About Isofol

About Isofol and Modufolin®

Isofol Medical AB was founded in 2008 based on the research of Professor Bengt Gustavsson and his collaboration with Merck & Cie, the world’s leading manufacturer of folate-based therapies. Isofol’s main objective is to improve the outlook for the majority of cancer patients undergoing chemotherapy treatments.

Isofol’s clinical lead candidate is Modufolin®, a novel folate-based therapy developed to increase the efficacy and reduce the side effects of antimetabolites used in cancer treatment. It is the key active metabolite of all clinically used folate-based drugs today, including leucovorin and levoleucovorin, and therefore does not require metabolic activation to exert its action. A majority of all patients treated for colorectal cancer with chemotherapy are also treated with folate-based therapies, and the combination of chemotherapy with folates is the most  commonly used cancer treatment in the world. The market opportunity for Modufolin® may therefore be measured in billions of US$.  Isofol is now conducting combined phase I and II clinical trials to verify the benefits of Modufolin® as a co-therapy in the treatment of cancer. To date, Modufolin® has been shown to be safe after treating numerous patients and Isofol is to commence the ISO-CC-006 study to prove the efficacy of Modufolin® in colorectal cancer patients.

Strategic collaborations

Isofol intends to take Modufolin® to market registration through a couple of clinical trials. Isofol will then follow the most favourable strategy to commercialise Modufolin® worldwide. To help achieve this, Isofol collaborates with a number of companies:

  • Isofol has a strategic R&D partnership with Merck & Cie, an affiliate of Merck KGaA, a leading science and technology company in healthcare, life science and performance materials and the world’s leading supplier of reduced folates such as Metafolin®and Leucovorin. Isofol holds an exclusive supply and license agreement for Modufolin® from Merck & Cie
  • A collaboration is in place with Recipharm for the exclusive commercial manufacture of Modufolin®. Recipharm is a leading European CDMO (Contract Development and Manufacturing Organization) in the pharmaceutical industry
  • Sahlgrenska University Hospital is an important clinical development platform for Isofol as it provides key clinical and medical competence to the company as well as offering state of the art facilities for Isofol’s clinical trials

Isofol has had successful meetings with regulatory authorities in Sweden, the US and Europe

In 2015, a meeting with the Swedish Medical Products Agency indicated that Modufolin® could be eligible for market approval if a clinical superiority program would be completed. This year (2016), Isofol met with both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). Both agencies endorsed the clinical development plan for Modufolin®, and were in agreement with Isofol regarding the requirements for the registration of Modufolin®. Isofol’s development plan aims for the completion of a proof-of-superiority program in 2018.