PRESS-RELEASE ·Filed Mar 20, 2026

PHVS

Pharvaris N.V.
BULLISH
Impact 8/10
Horizonmonths Processed6mo ago WireGlobeNewswire
Press release: m_and_a
Actionable Insight ▲ Bullish

Investors should monitor the upcoming Phase 3 CHAPTER-3 topline data in Q3 2026 as the next major catalyst; successful results could drive significant upside given the lack of oral options in HAE and strong Phase 2/3 signals to date.

DirectionBullish
Confidencehigh
Horizonmonths
Final — all horizons settled through T+60d
PHVS ▲ +21.31% at T+60d
LONG call ✓ call won +21.31% · α vs SPY +6.89% · entry $26.00 → $31.54
Entry anchored
Mar 19, 03:59 PM ET
via exchange tick
T+1d
-1.15%
call -1.15% · α -2.26%
$25.70
settled 6mo ago
T+5d
+5.19%
call +5.19% · α +7.34%
$27.35
settled 6mo ago
T+20d
+11.42%
call +11.42% · α +2.10%
$28.97
settled 6mo ago
T+60d
+21.31%
call +21.31% · α +6.89%
$31.54
settled 4mo ago

Price Chart

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Executive Summary

Pharvaris announced the publication of positive Phase 2 data from its CHAPTER-1 and RAPIDe-1 trials in The Lancet Haematology, showing deucrictibant's efficacy and safety as both a prophylactic and on-demand oral treatment for hereditary angioedema (HAE). The results support its potential as a first-in-class oral B2 receptor antagonist for end-to-end HAE management, with Phase 3 topline data expected in Q3 2026.

Key Facts

  • Phase 2 CHAPTER-1 trial showed statistically significant reduction in HAE attack frequency with deucrictibant for prophylaxis.
  • Phase 2 RAPIDe-1 trial demonstrated statistically significant reduction in attack severity and faster symptom relief for on-demand treatment.
  • Deucrictibant is an oral bradykinin B2 receptor antagonist, positioning it as a potential first-in-class oral therapy for both prevention and acute treatment of HAE.
  • Topline data from pivotal Phase 3 RAPIDe-3 trial already confirmed faster symptom relief and single-capsule resolution in most attacks.
  • Marketing authorization applications for deucrictibant immediate-release capsule are being prepared, with NDA submission expected in first half of 2026.
  • Deucrictibant has orphan drug designation in the U.S., EU, and Switzerland.

Financial Impact

Potential blockbuster revenue if approved, given deucrictibant's dual indication and oral convenience in a chronic, high-cost rare disease market.

revenuevaluationmarketCap

Risk Factors

  • Phase 3 data may not replicate Phase 2 results, particularly in larger, more diverse populations.
  • Regulatory delays or rejections despite strong data, especially given the novelty of the oral B2 antagonist mechanism.
  • Competition from existing injectable therapies and emerging oral kallikrein inhibitors.

Market Snapshot

Exchange
Nasdaq

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3259646
37 reports for PHVS
Performance horizon
89% Hit rate 8 of 9 directional calls best @ T+60▲ +19.66%Jun 15, 2026
Filters
Rows
Reports for PHVS — sortable, filterable
TypeNow
Sep 15, 2026
17d ago
Insider Cluster
BEARISH ★ 5/10
$38.06 $36.37▲ +4.44%▲ +5.26%$31.07 (+18.38%)
Sep 14, 2026
17d ago
144
NEUTRAL ★ 2/10
$38.06 $35.20▼ −7.51%▼ −9.63%$31.07 (−18.38%)
Sep 14, 2026
18d ago
Insider Cluster
NEUTRAL ★ 3/10
$38.86 $36.02▼ −7.31%▼ −7.41%$31.07 (−20.06%)
Sep 11, 2026
21d ago
Insider Cluster
NEUTRAL ★ 3/10
$38.02 $36.37▼ −4.34%▼ −4.12%$31.07 (−18.29%)
Sep 8, 2026
24d ago
6-K
BULLISH ★ 8/10
$37.84 $38.86▲ +2.70%▲ +3.36%$31.07 (−17.90%)
Aug 12, 2026
7w ago
6-K
NEUTRAL ★ 6/10
$36.46 $36.27▼ −0.52%▼ −0.08%$31.07 (−14.80%)
Aug 12, 2026
7w ago
Press Release
BULLISH ★ 7/10
$36.46 $36.27▼ −0.52%▼ −0.08%$31.07 (−14.80%)
Aug 6, 2026
8w ago
Press Release
NEUTRAL ★ 4/10
$34.45 $34.04▼ −1.19%▼ −2.40%$31.07 (−9.83%)
Jul 6, 2026
12w ago
Press Release
BULLISH ★ 6/10
$33.22 $35.07▲ +5.57%▲ +5.08%$31.07 (−6.49%)
Jul 1, 2026
13w ago
Insider Cluster
NEUTRAL ★ 3/10
$33.86 $35.96▲ +6.20%▲ +5.27%$31.07 (−8.25%)
Showing 10 of 37

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Report published Mar 20, 2026