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Patients Treated in Real Life With VEnetoclax for WAldenström Macroglobulinemia

Patients Treated in Real Life With VEnetoclax for WAldenström Macroglobulinemia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06200220
Enrollment
45
Registered
2024-01-10
Start date
2023-12-28
Completion date
2025-12-01
Last updated
2024-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Waldenstrom's Macroglobulinaemia Refractory

Brief summary

Waldenström macroglobulinemia (WM) is an incurable disease. BCL2 antagonist, an important anti-apoptosys molecule, is already approved for the treatment of chronic lymphocytic leukemia (CLL) and acute myeloid leukemia. Recently, a clinical trial including 32 patients with WM treated with Venetoclax showed an overall response rates of 84% and a major response rate of 81%. However, there is no in real life data, in the french population, of the efficiency of Venetoclax in WM. The aim of our multicentric retrospective study is to evaluate the efficiency and tolerance of Venetoclax in WM.

Interventions

DRUGVenetoclax

Observational study

Sponsors

Poitiers University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Waldenstrom's macroglobulinemia * Treatment with Venetoclax * Non opposition

Exclusion criteria

none

Design outcomes

Primary

MeasureTime frameDescription
Efficiency2018 to 2025ORR, MRR

Secondary

MeasureTime frameDescription
Efficiency in specific population2018 to 2025ORR in CXCR4 mutated patients, ORR in patients previously treated with BTK inhibitors
Tolerance2018 to 2025Adverse events

Countries

France

Contacts

Primary Contactcécile tomowiak, Dr
cecile.tomowiak@chu-poitiers.fr+33 (0)5.49.44.43.07
Backup ContactMathilde Vonfeld, Intern
mathilde.vonfeld@chu-poitiers.fr+33 (0)5.49.44.43.07

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026