Viewing Study NCT02975271



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Last Modification Date: 2024-10-26 @ 12:14 PM
Study NCT ID: NCT02975271
Status: TERMINATED
Last Update Posted: 2021-05-20
First Post: 2016-11-22

Brief Title: Study of the Efficacy Safety Tolerability of Serlopitant for Pruritus Itch After Burn Injury
Sponsor: Vyne Therapeutics Inc
Organization: Vyne Therapeutics Inc

Study Overview

Official Title: A Randomized Double-Blind Placebo-Controlled Study of the Efficacy Safety and Tolerability of Serlopitant for the Treatment of Pruritus Following Burn Injury
Status: TERMINATED
Status Verified Date: 2021-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Business Reasons
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: AUBURN
Brief Summary: Study of the Efficacy Safety Tolerability of Serlopitant for Pruritus Itch After Burn Injury
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None