Compare

4D Molecular Therapeutics/$FDMT

1D1W1M3M6MYTD1Y5YMAX

About 4D Molecular Therapeutics

4D Molecular Therapeutics Inc is biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. Companies focus is on advancing 4D-150 for wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME) through late-stage studies. It has built a portfolio of gene therapy product candidates focused on three therapeutic areas: Ophthalmology (intravitreal vector) includes 4D-150, 4D-710 and 4D-175; Cardiology (intravenous vector) includes 4D-710, 4D-725, and Pulmonology (aerosol vector).
Ticker
$FDMT
Sector
Health
Primary listing
NASDAQ
Employees
196

FDMT Metrics

BasicAdvanced
$718M
-
-$2.77
2.73
-

What the Analysts think about FDMT

Analyst ratings (Buy, Hold, Sell) for 4D Molecular Therapeutics stock.
Analyst projections of the future price of 4D Molecular Therapeutics stock.

Bulls say / Bears say

Two-year PRISM results showed stable vision and retinal measurements, with 78% fewer supplemental injections than an every-eight-week aflibercept schedule would imply. If larger controlled trials confirm this durability, 4D-150 could materially reduce treatment visits for wet AMD patients. (touchOPHTHALMOLOGY)
Both wet AMD Phase 3 trials have completed enrolment, and 4FRONT-2 finished about four months ahead of plan and enrolled more than expected. The first major efficacy readout is due in Q2 2027, giving investors a defined near-term clinical catalyst. (4D Molecular Therapeutics)
4D-150 has entered Phase 3 testing for DME as well as wet AMD, widening its potential use across two major retinal diseases. The company says the FDA and EMA have agreed that one DME Phase 3 trial, alongside existing clinical data, could support marketing applications. (4D Molecular Therapeutics)
PRISM was a small Phase 2b study, and its injection-burden reductions were compared with a projected dosing schedule rather than a concurrent control group. The Phase 3 trials must show that the benefit holds up in a larger, controlled comparison. (touchOPHTHALMOLOGY)
The DME evidence remains preliminary: the reported two-year efficacy at the Phase 3 dose came from only nine patients, without a control arm. The Phase 3 trial also requires patients to respond to aflibercept, so its results may not apply to those who respond poorly. (Ophthalmology Times)
FDMT remains pre-commercial and its second-quarter net loss widened to $72.9 million as research and development spending rose to $68.3 million. The company reported $430.6 million in cash and expects it to last into the second half of 2028, but ongoing trial costs leave limited room for setbacks or slower progress. (4D Molecular Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 23 Oct 2026.

FDMT Financial Performance

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

FDMT Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.