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A Study to Assess the Anti-Tumor Activity and Safety of Odronextamab in Adult Patients With B-cell Non-Hodgkin Lymphoma Who Have Been Previously Treated With Other Cancer Therapies

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NCT03888105

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

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
515actual
Sites
119
Countries
Australia, Canada, China +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
Start2019-11-13actualWhen the study began enrolling
Primary completion2026-06-17actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-12-15estimatedThe whole study's end, after follow-up
First posted2019-03-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-31actualThe 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)

Intervention

  • Drug: Odronextamab — also filed as REGN1979

Primary outcomes

what the primary-completion date above is the date OF
Objective Response Rate (ORR), as assessed by independent central review
measured Up to 52 weeks of study treatment
ORR, as assessed by independent central review
measured Up to 36 weeks of study treatment

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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