Fact CheckerSign in

NCT07567469Not yet recruitingPhase 1/2

A Safety and Efficacy Study of Combined Fianlimab + Cemiplimab in Children and Young Adults With Recurrent or Progressive High-Grade Glioma or Posterior Fossa-A Ependymoma

A Phase 1/2 Open-Label, Safety and Efficacy Study of Neoadjuvant Fianlimab (Anti-LAG-3 Antibody) in Combination With Cemiplimab (Anti-PD-1 Antibody) and Cemiplimab Alone Followed by Adjuvant Fianlimab in Combination With Cemiplimab in Pediatric and Young Adult Participants With Recurrent or Progressive High-Grade Glioma or Pediatric and Adult Participants With Recurrent or Progressive Posterior Fossa-A Ependymoma

Source: ClinicalTrials.gov · Last updated 5 May 2026

Brief summary (registry, in English)

This study is researching an experimental drug called cemiplimab (called "study drug") and the combination of experimental drugs of fianlimab and cemiplimab (called "study drugs"). The study is focused on children and young adults with recurrent or progressive High-Grade Glioma (HGG) or ependymoma. "Recurrent" means that the cancer came back after treatment. "Progressive" means that the tumor has grown or spread. The aim of the study is to see how safe, tolerable, and effective cemiplimab and the combination of fianlimab and cemiplimab are. The study is looking at several other research questions, including: * What side effects may happen from receiving the study drug(s) * Do the study drug(s) help study participants live longer without their tumors growing or spreading * How much of the study drug(s) is in the blood at different times * Whether the body makes antibodies against the study drug(s) (which could make the study drug\[s\] less effective or lead to side effects)

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
120 (estimated)
First submitted
28 Apr 2026
Start date
31 Aug 2026
Primary completion date
27 Aug 2032
Lead sponsor
Regeneron Pharmaceuticals
NCT number
NCT07567469
EU CT number
2025-521485-96-00

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 120
  • From 31 Aug 2026 to the primary completion date, 27 Aug 2032
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has not yet recovered from any acute toxicities resulting from prior therapy
  • Treatment with high dose systemic corticosteroids as described in the protocol

Other illness

  • Active autoimmune disease requiring systemic immunosuppressive therapy in the past 2 years
  • Active, serious medical illness, infection or other systemic illness which would limit participation in the trial
  • History of myocarditis
  • History of interstitial lung disease (eg, idiopathic pulmonary fibrosis, organizing pneumonia) or active, noninfectious pneumonitis that required immune-suppressive doses of glucocorticoids to assist with management
    • Note: Other protocol defined Inclusion/ Exclusion Criteria apply

Lab values

  • Prior treatment with antibodies to Programmed Cell Death Protein -1 (PD-1), Programmed Cell Death Protein Ligand -1 (PD-L1), Lymphocyte Activation Gene 3 (LAG3), or Cytotoxic T-Lymphocyte Associated protein 4 (CTLA-4)

Who the study is looking for

  • Participant must be diagnosed with recurrent/progressive HGG or PF-A ependymoma with unequivocal progression on Magnetic Resonance Imaging (MRI) as described in the protocol
  • Participant must have histologically confirmed (at initial diagnosis or relapse) HGG or PF-A ependymoma
  • Participant must be an adequate medical candidate for surgical resection as described in the protocol
  • Karnofsky Performance Status (KPS) score ≥50 (in participants ≥16 years) or Lansky Performance Status (LPS) score ≥50 (in participants \<16 years) as described in the protocol
  • Adequate organ function as described in the protocol

Age in the registry: 0 years to 39 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.