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Nanoform Finland (NANOFH) investor relations material
Nanoform Finland CMD 2025 Presentation summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.CMD 2025 Presentation summary16 Dec, 2025
Strategic vision and business targets for 2026–2030
Aims to break technological barriers in both small and large molecule drug development using CESS® for small molecules and BioLine for biologics, supporting the industry shift from IV to subcutaneous delivery.
Targets over 300 non-GMP projects and more than 30 GMP projects by 2030, with three nanoformed medicines launched by that year.
Sets ambitious financial goals: revenue exceeding €30 million, cumulative milestones over €30 million, and income growth above 50% CAGR from 2026–2030, with EBIT margin above 30%.
Cost growth is projected to remain below 5% CAGR due to prior investments in manufacturing scale-up and digital infrastructure.
Industry context and technology differentiation
Despite rising global pharma R&D spending, the number of new FDA drug approvals has remained flat, highlighting the need for innovative solutions.
Nanoform’s technology addresses low transition rates from preclinical to GMP projects, aiming to reach industry standards by 2030.
The CESS® process enables efficient, scalable nanoforming, with significant improvements in throughput and cost since 2021.
BioLine technology produces highly stable, high-concentration biologic suspensions, validated by large pharma partners for injectable and pulmonary delivery.
Product pipeline and partnerships
Pipeline includes nanoenzalutamide (prostate cancer), nanoapalutamide, nanoencorafenib (melanoma/colorectal cancer), and GLIORA (glioma), with launches targeted between 2028–2033.
Strategic partnerships with Helm Pharmaceuticals, Brafmed, and Revio Therapeutics support product development, regulatory submissions, and commercialization.
Nanoenzalutamide leverages a novel polymer-embedded nanoparticle platform to overcome existing patent and formulation hurdles, enabling smaller, patient-centric tablets.
GLIORA, a long-acting intra-tumoral hydrogel for glioma, combines nanoformed APIs for synergistic local therapy, with a de-risked development plan and strong IP protection.
How does PeN technology differentiate Nanoenzalutamide?
How does Nanoform address biologics SC delivery gap?
What drives the 2030 GMP project transition target?
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Next Nanoform Finland earnings date
Q4 202526 Feb, 2026
Next Nanoform Finland earnings date
Q4 202526 Feb, 2026
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Frequently asked questions
Nanoform provides nanotechnology and drug particle engineering services for the pharmaceutical industry. The company offers nanoparticle milling, a mechanical fragmentation process that reduces the particle size of APIs and enables the development of more bioavailable formulations. In addition, it provides physical characterization services for nanoparticles that comprises morphological analysis, including atomic force microscopy and scanning electron microscopy; elemental chemical analysis comprising inductively coupled plasma optical emission spectroscopy; and particle size distribution analysis comprising dynamic light scattering and laser diffraction, as well as supporting analytical equipment. The company was founded in 2008 and is headquartered in Helsinki, Finland.
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