Imara initiates Phase I clinical study of IMR-687 to treat sickle-cell disease

US-based biotechnology company Imara has initiated its Phase I clinical study of IMR-687 to treat patients with sickle-cell disease and other haemoglobinopathies.

IMR-687 is an orally administered, highly potent candidate developed to selectively inhibit phosphodiesterase-9 (PDE9i) in blood cells.

The inhibition of PDE9 reduces white blood cell stickiness that prevents blockage of blood vessels.

Sickle-cell disease is a rarely occurring, genetically inherited condition that alters haemoglobin, which is responsible for transporting oxygen throughout the body.

Altered haemoglobin distorts red blood cells into a stiff and inflexible sickle, or crescent, which gets stuck in small blood vessels.

The condition prevents blood carrying oxygen from reaching tissues and organs, thereby leading to vaso-occlusive crisis (VOC), acute chest syndrome (ACS), and permanent damage to organs including the liver, spleen, kidney and brain.

The Phase I clinical study is being conducted to assess the safety and tolerability of Imara’s lead product candidate, IMR-687.

Imara founder, president and CEO James McArthur said: “More than 160,000 individuals are living with sickle-cell disease in the United States and Europe with many more in Africa and Asia, yet, there remains a serious medical need facing those whose lives are burdened by this devastating disease.

“Initiating this first study in humans is a critically important milestone as we work to advance new therapies for people living with sickle-cell disease.”

Preclinical studies have suggested the efficacy of IMR-687 in reducing both the sickling of red blood cells and blood vessel occlusion.

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Image: Human blood with normal and sickle-shaped cells. Photo: courtesy of Dr Graham Beards.