WebFeb 23, 2024 · The median time to fluid-free subfield was 4 weeks for aflibercept 8mg vs 8 weeks for aflibercept 2mg. In PHOTON, DME patients treated with aflibercept 8mg 12- and 16-week dosing regimens had a ... WebSep 9, 2024 · The trials, called PHOTON in DME and PULSAR in wAMD, both showed the dosing regimens achieved non-inferiority in vision gains compared to the Eylea 8-week dosing regimen. Aflibercept 8 mg is being jointly developed by Regeneron and Bayer AG. In these trials, the safety of aflibercept 8 mg was consistent with the established safety …
阿柏西普(ZALTRAP/AFLIBERCEPT)在糖尿病黄斑水肿患者中的剂 …
WebFeb 10, 2024 · Berlin, February 10, 2024 - Bayer and Regeneron Pharmaceuticals, Inc., today announced two planned phase III studies, PHOTON and PULSAR, evaluating extended treatment intervals with a new aflibercept 8mg formulation for intravitreal injection in adults with visual impairment due to diabetic macular edema (DME) and wet age-related … WebSep 9, 2024 · The (PHOTON) & (PULSAR) study evaluates aflibercept (8mg, q12w or q16w) vs Eylea (q8w) in patients with DME & wAMD. Aflibercept is being jointly developed by Regeneron & Bayer Both the trial met their 1EPs i.e., patients treated with aflibercept (8mg, 12 & 16wk.) in DME & wAMD achieved non-inferiority in vision gains, and the safety results … church\u0027s chicken delivery trinidad
Aflibercept 8 mg Meets Primary Endpoints in Two Global Pivotal …
WebSep 8, 2024 · The PHOTON trial in DME and the PULSAR trial in wet AMD both demonstrated that aflibercept 8 mg 12- and 16-week dosing regimens achieved noninferiority in vision gains compared to the Eylea 8-week dosing regimen. In these trials, the safety of aflibercept 8 mg was consistent with the established safety profile of Eylea. WebSep 8, 2024 · The PHOTON trial in DME and the PULSAR trial in wAMD both demonstrated that aflibercept 8 mg 12- and 16-week dosing regimens achieved non-inferiority in vision gains compared to the EYLEA 8-week dosing regimen. In these trials, the safety of aflibercept 8 mg was consistent with the established safety profile of EYLEA. WebOct 3, 2024 · Aflibercept 8 mg is investigational, and its safety and efficacy have not been evaluated by any regulatory authority. About the Aflibercept 8 mg Trial Program. PHOTON in DME (N=658) and PULSAR in wAMD (N=1,009) are double-masked, active-controlled pivotal trials that are being conducted in multiple centers globally. church\u0027s chicken drive thru menu