A Study to Evaluate the Efficacy & Safety of INCB054707 in Participants

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT06113445` - A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V1)	Phase 3
	Recruiting	`NCT06113471` - A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)	Phase 3

See also

Status

Clinical Trial

Phase

Recruiting

NCT06113445 - A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V1)

Phase 3

Recruiting

NCT06113471 - A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)

Phase 3

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04818346
Study type	Interventional
Source	Incyte Corporation
Contact
Status	Completed
Phase	Phase 2
Start date	May 6, 2021
Completion date	May 24, 2023

A Study to Evaluate the Efficacy and Safety of INCB054707 in Participants With Vitiligo

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms