Sickle Cell Disease Market is Predicted to Exhibit Remarkable Growth at a CAGR of 22.1% During the Forecast Period (2025–2034) Across 6MM, Owing to the Increasing Prevalence, Awareness, and Advancements in Gene Therapies | DelveInsight
New York, USA, Dec. 03, 2025 (GLOBE NEWSWIRE) -- Sickle Cell Disease Market is Predicted to Exhibit Remarkable Growth at a CAGR of 22.1% During the Forecast Period (2025–2034) Across 6MM, Owing to the Increasing Prevalence, Awareness, and Advancements in Gene Therapies | DelveInsight
The sickle cell disease market is anticipated to grow by 2034, driven by advances in disease mechanisms that have yielded new diagnostic and therapeutic approaches, opening the way to more drug development. In addition, the increasing prevalence and the launch of emerging therapies, such as inclacumab (Pfizer), etavopivat (Novo Nordisk), mitapivat (Agios Pharmaceuticals), osivelotor (Pfizer), and others, will also contribute to the growing market size during the forecast period.
DelveInsight’s Sickle Cell Disease Market Insights report includes a comprehensive understanding of current treatment practices, emerging SCD drugs, market share of individual therapies, and current and forecasted SCD market size from 2020 to 2034, segmented into leading markets (the US, EU4, and the UK).
Sickle Cell Disease Market Summary
Discover which SCD medications are expected to grab the market share @ Sickle Cell Disease Market Report
Key Factors Driving the Growth of the SCD Market
Rising SCD Prevalence
According to DelveInsight’s assessment, in 2024, the total prevalent cases of sickle cell disease (SCD) in the 6MM were nearly 178.5K. These cases are anticipated to increase by 2034, with the majority occurring in individuals aged 18–44 years, followed by those aged 45–64 years, and fewer in younger (0–17 years) and older (65+ years) populations.
Current Standard of Care
The present treatment landscape for SCD includes NSAIDs, blood transfusions, chelating agents, nutritional supplements, and broad-spectrum antibiotics to manage complications. Established disease-modifying therapies include DROXIA (hydroxyurea), ENDARI (L-glutamine oral powder), and ADAKVEO (crizanlizumab-tmca). However, in September 2024, all lots of OXBRYTA were withdrawn across all markets, creating a treatment gap in the standard of care.
Launch of Emerging SCD Drugs
The SCD clinical trial landscape appears to be growing, with key players such as Novo Nordisk (etavopivat; NDec), Pfizer (osivelotor; inclacumab), Agios Pharmaceuticals (mitapivat), Fulcrum Therapeutics (pociredir), and others developing their assets in both early and late phases.
Sickle Cell Disease Market Analysis
Although sickle cell disease is widespread in the United States, many patients still receive inadequate care, particularly when treated by non-specialists. This highlights gaps within the healthcare system, leading to poor symptom control.
Management of SCD involves both drug-based and supportive therapies. Approved pharmacologic treatments include hydroxyurea, ENDARI (L-glutamine), ADAKVEO (crizanlizumab), CASGEVY (exagamglogene autotemcel), and LYFGENIA (lovotibeglogene autotemcel). Pain is commonly managed with opioids, NSAIDs, acetaminophen, and corticosteroids. Non-drug interventions, such as cognitive behavioral therapy, relaxation methods, biofeedback, and acupuncture, also play a supportive role.
Hydroxyurea remains the standard first-line option, while newer agents are being used to enhance symptom control. Therapies like ADAKVEO show strong adherence due to favorable dosing schedules and their ability to reduce vaso-occlusive crises.
Multiple next-generation treatments are progressing through the pipeline. Notable developers include Pfizer (inclacumab, GBT-601), Novo Nordisk (etavopivat), Bluebird Bio (lovo-cel), and Agios Pharmaceuticals (mitapivat). These emerging options aim to fill critical gaps by offering curative potential, improved safety, and greater convenience. With increasing disease burden and expected regulatory approvals, the SCD landscape is set for expansion and remains an attractive area for future investment.
Learn more about the SCD treatment options @ Sickle Cell Disease Treatment Market
Sickle Cell Disease Competitive Landscape
SCD clinical trial landscape possesses some drugs in mid- and late-stage development to be approved in the near future. The expected launch of therapies such as inclacumab (Pfizer), etavopivat (Novo Nordisk), mitapivat (Agios Pharmaceuticals), osivelotor (Pfizer), and others are anticipated to create a positive impact on the market.
Agios Pharmaceuticals’ Mitapivat is an innovative, first-in-class oral small molecule that acts as an allosteric activator of the pyruvate kinase enzyme. It has demonstrated the ability to markedly enhance the activity of both wild-type and various mutant forms of erythrocyte pyruvate kinase (PKR), leading to increased ATP generation and reduced concentrations of 2,3-diphosphoglycerate.
Pfizer’s Osivelotor is an advanced inhibitor of sickle hemoglobin (HbS) polymerization, designed with improved pharmacokinetic characteristics that help maintain hemoglobin in its oxygenated state and prevent polymer formation. The therapy may enable higher hemoglobin levels and greater target engagement at lower doses, potentially decreasing treatment burden and improving outcomes for individuals with sickle cell disease (SCD). In 2022, it received Orphan Drug Designation (ODD) and Rare Pediatric Disease Designation (RPDD) from the FDA.
CRISPR by Design refers to Scribe’s data-driven strategy for developing and refining its CRISPR-based technologies, including its X-Editing (XE) platform, to advance a new generation of transformative genetic therapies.
Sanofi and Scribe Therapeutics are working under an expanded collaboration initiated in September 2022, which includes an exclusive licensing agreement for CasXEditor (XE) genome-editing technology and associated guide RNAs across multiple targets, including sickle cell disease and other genetic disorders.
The anticipated launch of these emerging SCD therapies are poised to transform the SCD market landscape in the coming years. As these cutting-edge SCD therapies continue to mature and gain regulatory approval, they are expected to reshape the SCD market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth.
To know more about new treatment for SCD, visit @ Sickle Cell Disease Medication
Recent Developments in the SCD Market
What is Sickle Cell Disease?
Sickle cell disease (SCD) is a hereditary blood disorder caused by a mutation in the gene that produces hemoglobin, the oxygen-carrying protein in red blood cells. This mutation leads to the formation of abnormal “sickle-shaped” red blood cells that are stiff, sticky, and prone to clumping together. As a result, these misshapen cells can block blood flow in small vessels, leading to painful episodes, organ damage, an increased risk of infections, and chronic anemia. SCD is a lifelong condition that primarily affects individuals of African, Middle Eastern, and South Asian descent and requires ongoing medical care to manage symptoms and prevent complications.
Sickle Cell Disease Epidemiology Segmentation
The SCD epidemiology section provides insights into the historical and current SCD patient pool and forecasted trends for the leading markets. As per the estimates, the US accounted for approximately 73% of the total diagnosed prevalent cases of SCD in the 6MM.
The SCD market report proffers epidemiological analysis for the study period 2020–2034 in the leading markets segmented into:
Download the report to understand SCD management @ Sickle Cell Disease Treatment Options
Scope of the Sickle Cell Disease Market Report
Discover more about SCD drugs in development @ Sickle Cell Disease Clinical Trials
Table of Contents
Related Reports
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