TELO-SCOPE study: a randomised, double-blind, placebo-controlled, phase 2 trial of danazol for short telomere related pulmonary fibrosis

• Published in: BMJ open respiratory research 2021-12, Vol.8 (1), p.e001127
• Main Authors: Mackintosh, John A, Pietsch, Maria, Lutzky, Viviana, Enever, Debra, Bancroft, Sandra, Apte, Simon H, Tan, Maxine, Yerkovich, Stephanie T, Dickinson, Joanne L, Pickett, Hilda A, Selvadurai, Hiran, Grainge, Christopher, Goh, Nicole S, Hopkins, Peter, Glaspole, Ian, Reynolds, Paul N, Wrobel, Jeremy, Jaffe, Adam, Corte, Tamera J, Chambers, Daniel C
• Format: Article
• Language: English
• Subjects: Adults; Androgens; Anticoagulants; Australia; Birth control; Bone marrow; Breastfeeding & lactation; Carbon monoxide; Child; COVID-19; Danazol - therapeutic use; Double-blind studies; Humans; interstitial fibrosis; Interstitial Lung Disease; Lung diseases; Mutation; Ovaries; Patients; Pediatrics; Pneumonia; Pulmonary Fibrosis; Stem cell transplantation; Steroids; Telomerase; Telomere - genetics; Treatment Outcome
• ISSN: 2052-4439; 2052-4439
• DOI: 10.1136/bmjresp-2021-001127

IntroductionRecent discoveries have identified shortened telomeres and related mutations in people with pulmonary fibrosis (PF). There is evidence to suggest that androgens, including danazol, may be effective in lengthening telomeres in peripheral blood cells. This study aims to assess the safety and efficacy of danazol in adults and children with PF associated with telomere shortening.Methods and analysisA multi-centre, double-blind, placebo-controlled, randomised trial of danazol will be conducted in subjects aged >5 years with PF associated with age-adjusted telomere length ≤10th centile measured by flow fluorescence in situ hybridisation; or in children, a diagnosis of dyskeratosis congenita. Adult participants will receive danazol 800 mg daily in two divided doses or identical placebo capsules orally for 12 months, in addition to standard of care (including pirfenidone or nintedanib). Paediatric participants will receive danazol 2 mg/kg/day orally in two divided doses or identical placebo for 6 months. If no side effects are encountered, the dose will be escalated to 4 mg/kg/day (maximum 800 mg daily) orally in two divided doses for a further 6 months. The primary outcome is change in absolute telomere length in base pairs, measured using the telomere shortest length assay (TeSLA), at 12 months in the intention to treat population.Ethics and disseminationEthics approval has been granted in Australia by the Metro South Human Research Ethics Committee (HREC/2020/QMS/66385). The study will be conducted and reported according to Standard Protocol Items: Recommendations for Interventional Trials guidelines. Results will be published in peer-reviewed journals and presented at international and national conferences.Trial registration numbersNCT04638517; Australian New Zealand Clinical Trials Registry (ACTRN12620001363976p).