Middle East and Africa Hemoglobinopathies Market Report and Forecast 2025-2034

Middle East and Africa Hemoglobinopathies Market Analysis

Hemoglobinopathies comprise a group of genetic disorders affecting the structure, function, or production of hemoglobin. The advancements in the global hemoglobinopathies market are increasingly being introduced into the Middle East and African countries. The penetration of such new and innovative treatments in the regional market are positively impacting the standard of care and clinical outcomes for patients with conditions like sickle cell disease and thalassemia. Moreover, the increasing awareness campaigns and advocacy efforts coupled with the rising healthcare expenditure are leading to early diagnosis and better management of these inherited disorders which are poised to significantly contribute to the Middle East and Africa hemoglobinopathies market growth.

The high prevalence of hemoglobinopathies in the region which can be attributed to the genetic predisposition and high rates of consanguineous marriages directly affects the market dynamics. Recent data reveals that thalassemia and sickle cell anemia cause a substantial impact on morbidity and mortality among the affected individuals. Alpha-thalassemia is reported to be prevalent in the Middle Eastern countries. In Saudi Arabia, beta-thalassemia and sickle cell anemia are estimated to be 13.6 and 49.6 per 1000 population, respectively . The growing burden of these hemoglobin disorders is projected to fuel the need for effective diagnostics and treatment solutions to manage such conditions, thereby boosting the Middle East and Africa hemoglobinopathies market demand.

One of the major market trends is the surge in regulatory approvals of novel treatments by the health agencies in the region. In January 2024, the Saudi Food and Drug Authority (SFDA) approved Casgevy (exagamglogene autotemcel) which is a one-time gene-editing therapy leveraging a gene-editing tool called CRISPR/Cas9 to treat sickle cell disease (SCD) in adults and adolescents aged 12 and above who experience recurrent vaso-occlusive crises. Developed jointly by biotechnology companies Vertex Pharmaceuticals and CRISPR Therapeutics, this gene editing therapy represents the first medicine to receive and be approved via the SFDA Breakthrough Designation pathway. The presence of such regulatory reforms that accelerate the review of therapies that address unmet medical needs is likely to elevate the market value.

Middle East and Africa Hemoglobinopathies Report Snapshots

Middle East and Africa Hemoglobinopathies Size

Middle East and Africa Hemoglobinopathies Analysis

Middle East and Africa Hemoglobinopathies Companies