drugset / Trial / NCT00916747

Study of Zoledronic Acid, Pravastatin, and Lonafarnib for Patients With Progeria

NCT00916747

NaSingle-groupOpen-labelTreatment

Summary

Hutchinson-Gilford Progeria Syndrome (Progeria) is a rare autosomal disease that results in premature death at a median age of 13 years due to cardiovascular and cerebralvascular compromise. The mutation for this disease has been identified and results in a mutant form of lamin A that cannot be de-farnesylated. This study evaluates the combination of pravastain (a statin), lonafarnib (a farnesyltransferase inhibitor) and zoledronic acid (a bisphosphonate) in an open label phase II efficacy trial in children with Progeria. These agents all target farnesylation pathways at different points. Patients with genetically confirmed progeria will be eligible for this protocol. Treatment will be initiated for 24 months duration. Clinical and biologic parameters will be examined to assess response.

Timeline

Start
2009-08
Primary completion
2022-02
Completion
2023-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lonafarnib Small molecule 150 mg/m2 Oral
Subject Pravastatin Small molecule 5 mg Oral
Subject Pravastatin Small molecule 10 mg Oral
Subject Zoledronic acid Other / unclassified Intravenous