These Patients Struggle With Runaway Bones. Finally There’s Hope.
Why This Matters
Key context: Jordyn Bugarin, who lives with fibrodysplasia ossificans progressiva, or F.O.P., a rare genetic disorder that slowly turns muscle and connective tissue into bone, was in a clinical trial for a monoclonal antibody treatment for the condition. This development from The New York Times highlights ongoing changes in the sector.
Jordyn Bugarin, who lives with fibrodysplasia ossificans progressiva, or F.O.P., a rare genetic disorder that slowly turns muscle and connective tissue into bone, was in a clinical trial for a monoclonal antibody treatment for the condition.
Curation & Context
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