ong-Term Safety and Efficacy Study of Oral BG00012 Monotherapy in Relapsing-Remitting Multiple Sclerosis

Phase 1

• Conditions: Relapsing-Remitting Multiple Sclerosis; MedDRA version: 20.0Level: PTClassification code 10063399Term: Relapsing-remitting multiple sclerosisSystem Organ Class: 10029205 - Nervous system disorders; Therapeutic area: Diseases [C] - Nervous System Diseases [C10]

• Registration Number: EUCTR2008-004753-14-GB
• Lead Sponsor: Biogen Idec Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-11-09
• Last Update Posted: 25 May 2020

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 1700

Inclusion Criteria

1. Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local subject privacy regulations.

2. Subjects who participated in and completed as per protocol previous
BG00012 clinical studies 109MS301 or 109MS302, including those
subjects who received an open-label, approved MS therapy and
completed the modified visit schedule.

3. All male subjects and female subjects of childbearing potential must
practice effective contraception during the study and be willing and able
to continue contraception for 30 days after their last dose of study
treatment.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 1700
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1. Any significant change in medical history in subjects from 109MS301
or 109MS302, including laboratory tests, or current clinically significant
condition that in the opinion of the Investigator would have excluded the subjects' participation from their previous study. The Investigator must re-review the subject's medical fitness for participation and
consider any diseases that would preclude treatment.

2. Subjects from 109MS301 or 109MS302 who discontinued oral study
treatment due to an AE or due to reasons other than protocol-defined
relapse/disability progression.

3. Subjects from 109MS301 or 109MS302 who discontinued study
treatment due to disability progression or relapses and did not follow the modified visit schedule up to Week 96.

4. History of malignancy.

5. History of severe allergic or anaphylactic reactions.

6. Alanine transaminase (ALT), aspartate transaminase (AST), or
gamma-glutamyltransferase (GGT) >3 times the upper limit of normal
(ULN).

7. Female subjects considering becoming pregnant while in the study,
currently pregnant, or breast feeding.

8. Previous participation in this study (109MS303).

9. Unwillingness or inability to comply with the requirements of the
protocol including the presence of any condition (physical, mental, or
social) that is likely to affect the subject's ability to comply with the
protocol.

10. Other unspecified reasons that, in the opinion of the Investigator or
Biogen Idec, make the subject unsuitable for enrollment.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified