Fennec Pharmaceuticals Inc. commercializes PEDMARK, a sodium thiosulfate injection approved by the FDA as the first and only therapy to reduce the risk of ototoxicity from cisplatin in pediatric patients with localized, non-metastatic solid tumors. The company is a specialty pharmaceutical business that licensed the underlying technology exclusively from Oregon Health & Science University. Its sole marketed product addresses hearing protection in children undergoing platinum-based chemotherapy.
| Quarter | Revenue | YoY % | Earnings | YoY % |
|---|---|---|---|---|
| Q2 2025 | 9.7 | — | -3.1 | — |
| Q3 2025 | 12.5 | — | -0.6 | — |
| Q4 2025 | 13.8 | — | -4.8 | — |
| Q1 2026 | 15.1 | — | 0.2 | — |
| Q2 2026 | 17.9 | 85.2% | 2 | — |
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