Study in ALS With Abatacept & IL-2

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

October 28, 2021

Primary Completion Date

October 17, 2024

Study Completion Date

October 17, 2024

Conditions
Amyotrophic Lateral Sclerosis
Interventions
DRUG

Abatacept Injection [Orencia] and Proleukin (aldesleukin)

Abatacept (Orencia®) and recombinant human IL-2 (aldesleukin). Patients will receive a fixed dose of subcutaneous abatacept (125 mg/mL) at day 1. Two weeks later (day 15), patients will receive the second dose of subcutaneous abatacept (125 mg/mL). In addition, patients will receive subcutaneous IL-2 (1x106units /day) for 5 days (days 15-19). If this treatment regimen is tolerated, patients will receive 28 further similar treatment courses of abatacept and IL-2 every two weeks.

Trial Locations (1)

77030

Houston Methodist Research Institute, Houston

All Listed Sponsors
lead

The Methodist Hospital Research Institute

OTHER