Status:

COMPLETED

Dose Escalation Study of RSLV-132 in Subjects With Systemic Lupus Erythematosus

Lead Sponsor:

Resolve Therapeutics

Conditions:

Systemic Lupus Erythematosus

Eligibility:

All Genders

18-70 years

Phase:

PHASE1

Brief Summary

A one month multi-dose study will evaluate the safety and tolerability of 3 intravenous infusions of RSLV-132 in subjects with inactive to mild SLE.

Eligibility Criteria

Inclusion

  • Stable SLE with no anticipated change in medications for the next 60 days

Exclusion

  • Other biologic drugs

Key Trial Info

Start Date :

July 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2015

Estimated Enrollment :

32 Patients enrolled

Trial Details

Trial ID

NCT02194400

Start Date

July 1 2014

End Date

November 1 2015

Last Update

December 9 2015

Active Locations (4)

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Page 1 of 1 (4 locations)

1

Clinical Research of West Florida

Clearwater, Florida, United States, 33765

2

West Michigan Rheumatology

Grand Rapids, Michigan, United States, 49546

3

Altoona Center for Clinical Research

Duncansville, Pennsylvania, United States, 16635

4

Metroplex Clinical Research

Dallas, Texas, United States, 75231

Dose Escalation Study of RSLV-132 in Subjects With Systemic Lupus Erythematosus | DecenTrialz