Logotype for Herantis Pharma

Herantis Pharma (HRNTS) H1 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Herantis Pharma

H1 2026 earnings summary

20 Aug, 2026

Executive summary

  • HER-096 is advancing to a phase II trial as a potential first disease-modifying therapy for Parkinson's, supported by strong phase I/1b safety, biomarker, and translational data in both patients and healthy volunteers.

  • The phase II trial will be a randomized, placebo-controlled, double-blind study in early-stage Parkinson's, leveraging digital monitoring and biomarkers to assess efficacy.

  • HER-096 leverages CDNF biology for a broad, multimodal mechanism of action with neurorestorative potential, addressing a major unmet need in Parkinson's where no disease-modifying therapies exist.

  • The company operates in a large and growing market with high unmet need, as current therapies only address symptoms and lose effectiveness over time.

  • Positive FDA feedback, new leadership appointments, and collaborations for digital biomarker integration and CRO support have strengthened operational readiness.

Financial highlights

  • Operating expenses and cost base remained flat year-over-year, with spending focused on phase II preparations, biomarker development, and investor relations.

  • Net loss for 1H 2026 was EUR 3.3 million, compared to EUR 3.2 million in 1H 2025.

  • Cash and securities at June 30, 2026, ranged from EUR 3.5 million to EUR 4.6 million, with equity at EUR -0.7 million.

  • Long-term debt increased to EUR 3.4 million due to additional research and foundation funding.

  • EUR 4.2 million raised via share issue and EUR 8.0 million Horizon Europe grant secured for phase II trial.

Outlook and guidance

  • Clinical trial application for phase II is expected by year-end 2026, with first patient enrollment in 1H 2027 and interim efficacy data in 1H 2029.

  • Cash runway extends until end of 1H 2027, but additional capital is required to launch and complete the phase II trial.

  • R&D expenses and cash burn are expected to increase as phase II activities ramp up.

  • Active discussions are ongoing with potential pharma partners and investors for additional funding and development partnerships.

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