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NCT06792825

HM2023-43:Ph 2 Trial of Tafasitamab With Lenalidomide+Rituximab in Treatment-naive FL and MZL

Recruiting now Phase 2 Last updated 12 August 2025
What this trial tests

Phase 2 trial testing Tafasitamab in Follicular Lymphoma in 65 participants. Currently enrolling.

Timeline
7 August 2025
Primary endpoint
8 July 2029
8 July 2031

Quick facts

Lead sponsorMasonic Cancer Center, University of Minnesota
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment65
Start date7 August 2025
Primary completion8 July 2029
Estimated completion8 July 2031
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Masonic Cancer Center, University of Minnesota

Who can join

18 and older, any sex, with Follicular Lymphoma or Marginal Zone Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study follows a Simon's two-stage phase II trial design to evaluate the safety and efficacy of tafasitamab added to rituximab and lenalidomide for two treatment-naïve, parallel, independent cohorts: follicular lymphoma (FL) and marginal zone lymphoma (MZ). Each cohort, FL and MZ, will be evaluated separately. This study is presented to the patient and consent is signed prior to the initiation of treatment for their primary malignancy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Tafasitamab

Trials testing the same drug.

Other recruiting trials for Follicular Lymphoma

Currently open trials in the same condition.

Other Masonic Cancer Center, University of Minnesota 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/NCT06792825.

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