Ignite Creation Date:
2024-05-05 @ 12:07 PM
Last Modification Date:
2024-10-26 @ 9:20 AM
Study NCT ID:
NCT00240032
Status:
COMPLETED
Last Update Posted:
2011-04-11
First Post:
2005-10-13
Brief Title:
A Study to Evaluate the Impact on Skin Injection Site Reactions of Taking an Antihistamine Zyrtec or Placebo Prior to Daily Injections of Copaxone
Sponsor:
Organization:
Teva Branded Pharmaceutical Products RD Inc
Study Design
Study Type:
INTERVENTIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
None
Target Duration:
None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
None
Bio Spec Description:
None
Enrollment Count:
80
Enrollment Type:
ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
| Name |
|---|
| PHASE4 |
Observational Models:
Time Perspective List:
Who Masked List: