Idogen extends the project portfolio to projects in autoimmune diseases

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Idogen AB (”Idogen”) announces today that the company has decided to expand its project portfolio with a third therapeutic area; autoimmune diseases. Idogen´s research department is currently evaluating the potential of the company's technology in a group of autoimmune diseases where there is a major medical need, and where a treatment has the potential to be granted orphan drug status.

Idogen´s technology is designed for the development of tolerogenic cell therapy in a variety of areas, especially treatment of anti-drug antibodies, autoimmune diseases and organ rejection after transplantation.

Until now, Idogen's project portfolio consisted of the two product candidates IDO 8 and IDO T. IDO 8 is aimed at patients with severe haemophilia A affected by inhibitory antibodies against their vital treatment with coagulation factor VIII. An initial clinical trial of IDO 8 is scheduled to start in early 2020. IDO T is a treatment method aimed at preventing organ rejection in transplantation, primarily in renal transplantation. Preclinical proof of concept data for IDO T is expected to be presented within three to six months.

Idogen has now decided to expand the project portfolio with a third therapeutic area; autoimmune diseases. Patients with autoimmune diseases are often treated for prolonged periods with drugs that strongly suppress the immune system. However, the effect on the underlying disease is rarely optimal and treatment can lead to unwanted side effects. The medical need for improved therapies is therefore large. The purpose of Idogen's tolerogenic cell therapy is to dramatically reduce the need for immunosuppressive drugs by a short treatment with improvements for the patient as a result. Proof of principle data from a preclinical trial model relevant to a rare autoimmune disease is expected to be presented within three to six months.

“We are very excited about the opportunity to evaluate the potential of Idogen's technology platform in the field of autoimmune diseases. Today, there is a major unmet medical need in patients with current standard treatments, where we believe that Idogen's tolerogenic cell therapy can play an important role. Our focus will be on one or several rare diseases, which allows for the grant of orphan drug designation that can reduce both development costs and time until market approval, as well as extended market exclusivity”, CEO Lars Hedbys comments. 

For additional information, please contact:
Lars Hedbys, CEO Idogen AB
Tel: +46 (0)46-275 63 30
E-mail: lars.hedbys@idogen.com

This is an English version of an original Swedish press release communicated by Idogen AB. In case of interpretation issues or possible differences between the different versions, the Swedish version shall apply. This constitutes information that Idogen AB is required to publish under the EU’s Market Abuse Regulation. The information was submitted for publication through the above contact person on August 17 2018.

Idogen (Spotlight Stock Market: IDOGEN) develops tolerogenic cell therapies to prevent the patient’s immune system from attacking biological agents, transplanted organs or the body’s own cells or tissue. Idogen’s most advanced product candidate IDO 8 is designed for patients with severe haemophilia A who have developed anti-drug antibodies against their critical treatment with coagulation factor VIII (factor VIII). The company´s second project IDO T is developed to prevent kidney transplant rejection. The treatment is based on the patient's own cells and is expected to have a favorable safety profile and long-lasting effect. The fact that a short treatment has the potential to yield a long-lasting effect is another great advantage. For more information, visit www.idogen.com 

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We are very excited about the opportunity to evaluate the potential of Idogen's technology platform in the field of autoimmune diseases. Today, there is a major unmet medical need in patients with current standard treatments, where we believe that Idogen's tolerogenic cell therapy can play an important role. Our focus will be on one or several rare diseases, which allows for the grant of orphan drug designation that can reduce both development costs and time until market approval, as well as extended market exclusivity
Lars Hedbys, CEO Idogen