Clinical trial

Study To Evaluate The Immunogenicity And Safety Of r-hIFN Beta-1a (Rebif®) Using…

NCT00367484 · Merck KGaA, Darmstadt, Germany, Industry · Completed

Key facts

NCT number NCT00367484
Title Study To Evaluate The Immunogenicity And Safety Of r-hIFN Beta-1a (Rebif®) Using Clone 484-39 In Multiple Sclerosis
Official title Multicentre, Single Arm, Open, Phase IV Study To Evaluate Immunogenicity And Safety Of Subcutaneous r-hIFN Beta-1a (Rebif®) Using Clone 484-39 In The Treatment Of Relapsing Remitting Multiple Sclerosis
Lead sponsor Merck KGaA, Darmstadt, Germany, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Relapsing Remitting Multiple Sclerosis
Intervention type Biological
Interventions Rebif® (clone 484-39)
Enrollment 460
Start date May 1, 2004
Primary completion Jan 1, 2006
Completion Jan 1, 2006
First posted Aug 23, 2006
Last update posted Feb 27, 2014

At a glance

  • Yes 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:

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