Company profile / ANNX

Annexon, Inc.

Clinaptis stanceConstructive
ConvictionMedium
Ticker
ANNX
Exchange
NASDAQ
Coverage
Standard profile
Updated
Aug 28, 2026
Ophthalmology / Geographic Atrophy

Annexon is a clinical-stage biopharmaceutical company built on a single upstream target: C1q, the initiating molecule of the classical complement cascade. Vonaprument and tanruprubart are the same anti-C1q antibody deployed in two tissues — geographic atrophy (intravitreal) and Guillain-Barré syndrome (IV) — making the pipeline two shots on one biological thesis rather than two unrelated programs.

01 / Clinaptis view

The current read

We carry a central fair value of ~$8.5–9 per share against $5.07 spot, ~70–75% upside, on a regressed ARCHER II statistical case that clears the pooled Month-15 gate ~65–70% of the time — materially better odds than the raw 5-vs-19 event count implies. Downside is supported, not open-ended: a GA failure leaves ~$2.5–3.4 per share from tanruprubart (GBS), net cash and pipeline.

  1. The readout decides whether GA creates value; the quality of the win decides how much.
02 / Consensus gap

Where the market may differ

The tape prices ARCHER II close to a low-probability statistical coin flip on a fragile Phase 2 signal. Our bottom-up reconstruction of that signal, regressed for winner's-curse bias, implies materially better statistical odds than the "handful of events" framing suggests.

  1. The larger, underpriced gap is commercial: backing the GA probability-of-success out of the sum-of-the-parts implies only a ~17% market-assigned chance of category-maker economics, against our independent ~50% analytical PoS on the statistical gate — while the actual swing factor in value is whether a functional, patient-perceivable benefit changes physician treatment behavior after approval, a question the tape has largely left unpriced.
Coverage state
Standard profile
What the review turns on
Key variable

Whether a clean, uniform ARCHER II win translates into category-maker commercial behavior (dosing to label, durable persistence) or merely share-taker economics within the existing GA paradigm — the quality of the readout, not just its statistical pass/fail, sets what GA is worth.

Next catalyst

ARCHER II pooled Month-15 primary endpoint assessment, expected Q4 2026; if positive, the two-substudy consistency analysis follows in Q1 2027.

03 / Pipeline

Key programs

2 assets · 2 programs

AssetIndicationStageNext event
Vonaprument (ANX007)
Geographic atrophy
Phase 3
ARCHER II Month-15 assessment expected Q4 2026
Tanruprubart (ANX005)
Guillain-Barré syndrome
Phase 3 complete / Regulatory development
US BLA submission targeted after FDA review of FORWARD Western-bridge data (BLA timeline currently Q4 2026); EMA MAA under review following January 2026 acceptance
04 / Connected research

Published on ANNX

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  1. 01

    Annexon: ARCHER II Is More Than a Replication Bet in GA

    ARCHER II can survive heavy regression of the Phase 2 GA effect — RR ~0.5–0.6 still leaves a viable Phase 3, with replicated visual functional benefit offering genuine differentiation in GA

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