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AB SCIENCE (AB) investor relations material
AB SCIENCE H1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
H1 2026 revenue was €498k; operating loss widened to €10.4m and net loss to €9.0m, mainly reflecting a €6.5m CIR provision.
Clinical priorities shifted to AB8939 in AML and masitinib in ALS, with trial restarts planned for 2027 after quality-system work.
April–August private placements raised €19.7m; cash after the August raise was reported at ~€23m.
Financial highlights
Net sales were €498k in H1 2026 versus €515k in H1 2025, entirely from veterinary Masivet.
Operating loss was €10.4m versus €2.7m; net loss was €9.0m versus €5.2m, with the deterioration primarily reflecting the €6.5m CIR provision and higher employment-litigation provisions.
Net financial result improved to a €1.4m gain from a €2.4m loss, including a €2.0m ROMANE advance remeasurement benefit.
Cash and cash equivalents were €9.0m at June 30; shareholders’ equity was negative €22.5m.
Outlook and guidance
Cash needs were estimated to be covered through FY2026 and 2027, supported by July and August equity raises, an expected €1.1m CIR payment and deferred debt maturities; trailing 12-month cash burn averaged €9m/year.
A new quality-management system and external audit were planned by year-end 2026; AB8939 Phase 1 was targeted to resume in Q1 2027 and masitinib ALS Phase 3 in Q4 2027.
The AP-HP-sponsored masitinib sickle-cell study was expected to begin in early 2027 and was described as unaffected by inspection-related delays.
Strategic priorities include AB8939 in AML, masitinib in ALS, asset review, potential partnerships and veterinary sales development.
- Authorized Phase 3 programs advance masitinib across ALS, MS and Alzheimer’s disease.AB
Corporate presentation - Net loss fell 80% year-over-year as clinical focus narrowed to ALS and AML, with improved cash and financing.AB
H2 2025 - AB8939 plus venetoclax showed 100% response in high-risk AML with no hematological toxicity.AB
Status Update - Operating loss fell 24% but net loss rose; €6.3M raised for clinical and patent milestones.AB
H1 2025 - AB8939 shows strong efficacy in refractory and MECOM AML, with Phase II trials and funding secured.AB
Status Update - Net loss and operating deficit dropped, cash position improved, but regulatory risks persist.AB
H1 2024 - Operating loss halved and cash bolstered as clinical pipeline advances and IP portfolio grows.AB
H2 2024 - Masitinib advances in neurodegenerative diseases with new trials and a January 2025 update webcast.AB
Status Update
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