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NCT05740917UNKNOWNanonymous

A Multicenter, Open Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Initial Efficacy of XZB-0004 in the Treatment of Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome

Sponsor

Source record

Xuanzhu Biopharmaceutical Co., Ltd.

Phase

Source record

Phase 1

Modality

AI-normalized

small molecule

Target

AI-normalized

AXL receptor

Indication / condition

AI-normalized

AML

Intervention

Source record

XZB-0004

Source & freshness

Source record

NCT ID

NCT05740917

Original source

ClinicalTrials.gov

Source last updated

Feb 23, 2023

Ingested at

Jun 18, 2026

Internal sync

Jun 18, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT05740917

Title

A Multicenter, Open Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Initial Efficacy of XZB-0004 in the Treatment of Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome

Sponsor

Xuanzhu Biopharmaceutical Co., Ltd.

Status

UNKNOWN

Phase

Phase 1

Condition raw

AML, MDS

Condition normalized

AML, MDS

Modality raw

small molecule

Modality normalized

small molecule

Target raw

AXL receptor

Target normalized

AXL receptor

Interventions

XZB-0004

Public preview

Source record

XZB-0004, developed by Xuanzhu Biopharmaceutical Co., Ltd., is positioned to address the significant unmet medical need in relapsed/refractory Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS). The global market for AML therapies is projected to grow substantially, driven by increasing incidence rates and advancements in treatment options. The competitive landscape includes established therapies and emerging agents targeting similar pathways. Successful outcomes from this trial could enhance Xuanzhu's market position and attract potential partnerships or acquisitions, given the high-value nature of oncology assets. Diligence should focus on the robustness of the clinical data, regulatory pathways, and potential market access strategies.

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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