clinical-trial is the sole category represented across all 1 tracked stories. Aflibercept is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. The 8 average consequence score is above the beat benchmark of 5.9 in the same window.
Figures are computed live from our source-verified story record
— see our methodology for how impact and
sentiment are derived.
What the coverage shows about Efdamrofusp Alfa (IBI302)
clinical-trial is the sole category represented across all 1 tracked stories. Aflibercept is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. The 8 average consequence score is above the beat benchmark of 5.9 in the same window. Source depth averages 2 original sources per story, versus 2.5 across the same-window beat baseline. Efdamrofusp Alfa (IBI302) appears in 1 tracked Biotech story from March 24, 2026.
Stories tracked
1
Sources per story
2
Computed from the 1 stories linked to this entity, with beat comparisons drawn from all 20 Biotech stories published in the same date window. Shares are omitted below five stories and comparisons below a twenty-story baseline.
Coverage cohort
Appears alongside
Other entities that clear the same relevance threshold in stories also covering Efdamrofusp Alfa (IBI302). Shared-story counts are live from our verified record — not editorial picks.
Innovent Biologics' IBI302 (efdamrofusp alfa) successfully met its primary endpoint in the Phase 3 STAR registration trial for neovascular age-related macular degeneration. As the first domestically developed extended-interval treatment in China, it represents a significant shift toward reducing the injection burden for millions of patients.