Argenx's Vyvgart Long-Term Treatment Shows Improved gMG Disease Scores - argenx (NASDAQ:ARGX)

Argenx SE (NASDAQ:ARGX) announced interim results from ADAPT+ Phase 3 extension study evaluating Vyvgart (efgartigimod alfa-fcab) for generalized myasthenia gravis (gMG).

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Argenx SE (NASDAQ:ARGX) announced interim results from ADAPT+ Phase 3 extension study evaluating Vyvgart (efgartigimod alfa-fcab) for generalized myasthenia gravis (gMG).

The data from the three-year extension study will be presented at the 74th Annual Meeting of the American Academy of Neurology.
139 patients received at least one dose of Vyvgart in ADAPT+. As of the interim analysis, the mean treatment duration was 363 days. Efficacy analyses were based on 106 anti-acetylcholine receptor (AChR) antibody-positive patients.
Patients who continued long-term treatment with Vyvgart experienced consistent and clinically meaningful improvement on the Myasthenia Gravis Activities of Daily Living (MG-ADL) and Quantitative Myasthenia Gravis (QMG) scales.
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Mean improvements on MG-ADL and QMG scales from five treatment cycles were 5.1 and 4.7, respectively, and remained consistent.
The safety profile of long-term treatment (up to 10 treatment cycles) with Vyvgart continued to be favorable.
Vyvgart was well-tolerated with a consistent safety profile to the ADAPT trial and during the COVID-19 global pandemic.
The majority of adverse events were mild to moderate in severity.
Price Action: ARGX shares closed 0.30% lower at $324.41 on Monday.

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