An Open-label Study Investigating the Safety and Efficacy of rhPTH (1-84) in Subjects with Hypoparathyroidism
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
This study is designed to evaluate the safety and efficacy of 52 weeks of once-daily subcutaneous injections of rhPTH (1-84) for subjects who have previously been exposed to rhPTH (1-84) in the SHP634-101 (IRB 1701082476).
Description
This study is designed to evaluate the safety and efficacy of 52 weeks of once-daily subcutaneous injections of rhPTH (1-84) for subjects who have previously been exposed to rhPTH (1-84) in the SHP634-101 (IRB 1701082476).
Details
| Condition | hypoparathyroidism |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX8969 |
| Last Modified on | 19 February 2024 |
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