OBJECTIVES: I. Compare the rate of treatment failure in osteopetrosis patients receiving interferon gamma in combination with calcitriol to the rate of treatment failure in patients receiving calcitriol alone. II. Compare the number of adverse events or clinical manifestations of disease progression occurring in these patients. III. Assess the effects of interferon gamma on hematopoiesis, cranial nerve function, and rate of infection in these patients.

Condition	Treatment or Intervention	Phase
Osteopetrosis	Drug: calcitriol  Drug: interferon gamma	Phase III

Further Study Details: 

Expected Total Enrollment:  30

PROTOCOL OUTLINE: This is a randomized, placebo controlled, open label study. Patients are randomized to one of two arms (interferon gamma in combination with calcitriol or calcitriol alone). Arm I: Patients receive calcitriol once daily. Interferon gamma is administered by subcutaneous injection three times a week. Arm II: Patients receive calcitriol once daily. Patients may continue treatment in the absence of toxicity and disease progression. If disease progression is diagnosed in the control group, patients will then receive interferon gamma in combination with calcitriol. Patients are followed every 4 weeks.

Ages Eligible for Study:  up to  10 Years,  Genders Eligible for Study:  Both

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

• Biopsy and x-ray confirmed primary osteopetrosis
• Presence of anemia and/or cranial nerve compression

--Prior/Concurrent Therapy--

• Biologic therapy: No prior/concurrent bone marrow transplantation No prior interferon gamma No other investigational biologic agents
• Chemotherapy: No prior/concurrent chemotherapeutic agents for bone marrow transplantation
• Endocrine therapy: Prior/concurrent corticosteroid as supportive therapy allowed
• Radiotherapy: Not specified
• Surgery: At least 5 days since major surgery
• Other: Prior/concurrent calcitriol as supportive therapy allowed Prior/concurrent transfusion as supportive therapy allowed Prior/concurrent dietary therapy allowed

--Patient Characteristics--

• Age: 2 months to 10 years
• Performance status: Not specified
• Life expectancy: At least 6 months
• Hematopoietic: Not specified
• Hepatic: Bilirubin less than 2 mg/dL
• Renal: Creatinine less than 1.5 mg/dL OR Creatinine clearance greater than 50 mL/min
• Pulmonary: No uncorrected airway obstruction
• Other: No active infection requiring intravenous antibiotics No known seizure disorder not related to hypocalcemia No uncorrected hydrocephalus No MRI evidence of cerebral atrophy Must maintain or gain body weight No sleep apnea No thrombocytopenia No massive splenomegaly

Study chairs or principal investigators

L. Lyndon Key, Jr.,  Study Chair,  Medical University of South Carolina   

Study ID Numbers:  199/13284; MUSC-FDR000768
Record last reviewed:  January 2001
Last Updated:  October 13, 2004
Record first received:  October 18, 1999
ClinicalTrials.gov Identifier:  NCT00004402
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08