CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 54 enrolled
Drug / intervention
eltrombopag +1 moredrug
Likely dose
eltrombopag 12.5 mgfrom 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/NCT02998645
NCT02998645Phase 2Completed

SOAR, Interventional Phase II Single-arm Study to Assess Efficacy and Safety of Eltrombopag Combined With Cyclosporine as First Line Therapy in Adult Patients With Severe Acquired Aplastic Anemia

Novartis Pharmaceuticals·interventional·Posted Dec 20, 2016·Updated Dec 11, 2023

In Brief

A Phase 2 clinical trial evaluating eltrombopag and Cyclosporine for Severe Aplastic Anemia. Completed, enrolled 54 participants across 20 sites in 9 countries.

Detailed Summary

The purpose of this study was to evaluate the efficacy and safety of eltrombopag in combination with cyclosporine alone as first-line therapy on overall hematologic response

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil, Hong Kong, India, Italy, Mexico, South Korea, Spain, Thailand, Turkey (Türkiye)
Collaborators--

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedDec 20, 2016
Enrollment StartMay 11, 2017
Primary CompletionNov 3, 2020
Study CompletionMay 30, 2022
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 9.5 years ago

Interventions

eltrombopagdrug

Film-coated tablets (12.5 mg, 25 mg, 50 mg and 75 mg) administered orally, once daily for up to 6 months. East and Southeast Asian participants were treated with 100 mg once daily, to adjust for the lower apparent clearance of eltrombopag. All other participants were treated with 150 mg once daily.

Cyclosporinedrug

Supplied as oral soft gel capsules. The starting dose was based on body weight at 10.0 mg/kg/day (acceptable rounding range was from 9.5 to 10.5 mg/kg/day) in divided doses every 12 hours. After Day 1, dosing was titrated individually according to therapeutic trough level between 200 and 400 μg/L for 6 months. After 6 months (only for responders at Month 6), tapering of cyclosporine was done as follows: * 6-9 months: at the 6 months visit, the dose was reduced by 25% for 3 months * 9-12 months: at the 9 months visit, the dose was further reduced by 25% for another 3 months * 12-24 months: dose was maintained