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Kiniksa gets FDA orphan drug status for KPL-387, a monthly injectable for recurring pericarditis.
Kiniksa Pharmaceuticals has received FDA orphan drug designation for KPL-387, a potential monthly subcutaneous treatment for pericarditis, including recurrent cases.
The drug, a monoclonal antibody targeting interleukin-1 receptors, aims to address the unmet need in this rare condition.
The designation offers development incentives like tax credits and grant funding.
Phase 2 trial results are expected by late 2026.
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Kiniksa obtiene el estatus de fármaco huérfano de la FDA para KPL-387, una inyección mensual para la pericarditis recurrente.