Multiple Sclerosis Clinical Trial

A Study of Participants With Relapsing-Remitting Multiple Sclerosis (RRMS)

Summary

To look at the ability of LY2127399 to reduce magnetic resonance imaging (MRI) lesions at 12, 16, 20, and 24 weeks compared to placebo.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

18 through 64 years of age diagnosed with RRMS, who can walk without aid or rest for at least 200 meters (approximately 1/10 of a mile).
Women who can become pregnant must use birth control.

Exclusion Criteria:

Have had a live vaccination within 12 weeks before randomization, or intend to have a live vaccination during the course of the study.
Have had had recent surgery or are scheduled to have surgery during the study.
Are immunocompromised or have evidence of active infection [such as hepatitis, tuberculosis or, human immunodeficiency virus (HIV)].
Have been on certain drugs that are being studied for RRMS or have recently received prescription drugs to treat RRMS.
Have had a recent serious infection.
Have serious or uncontrolled illnesses other than RRMS.
Have clinically significant blood test values.
Have multiple or severe drug allergies.
Have contraindications for MRI "scanning" or claustrophobia (fear of an enclosed space) that cannot be managed.

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

245

Study ID:

NCT00882999

Recruitment Status:

Completed

Sponsor:

Eli Lilly and Company

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There are 63 Locations for this study

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For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Phoenix Arizona, 85013, United States
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Tucson Arizona, 85741, United States
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Fullerton California, 92835, United States
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Denver Colorado, 80220, United States
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Naples Florida, 34102, United States
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Plantation Florida, 33324, United States
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Sarasota Florida, 34239, United States
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Northbrook Illinois, 60062, United States
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Indianapolis Indiana, 46202, United States
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Kansas City Kansas, 66160, United States
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Lexington Kentucky, 40513, United States
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Biddeford Maine, 04005, United States
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Farmington Hills Michigan, 48334, United States
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Toms River New Jersey, 08755, United States
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Schenectady New York, 12308, United States
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Charlotte North Carolina, 28207, United States
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Raleigh North Carolina, 27607, United States
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Akron Ohio, 44320, United States
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Green Ohio, 44685, United States
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Greensburg Pennsylvania, 15601, United States
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Greenville South Carolina, 29615, United States
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Franklin Tennessee, 37064, United States
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Memphis Tennessee, 38120, United States
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Lubbock Texas, 79410, United States
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Round Rock Texas, 78681, United States
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Newport News Virginia, 23601, United States
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Roanoke Virginia, 24018, United States
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Sofia , 1407, Bulgaria
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Brno , 62500, Czechia
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Pardubice , 500 0, Czechia
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Prague , 140 5, Czechia
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Caen , 14033, France
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Montpellier , 34295, France
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Nimes , 30900, France
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Strasbourg , 67091, France
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Berlin , 13156, Germany
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Ulm , 89075, Germany
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Budapest , 1095, Hungary
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Gyor , 9023, Hungary
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Gyula , 5700, Hungary
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Tel Hashomer , 52621, Israel
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Gdansk , 80-95, Poland
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Gliwice , 44-10, Poland
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Grodzisk Mazowiecki , 05-82, Poland
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Krakow-Nowa Huta , PL-31, Poland
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Lodz , 90-54, Poland
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Lublin , 20-09, Poland
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Targu Mures , 54013, Romania
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Kazan , 44200, Russian Federation
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Kemerovo , 65006, Russian Federation
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Moscow , 11943, Russian Federation
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Belgrade , 11000, Serbia
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Nis , 18000, Serbia
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Bratislava , 833 0, Slovakia
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Kosice , 04011, Slovakia
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Spisska Nova Ves , 05201, Slovakia
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Zilina , 01001, Slovakia
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Dnepropetrovsk , 49027, Ukraine
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Donetsk , 83037, Ukraine
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Ivano-Frankivsk , 76008, Ukraine
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Kharkiv , 61000, Ukraine
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Vinnytsya , 21005, Ukraine
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Zaporizhzhya , 69057, Ukraine

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

245

Study ID:

NCT00882999

Recruitment Status:

Completed

Sponsor:


Eli Lilly and Company

How clear is this clinincal trial information?

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