GLAXF GSK plc

BULLISH Impact: 7/10 6-K
Horizon months Filed Apr 28, 2026 Processed 1mo ago SEC 0001654954-26-003977
Notable filing: 6-K
Latest settled — T+20d ⚠ clustered
GLAXF ▼ -6.37% at T+20d
LONG call ✗ call lost -6.37% · α vs SPY -11.83% · entry $27.31 → $25.57
Next anchor: T+60d in 6w
Last close $24.66 (close Jun 8) · -9.70% from $27.31 entry
Entry anchored
Apr 28, 2026
via day open
T+1d
-0.84%
call -0.84% · α -0.83%
$27.08
settled 6w ago
T+5d
-8.42%
call -8.42% · α -10.11%
$25.01
settled 5w ago
T+20d
-6.37%
call -6.37% · α -11.83%
$25.57
settled 14d ago
T+60d
call — · α —
in 6w

Price Chart

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Executive Summary

GSK announced FDA acceptance of its New Drug Application for bepirovirsen (chronic hepatitis B) with Priority Review and Breakthrough Therapy Designation, with a PDUFA date of October 26, 2026. The filing is supported by Phase III data showing statistically significant functional cure rates versus standard of care, addressing a large unmet need in a >250 million patient population. This is a positive regulatory milestone for a high-potential pipeline asset, though no financial terms or revenue estimates were disclosed.

Actionable Insight

The PDUFA date of October 26, 2026 provides a clear catalyst timeline. Traders should monitor for any FDA advisory committee meeting announcements and potential competitor developments (e.g., Arrowhead, Vir Biotechnology). Approval would unlock a significant new revenue stream for GSK's vaccines/specialty portfolio.

Key Facts

  • FDA accepted NDA for bepirovirsen with Priority Review and Breakthrough Therapy Designation
  • PDUFA goal date set for October 26, 2026
  • Phase III B-Well 1 and B-Well 2 trials showed statistically significant and clinically meaningful functional cure rates
  • Chronic hepatitis B affects >250 million people globally; current functional cure rates ~1%
  • Bepirovirsen licensed from Ionis Pharmaceuticals; not yet approved anywhere
  • Breakthrough Therapy Designation added to prior Fast Track Designation (Feb 2024)

Financial Impact

No financial figures disclosed; potential multi-billion-dollar peak sales if approved given large addressable patient population and high unmet need

revenuepipeline value

Risk Factors

  • Regulatory risk: FDA could issue Complete Response Letter or require additional trials
  • Commercial risk: pricing/reimbursement uncertainty and competition from other HBV curative approaches
  • Clinical risk: long-term durability data still pending; safety profile in broader populations unknown

Market Snapshot

Exchange
OTC
Sector
Pharmaceutical Preparations
Analyst Consensus
41% bullish (32 analysts)

Documents Analyzed

This report is based on 4 SEC documents filed with EDGAR.

DocumentAccession Number
6-K Filing (Primary)0001654954-26-003977
Document: 0001654954-26-003977-index-headers.html0001654954-26-003977
Document: 0001654954-26-003977-index.html0001654954-26-003977
Document: 0001654954-26-003977.txt0001654954-26-003977
50 reports for GLAXF
Performance horizon
45% Hit rate 5 of 11 directional calls best @ T+5▲ +7.60%Apr 1, 2026
Filters
Rows
Reports for GLAXF — sortable, filterable
Type Now
Jun 9, 2026
today
6-K
NEUTRAL ★ 1/10
awaiting T+5
Jun 9, 2026
today
6-K
BULLISH ★ 7/10
awaiting T+5
Jun 1, 2026
8d ago
6-K
NEUTRAL ★ 1/10
$24.25 $24.66▲ +1.69%▲ +4.44%$24.66 (+1.69%)
Jun 1, 2026
8d ago
6-K
NEUTRAL ★ 2/10
$24.25 $24.66▲ +1.69%▲ +4.44%$24.66 (+1.69%)
May 28, 2026
12d ago
6-K
BULLISH ★ 7/10
$24.58 $24.66▲ +0.33%▲ +0.01%$24.66 (+0.33%)
May 27, 2026
13d ago
6-K
NEUTRAL ★ 1/10
$25.57 $23.94▼ −6.37%▼ −7.58%$24.66 (−3.56%)
May 26, 2026
14d ago
6-K
NEUTRAL ★ 1/10
$25.50 $24.25▼ −4.90%▼ −5.99%$24.66 (−3.29%)
May 26, 2026
14d ago
6-K
NEUTRAL ★ 2/10
$25.50 $24.25▼ −4.90%▼ −5.99%$24.66 (−3.29%)
May 22, 2026
18d ago
6-K
NEUTRAL ★ 2/10
$26.00 $24.25▼ −6.73%▼ −8.39%$24.66 (−5.15%)
May 20, 2026
20d ago
6-K
NEUTRAL ★ 2/10
$25.70 $25.57▼ −0.51%▼ −1.74%$24.66 (−4.05%)
Showing 10 of 50

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