drugset / Trial / NCT01704404
7 Days of TD-4208 in Subjects With Chronic Obstructive Pulmonary Disease
RandomizedCrossoverQuadruple-blindTreatment
Summary
This study will characterize the dose response of TD-4208 after 7 days of dosing in subjects with Chronic Obstructive Pulmonary Disease (COPD).
Timeline
- Start
- 2012-12
- Primary completion
- 2013-11
- Completion
- 2013-12
Publications
- Lo A, Borin MT, Bourdet DL. Population Pharmacokinetics of Revefenacin in Patients with Chronic Obstructive Pulmonary Disease. Clin Pharmacokinet. 2021 Mar;60(3):391-401. doi: 10.1007/s40262-020-00938-3.
- Quinn D, Barnes CN, Yates W, Bourdet DL, Moran EJ, Potgieter P, Nicholls A, Haumann B, Singh D. Pharmacodynamics, pharmacokinetics and safety of revefenacin (TD-4208), a long-acting muscarinic antagonist, in patients with chronic obstructive pulmonary disease (COPD): Results of two randomized, double-blind, phase 2 studies. Pulm Pharmacol Ther. 2018 Feb;48:71-79. doi: 10.1016/j.pupt.2017.10.003. Epub 2017 Oct 4.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Revefenacin | Small molecule | 22 ug | Inhaled |
| Subject | Revefenacin | Small molecule | 44 ug | Inhaled |
| Subject | Revefenacin | Small molecule | 88 ug | Inhaled |
| Subject | Revefenacin | Small molecule | 175 ug | Inhaled |
| Subject | Revefenacin | Small molecule | 350 ug | Inhaled |
| Subject | Revefenacin | Small molecule | 700 ug | Inhaled |