Clinical trial

Immunogenicity and Safety of Concomitant Administration of MMR™ rHA and VARIVAX®…

NCT00432523 · Merck Sharp & Dohme LLC, Industry · Completed

Key facts

NCT number NCT00432523
Title Immunogenicity and Safety of Concomitant Administration of MMR™ rHA and VARIVAX® by Intramuscular Versus Subcutaneous Route (V205C-011)
Official title An Open, Randomised, Comparative, Multicentre Study of the Immunogenicity and Safety of M-M-R™II Manufactured With Recombinant Human Albumin (rHA) and VARIVAX® When Administered Concomitantly by Intramuscular (IM) Route or Subcutaneous (SC) Route at Two Separate Injection Sites in Healthy Subjects…
Lead sponsor Merck Sharp & Dohme LLC, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Measles, Mumps, Varicella
Intervention type Biological
Interventions M-M-R™II manufactured with recombinant Human Albumin (rHA) and VARIVAX®
Enrollment 752
Start date Jan 20, 2005
Primary completion Sep 5, 2005
Completion Sep 5, 2005
First posted Feb 8, 2007
Last update posted Oct 18, 2021
Countries France, Germany

At a glance

  • No 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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