CLINICAL TRIALS PROFILE FOR FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE
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All Clinical Trials for FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT02168478 ↗ | Neo-Synalar Modified 48 Hour Patch Test | Completed | Noah Rosenberg, MD | Phase 4 | 2014-06-01 | A 48 hour patch test performed in healthy volunteers to determine the presensitization (pre-existing allergy) of Neo-Synalar (neomycin sulfate 0.5%(0.35% neomycin base), fluocinolone acetonide 0.025%) Cream . Subjects also receive a positive control (Sodium Lauryl Sulfate) and a negative control (Saline). The primary objective of this study is to determine if any subjects exhibit an allergic reaction which may be indicative of a pre-existing sensitization. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE
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Clinical Trial Progress for FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE
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Clinical Trial Sponsors for FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE
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