Compare Bioavailability of RO7239361 After Subcutaneous Injection
Completed · Phase 1
Conditions studied: Healthy
In brief
Randomized study in healthy men and women. Assess the similarity of RO7239361 when injected into the arm, thigh, or the stomach. Collect data on safety of RO7239361.
Key facts
- Study ID
- NCT03100630
- Run by
- Hoffmann-La Roche
- People needed
- 99
- Starts
- 2017-05-09
- Expected to finish
- 2017-10-17
- Last updated by the study team
- 2019-08-07
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy participant as determined by no significant deviations in normal medical and surgical history and assessments
- Body Mass Index 18 kg/m2 to 32 kg/m2
- females must be of non-childbearing potential
You may not qualify if…
- tattoos or other skin findings on any of the potential injection sites
- history of chronic muscle pain within 30 days prior to study treatment
- prior history of IgG1 therapy
- Other protocol defined inclusion and exclusion criteria apply
Where it is running
- WCCT Global, Inc. — Cypress, California, United States
Full record on ClinicalTrials.gov
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