A Study of Efficacy and Safety of Ianalumab in Previously Treated Patients With Warm Autoimmune Hemolytic Anemia
Condition(s) studied
Investigational drug(s) / intervention(s)
Ianalumab: i.v. infusion, prepared from concentrate solution
Placebo: i.v. infusion, prepared from matching placebo
Study summary
The purpose of this study is to evaluate efficacy and safety of ianalumab compared to placebo in patients with warm autoimmune hemolytic anemia, who failed at least one line of treatment.
Eligibility
Primary outcome measure(s)
- Binary variable indicating whether a patient achieves a durable response — Randomization to Week 25
Durable response: hemoglobin level ≥10 g/dL and ≥2 g/dL increase from baseline, for a period of at least eight consecutive weeks between W9 and W25, in the absence of rescue medication or prohibited treatment
Trial sites (53)
| Facility | City | Region | Status |
|---|---|---|---|
| Michigan Center of Medical Research | Farmington Hills | Michigan | |
| University of Minnesota Med Center | Minneapolis | Minnesota | |
| Fred Hutchinson Cancer Center | Seattle | Washington | |
| Novartis Investigative Site | CABA | Buenos Aires | |
| Novartis Investigative Site | Buenos Aires | Argentina | |
| Novartis Investigative Site | Caba | Argentina | |
| Novartis Investigative Site | Garran | Australian Capital Territory | |
| Novartis Investigative Site | Melbourne | Victoria | |
| Novartis Investigative Site | Guangzhou | Guangdong | |
| Novartis Investigative Site | Hangzhou | Zhejiang | |
| Novartis Investigative Site | Dalian | China | |
| Novartis Investigative Site | Tianjin | China | |
| Novartis Investigative Site | Tianjin | China | |
| Novartis Investigative Site | Créteil | France | |
| Novartis Investigative Site | Lille | France | |
| Novartis Investigative Site | Nantes | France | |
| Novartis Investigative Site | Nice | France | |
| Novartis Investigative Site | Dresden | Germany | |
| Novartis Investigative Site | Essen | Germany | |
| Novartis Investigative Site | Giessen | Germany | |
| Novartis Investigative Site | Hanover | Germany | |
| Novartis Investigative Site | Debrecen | Hajdu Bihar Megye | |
| Novartis Investigative Site | New Delhi | National Capital Territory of Delhi | |
| Novartis Investigative Site | Madurai | Tamil Nadu | |
| Novartis Investigative Site | Hyderabad | Telangana | |
| Novartis Investigative Site | Lucknow | Uttar Pradesh | |
| Novartis Investigative Site | Kfar Saba | Israel | |
| Novartis Investigative Site | Petah Tikva | Israel | |
| Novartis Investigative Site | Milan | MI | |
| Novartis Investigative Site | Milan | MI | |
| Novartis Investigative Site | Bassano del Grappa | VI | |
| Novartis Investigative Site | Novara | Italy | |
| Novartis Investigative Site | Narita | Chiba | |
| Novartis Investigative Site | Matsuyama | Ehime | |
| Novartis Investigative Site | Gifu | Gifu | |
| Novartis Investigative Site | Kobe | Hyōgo | |
| Novartis Investigative Site | Isehara | Kanagawa | |
| Novartis Investigative Site | Suita | Osaka | |
| Novartis Investigative Site | Itabashi-ku | Tokyo | |
| Novartis Investigative Site | Shinjuku Ku | Tokyo |
+ 13 more sites — see the full list on the official registry below.
More Novartis Pharmaceuticals trials in Japan
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05648968 on ClinicalTrials.gov ↗ ← All trials in Japan