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Search / Trial NCT00035529

A Study to Evaluate the Preliminary Efficacy Pharmacokinetics and Immunogenicity of BMS-188667 Administered to Subjects With Relapsing-remitting Multiple Sclerosis

Launched by BRISTOL-MYERS SQUIBB · May 3, 2002

Trial Information

Current as of May 22, 2025

Terminated

Keywords

Ms

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion
  • relapsing-remitting MS
  • at least 1 exacerbation in preceding 2 years
  • at least 1 MRI lesion
  • stable for 2 months prior to dosing
  • Exclusion
  • progressive MS
  • currently treated with an immunomodulatory therapy
  • previously treated with an approved MS drug where treatment was discontinued for lack of efficacy
  • active bacterial or viral infections

About Bristol Myers Squibb

Bristol-Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a robust portfolio of products across multiple therapeutic areas, including oncology, immunology, cardiovascular, and fibrotic diseases, BMS emphasizes cutting-edge research and a commitment to advancing medical science through clinical trials. The company is driven by a mission to provide transformative therapies, leveraging collaboration and scientific expertise to address unmet medical needs and improve patient outcomes worldwide.

Locations

New Haven, Connecticut, United States

Louisville, Kentucky, United States

Worcester, Massachusetts, United States

Newark, New Jersey, United States

New York, New York, United States

Charlotte, North Carolina, United States

Philadelphia, Pennsylvania, United States

Dallas, Texas, United States

Burlington, Vermont, United States

Madison, Wisconsin, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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