drugset / Trial / NCT01474278
A Study of RO5028442 in Adult Male High-Functioning Autistic Patients
RandomizedCrossoverDouble-blind
Summary
This multi-center, randomized, double-blind study will evaluate exploratory biomarkers and the safety and tolerability of a single dose of RO5028442 in adult male high-functioning autistic patients. In a cross-over design, patients will be randomized to receive either a single dose of RO5028442 or matching placebo with a washout period of 7-14 days. Anticipated time on study is up to approximately 9 weeks.
Timeline
- Start
- 2011-12
- Primary completion
- 2013-03
- Completion
- 2013-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RO5028442 | Small molecule | 20 mg | Intravenous |