- Ascendis Pharma A/S' ASND stock is down 28% Monday morning as the FDA has notified deficiencies in its marketing application for TransCon PTH (palopegteriparatide) in hypoparathyroidism.
- The deficiencies were not disclosed in the letter. The FDA also stated that this does not reflect their final regulatory decision on the company's application.
- "This development a month from the agency's PDUFA action date may lead to a delay in the FDA's final regulatory decision on the TransCon PTH NDA," said Jan Mikkelsen, Ascendis Pharma's President and Chief Executive Officer.
- To date, 145 out of 154 clinical trial participants continue to be treated with TransCon PTH in Phase 2 and Phase 3 clinical trial open-label extensions.
- TransCon PTH has been generally well tolerated, with no discontinuations related to the study drug, the company said.
- As expected, Ascendis has received the comprehensive Day 120 response from the European Medicines Agency in Europe.
- The Copenhagen, Denmark-based company remains on track for a European Commission decision on the Marketing Authorisation Application for TransCon PTH during the fourth quarter of 2023.
- If approved, Ascendis expects its first European country launch in early 2024.
- Price Action: ASND shares are down 27.93% at $77.27 on the last check Monday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
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