Brodalumab in the Treatment of Immune-Related Adverse Events

PHASE1RecruitingINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

March 11, 2025

Primary Completion Date

May 31, 2026

Study Completion Date

November 30, 2026

Conditions
Breast CancerEsophageal CancerKidney CancerLung CancerThyroid CancerGynecologic CancerPancreatic CancerStomach CancerBrain TumorColon CancerRectal CancerHead and Neck CancerOral CancerLiver CancerSkin CancerProstate CancerTesticular CancerSolid Tumor
Interventions
DRUG

Brodalumab

Brodalumab 210 mg subcutaneous injection

RADIATION

CT scan

CT scans within 4 weeks of starting brodalumab and every 3 months during the study for tumor assessment

Trial Locations (1)

10032

RECRUITING

Columbia University Irving Medical Center, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bausch Health

UNKNOWN

lead

Brian Henick, MD

OTHER

NCT06673329 - Brodalumab in the Treatment of Immune-Related Adverse Events | Biotech Hunter | Biotech Hunter