Clinical trial
A Study of Plasma-Derived Human Butyrylcholinesterase Administered…
NCT00333528 · Baxalta now part of Shire, Industry · Completed
Key facts
| NCT number | NCT00333528 |
|---|---|
| Title | A Study of Plasma-Derived Human Butyrylcholinesterase Administered Intramuscularly |
| Official title | A Phase 1, Randomized, Observer-Blinded, Single Dose, Placebo Controlled Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Plasma-Derived Human Butyrylcholinesterase (HuBChE) Administered Intramuscularly (IM) |
| Lead sponsor | Baxalta now part of Shire, Industry |
| Collaborators | DynPort Vaccine Company LLC, A GDIT Company Industry |
| Status | Completed |
| Phase | Phase 1 |
| Study type | Interventional |
| Conditions | Healthy Volunteers |
| Intervention type | Drug |
| Interventions | Human butyrylcholinesterase (HuBChE) derived from human plasma, Placebo: Normal saline |
| Enrollment | 8 |
| Start date | Dec 1, 2007 |
| Primary completion | Apr 1, 2008 |
| Completion | Aug 1, 2008 |
| First posted | Jun 5, 2006 |
| Last update posted | May 5, 2021 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: