GLASSIA Infusion Rate Study
A Phase 4 Double-Blind Study to Assess the Safety and Tolerability of Intravenous Administration of GLASSIA in Healthy Adult Volunteers
Sponsor: Baxalta now part of Shire
A PHASE4 clinical study on Alpha1-antitrypsin Deficiency and Healthy Volunteers, this trial is completed. The trial is conducted by Baxalta now part of Shire and has accumulated 12 data snapshots since 2012. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
12 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE4
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE4
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Jan 2023 — Jul 2024 [monthly]
Completed PHASE4
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Dec 2022 — Jan 2023 [monthly]
Completed PHASE4
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Dec 2021 — Dec 2022 [monthly]
Completed PHASE4
▶ Show 7 earlier versions
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Jun 2021 — Dec 2021 [monthly]
Completed PHASE4
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Jan 2021 — Jun 2021 [monthly]
Completed PHASE4
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE4
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Mar 2018 — Jun 2018 [monthly]
Completed PHASE4
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Dec 2017 — Mar 2018 [monthly]
Completed PHASE4
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Feb 2017 — Dec 2017 [monthly]
Completed PHASE4
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE4
First recorded
Jul 2012
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Baxalta now part of Shire
For direct contact, visit the study record on ClinicalTrials.gov .