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Annexon Inc (ANNX)

Geographic Atrophy · registered primary completion 2026-10-31 · NCT06510816

Published 2026-09-02Market cap $942M7 sourced statements
A Study Investigating the Efficacy and Safety of Intravitreal (IVT) Injections of Vonaprument (Formerly ANX007) in Participants With Dry Age-Related Macular Degeneration (AMD) With Geographic Atrophy (GA) · PHASE3 · n=659 · active not recruiting

What this sheet is scored on

call

Cash of $209M against operating outflow of $53M per quarter gives roughly 3.9 quarters of runway, clearing the readout 0.7 quarters out but leaving under a year. On these figures the company raises capital within four quarters.

Share count and dilution

fact

38,563,565 shares outstanding against 64,156,074 if every outstanding option, warrant and convertible were exercised. In that case 39.9% of a gain in enterprise value would accrue to those holders rather than to current shareholders.

Market

fact

2 approved products already carry Geographic Atrophy on label, including IZERVAY, Syfovre. Approval would enter an occupied market.

Trial registry

fact

Registered design for NCT06510816: randomized, quadruple-masked, 659 participants (actual). Primary outcome: Proportion of Participants Experiencing a Best Corrected Visual Acuity (BCVA) ≥15-letter Loss from Baseline Through Month 15 as Assessed by .

Regulatory

fact

Designations disclosed: Breakthrough Therapy, Fast Track, Orphan Drug, PRIME (EU). These accelerate review and, for Orphan, confer exclusivity if approved; none is evidence of efficacy.

Pipeline

fact

2 distinct molecules in 2 active company-sponsored trials; Vonaprument accounts for 1 of them at Phase 3.

Ownership and proceedings

fact

Directors and executive officers as a group hold 10.31%.

This sheet is dated and will not be edited. When the registered primary completion passes, its outcome is recorded on the scoreboard and a new dated sheet is published if the filings change materially.