PRESS-RELEASE ·Filed Jun 16, 2026

IVVD

Invivyd
NEUTRAL
Impact 5/10
Horizonweeks Processed3mo ago WireGlobeNewswire
Press release: fda
Actionable Insight • Neutral

Monitor Q3 2026 for LIBERTY and DECLARATION topline data; positive safety/tolerability comparison could support BLA filing and differentiate VYD2311 from vaccines. Stock may trade on binary data readout risk.

DirectionNeutral
Confidencehigh
Horizonweeks
Final — all horizons settled through T+60d
IVVD ▼ -13.00% at T+60d
NEUTRAL call ✗ call lost -13.00% · α vs SPY -14.00% · entry $0.8918 → $0.7759
Entry anchored
Jun 16, 06:04 AM ET
via exchange tick
T+1d
+4.42%
call +4.42% · α +5.67%
$0.9312
settled 4mo ago
T+5d
+4.80%
call +4.80% · α +7.03%
$0.9346
settled 3mo ago
T+20d
-10.20%
call -10.20% · α -10.40%
$0.8008
settled 3mo ago
T+60d
-13.00%
call -13.00% · α -14.00%
$0.7759
settled 21d ago

Price Chart

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Executive Summary

Invivyd announced completion of enrollment in its Phase 3 LIBERTY trial comparing VYD2311 (monoclonal antibody) against an mRNA COVID vaccine, with topline data expected in Q3 2026. The trial is part of the broader REVOLUTION program aiming to position VYD2311 as an alternative to vaccines. This is a clinical milestone with no efficacy or safety data yet, so the immediate stock impact is limited.

Key Facts

  • Phase 3 LIBERTY trial enrollment complete; ~210 participants randomized, double-blind.
  • Primary endpoint: safety/tolerability of VYD2311 vs mRNA COVID vaccine through Day 6.
  • Topline data expected in Q3 2026, potentially alongside DECLARATION pivotal trial data.
  • VYD2311 is engineered from same backbone as pemivibart (EUA for immunocompromised PrEP) and adintrevimab.
  • DECLARATION trial (n~2,400) is placebo-controlled evaluating VYD2311 efficacy in preventing symptomatic COVID.
  • No efficacy or safety data released yet; forward-looking statements only.

Financial Impact

No financial data disclosed; clinical milestone with no revenue or cost figures.

Risk Factors

  • LIBERTY or DECLARATION may fail to show superiority or non-inferiority vs vaccine/placebo.
  • Regulatory pathway uncertain; FDA may require additional trials for BLA.
  • Viral evolution could reduce VYD2311 neutralizing activity.
  • Low historical win rate (29% T+20) on IVVD reports suggests market skepticism.

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
89% bullish (9 analysts)

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3312427
15 reports for IVVD
Performance horizon
75% Hit rate 3 of 4 directional calls best @ T+20▲ +35.85%Jul 6, 2026
Filters
Rows
Reports for IVVD — sortable, filterable
TypeNow
Sep 1, 2026
4w ago
8-K
NEUTRAL ★ 6/10
$0.8800 $0.8441▼ −4.08%▼ −5.26%$0.8221 (−6.58%)
Aug 17, 2026
6w ago
144
NEUTRAL ★ 2/10
$0.8680 $0.8198▼ −5.55%▼ −4.56%$0.8221 (−5.29%)
Jul 6, 2026
12w ago
8-K
BEARISH ★ 6/10
$0.8340 $0.5350▲ +35.85%▲ +35.29%$0.8221 (+1.43%)
Jun 16, 2026
15w ago
Press Release
NEUTRAL ★ 5/10
$0.8918 $0.8008▼ −10.20%▼ −10.40%$0.8221 (−7.82%)
Jun 11, 2026
16w ago
Institutional Cluster
MIXED ★ 4/10
$0.8125 $0.8037▼ −1.08%▼ −2.97%$0.8221 (+1.18%)
Jun 9, 2026
16w ago
Press Release
NEUTRAL ★ 4/10
$0.9900 $0.9418▼ −4.87%▼ −6.32%$0.8221 (−16.96%)
Jun 1, 2026
17w ago
Press Release
BULLISH ★ 5/10
$1.22 $0.8724▼ −28.49%▼ −27.19%$0.8221 (−32.61%)
May 14, 2026
20w ago
8-K
MIXED ★ 6/10
$1.16 $0.7700▼ −33.62%▼ −32.76%$0.8221 (−29.13%)
May 14, 2026
20w ago
Press Release
NEUTRAL ★ 5/10
$1.16 $0.7700▼ −33.62%▼ −32.76%$0.8221 (−29.13%)
Apr 9, 2026
25w ago
8-K
NEUTRAL ★ 5/10
$1.78 $1.46▼ −17.98%▼ −25.55%$0.8221 (−53.81%)
Showing 10 of 15

US Market Status

Market Closed — Opens Mon (64h 37m)

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Report published Jun 16, 2026