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Warm Autoimmune Hemolytic Anemia clinical trials

View clinical trials related to Warm Autoimmune Hemolytic Anemia.

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NCT ID: NCT04956276 Withdrawn - Clinical trials for Warm Autoimmune Hemolytic Anemia

Subcutaneous ALXN1830 in Adult Participants With Warm Autoimmune Hemolytic Anemia

Start date: January 1, 2022
Phase: Phase 2
Study type: Interventional

This is a Phase 2, multiple ascending, dose-finding, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety, health-related quality of life, tolerability, pharmacokinetic, pharmacodynamic, and immunogenicity, of up to 3 dose regimens of ALXN1830 administered subcutaneous(ly) (SC) in the treatment of WAIHA. This study will include 2 randomized, double-blind, placebo-controlled cohorts (Cohorts 1 and 2) to evaluate an 8-week treatment regimen, and an optional third open-label cohort (Cohort 3) to evaluate an alternative 12-week dosing regimen. Participants may continue participation in this study at the participant's and investigator's discretion in an open-label extension (OLE) period, consisting of monthly visits to observe participants for relapse, which will require going back on active treatment.

NCT ID: NCT04256148 Withdrawn - Clinical trials for Warm Autoimmune Hemolytic Anemia

ALXN1830 in Patients With Warm Autoimmune Hemolytic Anemia

Start date: July 2021
Phase: Phase 2
Study type: Interventional

The main objective of the study is to evaluate the safety and efficacy of ALXN1830 compared to placebo in adult participants with warm autoimmune hemolytic anemia (WAIHA).

NCT ID: NCT03965624 Withdrawn - Clinical trials for Immune Thrombocytopenia

Efficacy and Safety of Ixazomib and Dexamethasone Refractory Autoimmune Cytopenia

Ixa-Cyto
Start date: September 1, 2019
Phase: Phase 2
Study type: Interventional

Some patients with antibody-mediated autoimmune hematological diseases (warm autoimmune hemolytic anemia (wAIHA), cold agglutinin disease (cAIHA) and immune thrombocytopenia (ITP)) shows no or only minor and transient response to therapy despite several treatment-lines. Such patients are more likely to have a severe disease, with a higher morbidity and mortality. Hypothesis Effective depletion of autoreactive plasma cells might be the key for a curative approach of these diseases. Therefore, there is a rationale for using proteasome inhibitors (PIs) in these refractory patients. The rationale is that non-tumoral autoreactive plasma cells are rapidly targeted by proteasome inhibitors. It led us to propose a short course of dexamethasone and ixazomib (5 cycles), to evaluate the safety/efficacy of this innovative strategy of treatment. Method Prospective interventional uncontrolled single arm open study evaluating the rate of patients achieving 5 cycles of ixazomib and dexamethasone without severe toxicity and response on therapy.