Lonafarnib for Patients With Hutchinson-Gilford Progeria Syndrome or Progeroid Laminopathy
NCT ID: NCT03895528
Last Updated: 2021-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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APPROVED_FOR_MARKETING
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Brief Summary
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Detailed Description
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Conditions
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Interventions
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Lonafarnib
Farnesyl transferase inhibitor
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Adequate hepatic function as defined by SGPT (ALT) and SGOT (AST) ≤ 5 times upper limit of normal range for age
Exclusion Criteria
* Taking digoxin, a P-gp substrate with a narrow therapeutic window.
* Severe renal impairment (GFR \< 30 mL/min/1.73m2).
* Uncontrolled infection.
* Presence of any active clinically relevant medical condition that in the opinion of the treating physician would preclude patient from safely participating in the program.
* Pregnant or breast-feeding or plan to become pregnant while on therapy.
12 Months
ALL
No
Sponsors
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Eiger BioPharmaceuticals
INDUSTRY
Responsible Party
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References
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Gordon LB, Shappell H, Massaro J, D'Agostino RB Sr, Brazier J, Campbell SE, Kleinman ME, Kieran MW. Association of Lonafarnib Treatment vs No Treatment With Mortality Rate in Patients With Hutchinson-Gilford Progeria Syndrome. JAMA. 2018 Apr 24;319(16):1687-1695. doi: 10.1001/jama.2018.3264.
Other Identifiers
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EIG-EAP-LNF-001
Identifier Type: -
Identifier Source: org_study_id
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