Milestones

Hemerion team has been developing its technology since 2010 within the frame of scientific and clinical research teams located in Lille. Our endeavours led to a successful clinical validation in 2021.

2025
Hemerion opens a new clinical investigation site in Europe
Close-up of the Heliance device box in an operating room
Hemerion opens a new investigation site at Lille University Hospital dedicated to phase 1/2 clinical validation of its Pentalafen®/Heliance® therapy for the treatment of glioblastoma.
New €6.5 million funding round
Hemerion raises a new round of funding

Hemerion has completed a Series A financing round totaling more than €6.5 million, involving investment funds, public funding, business angels, and more than 260 private investors participating in a European crowdfunding campaign.

ISO13485 certification obtained
Hemerion achieves ISO 13485 Certification

Hemerion obtains ISO 13485:2016 certification for its quality management system for photonic medical devices from the British Standard Institute (BSI).

“Fast Track” status for Pentalafen® / Heliance® therapy
Hemerion receives FDA Fast Track Designation

Hemerion Therapeutics obtains “Fast Track” status from the FDA for its combined Pentalafen® / Heliance® therapy in the treatment of glioblastoma.

2024
Hemerion honored with the INPI 2024 Trophy in the “Research partnership” category
Hemerion wins the INPI 2024 Trophy

Hemerion wins the INPI 2024 Trophy in the “ Research Partnership” category. Created in 1991, this prestigious competition, organized by the French Institute of Industrial Property (INPI), recognizes exemplary companies in terms of intellectual property strategy.

First patient treated in the U.S.A. with the Pentalafen® / Heliance® therapy
Operating room

A first patient is treated in Pittsburgh, Pennsylvania as part of the new clinical trial sponsored by Hemerion. The study (HTX-GBM-01) is designed to confirm the safety and feasibility of the Pentalafen® / Heliance® combination therapy in the treatment of glioblastoma : a first in the USA.



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2023
The U.S. FDA authorizes Hemerion’s IND application for its Pentalafen® / Heliance® product combination
Hemerion addresses upfront management of newly diagnosed glioblastoma, during surgery, before any adjuvant treatment

The FDA authorization enables Hemerion to commence a Phase 1/2 clinical study at University of Pittsburgh Medical Center by Q4 2023 to evaluate the upgraded Pentalafen® / Heliance® platform.

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Last inclusion for the second clinical trial dedicated to Hemerion technology

The last patient included in the Dosindygo phase II clinical trial, led by the Lille University Hospital in partnership with Hemerion Therapeutics, was operated on in June 2023.

Hemerion receives the “Deeptech” label and an additional 2 million euros in funding from Bpifrance
Deeptech Connect 2023

Granted as part of Bpifrance’s Deeptech Plan, this financing allows Hemerion to accelerate the implementation of a new clinical trial.

2022
Hemerion raises €3.55 million to accelerate the implementation of international clinical trials for the treatment of glioblastoma
Fund raising

One year after the first round of funding, Hemerion’s new €3.55 million financing will accelerate the implementation of international clinical trials for the treatment of glioblastoma.

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2021
Hemerion awarded the Galien MedStartup Prize
Galien Prize MedStartup

Hemerion and Mount Sinai Health System (NYC) are collaborating to launch an ambitious clinical trial in 2022. This project has won the “Best Collaboration in the MedTech and Digital Health” award of the Galien Medstartup Prize: an international recognition that perfectly kickstarts the Hemerion development in the USA.

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Preliminary results published in Journal of Neuro-Oncology

Ground breaking preliminary results from the clinical study are published in the Journal of Neuro-Oncology. The Hemerion’s technology covered the 2018’s May issue.

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FDA grants Hemerion Orphan Drug designation

In the USA, the Hemerion’s technology becomes granted Orphan Drug Designation by the FDA.

Hemerion gathers 1.5M€ in funding
Hemerion Technology
For its preliminary funding round, Hemerion gathers 1.5M€ in dilutive and non-dilutive funding to further validate its therapeutic approach.
2020
Establishment of Hemerion Therapeutics
Surgeons

Hemerion Therapeutics is founded by the scientists and inventors of the technology, among them M. Vermandel, C. Dupont, N. Reyns, S. Mordon and M. Andraud gather deep scientific how-know and entrepreneurship skills to lead the company. In the mean time, Hemerion is awarded the French Tech Label that recognizes high potential start-up companies.

Logo La French Tech

2019
Introduction of the Hemerion technology in the USA
Introduction of the Hemerion technology in the USA

The Hemerion technology is demonstrated by Pr. N. Reyns at an international neurosurgery meeting in Cambridge – Boston (MA, USA) and in New-York (NY, USA) during Fluorescence-Guided Surgery Brain Tumor Symposiums hosted at The Icahn School of Medicine at Mount Sinai by Pr. C. G. Hadjipanayis.

2018
European Neurosurgery Congress
European Neurosurgery Congress

The Hemerion drug-device combination product is presented during the plenary session of annual congress of the European Association of the Neurosurgery Societies in Brussels (Be). First usability endpoints successfully collected during the Phase I INDYGO are reported to the European’s neurosurgeons community.

Nature highlights the world’s first clinical trial conducted with Hemerion technology

The use of Hemerion technology for the first time in the operating room, as part of a clinical trial, is detailed by the international magazine.

Patients enrollment successfully completed

The enrollment phase of the clinical trial INDYGO is successfully completed, after only one year. During this study sponsored by the University Hospital of Lille (France) and with  Pr. N. Reyns as the Principal Investigator, 10 patients included from may 2017 to June 2018 have been treated with the Hemerion’s technology.

2017
Awarded by world’s largest medical laser society

M. Vermandel becomes the first ever non-US resident of being the recipient of the ASLMS research grant (American Society of Lasers in Surgery and Medicine) for his work on drugs and laser technologies combination. ASLMS was founded in 1980 and is the world’s largest professional organization dedicated to the field of medical laser.

Kick-off of phase I clinical trial: INDYGO
Surgeons
For the first time, our technology combining a photosensitizing drug and an innovative photonic device is delivered upfront, during the surgery of patients newly diagnosed with glioblastoma. 
Indygo is a Phase I study sponsored by the University Hospital of Lille.
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