CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 41 enrolled
Drug / intervention
SAN-300 0.5 mg/kg QW +5 moredrug
Likely dose
SAN-300 0.5 mg/kg QWfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02047604
NCT02047604Phase 2Completed

A Randomized, Double-blind, Placebo-Controlled, Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of Escalating Doses of SAN-300 in Patients With Active Rheumatoid Arthritis With Inadequate Response to Disease-Modifying Anti-rheumatic Drug(s).

Bausch Health Americas, Inc.·interventional·Posted Jan 28, 2014·Updated Jun 21, 2021

In Brief

A Phase 2 clinical trial evaluating SAN-300 0.5 mg/kg QW, SAN-300 1.0 mg/kg QW, and 4 other interventions for Rheumatoid Arthritis. Completed, enrolled 41 participants across 12 sites.

Detailed Summary

A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of Escalating Doses of SAN-300 in Patients with Active Rheumatoid Arthritis with Inadequate Response to Disease-Modifying Anti-rheumatic Drug(s).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJan 28, 2014
Enrollment StartDec 1, 2013
Primary CompletionFeb 23, 2017
Study CompletionMar 23, 2017
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 12.4 years ago

Interventions

SAN-300 0.5 mg/kg QWdrug

SAN-300 1.0 mg/kg QWdrug

SAN-300 2.0 mg/kg QOWdrug

SAN-300 4.0 mg/kg QOWdrug

SAN-300 4.0 mg/kg QWdrug

Placebodrug