DelveInsight’s Sickle Cell Disease Market Insights report provides a thorough understanding of current treatment practices, emerging Sickle Cell Disease market share of the individual therapies, current and forecasted Sickle Cell Disease Market size from 2019 to 2032 segmented into 7MM (the USA, EU5 (the UK, Italy, Spain, France, and Germany), and Japan).
Sickle Cell Disease Overview
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS) which encodes hemoglobin subunit β. HbS is inherited in an autosomal recessive way and can occur due to homozygosity for HbS (HbSS). HbS is functional and soluble when oxygenated, but upon deoxygenation it polymerizes, leading to the generation of deformed red blood cells known as sickled cells and dense erythrocytes.
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Some of the key highlights of the Sickle Cell Disease Market Report
- According to DelveInsight’s analysis, no gender bias has been observed in case of Sickle cell disease.
- A 5-year study carried out using Florida Medicaid program data estimated that SCD patients had an average of 3.7 inpatient hospitalizations and 24.1 hospital days during the study period, with roughly 84% attributable to SCD-related diagnoses.
- “Sickle cell disease” quoted that demographical projections estimated that the annual number of newborn babies with SCA worldwide will exceed 400,000 by 2050.
- Sickle Cell Disease companies are included like Pfizer Inc., Micelle BioPharma Inc, AstraZeneca, BlueBird Bio, Agios Pharmaceuticals, Bristol-Myers Squibb, Emmaus Life Sciences lnc and many others.
- Sickle Cell Disease drugs are included like Droxia, Endari, Rivipansel, SC411 (Altemia), Ticagrelor, LentiGlobin BB305, AG-348, and many others.
Sickle Cell Disease Symptoms
- Anemia
- Episodes of pain
- Swelling of hands and feet
- Frequent infections
- Delayed growth or puberty
- Vision problems
Sickle Cell Disease Treatment
Sickle cell disease (SCD) is an umbrella term that defines a group of inherited diseases (including sickle cell anaemia (SCA), HbSC and HbSβ-thalassaemia,) characterized by mutations in the gene encoding the haemoglobin subunit β (HBB). The treatment starts with the recognition of pain in the sickle cell disease patients. Recurrent episodes of acute, severe pain are the hallmark of SCD. The pain is highly variable both within and among patients, and is the result of complex and poorly understood interactions between biological and psychosocial factors.
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Sickle Cell Disease Key Players
- Pfizer Inc.
- Micelle BioPharma Inc.
- AstraZeneca
- BlueBird Bio
- Agios Pharmaceuticals
- Bristol-Myers Squibb
- Emmaus Life Sciences lnc.
- And many others
- Droxia
- Endari
- Rivipansel
- SC411 (Altemia)
- Ticagrelor
- LentiGlobin BB305
- AG-348
- And many others
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Table of Content
- Key Insights
- Executive Summary
- Competitive Intelligence Analysis
- Market Overview at a Glance
- Disease Background and Overview
- Patient Journey
- Epidemiology and Patient Population
- Treatment Algorithm, Current Treatment, and Medical Practices
- Unmet Needs
- Key Endpoints of Sickle Cell Disease Treatment
- Marketed Products
- Emerging Therapies
- Seven Major Market Analysis
- Attribute analysis
- 7MM: Market Outlook
- Access and Reimbursement Overview
- KOL Views
- Market Drivers
- Market Barriers
- Appendix
- DelveInsight Capabilities
- Disclaimer
- About DelveInsight
About Us
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