Phase 2a Study of Interferon Gamma-1b for the Treatment of Autosomal Dominant Type 2 Osteopetrosis
This study is an open label use of ACTIMMUNE for patients with Autosomal Dominant Osteopetrosis Type 2(ADO2). Effects of treatment will be evaluated after 14 weeks on ACTIMMUNE by bone resorption markers. This study will treat 12 patients with ADO2 recruited from Indiana University and Riley Hospital for Children at Indiana University Health.
Indication: Autosomal Dominant Osteopetrosis Type 2
Modality: small molecule
Target: ACTIMMUNE
Sponsor: Indiana University
Source URL: ClinicalTrials.gov
Source updated: Jan 08, 2021
Ingested: May 21, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: ACTIMMUNE
View original source fields
Condition raw: Autosomal Dominant Osteopetrosis Type 2
Condition normalized: Autosomal Dominant Osteopetrosis Type 2
Modality raw: small molecule
Modality normalized: small molecule
Target raw: ACTIMMUNE
Target normalized: ACTIMMUNE