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NCT05845996 · ClinicalTrials.gov registry record · Phase 1
Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous and Subcutaneous Single and Repeated Doses of SAR441344 in Healthy Adult Subjects
A Phase 1 study, sponsored by Sanofi.
- Completed
- Registry status
- Phase 1
- Development phase
- 56
- Enrollment target
NCT05845996: Completed Phase 1 study, sponsored by Sanofi.
NCT05845996 is a Phase 1 study that has completed, run by Sanofi. The registered enrollment target is 56 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
NCT05845996, a Phase 1 study, has completed, sponsored by Sanofi.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 56 participants
- Enrollment target
Study Summary
Primary Objective is the tolerability and safety of ascending single and repeated intravenous infusion (IV) and/or subcutaneous (SC) administration of SAR441344
Primary Outcome
Number of participants with AE from baseline to day 127
Interventions
- DRUG placebo
- DRUG SAR441344
- BIOLOGICAL Keyhole limpet hemocyanin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2018-11-08 |
| Est. Completion | 2020-04-10 |
| Phase | Phase 1 |
What the finished NCT05845996 record still lists
NCT05845996 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 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 3 interventions - of which placebo is the first listed.
NCT05845996 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05845996 about?
NCT05845996 is a clinical study titled "Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous and Subcutaneous Single and Repeated Doses of SAR441344 in Healthy Adult Subjects". Primary Objective is the tolerability and safety of ascending single and repeated intravenous infusion (IV) and/or subcutaneous (SC) administration of SAR441344
What is the current status of trial NCT05845996?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 56 participants. The study started on 2018-11-08. Estimated completion is 2020-04-10.
What interventions are being tested in trial NCT05845996?
The interventions under investigation include: placebo (DRUG), SAR441344 (DRUG), Keyhole limpet hemocyanin (BIOLOGICAL).
Who is sponsoring clinical trial NCT05845996?
This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05845996's enrollment target sits among peer trials
56 902nd of 2000 higher than 1,083 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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