD

Phase

Source record

Phase 1/2

Modality

AI-normalized

small molecule

Target

AI-normalized

CD123 (targeted by Tagraxofusp), BCL-2 (targeted by Venetoclax), and cytidine nucleoside metabolism (targeted by Azacitidine)

Indication / condition

AI-normalized

Acute Myeloid Leukaemia (AML)

Intervention

Source record

Tagraxofusp, Azacitidine (AZA), Venetoclax

Source & freshness

Source record

NCT ID

NCT07148180

Original source

ClinicalTrials.gov

Source last updated

Feb 05, 2026

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT07148180

Title

A Multi-Site Break Through Cancer Trial: Targeting Measurable Residual Disease in Patients With Acute Myeloid Leukemia: A Phase 1/2 Study of Tagraxofusp, Azacitidine, and Venetoclax

Sponsor

Jacqueline Garcia, MD

Status

RECRUITING

Phase

Phase 1/2

Condition raw

Acute Myeloid Leukaemia (AML), Leukemia, Blood Cancer, Blood Cancers

Condition normalized

Acute Myeloid Leukaemia (AML), Leukemia, Blood Cancer, Blood Cancers

Modality raw

small molecule

Modality normalized

small molecule

Target raw

CD123 (targeted by Tagraxofusp), BCL-2 (targeted by Venetoclax), and cytidine nucleoside metabolism (targeted by Azacitidine)

Target normalized

CD123 (targeted by Tagraxofusp), BCL-2 (targeted by Venetoclax), and cytidine nucleoside metabolism (targeted by Azacitidine)

Interventions

Tagraxofusp, Azacitidine (AZA), Venetoclax

Public preview

Source record

This clinical trial investigates a novel combination therapy for Acute Myeloid Leukemia (AML) involving Tagraxofusp, Azacitidine, and Venetoclax. The trial is sponsored by Dr. Jacqueline Garcia at Dana-Farber Cancer Institute and is currently recruiting participants. The combination aims to address measurable residual disease (MRD) in AML patients, a significant unmet need in the market, as current therapies often fail to eliminate residual disease, leading to relapse. The FDA has previously approved Venetoclax and Azacitidine as a combination therapy for AML, while Tagraxofusp is approved for a different leukemia type. The success of this trial could enhance the competitive positioning of the involved companies, particularly Stemline Therapeutics, which supplies Tagraxofusp. The potential for market expansion hinges on demonstrating improved efficacy and safety over existing therapies, which could lead to significant commercial opportunities in the AML treatment landscape.

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

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