Macular Degeneration

Brolucizumab (RTH258) for the treatment of wet age-related macular degeneration

Brolucizumab for the treatment of wet age-related macular degeneration

Brolucizumab Reports Retinal Fluid Reduction in Phase 3 Analysis

New phase 3 trial data shows that brolucizumab (RTH258) 6 mg results in less instances of detected retinal fluid in treated patients versus those treated with aflibercept. The indication of treatment for the key marker of neovascular age-related macular degeneration (nAMD) lends to the hope that the humanized single-chain antibody fragment (scFv) can reach the market as a first-of-its-kind therapy.

Brolucizumab Reports Retinal Fluid Reduction in Phase 3 Analysis


New analysis of Novartis Phase III brolucizumab (RTH258) data reinforces superior reduction of retinal fluid

Novartis announced a new data analysis showing that retinal fluid was detected less often in patients treated with brolucizumab (RTH258) 6 mg versus aflibercept over four visits between weeks 36 to 48[1]. Retinal fluid is a key marker of disease activity in neovascular age-related macular degeneration (nAMD). The data, from pre-specified secondary endpoints of the Phase III HAWK and HARRIER trials, were presented at EURETINA 2018 as a follow-up to data presented in November 2017.

New analysis of Novartis Phase III brolucizumab (RTH258) data reinforces superior reduction of retinal fluid

Phase III clinical trials of brolucizumab in patients with neovascular age-related macular degeneration

What is brolucizumab (also known as RTH258)?

Phase III clinical trials of brolucizumab in patients with neovascular age-related macular degeneration


Übersicht Brolucizumab zur Behandlung der altersbedingten feuchten Makuladegeneration (AMD)


Wikipedia: https://en.wikipedia.org/wiki/Brolucizumab