Human medicines European public assessment report (EPAR): Yorvipath, Palopegteriparatide, Date of authorisation: 17/11/2023, Status: Authorised
Overview
On 14 September 2023, the Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Yorvipath1, intended for the treatment of chronic hypoparathyroidism in adults. The applicant for this medicinal product is Ascendis Pharma Bone Diseases A/S.
Yorvipath will be available as 168 µg/0.56 ml, 294 µg/0.98 ml and 420 µg/1.4 ml solutions for injection. The active substance of Yorvipath is palopegteriparatide, a transiently pegylated parathyroid hormone (ATC code: H05AA05) that in the body dissociates into parathyroid hormone and binds to and activates cell-surface parathyroid hormone receptors (PTH1R) similar to endogenous parathyroid hormone.
The benefits of Yorvipath are the achievement of serum and urinary calcium levels in the normal range and independence from conventional therapy, as observed in a phase 3, double blind, placebo controlled study in adult patients with hypoparathyrodism. The most common side effects are injection site reactions, headache, and paraesthesia. Hypercalcaemia may occur, especially when starting Yorvipath or when increasing the dose, and patients should be monitored for signs and symptoms of hypercalcaemia.
The full indication is:
Yorvipath is a parathyroid hormone (PTH) replacement therapy indicated for the treatment of adults with chronic hypoparathyroidism.
Yorvipath should be initiated and monitored by physicians experienced in the diagnosis and treatment of patients with hypoparathyroidism.
Detailed recommendations for the use of this product will be described in the summary of product characteristics (SmPC), which will be published in the European public assessment report (EPAR) and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.
1This product was designated as an orphan medicine during its development. EMA will now review the information available to date to determine if the orphan designation can be maintained
CHMP summary of positive for Yorvipath
DraftFirst published: Reference Number: EMA/CHMP/405555/2023
Product details
- Name of medicine
Yorvipath
- Active substance
palopegteriparatide
- International proprietary name (INN) or common name
Palopegteriparatide
- Therapeutic area (MeSH)
Hypoparathyroidism
- EMA product number
EMEA/H/C/005934
This medicine was designated an orphan medicine. This means that it was developed for use against a rare, life-threatening or chronically debilitating condition or, for economic reasons, it would be unlikely to have been developed without incentives. For more information, see Orphan designation.
- Marketing authorisation applicant
Ascendis Pharma Bone Diseases A/S
- Opinion adopted
14/09/2023
- Opinion status
Positive
This page was last updated on
Share this page
Legal Disclaimer:
EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.
