AnGes

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about AnGes

Aiming to be a global leader in genetic medicine

In December 1999, AnGes was founded with the aim of developing drugs based on the action of the hepatocyte growth factor (HGF) gene to regenerate blood vessels. The name AnGes was inspired by the English name Angiogenesis, meaning the creation of new blood vessels, and by the desire to be an Ange (French for angel) that delivers new and unprecedented drugs for intractable diseases. This desire has always been held by both the founder and employees.

The concept of treatment called angiogenesis was "unprecedented" at the time. In March 2019, after 20 years of challenges and hard work, AnGes received conditional and time-limited approval as the world's first genetic medicine product using plasmid DNA technology to regenerate blood vessels.
Meanwhile, based on the Global Vascular Guideline published by the Society of Vascular Surgeons of the United States, Europe, and Asia/Oceania in June 2019, we conducted a late stage Phase II clinical trial in mild to moderate arteriosclerosis obliterans with leg ulcers in the United States, and obtained favorable results.
Based on these results, we aim to file for approval in Japan for the treatment of ulcers in a wide range of patients with arteriosclerosis obliterans, regardless of the severity of the disease.

The probability of success in new drug development is said to be one in 30,000, but the fact that we were the first domestic bio-venture to bring an autologous product to market gives us great confidence and further encouragement. At the same time, I feel that it is an important mission to deliver this drug to patients suffering from ischemic diseases around the world, not only in Japan but also overseas.

In Japan, drug loss and drug lag have recently become an issue. While new drugs and treatment methods are being developed one after another in the world, there are many diseases for which there is no treatment available in Japan. As one response to this problem, we acquired the exclusive rights to market Zokinvy, a treatment for Progeria, in Japan, and began sales in May 2024.

In addition, at ACRL, which opened in 2021, We are engaged in screening tests to investigate the possibility of rare genetic diseases for which early detection and treatment are important. With a testing system based on global-standard target diseases, facilities, and technologies, we are increasing the number of orders every year.
In addition, ACRL began contract genetic testing in conjunction with the launch of Zokinvy, and is also engaged in biomarker testing.

At the forefront of research and development as a new treatment method is the technology of genome editing. We entered the development of genome editing by making EmendoBio a subsidiary in 2020. Genome editing is being developed mainly in the U.S. and has begun to be put to practical use as a treatment method for diseases for which there was no cure until now.
EmendoBio's proprietary OMNI nuclease technology is also being used in the development of cutting-edge cancer therapies.

We are committed to the development of genetic medicine with a global perspective and the introduction of therapeutic drugs in Japan, and to meeting the expectations of our stakeholders, including patients and their families who are waiting for new therapeutic drugs and methods of treatment, by developing genome editing technology, identifying diseases before they develop, and providing treatment opportunities. In addition to meeting the expectations of our stakeholders, including patients and their families who are waiting for new treatments and therapies, we will continue to contribute to the realization of healthy lifestyles.

Finally, we would like to thank you for your continued patronage and look forward to your continued support.

Ei Yamada, President & CEO

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