Clinical trial Recruiting at 7 sites Observational Ages 18 and up

Observatory of adults with Ph+ ALL receiving BCR-ABL1 inhibitors with chemotherapy, steroids, or monoclonal antibodies

Official title: AN OBSERVATORY FOR PATIENTS AGED 18 YEARS AND OVER WITH PHILADELPHIA CHROMOSOME POSITIVE (PH+ OR BCR::ABL1+) ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) AND TREATED WITH THE COMBINATION OF BCR::ABL1 INHIBITORS AND CHEMOTHERAPY AND/OR CORTICOSTEROIDS AND/OR A MONOCLONAL ANTIBODY.

Run by Versailles Hospital · NCT07684131 · Data updated 2026-11-12

This study follows adults with Philadelphia-positive acute lymphoblastic leukemia who are being treated with a combination of BCR-ABL1 inhibitors and other therapies to see how they fare in real-world practice.

More Acute Lymphoblastic Leukemia trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorVersailles Hospital
Academic / other
Drugs / interventionschemotherapy
Locations23 sites (Amiens and 22 other locations)
StatusRecruiting
StartedJanuary 15, 2024
Main results expectedJune 15, 2027
Study endsDecember 31, 2027
Registry record updatedJuly 6, 2026
Trial IDNCT07684131 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18 years and older) with Philadelphia chromosome–positive or BCR-ABL1–positive ALL who are being treated with a combination of BCR-ABL1 inhibitors and chemotherapy and/or corticosteroids and/or monoclonal antibodies.

Probably not a fit

Patients who do not consent to data collection or who are not treated in a participating center may not contribute information about possible benefits.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational study enrolling adults with Ph+ ALL who are treated with a combination of BCR-ABL1 inhibitors and chemotherapy and/or corticosteroids and/or monoclonal antibodies. Data will be collected to describe treatment patterns, real-world outcomes, and safety signals in routine clinical care. No experimental interventions are required beyond standard treatment, and no randomization is involved. Participation is limited to patients who consent to data collection and are treated at participating centers. The study aims to provide insights into how these combination regimens perform outside of controlled trials.

Why it matters

Potential benefit: The study could clarify real-world effectiveness and safety of combination therapies for Ph+ ALL, potentially guiding future treatment decisions.

How similar studies have gone: Observational data in similar real-world settings has helped characterize outcomes and safety for Ph+ ALL treatments, though this specific combination in routine practice is less documented.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male or female patients ≥ 18 years
2. Philadelphia chromosome or BCR::ABL1 positive acute lymphoblastic leukaemia
3. Treatment with the combination of BCR::ABL1 inhibitors and chemotherapy and/or corticotherapy and/or a monoclonal antibody

Exclusion Criteria:

1. Patients deceded and having previously refused data collection
2. Not included in a prospective clinical trial

Where it's running

  • CHU Bordeaux
    Bordeaux, France
    Recruiting
  • CHU clermont ferrand
    Clermont-Ferrand, France
    Recruiting
  • Centre Hospitalier sud francilien
    Corbeil-Essonnes, France
    Recruiting
  • CH Versailles
    Le Chesnay, France
    Recruiting
  • CH Le Mans
    Le Mans, France
    Recruiting
  • Hopital necker
    Paris, France
    Recruiting
Show 17 more locations
  • Hopital St Louis
    Paris, France
    Recruiting
  • Groupe hospitalier sud
    Amiens, France
    Not yet recruiting
  • CHU Angers
    Angers, France
    Not yet recruiting
  • CH de la cote basque
    Bayonne, France
    Not yet recruiting
  • Hopital Militaire Percy
    Clamart, France
    Not yet recruiting
  • CHU de grenoble
    Grenoble, France
    Not yet recruiting
  • CHU Sud Réunion
    La Réunion, France
    Not yet recruiting
  • Chu de Lille
    Lille, France
    Not yet recruiting
  • Hopital de la conception
    Marseille, France
    Not yet recruiting
  • Institut Paoli Calmettes
    Marseille, France
    Not yet recruiting
  • CHRU de Nancy
    Nancy, France
    Not yet recruiting
  • Centre Antoine Lacassagne
    Nice, France
    Not yet recruiting
  • Hopital Cochin
    Paris, France
    Not yet recruiting
  • CH de Lyon
    Pierre-Bénite, France
    Not yet recruiting
  • CH St Etienne
    Saint-Etienne, France
    Not yet recruiting
  • Icans
    Strasbourg, France
    Not yet recruiting
  • Hopital de Purpan
    Toulouse, France
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.