Your browser doesn't support javascript.
loading
Open-Label Pilot Study of Interferon Gamma-1b in Patients With Non-Infantile Osteopetrosis.
Nguyen, Andrew; Miller, Weston P; Gupta, Ashish; Lund, Troy C; Schiferl, Daniel; Lam, Lok Sze Kelvin; Arzumanyan, Zorayr; Orchard, Paul J; Polgreen, Lynda E.
Affiliation
  • Nguyen A; Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance CA USA.
  • Miller WP; Audentes Therapeutics, An Astellas Company San Francisco, (formerly at University of Minnesota) San Francisco CA USA.
  • Gupta A; University of Minnesota Minneapolis MN USA.
  • Lund TC; University of Minnesota Minneapolis MN USA.
  • Schiferl D; Bone Diagnostics Spring Branch TX USA.
  • Lam LSK; Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance CA USA.
  • Arzumanyan Z; Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance CA USA.
  • Orchard PJ; University of Minnesota Minneapolis MN USA.
  • Polgreen LE; Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance CA USA.
JBMR Plus ; 6(3): e10597, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35309862
The only treatment currently available for patients with severe infantile osteopetrosis is hematopoietic cell transplantation (HCT). HCT-related toxicity and mortality risks typically preclude its use in non-infantile patients, and other therapies are needed for these patients who have significant disease-related morbidity. Interferon gamma-1b is currently approved by the U.S. Food and Drug Administration (FDA) for treatment of severe infantile osteopetrosis (autosomal recessive osteopetrosis [ARO]). However, little is known about the effects of interferon gamma-1b in non-infantile osteopetrosis. Thus, this pilot study aimed at testing the safety and tolerability of interferon gamma-1b in patients with non-infantile osteopetrosis and assessing the clinical effects. We performed a 12-month, open-label, multi-center pilot study involving patients >1 year-old diagnosed radiographically with osteopetrosis. Patients were initiated on interferon gamma-1b subcutaneously 15 µg/m2 three times weekly, to be titrated over 3 weeks to a goal of 100 µg/m2 three times weekly. The primary aim was safety and tolerability. The secondary aims were to assess changes in peripheral quantitative computed tomography (pQCT), dual-energy x-ray absorptiometry (DXA) bone mineral density (BMD) Z-scores, bone biomarkers, and quality-of-life (QOL) measures. Four of the five participants enrolled withdrew from the study between 3 and 9 months due to intolerability of interferon gamma-1b-related flu-like symptoms. The last participant completed the study with the addition of prednisone on days of interferon gamma-1b administration. DXA and pQCT outcomes were stable over 6-12 months, and there were no clear trends in bone biomarkers or QOL measures. No serious drug-related adverse events were reported during this study. Interferon gamma-1b was only tolerable in one of five participants with the addition of prednisone. The stabilization of BMD and other measures of bone health during this study suggest possible positive effects of interferon gamma-1b on osteopetrosis; however, additional data are needed before conclusions on treatment efficacy can be made. © 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Aspects: Patient_preference Language: En Journal: JBMR Plus Year: 2022 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Aspects: Patient_preference Language: En Journal: JBMR Plus Year: 2022 Document type: Article Country of publication: