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6-K ·Filed May 14, 2026

GLMD

Galmed Pharmaceuticals Ltd.
BULLISH
Impact 7/10
Horizonweeks Processed5mo ago SEC0001493152-26-022873
Notable filing: 6-K
Actionable Insight ▲ Bullish

The ~500% bioavailability improvement is a significant technical milestone that de-risks the AM formulation and supports future clinical trials. However, with a $4M market cap and no revenue, the stock is highly speculative. Monitor AM-003 results and any partnership or financing announcements. The cross-filing 20-F indicates ongoing dilution risk via shelf registration and equity purchase agreements.

DirectionBullish
Confidencehigh
Horizonweeks
Final — all horizons settled through T+60d
GLMD ▼ -10.00% at T+60d
LONG call ✗ call lost -10.00% · α vs SPY -13.59% · entry $0.6590 → $0.5931
Entry = T+0 close
May 14, 2026
via day close
T+1d
-8.95%
call -8.95% · α -7.73%
$0.6000
settled 6mo ago
T+5d
-11.99%
call -11.99% · α -11.27%
$0.5800
settled 5mo ago
T+20d
-7.13%
call -7.13% · α -6.27%
$0.6120
settled 5mo ago
T+60d
-10.00%
call -10.00% · α -13.59%
$0.5931
settled 3mo ago

Price Chart

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Executive Summary

Galmed announced positive Phase 1 PK results for its oral Aramchol Meglumine (AM) formulation, showing ~500% bioavailability increase at 400mg vs. Aramchol Free Acid 300mg, enabling a once-daily lower dose. This is a meaningful pipeline de-risking event for a $4M market cap clinical-stage biotech, but the company remains pre-revenue with no near-term revenue catalyst.

Key Facts

  • Phase 1 PK study (AM-001) showed 400mg AM granules for oral suspension increases bioavailability by ~500% vs. 300mg AA tablets.
  • 200mg AM showed ~3-fold bioavailability increase vs. 300mg AA.
  • Transition to once-daily 400mg AM dose enables GMP clinical batch production, solidifies IP protection, and may reduce drug CoGs by ~50%.
  • Additional PK study (AM-003) comparing AM 400mg tablets once daily vs. AA 300mg twice daily is ongoing.
  • Company is a clinical-stage biopharma with $4M market cap, pre-revenue, and no approved products.

Financial Impact

No financial figures provided; potential cost of goods reduction of ~50% and improved patient compliance upon commercialization, but no revenue or earnings data.

bioavailabilitydosing frequencycost of goods

Risk Factors

  • Pre-revenue clinical-stage company with no approved products and high cash burn.
  • Ongoing dilution risk from existing shelf registration and standby equity purchase agreement.
  • Clinical and regulatory uncertainty for MASH and GI oncology indications.
  • Low market cap and liquidity risk; stock may be volatile on news flow.

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations
Analyst Consensus
0% bullish (6 analysts)

Investment Themes

Documents Analyzed

This report is based on 5 SEC documents filed with EDGAR.

DocumentAccession Number
6-K Filing (Primary)0001493152-26-022873
Exhibit: ex99-1.htm0001493152-26-022873
Document: 0001493152-26-022873-index-headers.html0001493152-26-022873
Document: 0001493152-26-022873-index.html0001493152-26-022873
Document: 0001493152-26-022873.txt0001493152-26-022873
15 reports for GLMD
Performance horizon
67% Hit rate @ T+5 4 of 6 directional calls Went positive at some point 6 of 7 best @ T+5▲ +31.26%Jun 8, 2026
Filters
Rows
Reports for GLMD — sortable, filterable
TypeNow
Sep 9, 2026
6w ago
6-K
NEUTRAL ★ 4/10
$4.63 $3.63▼ −21.71%▼ −21.37%—
Sep 4, 2026
7w ago
EFFECT
BEARISH ★ 5/10
$3.88 $4.63▼ −19.33%▼ −20.54%—
Sep 3, 2026
7w ago
6-K
NEUTRAL ★ 2/10
$3.88 $4.63▲ +19.33%▲ +20.54%—
Sep 2, 2026
7w ago
6-K
NEUTRAL ★ 2/10
$3.92 $4.63▲ +18.11%▲ +19.26%—
Aug 19, 2026
9w ago
6-K
NEUTRAL ★ 4/10
$4.77 $4.33▼ −9.22%▼ −8.84%—
Aug 17, 2026
10w ago
6-K
BULLISH ★ 6/10
$0.5134awaiting T+5——
Jul 28, 2026
13w ago
6-K
NEUTRAL ★ 4/10
$0.5340 $0.5754▲ +7.75%▲ +3.64%—
Jul 16, 2026
14w ago
6-K
BULLISH ★ 6/10
$0.5501 $0.5530▲ +0.53%▲ +2.20%—
Jun 22, 2026
18w ago
6-K
BULLISH ★ 7/10
$0.5641 $0.5709▲ +1.21%▲ +1.66%—
Jun 8, 2026
20w ago
6-K
BULLISH ★ 7/10
$0.4693 $0.6160▲ +31.26%▲ +29.15%—
Showing 10 of 15

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Report published May 14, 2026