Argenx looks for quick label expansion for subcutaneous Vyvgart with PhII data — shares soar
Less than a month after argenx first landed approval of the subcutaneous version of its top drug, the Dutch biotech has notched another win in another rare disease.
The positive data come from a Phase II study of Vyvgart Hytrulo in chronic inflammatory demyelinating polyneuropathy (CIDP), where the drug slashed the risk of relapse by 61% versus placebo (p=0.000039), meeting the primary endpoint in Stage B of the trial, which involved 221 patients.
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