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Clinical Trials/NCT02651662
NCT02651662
Active, not recruiting
Phase 1

A Phase 1 Study to Assess Safety and Tolerability of Odronextamab (REGN1979) an Anti-CD20 x Anti-CD3 Bispecific Monoclonal Antibody, and Cemiplimab (REGN2810), an Anti-Programmed Death-1 Monoclonal Antibody in Patients With B-Cell Malignancies (CLIO-1)

Regeneron Pharmaceuticals30 sites in 6 countries105 target enrollmentJanuary 11, 2016

Overview

Phase
Phase 1
Intervention
cemiplimab
Conditions
Relapsed/Refractory Aggressive B-Cell Lymphoma
Sponsor
Regeneron Pharmaceuticals
Enrollment
105
Locations
30
Primary Endpoint
Incidence of dose limiting toxicities (DLTs) of cemiplimab in combination with odronextamab
Status
Active, not recruiting
Last Updated
2 months ago

Overview

Brief Summary

This study is researching a combination of 2 experimental drugs, referred to as "study drugs", called odronextamab (also known as REGN1979) and cemiplimab (also known as REGN2810). The study is focused on patients who have relapse/refractory aggressive B-cell lymphoma. The aim of the study is to see how safe and tolerable the study drugs are, and to define the recommended dose regimen for the combination with odronextamab.

This study is also looking at several other research questions, including:

  • What side effects may happen from taking the study drugs
  • How effective the study drugs are against the disease
  • How much study drug is in the blood at different times
  • Whether the body makes substances or protein called antibodies against the study drugs (that could make the drugs less effective or could lead to side effects)
Registry
clinicaltrials.gov
Start Date
January 11, 2016
End Date
May 31, 2026
Last Updated
2 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Have documented CD20+ aggressive B-cell NHL that is either not responsive to or relapsed after at least 2 prior lines of systemic therapy, for whom treatment with an anti-CD20 antibody may be appropriate. In addition, prior treatments should at least contain an anti-CD20 antibody and an alkylating agent.
  • Must have at least 1 nodal lesion (≥1.5 cm), or at least one extranodal lesion with longest transverse diameter (LDi) greater than 1.0 cm, documented by diagnostic imaging (computed tomography \[CT\] or magnetic resonance imaging \[MRI\]).
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤1
  • Adequate bone marrow and hepatic function, as defined in the protocol
  • Willing and able to comply with clinic visits and study-related procedures
  • Provide signed informed consent

Exclusion Criteria

  • Primary central nervous system (CNS) lymphoma, or known or suspected CNS involvement by non-primary CNS NHL
  • History of or current relevant CNS pathology, as described in the protocol
  • Ongoing or recent (within 2 years) evidence of significant autoimmune disease that required treatment with systemic immunosuppressive treatments, which may suggest risk for immune-mediated adverse events (iAEs)
  • Prior therapies, as described in the protocol
  • Uncontrolled infection with human immunodeficiency virus (HIV), hepatitis B or hepatitis C infection or other uncontrolled infection
  • Cytomegalovirus infection as noted by detectable levels on peripheral blood polymerase chain reaction (PCR) assay until the infection is well controlled.
  • Known hypersensitivity to both allopurinol and rasburicase
  • Pregnant or breastfeeding women
  • Women of childbearing potential, or men who are unwilling to practice highly effective contraception prior to the initial dose/start of the first treatment, during the study, and for at least 6 months after the last dose, as defined in the protocol
  • Patients prior diagnosis of hemophagocytic lymphohistiocytosis (HLH) or macrophage activation syndrome (MAS)

Arms & Interventions

Dose escalation phase

Safety assessment of odronextamab in combination with cemiplimab and selection of recommended phase 2 dose (RP2D) regimen(s) for the combination of odronextamab and cemiplimab.

Intervention: cemiplimab

Dose escalation phase

Safety assessment of odronextamab in combination with cemiplimab and selection of recommended phase 2 dose (RP2D) regimen(s) for the combination of odronextamab and cemiplimab.

Intervention: odronextamab

Dose expansion phase

RP2D administration of the combination treatment.

Intervention: cemiplimab

Dose expansion phase

RP2D administration of the combination treatment.

Intervention: odronextamab

Outcomes

Primary Outcomes

Incidence of dose limiting toxicities (DLTs) of cemiplimab in combination with odronextamab

Time Frame: Up to 28 days

Incidence of treatment emergent adverse events (TEAEs) of cemiplimab in combination with odronextamab

Time Frame: Up to 18 months

Incidence of adverse events of special interest (AESIs) of cemiplimab in combination with odronextamab

Time Frame: Up to 18 months

Severity of AESIs of cemiplimab in combination with odronextamab

Time Frame: Up to 18 months

Severity of TEAEs of cemiplimab in combination with odronextamab

Time Frame: Up to 18 months

Secondary Outcomes

  • Odronextamab and cemiplimab concentrations in serum(Up to 18 months)
  • Titer of ADAs to odronextamab and cemiplimab over time(Up to 18 months)
  • Complete response (CR) rate as assessed by investigator(Up to 18 months)
  • Incidence of anti-drug antibodies (ADAs) to odronextamab and cemiplimab over time(Up to 18 months)
  • Duration of response as assessed by investigator(Up to 18 months)
  • Incidence of neutralizing antibodies (Nabs) to odronextamab and cemiplimab over time(Up to 18 months)
  • Titer of Nabs to odronextamab and cemiplimab over time(Up to 18 months)
  • Overall response rate as assessed by investigator(Up to 18 months)

Study Sites (30)

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