EyePoint Pharmaceuticals/$EYPT

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About EyePoint Pharmaceuticals

EyePoint Inc focuses is a clinical-stage biopharmaceutical company committed to developing and commercializing therapeutics to improve the lives of patients with serious retinal diseases, that may reduce the frequency of follow-up care. The company's pipeline program includes i) DURAVYU: a sustained-release product candidate for retinal diseases, with the potential to provide patients with improved visual outcomes with less burden. ii) EYP-2301: early-stage program using Durasert E technology to deliver razuprotafib, a TIE-2 agonist targeting VE-PTP for vascular stability in retinal diseases like wet AMD.
Ticker
$EYPT
Sector
Health
Primary listing
NASDAQ
Employees
-

EYPT Metrics

BasicAdvanced
$366M
-
-$3.76
1.74
-

What the Analysts think about EYPT

Analyst ratings (Buy, Hold, Sell) for EyePoint Pharmaceuticals stock.
Analyst projections of the future price of EyePoint Pharmaceuticals stock.

Bulls say / Bears say

Despite the LUGANO primary-endpoint miss, DURAVYU produced a 42% reduction in treatment burden versus aflibercept, with 54% of patients remaining supplement-free through Week 56 and 79% receiving zero or one supplemental injection. These results could support meaningful differentiation if confirmed in LUCIA and accepted by regulators. (EyePoint)
EyePoint completed enrollment in both pivotal Phase 3 DME trials in only five months, enrolling more than 480 patients. Rapid enrollment and a second large retinal-disease opportunity preserve upside beyond wet AMD, although topline DME data are not expected until Q4 2027. (EyePoint)
The company reported $180 million in cash, cash equivalents, and marketable securities as of June 30, 2026, and expects this balance to fund operations into Q4 2027 beyond key wet-AMD milestones. That runway reduces near-term financing pressure while investors await LUCIA and further clinical data. (SEC filing)
DURAVYU failed to meet the full-dataset primary endpoint in the pivotal LUGANO wet-AMD trial, despite passing an ad hoc analysis that excluded an asymmetric group of patients. This materially raises regulatory and investor risk ahead of the second pivotal readout. (Reuters)
EyePoint remains deeply loss-making while spending escalates: Q2 operating expenses rose to $97.9 million, net loss reached $94.5 million, and cash and marketable securities fell to $180 million from $223 million in the prior quarter. Continued development and manufacturing investment could increase dilution or financing risk if milestones are delayed. (SEC filing)
The investment case remains heavily dependent on DURAVYU, which is still unapproved; after the LUGANO miss, the company needs supportive LUCIA results expected in Q4 2026, while DME efficacy data are not expected until Q4 2027. Any further setback could materially weaken the company’s path to commercialization. (EyePoint)
Data summarised monthly by Lightyear AI. Last updated on 13 Sept 2026.

EYPT Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

EYPT Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

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