RSLV-132
Biological0.3 - 10.0 mg/kg RSLV-132 weekly for 4 weeks
NCT Number: NCT02194400
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.
Looking for future studies?
Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Clinical Research of West Florida, Clearwater, Florida, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.3 - 10.0 mg/kg RSLV-132 weekly for 4 weeks
Time frame: 30 days
Looking for future studies?
Notify MeResolve Therapeutics
Industry
A Double-Blind, Placebo-Controlled Dose Escalation Study of the Administration of Multiple Intravenous Doses of RSLV-132 in Subjects With Systemic Lupus Erythematosus
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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