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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
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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