Long-term safety of tiotropium/olodaterol in older patients with moderate-to-very-severe COPD in the TONADO® studies.
Gary T FergusonFrançois MaltaisJill KarpelUlrich BothnerIsabel KloerMatthias TrampischRoland BuhlPublished in: NPJ primary care respiratory medicine (2020)
Older patients with chronic obstructive pulmonary disease (COPD) may be at increased risk of adverse events (AEs) due to decreased protective organ function and increased comorbidities. TONADO® 1 + 2 were replicate, randomized, double-blind, parallel-group, 52-week, Phase III trials comparing the efficacy and safety of tiotropium/olodaterol (5/5 µg) versus the monocomponents via the Respimat® inhaler in patients with moderate-to-very-severe COPD. In this prespecified safety analysis, patients were grouped by age. Of 3100 patients, 1585 (51.1%) were aged <65 years, 1198 (38.7%) 65-<75 years, 309 (10.0%) 75-<85 years, and eight (0.3%) ≥85 years. At baseline, 23.4% had a pre-existing cardiac disorder, 45.6% had hypertension, and 13.3% had glucose metabolism disorders, including diagnosed diabetes. Overall, there was no increase in major adverse cardiac events, other AEs, or serious AEs with tiotropium/olodaterol versus the monocomponents in any age group, supporting the safety of tiotropium/olodaterol in older patients with COPD.
Keyphrases
- phase iii
- double blind
- chronic obstructive pulmonary disease
- placebo controlled
- end stage renal disease
- ejection fraction
- clinical trial
- newly diagnosed
- chronic kidney disease
- open label
- physical activity
- type diabetes
- blood pressure
- middle aged
- high intensity
- heart failure
- early onset
- community dwelling
- prognostic factors
- cystic fibrosis
- metabolic syndrome
- patient reported outcomes
- study protocol
- data analysis
- drug induced
- adverse drug