A Multi-Center, Randomized, Open-Label, Single-Dose, Parallel Group Study to Investigate the Relative Bioavailability of Gantenerumab Produced With the G4 Process in Comparison to Gantenerumab Produced With the G3 Process Following Administration by Subcutaneous Injection in Healthy Volunteers
Latest Information Update: 17 Jan 2020
At a glance
- Drugs Gantenerumab (Primary)
- Indications Alzheimer's disease
- Focus Pharmacokinetics
- Sponsors Roche
- 15 Jan 2018 Status changed from active, no longer recruiting to completed.
- 30 Oct 2017 Planned End Date changed from 27 Dec 2017 to 8 Dec 2017.
- 30 Oct 2017 Planned primary completion date changed from 27 Dec 2017 to 8 Dec 2017.