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Ascendis Pharma A/S Announces Phase 3 PaTHway Trial of TransCon™ PTH in Adults with Hypoparathyroidism Met Primary and All Key Secondary Endpoints

– For the primary composite endpoint, TransCon PTH demonstrated a response rate of 78.7% compared to 4.8% for control . – TransCon PTH demonstrated statistically. | March 13, 2022

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Ascendis Pharma A/S Announces Phase 3 PaTHway Trial of

– For the primary composite endpoint, TransCon PTH demonstrated a response rate of 78.7% compared to 4.8% for control (p-value <0.0001). – TransCon.

United statesNew jerseyPalo altoRedwood cityBaden wübergAimee shuAscendis pharmaOutcomes trust incAscendis pharma groupDial in internationalAscendis pharma hp patient experience researchExchange commissionUs food drug administration for transconEuropean unionEuropean medicines agencyClinical development

Ascendis Pharma A/S Announces Mean Bone Mineral Density

Ascendis Pharma A/S Announces Mean Bone Mineral Density
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Ascendis Pharma A/S Announces Expansion of Global Clinical Reach for TransCon™ PTH with Filing of the Clinical Trial Notification for Phase 3 Clinical Trial in Adults with Hypoparathyroidism in Japan

Ascendis Pharma A/S Announces Expansion of Global Clinical Reach for TransCon™ PTH with Filing of the Clinical Trial Notification for Phase 3 Clinical Trial in Adults with Hypoparathyroidism in Japan
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Ascendis Pharma A/S Presents 6-Month Open-Label Extension Data from Phase 2 PaTH Forward Trial

Ascendis Pharma A/S Presents 6-Month Open-Label Extension Data from Phase 2 PaTH Forward Trial
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