ANNX Annexon Biosciences

NEUTRAL Impact: 4/10 PRESS-RELEASE
Horizon months Filed Mar 30, 2026 Processed 2mo ago Wire GlobeNewswire
Press release: earnings
Latest settled — T+20d
ANNX ▲ +8.48% at T+20d
NEUTRAL call ✓ call won +8.48% · α vs SPY -0.94% · entry $5.54 → $6.01
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Last close $5.12 (close Jun 8) · -7.58% from $5.54 entry
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Executive Summary

Annexon Biosciences reported fourth quarter and full year 2025 financial results, highlighting a strong cash position of $238.3 million and progress in its late-stage clinical programs for vonaprument (GA) and tanruprubart (GBS). The company expects topline Phase 3 data for vonaprument in Q4 2026 and plans a U.S. BLA submission for tanruprubart in 2026 based on FORWARD study data.

Key Financial Metrics

EPS
$-1.34

Actionable Insight

Investors should monitor upcoming topline data from the Phase 3 ARCHER II trial in Q4 2026, which could be a major value driver. The MAA filing in Europe for tanruprubart represents near-term regulatory risk/reward, while the planned 2026 U.S. BLA submission depends on FORWARD study outcomes.

Key Facts

  • Cash, cash equivalents, and short-term investments totaled $238.3 million as of December 31, 2025, providing runway into the second half of 2027.
  • R&D expenses increased to $184.7 million in 2025 from $119.4 million in 2024, driven by advancement of the Phase 3 ARCHER II trial and regulatory filings for tanruprubart.
  • Net loss attributable to common stockholders was $208.5 million in 2025, up from $138.2 million in 2024.
  • Topline Phase 3 ARCHER II data for vonaprument in geographic atrophy (GA) expected in Q4 2026.
  • Marketing Authorization Application (MAA) filed in Europe for tanruprubart in Guillain-Barré Syndrome (GBS); U.S. BLA submission anticipated in 2026.

Financial Impact

Increased R&D spending by $65.3 million YoY to $184.7 million; net loss widened to $208.5 million in 2025 from $138.2 million in 2024.

r_d_expensesnet_losscash_runway

Risk Factors

  • Clinical trial results may not meet endpoints, particularly the primary endpoint of visual acuity preservation in the ARCHER II trial.
  • Regulatory delays or rejections for tanruprubart in Europe or the U.S. could negatively impact valuation.
  • Cash runway extends into H2 2027, but additional financing may be required depending on development timelines and commercialization plans.

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3264990
7 reports for ANNX
Performance horizon
80% Hit rate 4 of 5 directional calls best @ T+20▲ +32.68%May 16, 2026
Filters
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Reports for ANNX — sortable, filterable
Type Now
May 16, 2026
24d ago
ANALYST-UPGRADE
BULLISH ★ 3/10
$5.11 $5.02▼ −1.76%▼ −0.93%$5.12 (+0.20%)
May 12, 2026
28d ago
ANALYST-UPGRADE
BEARISH ★ 4/10
$5.44 $4.96▲ +8.82%▲ +8.90%$5.12 (+5.88%)
May 7, 2026
4w ago
Press Release
BULLISH ★ 6/10
$5.69 $5.37▼ −5.62%▼ −7.09%$5.12 (−10.02%)
Apr 16, 2026
7w ago
ANALYST-UPGRADE
BULLISH ★ 8/10
$6.33 $6.06▼ −4.27%▼ −5.25%$5.12 (−19.12%)
Apr 16, 2026
7w ago
ANALYST-UPGRADE
BULLISH ★ 7/10
$6.33 $6.06▼ −4.27%▼ −5.25%$5.12 (−19.12%)
Mar 30, 2026
10w ago
Press Release
NEUTRAL ★ 4/10
$5.54 $6.05▲ +9.21%▲ +5.26%$5.12 (−7.58%)
Mar 2, 2026
14w ago
Insider Cluster
NEUTRAL ★ 3/10
$5.52 $5.59▲ +1.27%▲ +2.48%$5.12 (−7.25%)
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