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Search / Trial NCT00292253

Tolerability of Rebif® Injection With and Without the Use of Rebiject™Mini in Relapsing-Remitting Multiple Sclerosis Subjects

Launched by EMD SERONO · Feb 13, 2006

Trial Information

Current as of June 01, 2025

Completed

Keywords

Ms

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Greater than or equal to 18 years of age
  • Has relapsing-remitting MS
  • Are willing and able to comply with the protocol for the duration of the study
  • Exclusion Criteria:
  • Has significant leukopenia/lymphopenia (white blood cell count less than (\<) 0.5 times the lower limit of normal)
  • Has elevated liver function tests (aspartate aminotransferase \[AST\], Alanine transaminase \[ALT\], or alkaline phosphatase greater than (\>) 2 times the upper limit of normal or total bilirubin \> 1.5 times the upper limit of normal)
  • Has an allergy to human serum albumin or mannitol
  • Had treatment with an investigational product or procedure within 3 months
  • Has the presence of systemic disease or abnormal laboratory findings that might interfere with subject safety, compliance or evaluation of the condition under study
  • Has concomitant use of Avonex®, Betaseron®, Copaxone®, or Novantrone®

About Emd Serono

EMD Serono, a subsidiary of Merck KGaA, Darmstadt, Germany, is a leading global biopharmaceutical company dedicated to advancing patient care through innovative therapies in oncology, neurology, and endocrinology. Committed to scientific excellence and patient-centered approaches, EMD Serono focuses on developing cutting-edge medicines and solutions that address unmet medical needs. With a robust pipeline and a strong emphasis on research and development, the company collaborates with healthcare professionals and stakeholders worldwide to enhance treatment options and improve outcomes for patients.

Locations

Patients applied

0 patients applied

Trial Officials

Maria Lopez-Bresnahan, M.D.

Study Director

Merck Serono International SA

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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