A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ABT-199 in Female Patients With Systemic Lupus Erythematosus (SLE)

PHASE1CompletedINTERVENTIONAL
Enrollment

97

Participants

Timeline

Start Date

November 30, 2012

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Lupus Erythematosus
Interventions
DRUG

ABT-199

Tablet

OTHER

Placebo

Tablet

Trial Locations (15)

10117

Site Reference ID/Investigator# 107896, Berlin

11030

Site Reference ID/Investigator# 89773, Manhasset

16635

Site Reference ID/Investigator# 78254, Duncansville

32713

Site Reference ID/Investigator# 131720, DeBary

32806

Site Reference ID/Investigator# 89693, Orlando

33016

Site Reference ID/Investigator# 124116, Miami Lakes

33136

Site Reference ID/Investigator# 118637, Miami

33765

Site Reference ID/Investigator# 89694, Clearwater

55905

Site Reference ID/Investigator# 129826, Rochester

66212

Site Reference ID/Investigator# 78256, Overland Park

75231

Site Reference ID/Investigator# 123335, Dallas

Site Reference ID/Investigator# 78253, Dallas

CP 14050

Site Reference ID/Investigator# 116395, Distrito Federal

C.P. 64000

Site Reference ID/Investigator# 112555, Monterrey

00909-3004

Site Reference ID/Investigator# 132009, San Juan

All Listed Sponsors
lead

AbbVie (prior sponsor, Abbott)

INDUSTRY

NCT01686555 - A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ABT-199 in Female Patients With Systemic Lupus Erythematosus (SLE) | Biotech Hunter | Biotech Hunter