Clin2
NCT05581030Possibly a fitRecruiting

Newly diagnosed ALL: testing a treatment after Hyper-CVAD

Acute Lymphoblastic Leukemia

Treatments studied

Part of Blood & lymphatic, Cancer, Immune system & allergy clinical trials.

This Phase 1 study looks at a treatment approach for people newly diagnosed with Philadelphia-negative B- or T-cell acute lymphoblastic leukemia (ALL) after completing a specific chemotherapy course called Hyper-CVAD 1A. It aims to see if the treatment can be given safely and how well it may work for this type of leukemia.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
7 people
Ages
18 years to 50 years
Study type
Interventional

Who can take part

  • You have Philadelphia-negative B- or T-cell ALL confirmed by lab testing, with more than 10% leukemia cells in blood or bone marrow at diagnosis
  • You finished Hyper-CVAD arm 1A and fully recovered from it before starting this trial
  • You can follow the study schedule and give informed consent (or assent, if applicable)
  • Your energy level is fairly good (ECOG 0 to 1) and your heart function is strong (ejection fraction at least 50%)
  • Your liver and kidney tests are within allowed ranges (bilirubin/creatinine under 1.5 times normal; AST/ALT under 3 times normal)
  • If you can become pregnant (or can father children), you must use strict non-hormonal contraception and have a negative pregnancy test; you also cannot donate sperm during the study and for 3 months after

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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