A Study to Evaluate the Effectiveness, Tolerability and Safety of Laquinimod
Launched by TEVA BRANDED PHARMACEUTICAL PRODUCTS R&D, INC. · Jul 5, 2006
Trial Information
Current as of July 22, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Willing and able to give written informed consent
- • 2. Confirmed MS diagnosis as defined by the McDonald criteria
- • 3. R-R MS disease course.
- • 4. At least one gadolinium-enhanced lesion on screening MRI
- • 5. Women of child-bearing potential must practice a reliable method of birth control.
- • 6. Must understand the requirements of the study and agree to comply with the study protocol.
- Exclusion Criteria:
- • 1. Subjects who suffer from any form of progressive MS.
- • 2. Any condition which the investigator feels may interfere with participation in the study.
- • 3. Subjects with a clinically significant or unstable medical or surgical condition that would preclude safe and complete study participation,
- • 4. Subjects who received any investigational medication, immunosuppressives or cytotoxic agents within 6 months prior to screening
- • 5. Previous treatment with immunomodulators within two months prior to screening
About Teva Branded Pharmaceutical Products R&D, Inc.
Teva Branded Pharmaceutical Products R&D, Inc. is a leading global pharmaceutical company dedicated to the research, development, and commercialization of innovative therapeutic solutions. With a strong emphasis on delivering high-quality medicines across various therapeutic areas, Teva leverages its extensive expertise in drug development and manufacturing to advance healthcare outcomes. The company's commitment to scientific excellence and patient-centric approaches drives its clinical trial initiatives, focusing on addressing unmet medical needs and improving the quality of life for patients worldwide. Through robust partnerships and a comprehensive portfolio, Teva continues to play a pivotal role in the pharmaceutical landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Prof. Giancarlo Comi
Study Chair
Teva Pharmaceutical Industries, Ltd.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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