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NCT01756950 · ClinicalTrials.gov registry record · Phase 1
Assessment of CR8020, a Monoclonal Antibody Against Influenza A Viruses
A Phase 1 study, sponsored by Crucell Holland.
- Completed
- Registry status
- Phase 1
- Development phase
- 64
- Enrollment target
NCT01756950: Completed Phase 1 study, sponsored by Crucell Holland.
NCT01756950 is a Phase 1 study that has completed, run by Crucell Holland. The registered enrollment target is 64 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01756950, a Phase 1 study, has completed, sponsored by Crucell Holland.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 64 participants
- Enrollment target
Study Summary
The purpose of this study is to assess in healthy subjects the safety, tolerability, pharmacokinetics and immunogenicity of single escalating doses of CR8020, a monoclonal antibody against influenza A viruses.
Interventions
- BIOLOGICAL 2 mg/kg CR8020
- BIOLOGICAL 5 mg/kg CR8020
- BIOLOGICAL 15 mg/kg CR8020
- BIOLOGICAL 30 mg/kg CR8020
- BIOLOGICAL 50 mg/kg CR8020
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2013-01 |
| Est. Completion | 2013-11 |
| Phase | Phase 1 |
What the finished NCT01756950 record still lists
NCT01756950 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 5 interventions - of which 2 mg/kg CR8020 is the first listed.
NCT01756950 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01756950 about?
NCT01756950 is a clinical study titled "Assessment of CR8020, a Monoclonal Antibody Against Influenza A Viruses". The purpose of this study is to assess in healthy subjects the safety, tolerability, pharmacokinetics and immunogenicity of single escalating doses of CR8020, a monoclonal antibody against influenza A viruses.
What is the current status of trial NCT01756950?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2013-01. Estimated completion is 2013-11.
What interventions are being tested in trial NCT01756950?
The interventions under investigation include: 2 mg/kg CR8020 (BIOLOGICAL), 5 mg/kg CR8020 (BIOLOGICAL), 15 mg/kg CR8020 (BIOLOGICAL), 30 mg/kg CR8020 (BIOLOGICAL), 50 mg/kg CR8020 (BIOLOGICAL).
Who is sponsoring clinical trial NCT01756950?
This trial is sponsored by Crucell Holland, which has 10 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01756950's enrollment target sits among peer trials
64 808th of 2000 higher than 1,181 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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