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A Trial to Learn How Effective and Safe Odronextamab is Compared to Standard of Care for Adult Participants With Previously Treated Aggressive B-cell Non-Hodgkin Lymphoma

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NCT06230224 · readout in 649 d

Sponsored by Regeneron Pharmaceuticals (industry) · REGN — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
216actual
Sites
81
Countries
Argentina, Australia, Brazil +11

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
Start2024-02-15actualWhen the study began enrolling
Primary completion2028-05-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-05-29estimatedThe whole study's end, after follow-up
First posted2024-01-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • B-Cell Non-Hodgkin Lymphoma (B-NHL)

Interventions

  • Drug: Odronextamab — also filed as R1979
  • Drug: Ifosfamide — also filed as Ifex
  • Drug: Carboplatin — also filed as Paraplatin
  • Drug: Etoposide — also filed as Etopophos
  • Drug: Rituximab — also filed as Rituxan
  • Drug: Dexamethasone — also filed as Decadron
  • Drug: Cisplatin — also filed as Platinol
  • Drug: Cytarabine — also filed as Cytosar-U
  • Drug: Gemcitabine — also filed as Gemzar

Primary outcome

what the primary-completion date above is the date OF
Event-free survival (EFS) as assessed by independent central review (ICR)
measured Assessed up to 3 years

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