FENCNasdaqBiological Products, (No Diagnostic Substances)US GAAP · USD

Fennec Pharmaceuticals Inc

Fennec Pharmaceuticals is a U.S.-based commercial-stage biopharmaceutical company focused on PEDMARK® (sodium thiosulfate injection), a therapy used to reduce cisplatin-induced hearing loss in pediatric cancer patients. The company also monetizes its asset through licensing arrangements, including commercialization rights outside the U.S. for PEDMARQSI®/PEDMARK®.

Liikevaihto44,6milj. USD
−6,1 %v/v
Liikevoitto (EBIT)−6,3milj. USD
−344,6 %v/v
EBIT-marginaali−14,1%
−19,5 %-yks.v/v
Nettotulos−9,7milj. USD
−2 134,2 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−40−200204060milj. USD2020: 0,17 milj. USD2020: EBIT −18 milj. USD20202021: 0,17 milj. USD2021: EBIT −17 milj. USD20212022: 1,5 milj. USD2022: EBIT −23 milj. USD20222023: 21 milj. USD2023: EBIT −13 milj. USD20232024: 48 milj. USD2024: EBIT 2,6 milj. USD20242025: 45 milj. USD2025: EBIT −6,3 milj. USD202545−6,3
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Commercial product sales55 %

Sales of PEDMARK® in the U.S. and related branded product commercialization.

International licensing35 %

Out-licensing of PEDMARQSI® rights to partners for Europe, Australia and New Zealand.

Milestones and upfront fees10 %

Non-refundable upfront payments and milestone receipts under collaboration agreements.

Asiakkaat

Fennec sells primarily into the life sciences and pharmaceutical ecosystem rather than to mass-market consumers. Its direct customers include hospitals, oncology treatment centers, and pharmaceutical partners that commercialize or license PEDMARK/PEDMARQSI in specific territories.

Pediatric oncology providers

Hospitals and cancer centers buy PEDMARK for children receiving cisplatin to reduce hearing-loss risk.

Pharmaceutical commercialization partners

Partners license rights to market PEDMARQSI/PEDMARK in defined territories and pay milestones or royalties.

Specialty pharmacy and distribution channels

Channel partners distribute the product to treatment sites and support access and reimbursement.

International oncology markets

Ex-U.S. markets buy through local commercialization partners as approvals and launches expand.

Strategia

Fennec is pursuing commercialization of its single approved product while broadening access through regional licensing partnerships. Management is also actively evaluating strategic alternatives and collaborations to secure funding, extend runway, and support future development and commercialization efforts.

Grow PEDMARK adoption in the U.S.Lyhyt aikaväli

The company depends heavily on one commercial asset, so uptake drives revenue and operating leverage.

Scale ex-U.S. commercialization through partnersKeskipitkä aikaväli

Licensing reduces direct operating burden while expanding market reach and potential royalty streams.

Secure additional capital and strategic optionsLyhyt aikaväli

Working capital needs remain uncertain and the company references further capital requirements.

Maantiede

The company is headquartered in the United States, where PEDMARK was first approved and where commercial activity is centered. Outside the U.S., Fennec has expanded through licensing, with PEDMARQSI approved in the EU and U.K. and launched in Germany and the U.K. through Norgine. This makes the business dependent on regulatory approvals and partner execution in Europe and other ex-U.S. markets.

Riskit

Fennec is highly concentrated in a single product and therefore exposed to adoption, reimbursement, and regulatory execution risk. Its partner-led international expansion reduces direct investment needs but increases dependence on third parties, while ongoing capital needs and clinical/regulatory uncertainty remain material for a small biopharma company.

Järjestetty vakavuuden mukaan
Single-product concentrationKorkea

Revenue and strategic value are tied primarily to PEDMARK/PEDMARQSI, so any setback would materially affect the business.

Kohdistuu: PEDMARK commercialization

Partner dependenceKorkea

International growth relies on Norgine and other collaborators to launch, market, and distribute the product.

KohdistuuEuropeAustraliaNew Zealand
Financing and liquidity riskKorkea

Management states future capital requirements are uncertain and may depend on collaboration proceeds or financing.

Kohdistuu: Working capital and runway

Regulatory and market access riskKeskitaso

Approvals, label scope, and reimbursement determine whether hospitals can adopt the therapy at scale.

KohdistuuU.SEUU.K

Kirjanpito

Harkinnanvaraiset erät
ASC 606 license revenue

Upfront fees, milestones, and royalties require allocation and judgment on when obligations are satisfied.

Vaikutus: Can shift revenue between periods and affect comparability.

Expected credit losses

Receivables are evaluated using customer history, macro factors, and industry conditions.

Vaikutus: Affects bad debt expense and net receivables.

Performance-based equity awards

PSU vesting depends on revenue milestones and is expensed when probable.

Vaikutus: Can increase compensation expense if milestones are expected to be achieved.

Fair value of cash equivalents

Money market balances are exposed to fair value and liquidity considerations.

Vaikutus: Minor but relevant for treasury and liquidity analysis.

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026