Equillium

EQ · NASDAQ

$1.38+$0.14 (+11.29%)TodayMarket closed ·
Prev close $1.24

EQ analyst rating

BuyConsensus of 6 analysts over the last 12 months. 100% rate it a buy.
  • Strong buy1
  • Buy5
  • Hold0
  • Underperform0
  • Sell0

12-month price target · 12 analysts

Average $9.29 (+573.4% upside)

Low
$5.05
Now
$1.38
High
$21.00

Upgrades and downgrades

The latest rating actions, newest first

EQ analyst upgrades, downgrades and rating actions
FirmDateActionRating
Leerink PartnersOct 12, 2026InitiatesOutperform
Roth CapitalSep 4, 2026MaintainsBuy
Piper SandlerJul 13, 2026InitiatesOverweight
Roth CapitalJun 2, 2026MaintainsBuy
Leerink PartnersMay 28, 2026UpgradeMarket Perform → Outperform
Roth CapitalMay 28, 2026MaintainsBuy
Roth CapitalApr 17, 2026MaintainsBuy
B. Riley SecuritiesApr 16, 2026InitiatesBuy
Raymond JamesApr 14, 2026InitiatesStrong Buy
Roth CapitalMar 13, 2026InitiatesBuy

The case for and against

Updated Oct 21, 2026

Bull case

Equillium is attractive because its lead asset EQ504 targets a clinically validated AhR pathway in ulcerative colitis with strong mechanistic support from 4 studies, 12 ex vivo assays, 1 intestinal organoid assay, and 1 murine model, all pointing to barrier protection and anti-inflammatory effects. The thesis is further strengthened by differentiated design features—colon-targeted delivery, high potency, and selectivity—which aim to improve safety versus more systemically absorbed or less selective AhR agents, while still addressing a large ~180K US patient population and multiple treatment settings. EQ302 adds optionality as a wholly owned oral IL-15/21 inhibitor, and Teva’s positive Phase 2a celiac data plus argenx’s $2.2 billion IL-15 transaction support the mechanism, but EQ504 remains the primary value driver with Phase 1 initiation on-track for mid-2026 and biomarker data in 2Q27E.

Bear case

Equillium is a clinical-stage biotechnology company whose valuation is heavily dependent on EQ504, yet the program has not entered human testing and Phase 1 biomarker data may fail to show adequate target engagement or reveal safety concerns, including a potential PAH signal. The investment case is further weakened by the uncertainty of translating surrogate biomarkers such as CYP1A1, IL-10, and IL-22 into meaningful UC outcomes, especially when regulators will demand remission and mucosal healing in later studies. Financially, cash of $61.3M as of March 31, 2026 and an additional $20M contingent financing may not be enough to avoid dilutive capital raises if Phase 1 is negative or ambiguous, while competition and a weaker M&A backdrop could further pressure equity value.

Information on this page is provided for informational purposes only and is not a recommendation to buy, sell or hold any security. Investing involves risk, including possible loss of principal. Market data is delayed at least 15 minutes and is provided without warranty. Analyst ratings, price targets and company data come from third-party sources. Past performance does not guarantee future results.