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Definium Therapeutics/$DFTX

1D1W1M3M6MYTD1Y5YMAX

About Definium Therapeutics

Definium Therapeutics Inc is developing inventive, next-generation therapeutics intended to solve the underlying causes of psychiatric and neurological disorders and offer patients long-term remission rather than transient symptom reduction. Its late-stage pipeline includes four Phase 3 trials-two each for GAD and MDD-anchored by its candidate, DT120 ODT, which has received FDA Breakthrough Therapy Designation for GAD. In parallel, the Company is advancing its commercial and operational readiness to support a care model and prepare for the potential launch of DT120 ODT, if approved and marketed. The company operates in one reportable segment relating to the research and development of the company's neurological drug development platform.
Ticker
$DFTX
Sector
Health
Primary listing
NASDAQ
Employees
-

DFTX Metrics

BasicAdvanced
$5.1B
-
-$3.48
2.24
-

What the Analysts think about DFTX

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

Bulls say / Bears say

DT120 has cleared two Phase 3 trials in GAD: it beat placebo by 5.4 points in Voyage and 5.1 points in Panorama on the HAM-A at week 12, with both results highly statistically significant. Replication across separate studies makes the anxiety result more convincing. (Definium Therapeutics, Definium Therapeutics)
In MDD, Emerge showed an 8.1-point placebo-adjusted improvement on the MADRS at week six, with benefit still evident at week 12. The FDA’s Breakthrough Therapy designation for MDD adds regulatory momentum in a second major indication. (Definium Therapeutics, Definium Therapeutics)
Definium reported about $1.1 billion in cash, cash equivalents and investments at the end of June and expects it to fund operations into 2030. That gives the company substantial room to advance its late-stage trials and prepare for a potential launch without an immediate need for more capital. (Definium Therapeutics)
The psychedelic effects may compromise blinding: in Panorama, 95% of high-dose participants and 91% of low-dose participants correctly guessed their assignment. That could make symptom ratings more vulnerable to expectancy effects, even if other trial features support a genuine treatment effect. (Mugglehead, Definium Therapeutics)
Treatment may be difficult to scale in ordinary clinics: in Panorama, treatment-emergent adverse events affected 94.8% of the 100 µg group versus 62.9% on placebo, including illusions in 68% of treated participants. Participants took an average of 6.2 hours to meet end-of-session clearance criteria, which may constrain clinic throughput and patient acceptance. (Definium Therapeutics, earningscalls.dev)
The approval route and timing remain uncertain: Definium says it will discuss the GAD and MDD regulatory strategy with the FDA at a pre-NDA meeting in the fourth quarter, and it is targeting an NDA filing in the first half of 2027. The agency’s feedback could affect the filing plan and how quickly DT120 reaches the market. (Definium Therapeutics, Definium Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 9 Oct 2026.

DFTX Financial Performance

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

DFTX 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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