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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Versailles Hospital Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 23 sites (Amiens and 22 other locations) |
| Status | Recruiting |
| Started | January 15, 2024 |
| Main results expected | June 15, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | July 6, 2026 |
| Trial ID | NCT07684131 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
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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
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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
- Study coordinator: Sandrine Roux
- Email: sroux@ght78sud.fr
- Phone: +33139239777
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.