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What Progress In The Rare Disease, Osteogenesis Imperfecta?

 
• By John Davis

Two-year-old biotech Mereo BioPharma Group plc is planning to start a pivotal Phase IIb study in osteogenesis imperfecta patients in the first-half of this year with its anti-sclerostin antibody, BPS-804, and if the results are promising, EU patients could gain early access through the region’s adaptive pathways program.

Bone structure

Osteogenesis imperfecta, or brittle bone disease, is a rare condition that is more familiar than most to the general public, as it can have a debilitating effect on younger children and be distressing to parents, patients and family members. But the condition has few if any effective therapies on the market or in development, a fact that backs the acceptance of Mereo BioPharma Group Ltd.’s investigational osteogenesis imperfecta product BPS-804 into the European Medicines Agency’s adaptive pathways program, announced Feb. 20.

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