An ascending multiple dose study of the safety, tolerability, pharmacokinetics, pharmacodynamics, and clinical efficacy of ILV-094 administered subcutaneously or intravenously to subjects with psoriasis
Abstract
The purpose of this study is to assess safety, and tolerability of multiple doses of ILV-094 administered to subjects with psoriasis
Conditions: Psoriasis.
Primary outcome: Number of Participants With Treatment-Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs); Number of Participants With Clinically Significant Changes in Electrocardiogram (ECG) Parameters; Number of Participants With Vital Sign Values of Potential Clinical Importance (PCI); Number of Participants With Laboratory Test Values of Potential Clinical Importance.
Enrollment: 76 participants.
How strong is the evidence?
Evidence Hub reads this as a clinical trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 76 participants or records.
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