NCT05473715 is XPAND, Bayer's phase IV aflibercept-interval study in neovascular age-related macular degeneration, protocol BAY86-5321/21912. It compared customized proactive intervals with standard treat-and-extend after initial treatment, with a planned noninferiority comparison of change in best-corrected visual acuity at week 36. 12
The posted EU results, not just the registration, show four people screened and three randomized/treated: two in the customized group and one in the standard group. None completed the study, and zero participants were analyzed for the primary visual-acuity endpoint. The trial started on April 25, 2023 and ended early on July 11, 2023; the results were posted in July 2024. 2
Accordingly, XPAND produced no usable primary comparison establishing that customized intervals preserved vision as well as the standard approach. That is a specific limitation of this prematurely ended three-person study—not evidence that aflibercept generally fails in wet AMD. Bayer's official page labels the program terminated/withdrawn. 23