Aquestive Therapeutics/$AQST

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About Aquestive Therapeutics

Aquestive Therapeutics Inc is a specialty pharmaceutical company engaged in developing and commercializing differentiated products to meet medical needs. Its later-stage product pipeline focuses on the treatment of diseases of the Central Nervous System (CNS), and an earlier-stage pipeline for the treatment of severe allergic reactions, including anaphylaxis. Its commercial product portfolio includes Suboxone, Emylif, Ondif, and Sympazan. The product pipeline includes Libervant Buccal Film, AQST-108. The majority of its revenue comes from the United States.
Ticker
$AQST
Sector
Health
Primary listing
NASDAQ
Employees
147

AQST Metrics

BasicAdvanced
$612M
-
-$0.65
1.43
-

What the Analysts think about AQST

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

Bulls say / Bears say

Aquestive completed the new human-factors and pharmacokinetic studies for Anaphylm, with materially better packaging results and no administration errors in the self-administration arm. The company remains on track to resubmit the NDA in the third quarter, while the earlier FDA rejection did not question manufacturing controls or clinical comparability with auto-injectors. (Aquestive Therapeutics, Last10K)
If approved, Anaphylm could be the first non-invasive, orally delivered epinephrine product, giving Aquestive a differentiated route into a sizeable rescue market. The company also expects up to $75 million from RTW and $20 million from Oaktree for the launch, subject to approval and other conditions. (BioSpace, StockAnalysis)
The existing business is improving while the pipeline is being prepared: second-quarter revenue rose 38% year on year to $13.8 million, and the six-month adjusted EBITDA loss narrowed sharply. Aquestive ended June with $98.5 million of cash and has refinanced its debt, extending financial flexibility towards a potential launch. (StockAnalysis, StockTitan)
Anaphylm remains a binary regulatory bet after the FDA issued a Complete Response Letter over pouch-opening and administration problems. A resubmission is only planned, and the company cannot guarantee the accelerated review it intends to request. (Last10K, MarketBeat)
The company is still loss-making and consuming cash: its second-quarter filing showed $24.2 million of operating cash use over six months and a $56.6 million stockholders’ deficit, while 2026 guidance still implies a $30 million to $35 million adjusted EBITDA loss. Much of the planned launch funding is conditional on Anaphylm approval, leaving delay or financing risk for shareholders. (StockTitan, StockAnalysis)
Near-term proprietary diversification is limited. Libervant is only tentatively approved for patients aged 12 and over and is not expected to become eligible for full approval until January 2027, while its younger-patient filing is still under review. (StockTitan, Last10K)
Data summarised monthly by Lightyear AI. Last updated on 15 Sept 2026.

AQST Financial Performance

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

AQST Earnings Performance

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

Funds containing AQST

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