A Study Evaluating the Real World Experience of Participants Treated With BRIUMVI® (Ublituximab-xiiy) for Relapsing Multiple Sclerosis (RMS) (ENABLE)
REal World ExperieNce With BRIUMVI® (UblituximAB-xiiy) Treated Patients: A Longitudinal REgistry Study (ENABLE)
The purpose of this study is to evaluate safety, effiectiveness, and to gain insight into the treatment experience of participants prescribed BRIUMVI® (ublituximab-xiiy) in the real-world setting
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: TG Therapeutics Clinical Support Team
- Phone Number: 1-877-575-8489
- Email: clinicalsupport@tgtxinc.com
Study Locations
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Guaynabo, Puerto Rico, 00968
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- TG Therapeutics Investigational Trial Site
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London, United Kingdom, SW170QT
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Alabama
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Birmingham, Alabama, United States, 35209
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Cullman, Alabama, United States, 35058
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Huntsville, Alabama, United States, 35802
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Mobile, Alabama, United States, 36604
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Arizona
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Gilbert, Arizona, United States, 85297
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Phoenix, Arizona, United States, 85032
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Scottsdale, Arizona, United States, 85253
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California
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Fresno, California, United States, 93720
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Newport Beach, California, United States, 92663
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Orange, California, United States, 68130
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West Hollywood, California, United States, 90048
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Colorado
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Aurora, Colorado, United States, 80045
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Basalt, Colorado, United States, 81621
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Colorado Springs, Colorado, United States, 80918
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Colorado Springs, Colorado, United States, 80920
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Denver, Colorado, United States, 80222
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Fort Collins, Colorado, United States, 80528
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Grand Junction, Colorado, United States, 81501
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Connecticut
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Farmington, Connecticut, United States, 06032
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Hartford, Connecticut, United States, 06112
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District of Columbia
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Washington D.C., District of Columbia, United States, 20010
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Florida
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Altamonte Springs, Florida, United States, 32714
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Boca Raton, Florida, United States, 33486
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Clearwater, Florida, United States, 33761
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Gainesville, Florida, United States, 32611
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Maitland, Florida, United States, 32751
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Miami, Florida, United States, 33176
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Naples, Florida, United States, 34105
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Orlando, Florida, United States, 32806
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Pensacola, Florida, United States, 32504
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Weston, Florida, United States, 33331
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Georgia
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Atlanta, Georgia, United States, 30309
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Atlanta, Georgia, United States, 30327
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Savannah, Georgia, United States, 31406
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Smyrna, Georgia, United States, 30080
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Hawaii
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Honolulu, Hawaii, United States, 96817
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Idaho
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Coeur d'Alene, Idaho, United States, 83814
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Illinois
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Chicago, Illinois, United States, 60612
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Chicago, Illinois, United States, 60611
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Evanston, Illinois, United States, 60201
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Urbana, Illinois, United States, 61801
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Indiana
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Avon, Indiana, United States, 46123
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Kansas
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Roeland Park, Kansas, United States, 66205
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Kentucky
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Lexington, Kentucky, United States, 40504
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Louisville, Kentucky, United States, 40202
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Maryland
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Baltimore, Maryland, United States, 21237
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Glen Burnie, Maryland, United States, 21061
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Massachusetts
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Boston, Massachusetts, United States, 02215
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Burlington, Massachusetts, United States, 01805
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Norfolk, Massachusetts, United States, 02481
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Michigan
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Ann Arbor, Michigan, United States, 48019
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Detroit, Michigan, United States, 48202
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Farmington, Michigan, United States, 48334
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Owosso, Michigan, United States, 48867
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Rochester Hills, Michigan, United States, 48307
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Minnesota
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Golden Valley, Minnesota, United States, 55422
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Plymouth, Minnesota, United States, 55446
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Montana
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Billings, Montana, United States, 59101
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Nebraska
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Lincoln, Nebraska, United States, 68502
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Omaha, Nebraska, United States, 68154
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Nevada
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Las Vegas, Nevada, United States, 89106
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New Jersey
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Bridgewater, New Jersey, United States, 08807
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Cherry Hill, New Jersey, United States, 08002
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Freehold, New Jersey, United States, 07728
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Livingston, New Jersey, United States, 07039
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Neptune City, New Jersey, United States, 00753
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Paramus, New Jersey, United States, 07652
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Teaneck, New Jersey, United States, 07666
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New York
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Amherst, New York, United States, 14226
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Lake Success, New York, United States, 11042
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New York, New York, United States, 11501
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The Bronx, New York, United States, 10467
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North Carolina
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Charlotte, North Carolina, United States, 28210
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New Bern, North Carolina, United States, 28562
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Raleigh, North Carolina, United States, 27607
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Ohio
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Centerville, Ohio, United States, 45429
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Centerville, Ohio, United States, 45459
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Cincinnati, Ohio, United States, 45212
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Cleveland, Ohio, United States, 44195
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Columbus, Ohio, United States, 43214
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Columbus, Ohio, United States, 43235
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Toledo, Ohio, United States, 43608
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Oklahoma
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Norman, Oklahoma, United States, 73019
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Oregon
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Portland, Oregon, United States, 97225
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Pennsylvania
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Bethlehem, Pennsylvania, United States, 18017
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Tennessee
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Franklin, Tennessee, United States, 37067
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Knoxville, Tennessee, United States, 37996
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Mount Juliet, Tennessee, United States, 37122
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- TG Therapeutics Investigational Trial Site
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Nashville, Tennessee, United States, 37215
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Spring Hill, Tennessee, United States, 37174
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Texas
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Austin, Texas, United States, 78723
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Austin, Texas, United States, 78712
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- TG Therapeutics Investigational Trial Site
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Austin, Texas, United States, 78758
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Dallas, Texas, United States, 75206
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Dallas, Texas, United States, 75243
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Edinburg, Texas, United States, 78572
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Frisco, Texas, United States, 75035
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- TG Therapeutics Investigational Trial Site
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Lubbock, Texas, United States, 79414
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San Antonio, Texas, United States, 78229
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Utah
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Ogden, Utah, United States, 84403
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Salt Lake City, Utah, United States, 84103
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Virginia
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Charlottesville, Virginia, United States, 22908
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Salem, Virginia, United States, 24153
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Vienna, Virginia, United States, 22182
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Virginia Beach, Virginia, United States, 23456
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Washington
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Kirkland, Washington, United States, 98034
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West Virginia
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Morgantown, West Virginia, United States, 26506
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Wisconsin
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Greenfield, Wisconsin, United States, 53228
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Milwaukee, Wisconsin, United States, 53226
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Neenah, Wisconsin, United States, 54956
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Waukesha, Wisconsin, United States, 53188
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
The study population will include participants with RMS who are receiving BRIUMVI® (ublituximab-xiiy).
Description
Inclusion Criteria:
- Confirmed Multiple Sclerosis (MS) diagnosis.
- Participants who have not received any BRIUMVI® (ublituximab-xiiy) infusion prior to study start. Participants who have been prescribed BRIUMVI® (ublituximab-xiiy) but have not yet received their first infusion on Day 1 of 150 milligrams (mg) can be included.
Exclusion Criteria:
- Have received any live or live-attenuated vaccines (including for varicella-zoster virus or measles) within 4 weeks prior to first BRIUMVI® (ublituximab-xiiy) administration or any non-live vaccines within 2 weeks prior to first BRIUMVI® (ublituximab-xiiy) administration.
- Any active infection (e.g., active Hepatitis B virus [HBV])
- Concurrent participation in any interventional MS trials, or planned concurrent treatment with other Multiple Sclerosis Disease Modifying Therapy (MS DMT) during the study period.
Study Plan
How is the study designed?
Design Details
- Observational Models: CASE_ONLY
- Time Perspectives: PROSPECTIVE
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
Intervention / TreatmentIntervention / Treatment |
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BRIUMVI® (Ublituximab-xiiy)
Participants will receive BRIUMVI® (Ublituximab-xiiy) intravenous (IV) infusion for the treatment of RMS. |
No Intervention |
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Annualized Relapse Rate (ARR)
Time Frame: Up to Week 96
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Up to Week 96
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
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Percentage of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: Up to Week 96
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Up to Week 96
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Number of Participants with Infusion Related Reaction (IRR) at Each Infusion
Time Frame: Up to Week 96
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Up to Week 96
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Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- TG1101-RMS406
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.