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NCT00043329COMPLETEDanonymous

Post-Marketing Surveillance Study of Actimmune (Interferon Gamma-1b) in Patients With Severe Malignant Osteopetrosis

Sponsor

Source record

InterMune

Phase

Source record

Not classified

Modality

AI-normalized

small molecule

Target

AI-normalized

Actimmune Registry

Indication / condition

AI-normalized

Osteopetrosis

Intervention

Source record

Actimmune Registry

Source & freshness

Source record

NCT ID

NCT00043329

Original source

ClinicalTrials.gov

Source last updated

Nov 01, 2007

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT00043329

Title

Post-Marketing Surveillance Study of Actimmune (Interferon Gamma-1b) in Patients With Severe Malignant Osteopetrosis

Sponsor

InterMune

Status

COMPLETED

Phase

Detailed source ingestion pending

Condition raw

Osteopetrosis

Condition normalized

Osteopetrosis

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Actimmune Registry

Target normalized

Actimmune Registry

Interventions

Actimmune Registry

Public preview

Source record

The purpose of this study is to establish a registry of all children with severe, malignant osteopetrosis who are treated with Actimmune (IFN-g 1b or Interferon gamma-1b) to monitor the effects of IFN-g 1b on preventing progression of this disease and to follow the safety of patients receiving it on a long-term basis. In addition, evaluation of the possible effect of Actimmune therapy on the humoral response to normal childhood vaccinations in this same patient population will be examined.Interferon gamma is a substance that the body makes naturally.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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