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Completed Phase 1 Interventional

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

ClinicalTrials.gov ID: NCT01686555

Public ClinicalTrials.gov record NCT01686555. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 5:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Assessment of the Safety, Tolerability, and Pharmacokinetics of ABT-199 After Single and Multiple Ascending Doses in Female Subjects With Systemic Lupus Erythematosus (SLE)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To assess the safety, tolerability and pharmacokinetics of ABT-199 in female subjects with Systemic Lupus Erythematosus.

Study identification

NCT ID
NCT01686555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
97 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2012 (Type not available)
Primary completion
Jun 2015 (Actual)
Completion
Jun 2015 (Actual)
Last update posted
Nov 20, 2017

2012 – 2015

United States locations

U.S. sites
11
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Site Reference ID/Investigator# 89694 Clearwater Florida 33765 —
Site Reference ID/Investigator# 131720 DeBary Florida 32713 —
Site Reference ID/Investigator# 118637 Miami Florida 33136 —
Site Reference ID/Investigator# 124116 Miami Lakes Florida 33016 —
Site Reference ID/Investigator# 89693 Orlando Florida 32806 —
Site Reference ID/Investigator# 78256 Overland Park Kansas 66212 —
Site Reference ID/Investigator# 129826 Rochester Minnesota 55905 —
Site Reference ID/Investigator# 89773 Manhasset New York 11030 —
Site Reference ID/Investigator# 78254 Duncansville Pennsylvania 16635 —
Site Reference ID/Investigator# 123335 Dallas Texas 75231 —
Site Reference ID/Investigator# 78253 Dallas Texas 75231 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01686555, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 20, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01686555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →