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Tafasitamab + Lenalidomide + R-CHOP Versus R-CHOP in Newly Diagnosed High-intermediate and High Risk DLBCL Patients

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NCT04824092 · readout in 13 d

Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
899actual
Sites
307
Countries
Argentina, Australia, Austria +26

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-05-11actualWhen the study began enrolling
Primary completion2026-09-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-11-01estimatedThe whole study's end, after follow-up
First posted2021-04-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Diffuse Large B-cell Lymphoma

Interventions

  • Drug: Tafasitamab — also filed as Monjuvi
  • Drug: Lenalidomide
  • Drug: Rituximab
  • Drug: Cyclophosphamide
  • Drug: Doxorubicin
  • Drug: Vincristine
  • Drug: Prednisone
  • Drug: Tafasitamab placebo
  • Drug: Lenalidomide placebo

Primary outcome

what the primary-completion date above is the date OF
PFS-INV
measured Time from date of randomization until Progressive Disease or death from any cause. In this trial, the primary endpoint is PFS as assessed by the investigator (up to 43 months)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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