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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT00043329
Date of registration: 07/08/2002
Prospective Registration: No
Primary sponsor: InterMune
Public title: Post Marketing Surveillance Study of Actimmune in Patients With Severe, Malignant Osteopetrosis
Scientific title: Post-Marketing Surveillance Study of Actimmune (Interferon Gamma-1b) in Patients With Severe Malignant Osteopetrosis
Date of first enrolment: January 2002
Target sample size: 6
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00043329
Study type:  Observational
Study design:  Time Perspective: Retrospective  
Phase: 
Countries of recruitment
United States
Contacts
Name:     Steven Porter, MD
Address: 
Telephone:
Email:
Affiliation:  InterMune
Key inclusion & exclusion criteria

- Male or female

- Diagnosis of severe, malignant osteopetrosis

- Currently receiving or planning to initiate therapy with Actimmune (Interferon
gamma-1b)

- Willing to attend follow-up appointments every 6 months following enrollment into the
study, if clinically indicated



Age minimum: N/A
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Osteopetrosis
Intervention(s)
Drug: Actimmune Registry
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
GIOS-003
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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