drugset / Trial / NCT02176252
Safety, Tolerability, Pharmacokinetics and Pharmacodynamic of AZD1722 in Healthy Male and Female Japanese Subjects
NaSingle-groupQuadruple-blindTreatment
Summary
The study is designed to evaluate the safety, tolerability, pharmacodynamics and pharmacokinetics of AZD1722 in healthy Japanese subjects at increasing doses given for 7 days in order to allow for including Japanese subjects in future global studies. A cohort of Caucasian subjects will be included in the study to evaluate cardiac effects, assessed by digital ECGs (dECG) recordings, also in Caucasian subjects.
Timeline
- Start
- 2013-07
- Primary completion
- 2013-12
- Completion
- 2013-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tenapanor | Small molecule | 15 mg | — |
| Subject | Tenapanor | Small molecule | 30 mg | — |
| Subject | Tenapanor | Small molecule | 60 mg | — |
| Subject | Tenapanor | Small molecule | 90 mg | — |
| Subject | Tenapanor | Small molecule | 180 mg | — |
Indications
No indication recorded.