US FDA approves Bluebird Bio’s gene therapy for rare neurological disorder

The approval was largely expected after the drug received unanimous endorsement from a panel of outside advisers to the FDA in June
US FDA approves Bluebird Bio’s gene therapy for rare neurological disorder

Bluebird said it anticipates commercial product will be available by the end of 2022 through a limited number of qualified treatment centres in the US.

In August, the company’s beti-cel therapy secured FDA approval to treat a rare blood disorder that was priced at a record $2.8 million, the most expensive treatment to date.

CALD is caused by mutations in a gene called ABCD1 that leads to the buildup of very long-chain fatty acids in the brain and spinal cord. It typically occurs in boys between the ages of three and 12 years.

Eli-cel adds functional copies of the ABCD1 gene in a patient’s stem cells to help produce a protein required to break down the long-chain fatty acids.

The approval was largely expected after the drug received unanimous endorsement from a panel of outside advisers to the FDA in June.

Bluebird biogene therapyUS FDA approval
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