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NCT02089087 · ClinicalTrials.gov registry record · Phase 1
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Dose CFZ533 in Rheumatoid Arthritis Patients
A Phase 1 study of Rheumatoid Arthritis, sponsored by Novartis Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 75
- Enrollment target
- 6
- Study locations
NCT02089087 is a Phase 1 study of Rheumatoid Arthritis that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 75 participants, below the 4,690-participant average among 197 other Rheumatoid Arthritis trials with a reported enrollment target (98% lower). The trial reports 6 study locations across 5 states.
The verdict
NCT02089087, a Phase 1 study of Rheumatoid Arthritis, has completed, sponsored by Novartis Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 75 participants
- Enrollment target
- 6
- Study locations
Study Summary
This is a first-in-human study to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous and subcutaneous doses of CFZ533 in healthy subjects and intravenous doses in rheumatoid arthritis patients.
Conditions Studied
Interventions
- DRUG Placebo
- BIOLOGICAL CFZ533
Study Locations (6)
Florida
- Novartis Investigative Site - Miami
- Novartis Investigative Site - South Miami
Alabama
- Novartis Investigative Site - Anniston
Nebraska
- Novartis Investigative Site - Lincoln
Pennsylvania
- Novartis Investigative Site - Duncansville
Other
- Novartis Investigative Site - Taipei
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2013-01-07 |
| Est. Completion | 2017-02-03 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02089087
The ClinicalTrials.gov registry entry for NCT02089087 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,690-participant average among 197 other Rheumatoid Arthritis trials with a reported enrollment target (98% lower). The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Rheumatoid Arthritis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT02089087 reports 6 study locations spanning 5 distinct geographic areas - top geographies include Florida, Alabama, Nebraska.
Frequently Asked Questions
What is clinical trial NCT02089087 about?
NCT02089087 is a clinical study titled "Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Dose CFZ533 in Rheumatoid Arthritis Patients". This is a first-in-human study to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous and subcutaneous doses of CFZ533 in healthy subjects and intravenous doses in rheumatoid arthritis patients.
What is the current status of trial NCT02089087?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 75 participants. The study started on 2013-01-07. Estimated completion is 2017-02-03.
What conditions does trial NCT02089087 study?
This clinical trial studies the following conditions: Rheumatoid Arthritis.
What interventions are being tested in trial NCT02089087?
The interventions under investigation include: Placebo (DRUG), CFZ533 (BIOLOGICAL).
Who is sponsoring clinical trial NCT02089087?
This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02089087 being conducted?
This trial has 6 study locations across Alabama, Florida, Nebraska, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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