This multicenter, non-randomized, open-label, single- and multiple-ascending-dose study will investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of RO6867461 in patients with wet age-related macular degeneration.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Single or multiple ascending dose by intravitreal injection
Unnamed facility
Colorado Springs, Colorado, United States
Unnamed facility
Baltimore, Maryland, United States
Unnamed facility
Dallas, Texas, United States
Unnamed facility
Houston, Texas, United States
Ocular safety, assessed by BCVA (EDTRS chart), slitlamp examination, ophthalmoscopy, IOP, fundus photography, SD-OCT, angiography
Time frame: Part A, 12 weeks; Part B, 20 weeks
Safety: Incidence of adverse events
Time frame: Part A, 12 weeks; Part B, 20 weeks
Pharmacokinetics: Area under the concentration time curve (AUC)
Time frame: Part A, 12 weeks; Part B, 20 weeks
Pharmacokinetics: Maximum plasma concentration (Cmax)
Time frame: Part A, 12 weeks; Part B, 20 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Charlottesville, Virginia, United States
Unnamed facility
Belfast, United Kingdom
Unnamed facility
Bristol, United Kingdom
Unnamed facility
London, United Kingdom