Evaluating the Safety and Efficacy of Deucravacitinib Compared to Placebo Hidradenitis Suppurativa (HS).

PHASE2TerminatedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

November 30, 2023

Primary Completion Date

February 25, 2025

Study Completion Date

April 10, 2025

Conditions
Hidradenitis Suppurativa
Interventions
DRUG

Deucravacitinib

Deucravacitinib is a stable deuterium-containing compound (where deuterium is a stable, nonradioactive isotope of hydrogen) and a potent, highly selective small molecule inhibitor of TYK2. Deucravacitinib has a unique mode of binding that provides the high selectivity over the other members of the JAK family of nonreceptor tyrosine kinases. 1 active oral tablet (6mg) in the morning and evening for 16weeks.

DRUG

Placebo

Placebo will consist of a tablet (0mg) and will be administered orally BID for 16weeks.

Trial Locations (1)

02215

Beth Israel Deaconess Medical Center, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

Beth Israel Deaconess Medical Center

OTHER

NCT05997277 - Evaluating the Safety and Efficacy of Deucravacitinib Compared to Placebo Hidradenitis Suppurativa (HS). | Biotech Hunter | Biotech Hunter