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Fennec Pharmaceuticals/$FENC

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About Fennec Pharmaceuticals

Fennec Pharmaceuticals Inc is a commercial-stage biopharmaceutical company. Its product candidate is PEDMARK which is sodium thiosulfate in a novel formulation for the prevention of cisplatin-induced hearing loss, or ototoxicity in children. The company principally operates in the United States.
Ticker
$FENC
Sector
Health
Primary listing
NASDAQ
Employees
35

FENC Metrics

BasicAdvanced
$344M
-
-$0.10
1.07
-

What the Analysts think about FENC

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

Bulls say / Bears say

PEDMARK sales rose 78% year on year to $17.1 million in the second quarter, with adjusted EBITDA of $2.8 million and cash of $41.2 million. That suggests the growing commercial business is beginning to generate profits and fund itself. (Fennec Pharmaceuticals Inc.)
An investigator-led Phase 2 study in Japan met its primary endpoint, showing significant hearing protection without evidence of interference with cisplatin’s anti-cancer activity. This supports the case for seeking Japanese registration and a commercial partner. (U.S. Securities and Exchange Commission)
International licensing offers a route to growth beyond US sales: management said Norgine planned to launch PEDMARQSI in ten markets during the second half of 2026. Successful launches could bring Fennec royalties and milestone payments without requiring it to build its own sales operation in those territories. (StockAnalysis, U.S. Securities and Exchange Commission)
Commercial expansion is costly: second-quarter selling and marketing expense more than doubled year on year to $10.7 million, against $17.1 million of PEDMARK sales. If sales growth slows, those higher costs could weigh on margins. (Fennec Pharmaceuticals Inc.)
Fennec depends on a single product, and PEDMARK’s approved use is limited to children with localised, non-metastatic solid tumours. Broader adult and metastatic uses remain exploratory and would need further clinical evidence and regulatory approval, limiting how quickly the company can expand its market. (U.S. Securities and Exchange Commission)
Cipla could enter the US market with a generic version from 1 September 2033, or earlier in specified circumstances. Generic competition would put pressure on Fennec’s key revenue source, and its filings also warn that patent protection could be challenged or circumvented. (U.S. Securities and Exchange Commission)
Data summarised monthly by Lightyear AI. Last updated on 28 Oct 2026.

FENC Financial Performance

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

FENC Earnings Performance

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

Funds containing FENC

Funds
Fund name
Fund size
$FENC weighting
SPDR Russell 2000 US Small Cap€R2US
$5.3B0.01%
SPDR Russell 2000 US Small Cap£R2SC
$5.3B0.01%
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