A Phase III, Multicenter, Randomized, Double-Masked, Sham-Controlled Study to Investigate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Vamikibart Administered Intravitreally in Patients With Uveitic Macular Edema
Latest Information Update: 08 Jan 2025
At a glance
- Drugs Vamikibart (Primary)
- Indications Retinal oedema
- Focus Registrational; Therapeutic Use
- Acronyms Sandcat
- Sponsors Roche
- 06 Jan 2025 Planned End Date changed from 30 Jun 2025 to 31 Dec 2025.
- 06 Jan 2025 Planned primary completion date changed from 30 Jun 2025 to 31 Dec 2025.
- 06 Jan 2025 Status changed from recruiting to active, no longer recruiting.