Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07231952

A Study of Pirtobrutinib, Venetoclax, and Rituximab in People With Waldenström's Macroglobulinemia (WM)/Lymphoplasmacytic Lymphoma (LPL)

A Phase II Study of Time-limited Combination of Pirtobrutinib, Venetoclax, and Rituximab in Treatment Naïve Patients With Waldenström's Macroglobulinemia (WM) / Lymphoplasmacytic Lymphoma (LPL) (PRoVen)

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to find out if the combination of pirtobrutinib, venetoclax, and rituximab is an effective treatment for participants with Waldenström's macroglobulinemia (WM)/lymphoplasmacytic lymphoma (LPL)

Conditions

Interventions

TypeNameDescription
DRUGPirtobrutinibPO QD
DRUGVenetoclaxPO QD
DRUGRituximabIV or SC

Timeline

Start date
2025-11-11
Primary completion
2028-04-11
Completion
2028-04-11
First posted
2025-11-17
Last updated
2025-11-17

Locations

8 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07231952. Inclusion in this directory is not an endorsement.