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According to the National Organisation for Rare Disorders, warm autoimmune hemolytic anemia (wAIHA) is the most common subtype of autoimmune hemolytic anemia, affecting approximately 1 to 3 per 100,000 people every year. The disease can occur at any age, therefore, there is a significant focus on designing effective drugs that help in successfully managing and treating the disease.
The Warm Autoimmune Hemolytic AnemiaDrug Pipeline Insight Report by Expert Market Research gives comprehensive insights into warm autoimmune hemolytic anemiadrugs currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for warm autoimmune hemolytic anemia. The report includes the analysis of over 100 pipeline drugs and 50+ companies. The warm autoimmune hemolytic anemia pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials including their adverse effects on patients suffering from warm autoimmune hemolytic anemia.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration and ongoing product development activities related to warm autoimmune hemolytic anemia.
Warm autoimmune hemolytic anemia is an autoimmune condition that leads to premature death of red blood cells in the body. It is the most common type of autoimmune hemolytic anemia. Normally, red blood cells have a lifespan of 120 days before they are ultimately destroyed by the spleen. However, individuals affected by this condition witness sudden death of RBCs at a rapid pace and to an extent wherein the body cannot compensate for the drastic loss. Symptoms may include tiredness, dizziness, jaundice or heart palpitations.
The first-line therapy for warm autoimmune hemolytic anemia involves corticosteroids. These drugs are successful in about 65-70% of the patients. In relapsed cases, splenectomy, rituximab or other immunosuppressive drugs are advised. In December 2023, researchers at the American Journal of Hematology revealed that Fostamatinib, a spleen tyrosine kinase inhibitor, previously used for the treatment of patients with chronic immune thrombocytopenia in the United States can be found successful in managing warm antibody autoimmune hemolytic anemia (wAIHA) effectively. Such initiatives aimed at developing high-efficacy drugs are amongst major trends, impacting the drug pipeline outlook positively.
This section of the report covers the analysis of warm autoimmune hemolytic anemiadrugs based on several segmentations including:
By Phase
EMR’s pipeline assessment report covers 50+ drug analyses based on phase.
By Drug Class
EMR’s pipeline assessment report covers 50+ drug analyses based on drug classes:
By Route of Administration
EMR’s pipeline assessment report covers 50+ drug analyses based on the route of administration.
The report covers phase I, phase II, phase III, phase IV, and early phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total clinical trials for warm autoimmune hemolytic anemia. There are around 20 drugs in phase II of warm autoimmune hemolytic anemia drugs.
The drug molecules categories covered under warm autoimmune hemolytic anemiapipeline analysis include corticosteroids, immunosuppressive agents, intravenous immunoglobulins (IVIG), cytotoxic agents and monoclonal antibodies. These drugs can be used in combination, based on the patient’s response to treatment, symptoms and severity of the condition.
The EMR report for the warm autoimmune hemolytic anemiadrug pipeline covers the profile of key companies involved in clinical trials and their drugs under development. Below is the list of a few players involved in warm autoimmune hemolytic anemia clinical trials:
ALXN1830
Sponsored by Alexion Pharmaceuticals, Inc., the drug is under trials to assess its efficacy and safety in treating warm autoimmune hemolytic anemia (WAIHA). It is currently in Phase 2 of a randomised double-blind study.
M281
As a part of the 24-week double-blind study, M281 is under examination for its efficacy and safety against warm autoimmune hemolytic anemia (wAIHA). It will be administered every 4 weeks during the 24-week double-blind period.
Rilzabrutinib
This oral drug is being evaluated to check the efficacy, safety and pharmacokinetics in patients affected with warm autoimmune hemolytic anemia. Sponsored by Sanofi, Rilzabrutinib is in Phase 2 of an open-label study.
Obexelimab
Zenas BioPharma (USA), LLC is conducting a study to examine the safety and efficacy of obexelimab against warm autoimmune hemolytic anemia (wAIHA) in about 134 participants enrolled in the study.
The Warm Autoimmune Hemolytic Anemia Drug Pipeline Insight Report provides a strategic overview of the latest and future landscape of treatments for warm autoimmune hemolytic anemia. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into market trends, regulatory environments, and potential growth opportunities within warm autoimmune hemolytic anemia pipeline insights.
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*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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