Rituximab and Abatacept Effectiveness in Differential Treatment of Interstitial Lymphocytic Lung Disease in Children With Primary Immunodeficiencies.
- Sponsor
- Federal Research Institute of Pediatric Hematology, Oncology and Immunology
- Study ID
- NCT04572620
- Status
- Unknown
Conditions
- Interstitial Lymphocytic Lung Disease
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- Rituximab — DRUG375 mg/m2 as 4 weekly consecutive i.v. infusions with subsequent infusions of 375 mg/m2 performed every 3 months for 12 months.
- Abatacept — DRUG10 mg/kg i.v. every 2 weeks twice, then every 4 weeks for 12 months.
Study Details
The rationale for this retrospective study is to evaluate the efficacy and safety of abatacept and rituximab treatment of ILLD in a cohort of pediatric patients with different forms of PID, who received one of the two therapy regimens predominantly based on the lesions histopathology.
Key Dates
- Start date
- Sep 7, 2020
- Status verified
- Sep 2020
- Primary completion
- Sep 30, 2021
- Completion
- Sep 30, 2021
Study Design
- Enrollment
- 30 participants (estimated)
Arms
- Arm: group 1(rituximab)
- Arm: group 2 (abatacept)
Primary Outcome Measure
Dynamics of severity clinical and radiological symptoms [ Time Frame: before the time the first dose of study treatment was administered ]
Central Contacts
- Anna Shcherbina, MD, PhD+7(495)2876570