Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Prurigo Nodularis

Completed · Phase 3 · Has a placebo group

Conditions studied: Pruritus, Prurigo Nodularis

In brief

Study of the efficacy, safety, and tolerability of serlopitant for the treatment of pruritus in adults with prurigo nodularis

Key facts

Study ID

NCT03546816

Run by

Vyne Therapeutics Inc.

People needed

285

Starts

2018-05-02

Expected to finish

2020-02-14

Last updated by the study team

2021-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Study Site 504 — Birmingham, Alabama, United States
• Study Site 533 — Rogers, Arkansas, United States
• Study Site 204 — Fremont, California, United States
• Study Site 383 — North Hollywood, California, United States
• Study Site 356 — San Diego, California, United States
• Study Site 514 — Santa Ana, California, United States
• Study Site 501 — Aventura, Florida, United States
• Study Site 210 — Coral Gables, Florida, United States
• Study Site 534 — Fort Lauderdale, Florida, United States
• Study Site 531 — Miami, Florida, United States
• Study Site 530 — Miami, Florida, United States
• Study Site 222 — North Miami Beach, Florida, United States
• Study Site 510 — Newnan, Georgia, United States
• Study Site 388 — Skokie, Illinois, United States
• Study Site 228 — Louisville, Kentucky, United States
• Study Site 527 — New Orleans, Louisiana, United States
• Study Site 525 — Glenn Dale, Maryland, United States
• Study Site 379 — Boston, Massachusetts, United States
• Study Site 506 — Ann Arbor, Michigan, United States
• Study Site 515 — Detroit, Michigan, United States
• Study Site 371 — Saint Joseph, Missouri, United States
• Study Site 528 — St Louis, Missouri, United States
• Study Site 227 — Omaha, Nebraska, United States
• Study Site 526 — Henderson, Nevada, United States
• Study Site 201 — East Windsor, New Jersey, United States

Full record on ClinicalTrials.gov

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