NDASUBCUTANEOUSSOLUTION
Approved
Nov 2002
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
Drug data last refreshed 4h ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
FORTEO (teriparatide) is a subcutaneous parathyroid hormone analog approved by the FDA in November 2002 for osteoporosis treatment. It works by stimulating bone formation through PTH receptor activation, differentiating it from antiresorptive agents that primarily slow bone loss. FORTEO is indicated for patients with osteoporosis at high risk of fracture, particularly those who have failed or are intolerant to other therapies. It represents a unique anabolic mechanism in the osteoporosis treatment landscape.
$0.4BPart D
Mechanism of Action
Pharmacologic Class:
Parathyroid Hormone Analog
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
A Phase 3 Randomized Clinical Trial to Investigate the Safety and Efficacy of Palopegteriparatide at Doses Greater Than 30 μg/Day in Adult Participants With Hypoparathyroidism
Started Apr 2026
36 enrolled
HypoparathyroidismEndocrine System DiseasesParathyroid Diseases
A Study to Assess the Amount of Palopegteriparatide in Breast Milk of Lactating Females Requiring YORVIPATH® (Palopegteriparatide)
Started Mar 2026
10 enrolled
Hypoparathyroidism
A Global Pregnancy Registry to Assess Maternal, Fetal, and Infant Outcomes Following Exposure to YORVIPATH® (Palopegteriparatide) During Pregnancy and Breastfeeding
Started Feb 2026
50 enrolled
Hypoparathyroidism
Assess Safety and Compare PK of New Oral hPTH(1-34) Tablet Formulations vs. EBP05 Tablets and Subcutaneous Forteo
Started May 2023
45 enrolled
HypoparathyroidismOsteoporosisFractures, Bone+1 more
Fracture Recovery for Returning to Duty (Teriparatide STRONG)
Started Dec 2022
183 enrolled
Stress Fracture of Tibia or Fibula
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.