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Herantis H2'25 preview: Blood-brain barrier passed and financial barriers lowered

HRTISAnalyst Comment02.03.2026, 08.19
Antti SiltanenAnalyst
Discuss

Summary

  • Herantis Pharma is set to release its 2025 results on March 5, 2026, with a focus on the progress of the HER-096 drug candidate's Phase II clinical trials, supported by secured funding from a share issue and EU grant.
  • The Phase I study of HER-096 showed the drug candidate is safe, well-tolerated, and capable of crossing the blood-brain barrier, establishing a strong scientific basis for Phase II trials planned for H2’26.
  • Herantis has secured 8 MEUR from the Horizon Europe program and 4.2 MEUR from a share issue, reducing financial risk and positioning the company favorably for partnership negotiations, though an additional 8–12 MEUR is estimated to be needed for Phase II.
  • Herantis, an early-stage drug development company, reported an estimated H2 EBIT of -2.6 MEUR and a full-year 2025 adjusted EBIT of -5.5 MEUR, with costs rising due to clinical trial activities, yet maintaining a moderate cost structure relative to development progress.

This content is generated by AI. You can give feedback on it in the Inderes forum.

Translation: Original published in Finnish on 3/2/2026 at 7:00 am EET.

Estimates H2'24H2'25H2'25e2025e
MEUR/EUR ComparisonRealizedInderesInderes
Revenue 0 00
EBIT -2.27 -2.56-5.51
EPS (reported) -0.11 -0.12-0.25

Source: Inderes

Herantis Pharma will publish its 2025 result on Thursday, March 05, 2026, and the company's earnings release can be followed here at 10:00 am EET. We will pay particular attention in the report to the progress of preparations for the second phase of clinical trials of the HER-096 drug candidate. Funding for the upcoming trial has been secured through a recently announced share issue and EU grant. Any additional information on securing the remaining financing needs will also be a focal point of the report.

Scientific basis solid for the future

In October 2025, Herantis published the main results of the Phase I study. Based on these results, the Parkinson's disease drug candidate, HER-096, was deemed safe and well-tolerated in short-term dosing. The candidate also crossed the blood-brain barrier, reaching its target in the central nervous system. In January, the company supplemented the results with a biomarker analysis, which suggested that the candidate has biological activity as well. Overall, the results achieved the objectives of Phase I, creating a strong scientific basis for the next Phase II study. Herantis plans to initiate Phase II in H2’26.

Funding has already been partially arranged

Herantis’ financial position has recently shown positive development. The company has secured 8 MEUR in EU funding from the Horizon Europe program, which will cover a significant portion of the upcoming HER-096 Phase II trial costs as a grant. Additionally, the company collected 4.2 MEUR in gross assets from a directed share issue in February. These arrangements reduce the company's financial risk significantly and improve its position in ongoing partnership negotiations. We estimate the direct costs of the Phase II trial to be around 15–20 MEUR. In addition, the company will require funding for administrative expenses and potential R&D activities. According to our rough estimate, the company still needs around 8–12 MEUR in funding to carry out Phase II. We believe this is also achievable through equity financing without significant issues. The company is still aiming to secure financing through a partnership agreement during the spring, which we believe would be the most desirable option.

Cost-effective drug development

Herantis is an early-stage drug development company with no products on the market yet. The company's business model is based on developing drug candidates and increasing their value through clinical trials. Actual future revenue would consist of advance and milestone payments from potential partnership agreements or, later on, royalty income. We estimate Herantis’ H2 EBIT to be -2.6 MEUR. For the full year 2025, we expect adjusted EBIT to have settled at -5.5 MEUR. During the review period, expenses increased particularly due to the completion of the Phase Ib clinical trial of the HER-096 candidate and the publication of the biomarker analysis in January. We expect earnings per share of EUR -0.12 in H2. Although the result is negative, we believe the company's cost structure has remained very moderate relative to the progress of the drug development program.

Herantis Pharma Plc is a clinical-stage biotechnology company developing disease modifying therapies for Parkinson’s disease. Herantis’ lead product HER-096 is a small synthetic chemical peptidomimetic molecule developed based on the active site of the CDNF protein. HER-096 combines the mechanism of action of CDNF with subcutaneous administration. The Phase 1a clinical trial demonstrated a good safety and tolerability profile as well as blood-brain barrier penetration of subcutaneously administered HER-096. The shares of Herantis are listed on the Nasdaq First North Growth Market Finland.

Read more on company page

Key Estimate Figures08.01

202425e26e
Revenue0.00.00.0
growth-%150.0 %
EBIT (adj.)-5.0-5.5-6.6
EBIT-% (adj.)-50,270.0 %-55,119.0 %-66,408.0 %
EPS (adj.)-0.25-0.25-0.28
Dividend0.000.000.00
Dividend %
P/E (adj.)neg.neg.neg.
EV/EBITDAneg.neg.neg.

Forum discussions

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57 minutes ago
by Oxymoron 007
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An example of successful drug development, obtaining the necessary approvals, and commercialization. https://www.barrons.com/articles/uniqure...
6/22/2026, 8:20 PM
by Oxymoron 007
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6/21/2026, 11:07 AM
by Oxymoron 007
3
Jun 2026 Herantis Pharma Q&A video 8 min https://x.com/ristopar/status/2067446794787692743/video/1?s=46
6/18/2026, 3:34 AM
by Oxymoron 007
0
Partnership between Herantis Pharma and Individ in the drug development of HER-096 for PD https://x.com/ristopar/status/2061863099800408356?...
6/17/2026, 2:38 PM
by Oxymoron 007
0
Could you provide a brief summary instead of just a link? I’m personally banned from X, so it’s difficult to read. And just in general, too.
6/14/2026, 2:47 PM
by Hetki on nyt
9
Herantis received positive feedback from the FDA regarding the study design for the HER-096 drug candidate, but Inderes lowered the target price...
6/5/2026, 9:19 AM
by Oxymoron 007
2