Efficacy and Safety of BBT-401-1S in Ulcerative Colitis

PHASE2TerminatedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

April 22, 2019

Primary Completion Date

May 18, 2020

Study Completion Date

July 31, 2020

Conditions
Ulcerative Colitis
Interventions
DRUG

BBT-401-1S first and then Placebo

Total 16 week treatment period: The subject takes BBT-401-1S, QD for the first 12 weeks, then placebo for the last 4 weeks.

DRUG

Placebo first and then BBT-401-1S

Total 16 week treatment period: The subject takes the placebo, QD for the first 8 weeks, then BBT-401-1S for the last 8 weeks.

Trial Locations (11)

20850

Site 04, Rockville

28112

Site 02, Monroe

33029

Site 12, Pembroke Pines

33487

Site 11, Boca Raton

37421

Site 08, Chattanooga

48109

Site 10, Ann Arbor

78503

Site 13, McAllen

78705

Site 05, Austin

93003

Site 01, Ventura

95821

Site 03, Sacramento

98195

Site 09, Seattle

Sponsors
All Listed Sponsors
collaborator

KCRN Research, LLC

INDUSTRY

lead

Bridge Biotherapeutics, Inc.

INDUSTRY

NCT03800420 - Efficacy and Safety of BBT-401-1S in Ulcerative Colitis | Biotech Hunter | Biotech Hunter