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Analyst Comment

Herantis' Phase I trial achieved all its objectives

By Antti SiltanenAnalyst
Herantis Pharma

Translation: Original published in Finnish on 10/8/2025 at 7:25 am EET.

Herantis Pharma issued a press release on Tuesday evening regarding the main results of its clinical Phase Ib trial of HER-096, its drug candidate for Parkinson's disease. The study achieved all primary and secondary objectives set for it. The results thus clearly support moving to the next research phase and were also in line with previous data and our expectations. The company will hold a press conference on the results on Wednesday at 1 pm EEST. The event can be followed here. We will update our view by Thursday morning, once all information from the press conference is available. Based on our preliminary assessment, the stock's risk level decreases by one notch due to the positive results.

Trial objectives were met and there were no surprises

The primary objective of the study was to demonstrate the safety and tolerability of the drug candidate. According to Herantis, repeated doses of HER-096 were generally safe and well tolerated in patients with Parkinson's disease. The secondary objective was to determine the pharmacokinetics, i.e., the behavior of the drug in the body. The results confirmed that the drug effectively crosses the blood-brain barrier, meaning it reaches its target in the central nervous system. This is a critical feature for the drug's function, for which preliminary promising results were obtained earlier. According to the company, the concentrations achieved in the cerebrospinal fluid were at a level where pharmacological effects can be expected. In other words, the drug candidate reaches its target and remains there long enough for potential therapeutic effects to be achieved in the future. Regarding dosage, 300 mg/kg administered subcutaneously twice a week appears to have been selected as the best option for the next phase, according to the release. The trial was not designed to assess efficacy, so evidence in this regard will have to await the next phase.

Financing solution paves the way for the next clinical phase

According to the company, the results support the progression of HER-096 to a Phase II trial, which the company plans to initiate during 2026. We have already stated in our previous reports that the results support the continuation of the study. Reflecting this, in our H1’25 report, we had already raised the probability of Phase 1 success in our model to a rather high 75%. The results now obtained are thus in line with previously obtained results and our expectations. With good results, the risk profile of drug development will, in our view, decrease by one notch, although the overall risk level remains quite high. Herantis expects the entire study dataset, including exploratory biomarker results, to be completed by the end of 2025. These may provide additional information on the drug's behavior and effects, but in our opinion, the main results now published were the most important prerequisite for the project's continuation.

The next significant step for the company is securing funding for the Phase II trial. The company has previously stated that it aims to enter into a partnership agreement with a larger pharmaceutical company. In our view, the strong results now obtained support Herantis' negotiating position for a potential partnership agreement.

 

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 Figures22.08

202425e26e
Revenue0.00.00.0
growth-%150.0 %
EBIT (adj.)-5.0-5.5-5.9
EBIT-% (adj.)-50,270.0 %-55,119.0 %-59,321.2 %
EPS (adj.)-0.25-0.25-0.25
Dividend0.000.000.00
Dividend %
P/E (adj.)neg.neg.neg.
EV/EBITDAneg.neg.neg.

Forum discussions

Note, latest timing info! Herantis expects to report the Phase 1b biomarker data by mid-January 2026, in advance of the JP Morgan Healthcare...
12/1/2025, 5:25 PM
by Oxymoron 007
3
This link contains key information about an approved, commonly used medication for the “treatment” of Parkinson’s disease. Much seems to be ...
12/1/2025, 10:44 AM
by Oxymoron 007
3
Yeah, exactly. In principle, it goes like this: In the analysis, a required rate of return (WACC) is given to the shares. If the difference ...
12/1/2025, 6:24 AM
by Antti Siltanen
4
Herantis Pharma | Edison webinar https://youtu.be/OZbyxHiHc0w?si=tk6Czn33xwUvMKc6
11/28/2025, 4:51 AM
by Oxymoron 007
1
Herantis Pharma Plc | Press release | 26 November 2025, at 12:00 EET Herantis Pharma announces successful completion of six-month GLP toxicology...
11/26/2025, 3:56 PM
by Oxymoron 007
4
Approximately 30-60 days were supposed to be spent on marker counting. October 25th was likely the day the phase ended. Perhaps they will hold...
11/26/2025, 3:37 PM
3
Can’t you read “between the lines” from that, that the biomarker results were good? It had surprisingly little effect on the stock price, as...
11/26/2025, 3:27 PM
by Buy and Hold Is Eternal
4
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