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NCT07231952

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

Recruiting now Phase 2 Last updated 17 November 2025
What this trial tests

Phase 2 trial testing Pirtobrutinib in Waldenstrom Macroglobulinemia in 40 participants. Currently enrolling.

Timeline
11 November 2025
Primary endpoint
11 April 2028
11 April 2028

Quick facts

Lead sponsorMemorial Sloan Kettering Cancer Center
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date11 November 2025
Primary completion11 April 2028
Estimated completion11 April 2028
Sites8 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Memorial Sloan Kettering Cancer Center — full company profile →

Who can join

18 and older, any sex, with Waldenstrom Macroglobulinemia or Lymphoplasmacytic Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Pirtobrutinib

Trials testing the same drug.

Other recruiting trials for Waldenstrom Macroglobulinemia

Currently open trials in the same condition.

Other Memorial Sloan Kettering Cancer Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07231952.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing