A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability and Efficacy of NBI-5788 in Patients With Relapsing Multiple Sclerosis
Data Collection
Autoimmune Diseases+6
+ Demyelinating Diseases
+ Immune System Diseases
Treatment Study
Summary
Study start date: July 1, 2003
Actual date on which the first participant was enrolled.This is a multicenter, randomized, double-blind, placebo-controlled trial in which qualifying patients will be randomized 2:1 to receive active drug or placebo. Eligible patients must have MS with relapse, have had one or more relapses during the prior 2 years, 1-10 gadolinium (Gd)-enhancing lesions on the Run-in MRI, and an EDSS of 6.5 or less. There are exclusions for certain prior MS treatments and medical / psychiatric conditions. Following a 4-week run-in phase in which patients will have a baseline MRI, patients will enter a 4 week induction phase, during which they will be receive injections weekly (5 doses), then a 32-week maintenance phase during which injections are monthly (8 doses). A final follow-up visit will be conducted 4 weeks after the last injection. The primary efficacy parameter is a summary change score of the mean number of total Gd-enhancing lesions at weeks 36 and 40 minus the mean number for the two baseline scans. Safety monitoring will include AE/SAE reporting, physical exams, vital signs, ECG. CXR, laboratory tests, neurologic evaluations, and systemic hypersensitivity and injection site assessments. All study medications will be administered by study personnel and patients will remain under observation for a minimum of 2 hours post-injection. An independent Data Safety and Monitoring Board will oversee the safety of the trial.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.150 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 55 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Male or female, 18 to 55 years of age * Diagnosed with relapsing multiple sclerosis, with at least one relapse in the last two years * Females must not plan on becoming pregnant * Females must either be post-menopausal, surgically incapable of bearing children, or practicing an acceptable method of birth control and willing to continue birth control until 30 days after the last dose of study drug * Males must not intend to impregnate a partner during the study or for 30 days after the study and must also practice acceptable birth control with their partners Exclusion Criteria: * Significant long-lasting disease of the immune system other than multiple sclerosis * Past or current medical disease (heart, liver, kidney, etc.) including severe asthma, cancer or advancing brain or spinal cord disorder * Known or suspected long-lasting infectious disease including HIV, hepatitis B, or hepatitis C * Treatment with certain steroid or hormone medications within 30 days before the pre-study MRI scan * Treatment with other medications that suppress the immune system within 6 months before the pre-study MRI scan * Certain treatments and medications are not allowed * Laboratory and other tests will be performed to determine further eligibility * History of drug or alcohol abuse in the last year * History of medical or psychiatric condition that could pose a risk for participation in the study * Females who are pregnant or breast feeding * Participation in any other trial of an investigational agent within 90 days before the start of the study * History of not following instructions with past therapy.