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
| Type | Name | Description |
|---|---|---|
| DRUG | Pirtobrutinib | PO QD |
| DRUG | Venetoclax | PO QD |
| DRUG | Rituximab | IV 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07231952. Inclusion in this directory is not an endorsement.