drugset / Trial / NCT06531941
Extension Study to Evaluate the Long-Term Safety and Tolerability of MBX 2109 in Patients With Hypoparathyroidism
Non-randomizedCrossoverOpen-labelTreatment
Summary
The purpose of this study is to evaluate the long-term safety and tolerability of MBX 2109 in patients with hypoparathyroidism who completed the 12-week treatment period in the Phase 2 study, MBX-2H1002.
Timeline
- Start
- 2024-10-31
- Primary completion
- 2027-05-27
- Completion
- 2027-05-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Canvuparatide | Protein / enzyme biologic | 200 ug | Subcutaneous |
| Subject | Canvuparatide | Protein / enzyme biologic | 400 ug | Subcutaneous |
| Subject | Canvuparatide | Protein / enzyme biologic | 1600 ug | Subcutaneous |