PCVX Vaxcyte, Inc.

NEUTRAL Impact: 4/10 PRESS-RELEASE
Horizon months Filed Mar 23, 2026 Processed 2mo ago Wire GlobeNewswire
Press release: fda
Latest settled — T+20d
PCVX ▲ +8.24% at T+20d
NEUTRAL call ✓ call won +8.24% · α vs SPY +0.82% · entry $55.94 → $60.55
Next anchor: T+60d in 7d
Last close $46.33 (close Jun 8) · -17.18% from $55.94 entry
Entry anchored
Mar 23, 08:15 AM ET
via Databento tick
T+1d
-2.27%
call -2.27% · α -1.91%
$54.67
settled 3mo ago
T+5d
-1.75%
call -1.75% · α +1.81%
$54.96
settled 2mo ago
T+20d
+8.24%
call +8.24% · α +0.82%
$60.55
settled 7w ago
T+60d
call — · α —
in 7d

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Executive Summary

Vaxcyte announced completion of enrollment in the OPUS-1 and OPUS-2 Phase 3 trials for its investigational 31-valent pneumococcal vaccine VAX-31. Topline data from OPUS-1 is expected in Q4 2026, with OPUS-2 and OPUS-3 results anticipated in H1 2027. The trials are designed to support a future Biologics License Application (BLA) submission to the FDA, building on prior Breakthrough Therapy designation for VAX-31 in preventing invasive pneumococcal disease and pneumonia.

Actionable Insight

Monitor for topline data from OPUS-1 in Q4 2026, which could be a major catalyst. Until then, no new efficacy or safety data to assess; current market cap reflects future potential, not near-term fundamentals.

Key Facts

  • Enrollment completed in OPUS-1 (n≈4,000) and OPUS-2 (n≈1,300) Phase 3 trials for VAX-31.
  • Topline data from OPUS-1 expected in Q4 2026; OPUS-2 and OPUS-3 results expected in H1 2027.
  • OPUS-1 is a pivotal noninferiority trial comparing VAX-31 to Capvaxive® (PCV21) and Prevnar 20® (PCV20) in adults ≥50 years.
  • VAX-31 has FDA Breakthrough Therapy Designation for prevention of both IPD and pneumococcal pneumonia in adults.
  • No clinical results or financial figures reported — this is a program update on trial enrollment.

Financial Impact

No immediate financial impact; potential long-term value if VAX-31 demonstrates superiority and gains approval.

revenuevaluationR&D spend

Risk Factors

  • Clinical trial results may not meet endpoints despite favorable Phase 1/2 data.
  • Regulatory delays or failure to obtain BLA approval even with positive data.
  • High market expectations already priced in given $7.9B market cap despite being pre-revenue.

Market Snapshot

Exchange
Nasdaq

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3260381
7 reports for PCVX
Performance horizon

Track record builds as more directional reports settle.

Filters
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Reports for PCVX — sortable, filterable
Type Now
Jun 2, 2026
7d ago
Press Release
NEUTRAL ★ 4/10
$46.93 $48.76▲ +3.90%▲ +3.49%$46.33 (−1.28%)
May 6, 2026
4w ago
8-K
BEARISH ★ 7/10
$51.48 $53.01▼ −2.97%▼ −2.14%$46.33 (+10.00%)
Apr 23, 2026
6w ago
DEFA14A
NEUTRAL ★ 3/10
$59.49 $59.72▲ +0.39%▲ +0.22%$46.33 (−22.12%)
Apr 1, 2026
10w ago
Insider Cluster
NEUTRAL ★ 3/10
$58.50 $58.38▼ −0.21%▼ −0.28%$46.33 (−20.80%)
Mar 23, 2026
11w ago
Press Release
NEUTRAL ★ 4/10
$55.94 $54.67▼ −2.27%▼ −1.91%$46.33 (−17.18%)
Feb 24, 2026
15w ago
8-K
NEUTRAL ★ 4/10
$63.04 $60.00▼ −4.82%▼ −4.28%$46.33 (−26.51%)
Feb 24, 2026
15w ago
8-K
NEUTRAL ★ 5/10
$63.04 $60.00▼ −4.82%▼ −4.28%$46.33 (−26.51%)
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