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Study to Investigate the Safety and Tolerability of Odronextamab in Patients With CD20+ B-Cell Malignancies

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NCT02290951

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
200actual
Sites
22
Countries
France, Germany, Israel +2

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
Start2015-01-09actualWhen the study began enrolling
Primary completion2025-08-21actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-08-21actualThe whole study's end, after follow-up
First posted2014-11-14estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non-Hodgkin Lymphoma
  • Chronic Lymphocytic Leukemia

Interventions

  • Drug: Odronextamab multiple dose levels — also filed as REGN1979
  • Drug: Odronextamab multiple dose levels — also filed as REGN1979

Primary outcomes

what the primary-completion date above is the date OF
Safety/overall frequency of adverse events (AEs)
measured Up to 24 months
Safety/dose limiting toxicities (DLTs)
measured Up to 28 days
Antitumor activity as measured by the objective response rate (ORR)
measured Through study completion, an average of 24 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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