APTADIR RAISES A €40M ($45M) SEED FINANCING TO ADVANCE FIRST-IN-CLASS DEMETHYLATING MEDICINES

• Funds will advance novel class of RNA inhibitors to reverse intractable genetic conditions
• Seed is led by 4BIO Capital with follow-on participation from the company's original pre-seed investor EXTEND (CDP Venture Capital SGR, Angelini Ventures and Evotec SE)
• Science originates from three leading institutions – the Beth Israel Deaconess Medical Center, the Italian Research National Council (CNR) and the Cancer Science Institute of Singapore

Milan, Italy – 29 September 2026 – Aptadir Therapeutics (Aptadir), a biotech company developing a novel class of RNA inhibitor-based therapeutics for treating intractable genetic conditions, announces the closing of its EUR 40M Seed round.

The round was led by 4BIO Capital, with follow-on participation from the company’s original pre-seed investor, EXTEND, Italy’s National Technology Transfer Hub, launched by CDP Venture Capital SGR and jointly funded by Angelini Ventures and Evotec SE.

The seed round was also supported by CDP Venture Capital, through the Digital Transition Fund, Indaco Venture Partners (Indaco Bio Structure and Indaco Bio Parallel Lombardia),  XGEN Venture and CE-Ventures. Additional participants included Angelini Ventures, through a direct investment, Kerna Ventures, Italian Angels for Biotech, and Club degli Investitori.

The funds will be used to advance the company’s pipeline of disease-modifying investigational RNA therapeutics, including its lead candidate, CAP1-FMR1 for Fragile X Syndrome. The Company’s technology is based on the landmark discovery of a new class of RNAs which are capable of blocking aberrant DNA methylation at a single gene level^1,2. By reversing this abnormal gene silencing, Aptadir’s RNA inhibitors can reactivate gene expression and restore normal biological function, an effect the Company has demonstrated in patient-derived disease models. Aptadir is developing a portfolio of drug candidates based on this proprietary technology. The molecules, called DNMTs Interacting RNAs (DiRs), target specific genes that are silenced in cancer and genetic disorders. The technology is based on the findings of an international group of renowned scientists in the fields of RNA and DNA biology, genetic disorders, leukemia and immunotherapeutics including Annalisa Di Ruscio and Daniel Tenen from the Beth Israel Deaconess Medical Center, Vittorio de Franciscis of the Italian Research National Council, Marcin Kortylewsky of City of Hope National Medical Center. 

Giovanni Amabile, Founder and CEO, said: “The magnitude of this seed round reflects the exciting potential of our DiRs technology and the quality of a truly international scientific team. Originating from world-class institutions, the discovery of this new class of RNA inhibitors was a landmark event not only from a scientific point of view, but also for providing newfound hope for patients affected by intractable disorders. With the backing of our investors, we now have the opportunity to develop a pipeline of drug candidates with the potential to restore genetic pathways that, for decades, have been considered irreversibly silenced.”

Dima Kuzmin, Managing Partner of lead investor, 4BIO Capital, added: “Finding truly innovative new science with such potential is a rare event. We are delighted to back this novel modality that can give rise to multiple therapeutics addressing previously entirely undruggable disease mechanisms. The group of founders behind the science are world-renowned and the potential of the technology could be life changing. We are confident that the right factors are in place, from the science to the management team, to take this technology forward into the clinic.”

Claudia Pingue, Head of Technology Transfer fund at CDP Venture Capital and Chairman of EXTEND said: “Our purpose at EXTEND is to identify and help develop translational drug discovery opportunities. We recognized how powerful Aptadir’s science could be from the outset, and this was the rationale for us to spinning out the company and investing from the very earliest, highest risk stages, first at the pre-seed and follow through with this significant seed round. We are proud that this science is now attracting further investment from international partners, and we will continue to support the Company as it develops.”

-Ends-

1. Di Ruscio A et al 2013, Nature
2. Esposito CL et al 2023, Nature Communication

Aptadir Therapeutics	info@aptadir.com
Giovanni Amabile, CEO
Vigo Consulting (Biopharma media)	+44 (0)7890 022 814
Melanie Toyne-Sewell / Rozi Morris	Aptadir@vigoconsulting.com
JET’S PR (Italian media) Ernesto Bonetti	e.bonetti@jetsgroup.it

Notes to Editors

About Aptadir Therapeutics

Aptadir Therapeutics is a preclinical biotech company developing a new class of RNA therapeutics. The Company’s therapeutic focus is underserved intractable cancers and genetic conditions, including underserved intractable conditions in the oncology and rare diseases fields such as Fragile X Syndrome and Myelodysplastic Syndrome.

The technology was developed and validated by a group of key opinion leaders in the field of RNA therapeutics based at three world class institutions: the Harvard Medical School, Cancer Science institute of Singapore, Italian CNR Institute and City of Hope National Medical Center. The platform is based on a landmark discovery of a new class of RNA inhibitors called DNMTs Interacting RNAs (DiRs)^1,2. DiRs are capable of blocking aberrant DNA methylation at a single gene level reactivating previously hypermethylated genes – a key feature in cancer and genetic disorders.

The first programme is developing a treatment for Fragile X Syndrome, a genetic condition that causes intellectual disability, learning difficulties and developmental delays. Fragile X Syndrome is caused by the silencing of the FMR1 gene on the X chromosome, resulting in the loss or significant reduction of FMRP, a protein essential for normal brain development and function.

To find out more, please see: www.aptadir.com and on LinkedIn.

About 4BIO Capital

4BIO Capital is a global specialist biotech venture firm investing in breakthrough technologies that solve critical healthcare challenges. 4BIO partners with visionary biotech founders, investing with conviction and serving as a therapeutic navigator to guide the transformation of scientific innovation into life-changing therapies. The 4BIO team are specialists with deep scientific expertise and proven commercial track records, strategically matched to portfolio companies that align with their specific areas of knowledge.

For more information, connect with us on LinkedIn and X @4biocapital and visit www.4biocapital.com.

About EXTEND

EXTEND is the Italian National Technology Transfer Hub solely dedicated to the biopharmaceutical sector, established on the initiative of CDP Venture Capital through its Technology Transfer Fund to translate scientific research outcomes into new companies developing novel therapeutic approaches.

Alongside CDP Venture Capital, Extend is funded by co‑investors Evotec and Angelini Ventures. The scientific promoters of the initiative are IRCCS San Raffaele Hospital (Milan); the Universities of Milan, Florence, Modena and Reggio Emilia, Padua, Trento, and La Sapienza (Rome); the regional research district of Puglia through H‑Bio; and Human Technopole.To learn more, please visit:  extend-tt.vc

To learn more about Aptadir’s investors, please visit:

• CDP Venture Capital SGR — cdpventurecapital.it
• XGEN Venture — xgenventure.com
• Indaco Venture Partners — indacosgr.com
• CE- Ventures — crescententerprises.com
• Angelini Ventures — angeliniventures.com
• Kerna Ventures — kerna.vc
• Italian Angels for Biotech (IAB) — italianab.it
• Club degli Investitori — clubdeglinvestitori.it

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• Giovanni Amabile, Founder and CEO