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A Study of the Safety and Tolerability of MEDI-551 in Scleroderma


A Phase 1, Randomized, Double-blind, Placebo-controlled Study of the Safety and Tolerability of MEDI-551 in Scleroderma




The primary objective of this study is to evaluate the safety and tolerability of intravenously administered MEDI-551 over escalating single doses in adult subjects with Scleroderma

Study Status: Recruiting

Tara Barker 216-445-6139

Condition Intervention Phase
Scleroderma Biological: MEDI-551
Biological: Placebo
Biological: MEDI-551
Biological: MEDI-551
Biological: MEDI-551
Other: Placebo
Phase 1

Verified by MedImmune LLC August, 2011

Sponsored by: MedImmune LLC
Information provided by: MedImmune LLC identifier: NCT00946699

Study Type: Interventional

Study Design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Dominique Ethgen, M.D.., Study Director

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