CLINICAL TRIALS PROFILE FOR SERLOPITANT
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Clinical Trials for Serlopitant
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT01951274 ↗ | VPD-737 for Treatment of Chronic Pruritus | Completed | Menlo Therapeutics Inc. | Phase 2 | A study of a several doses of a novel treatment for chronic itch compared to placebo for patients whose condition has not responded to other treatments |
NCT01951274 ↗ | VPD-737 for Treatment of Chronic Pruritus | Completed | Vyne Therapeutics Inc. | Phase 2 | A study of a several doses of a novel treatment for chronic itch compared to placebo for patients whose condition has not responded to other treatments |
NCT02196324 ↗ | A Randomized Placebo-Controlled Study of the Neurokinin-1 (NK1) Receptor Antagonist Serlopitant Prurigo Nodularis (PN) | Completed | Menlo Therapeutics Inc. | Phase 2 | The purpose of this study is to demonstrate whether or not VPD-737, an NK1 receptor antagonist is safe and effective for treatment of prurigo nodularis versus placebo. |
NCT02196324 ↗ | A Randomized Placebo-Controlled Study of the Neurokinin-1 (NK1) Receptor Antagonist Serlopitant Prurigo Nodularis (PN) | Completed | Vyne Therapeutics Inc. | Phase 2 | The purpose of this study is to demonstrate whether or not VPD-737, an NK1 receptor antagonist is safe and effective for treatment of prurigo nodularis versus placebo. |
NCT02654483 ↗ | Neurokinin-1 Receptor Antagonist for the Treatment of Itch in EB Patients | Completed | Epidermolysis Bullosa Research Partnership | Phase 2 | Our goal is to determine whether daily oral administration of VPD-737 (5 mg) is effective and safe in treating moderate to severe pruritus in patients with Epidermolysis Bullosa (EB). |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for Serlopitant
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Clinical Trial Locations for Serlopitant
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Clinical Trial Progress for Serlopitant
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Clinical Trial Sponsors for Serlopitant
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