TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

YORVIPATH

PALOPEGTERIPARATIDE
Metabolic Approved 2024-08-09
1
Indication
--
Phase 3 Trials
1
Priority Reviews
1
Years on Market

Details

Status
Prescription
First Approved
2024-08-09
Routes
SUBCUTANEOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: PALOPEGTERIPARATIDE

YORVIPATH Approval History

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What YORVIPATH Treats

1 indications

YORVIPATH is approved for 1 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Hypoparathyroidism
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

YORVIPATH FDA Label Details

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Indications & Usage

FDA Label (PDF)

YORVIPATH is indicated for the treatment of hypoparathyroidism in adults. YORVIPATH is a parathyroid hormone analog (PTH(1-34)) indicated for the treatment of hypoparathyroidism in adults. Limitations of Use : Not studied for acute post-surgical hypoparathyroidism. Titration scheme only evaluated in adults who first achieved an albumin-corrected serum calcium of at least 7.8 mg/dL using calcium and active vitamin D treatment. Limitations of Use YORVIPATH was not studied for acute post-surgical hypoparathyroidism. YORVIPATH's titration scheme was only evaluated in adults who first achieved an a...

YORVIPATH Patents & Exclusivity

Latest Patent: Nov 2042
Exclusivity: Aug 2031

Patents (81 active)

US12403182 Expires Nov 12, 2042
US12453778 Expires Sep 28, 2037
US12295989 Expires Sep 28, 2037
US11857603 Expires Sep 28, 2037
US11590207 Expires Sep 28, 2037
US11890326 Expires Sep 28, 2037
US11759504 Expires Sep 28, 2037
US11918628 Expires Sep 28, 2037
US8906847 Expires Apr 30, 2031
+ 71 more patents

Exclusivity

NCE Until Aug 2029
ODE-492 Until Aug 2031
NCE Until Aug 2029
ODE-492 Until Aug 2031
NCE Until Aug 2029
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.