Calliditas Therapeutics (CALT) has released an update.
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Calliditas Therapeutics has announced that the EMA’s CHMP has recommended full marketing authorization for Kinpeygo in the EU for treating primary IgA nephropathy (IgAN), a rare kidney disease. This endorsement follows the initial conditional approval granted in July 2022, aiming to broaden the treatment to a wider patient population. The European Commission is expected to finalize the decision on marketing authorization by August 2024.
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