Report workspace

Add to folder
NCT06765876RECRUITINGanonymous

Safety and Efficacy of Anti-CD123 Chimeric Antigen Receptor-Modified Autologous T Cells (CART123) in Patients With Relapsed/Refractory CD123+ Hematologic Malignancies: A Dose Escalation, Open-Label, Phase I Study

Sponsor

Source record

Institute of Hematology and Blood Transfusion, Czech Republic

Phase

Source record

Phase 1

Modality

AI-normalized

protein therapy

Target

AI-normalized

CD123 antigen on malignant hematologic cells

Indication / condition

AI-normalized

Leukemia, Myeloid, Acute(AML)

Intervention

Source record

Autologous CAR123 T lymphocytes

Source & freshness

Source record

NCT ID

NCT06765876

Original source

ClinicalTrials.gov

Source last updated

Jan 12, 2026

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT06765876

Title

Safety and Efficacy of Anti-CD123 Chimeric Antigen Receptor-Modified Autologous T Cells (CART123) in Patients With Relapsed/Refractory CD123+ Hematologic Malignancies: A Dose Escalation, Open-Label, Phase I Study

Sponsor

Institute of Hematology and Blood Transfusion, Czech Republic

Status

RECRUITING

Phase

Phase 1

Condition raw

Leukemia, Myeloid, Acute(AML), Precursor Cell Lymphoblastic Leukemia-Lymphoma, Myelodysplastic Syndromes (MDS), Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

Condition normalized

Leukemia, Myeloid, Acute(AML), Precursor Cell Lymphoblastic Leukemia-Lymphoma, Myelodysplastic Syndromes (MDS), Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

CD123 antigen on malignant hematologic cells

Target normalized

CD123 antigen on malignant hematologic cells

Interventions

Autologous CAR123 T lymphocytes

Public preview

Source record

The CART123 trial, sponsored by the Institute of Hematology and Blood Transfusion in the Czech Republic, targets relapsed/refractory CD123+ hematologic malignancies, including AML, MDS, ALL, and BPDCN. The trial's focus on a personalized CAR T-cell therapy approach positions it within a rapidly growing market for immunotherapies in hematologic cancers. Given the high unmet need in this patient population, successful outcomes could lead to significant commercial opportunities, particularly if the therapy demonstrates a favorable safety and efficacy profile compared to existing treatments. The trial's design includes a dose escalation strategy, which may provide insights into optimal dosing for future studies and potential market entry. Competitive landscape considerations include other CAR T-cell therapies targeting similar malignancies, necessitating a robust differentiation strategy based on clinical outcomes and safety profiles.

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.

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.