Actively Recruiting

Phase 2
Age: 14Years - 74Years
All Genders
NCT06742463

VHAG in Treating R/R T-ALL/LBL

Led by First Affiliated Hospital of Zhejiang University · Updated on 2024-12-19

50

Participants Needed

1

Research Sites

186 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Acute T cell lymphoblastic leukemia/lymphoma (T-ALL/LBL) is an aggressive type of leukemia that results from the malignant evolution of T-lineage progenitor cells at different differentiation stages. After induction chemotherapy and consolidation chemotherapy, there are still about 30% of patients who cannot achieve complete remission of clinical symptoms or negative MRD. This is also an important factor for the recurrence of ALL patients. In addition, most relapsed T-ALL/LBL patients relapse during first-line treatment. Once the disease relapses, it is difficult to cure for most young and adult patients, and the overall survival rate of patients is less than 10%.

CONDITIONS

Official Title

VHAG in Treating R/R T-ALL/LBL

Who Can Participate

Age: 14Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of newly diagnosed T-cell acute leukemia/lymphoma based on 2022 WHO classification
  • Age 14 years or older and under 75 years
  • Clinically diagnosed as relapsed or refractory T-ALL/LBL
  • ECOG performance status score of 0 to 2
  • Expected survival time of 2 months or more
  • No organ dysfunction restricting protocol use during screening
  • Able to understand the study and provide informed consent
Not Eligible

You will not qualify if you...

  • Known central nervous system involvement of T-ALL/LBL
  • Abnormal heart, lung, liver, kidney, or other organ functions limiting trial participation
  • Cardiac ultrasound showing left ventricular ejection fraction (LVEF) below 45%
  • History of other malignancies within the past 5 years except localized thyroid cancer or in situ skin cancer
  • Serum total bilirubin over 1.5 times the upper limit of normal
  • ALT or AST over 2.5 times the upper limit of normal
  • Serum creatinine over 1.5 times the upper limit of normal
  • Known HIV infection
  • Conditions affecting use of the study drug as judged by the investigator
  • Inability to understand or comply with the study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, Zhejiang, China, 310003

Actively Recruiting

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Research Team

J

Jie Jin, M.D.

CONTACT

C

Chenying Li, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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