Aperçu

Éligibilité

Détails de la conception

Bras et interventions

Mesures des résultats

Sites d'essai

Source : NCT05901974

Recrutement en cours

Venetoclax Combined With Azactidine in the Treatment of ALAL

Interventionnel

Phase 2

The First Affliated Hospital of Soochow University

Sponsor: Sheng-Li Xue, MD

Dernière synchronisation : 16 décembre 2025
Avis - Les informations proviennent de registres publics et peuvent ne pas refléter les changements en temps réel sur le site local.

The prognosis of acute leukaemias of ambiguous lineage is poor. The effect of chemotherapy regimen and hematopoietic stem cell transplantation are still unclear. Therefore, we will explore new therapy to improve the remission rate of acute leukaemias of ambiguous lineage. Venetoclax can significantly improve the remission rate and prolong PFS and OS. At present, venetoclax combined with azacitidine or decitabine has become the preferred treatment regimen for elderly AML patients. It also shows a high response rate in relapsed/refractory AML or MDS patients. There are few clinical studies on the treatment of ALAL. The purpose of this study is to explore the efficacy and safety of venetoclax combined with azacitidine in the treatment of newly diagnosed ALAL patients.

Catégorie de traitement

Thérapie ciblée, Autres médicaments

Mutations requises

Aucun

Essai commencé

1 juillet 2023

Dernière mise à jour par le sponsor

16 décembre 2025

Achèvement estimé

1 mars 2026

Contact de l'étude

Nom:Sheng-Li Xue, MD

E-mail:slxue@suda.edu.cn

Téléphone:0086-0512-67781139

Éligibilité

Critères d'inclusion

1. Patients aged ≥ 15 years.

2. Patients diagnosed with ALAL according to 5th edition of WHO Acute Leukaemias of Ambiguous Lineage diagnosis standard.

3. New diagnosed patients.

4. ECOG performance status score less than 3.

5. Expected survival time ≥3 months.

6. Patients without serious heart, lung, liver, or kidney disease.

7. Ability to understand and voluntarily provide informed consent.

Critères d'exclusion

1. Patients who are allergic to the study drug or drugs with similar chemical structures.

2. Pregnant or lactating women, and women of childbearing age who do not want to practice effective methods of contraception.

3. Active infection.

4. Active bleeding.

5. Patients with new thrombosis, embolism, cerebral hemorrhage, or other diseases or a medical history within one year before enrollment.

6. Patients with mental disorders or other conditions whereby informed consent cannot be obtained and where the requirements of the study treatment and procedures cannot be met.

7. Liver function abnormalities (total bilirubin > 1.5 times the upper limit of the normal range, ALT/AST > 2.5 times the upper limit of the normal range or patients with liver involvement whose ALT/AST > 1.5 times the upper limit of the normal range), or renal anomalies (serum creatinine > 1.5 times the upper limit of the normal value).

8. Patients with a history of clinically significant QTc interval prolongation (male > 450 ms; female > 470 ms), ventricular heart tachycardia and atrial fibrillation, II-degree heart block, myocardial infarction attack within one year before enrollment, and congestive heart failure, and patients with coronary heart disease who have clinical symptoms and requiring drug treatment.

9. Surgery on the main organs within the past six weeks.

10. Drug abuse or long-term alcohol abuse that would affect the evaluation results.

11. Patients who have received organ transplants (excepting bone marrow transplantation).

12. Patients not suitable for the study according to the investigator's assessment.

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Détails de la conception

AllocationN/A

Modèle d'interventionSingle Group Assignment

MasquageNone (Open Label)

Nombre à inscrire23

Bras et interventions

Bras

Interventions

Type : Experimental

Description : Venetoclax combined with azacitidine regimen. Venetoclax orally once daily (100 mg d1, 200 mg d2, 400 mg d3-28); azacitidine 75 mg/m2 subcutaneously once daily on days 1-7 .

Interventions :

Venetoclax
azactidine

Mesures des résultats

Mesures des résultats primaires

Overall Response Rate (ORR)At the end of Cycle 1 (each cycle is 28 days)

The overall response (complete remission, complete remission with incomplete blood count recovery) rate achieved after one or two courses (28 days) induction therapy by venetoclax combined azacitidine regimen.

Complete Remission Rate (CRR)At the end of Cycle 1 (each cycle is 28 days)

The complete remission rate achieved after one or two courses (28 days) induction therapy by venetoclax combined azacitidine regimen.

Mesures des résultats secondaires

Progression-Free Survival (PFS)1 year

It is measured from the date of entry into this trial to the date of progression or death.

Adverse events in hematological system1 year

Record of adverse events in hematological system during and after designed venetoclax combined azacitidine regimen induction.

Overall survival (OS)1 year

It is measured from the date of entry into this trial to the date of death from any cause; patients not known to have died at last follow-up are censored on the date they were last known to be alive.

Adverse events in other organs or systems1 year

Record of adverse events in other organs or systems during and after designed venetoclax combined azacitidine regimen induction.

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Sites d'essai

Cette étude compte 1 site d'essai

The First Affliated Hospital of Soochow University

Suzhou, CN

Nom:Sheng-Li Xue

Recrutement en cours

Suzhou, CN

The First Affliated Hospital of Soochow University

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