drugset / Trial / NCT01967966
A Bioavailability and Pharmacokinetic Study of GDC-0032 in Healthy Volunteers
RandomizedParallel-groupOpen-labelBasic science
Summary
This 2-arm, open-label, non-randomized study will investigate the absolute bioavailability, pharmacokinetics, mass balance, and routes of elimination of GDC-0032 as well as its safety in healthy volunteers. Patients will receive either a single oral dose of GDC-0032 followed by a 14C-labeled IV dose of GDC-0032 or a single oral dose of 14C-labelled GDC-0032.
Timeline
- Start
- 2013-11
- Primary completion
- 2013-12
- Completion
- 2013-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Taselisib | Small molecule | — | Oral |
Indications
No indication recorded.