The Hemoglobin Subunit Beta pipeline drugs market research report outlays comprehensive information on the Hemoglobin Subunit Beta targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Hemoglobin Subunit Beta pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
The report also covers products from therapy areas such as Hematological Disorders, Oncology, and Metabolic Disorders which include the indications Sickle Cell Disease, Beta Thalassaemia, Blood Cancer, and Fabry Disease. It also reviews key players involved in Hemoglobin Subunit Beta targeted therapeutics development with respective active and dormant or discontinued products.
The Hemoglobin Subunit Beta pipeline targets constitutes close to 20 molecules. Out of which, approximately 15 molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase I, Phase 0, Preclinical, and Discovery stages are 1, 1, 2, 7, and 4 respectively. Similarly, the universities portfolio in Phase II, and Preclinical comprises 2, and 3 molecule.
Hemoglobin Subunit Beta overview
Hemoglobin subunit beta (HBB) is a critical protein component of hemoglobin, the oxygen-carrying protein found in red blood cells. Encoded by the HBB gene, β-globin plays a pivotal role in transporting oxygen throughout the body. In adults, hemoglobin A (HbA), the predominant form of hemoglobin, consists of four subunits: two α-globin chains and two β-globin chains. Each β-globin chain contains an iron-binding heme group, enabling the reversible binding of oxygen molecules.
For a complete picture of Hemoglobin Subunit Beta’s drug pipeline, buy the report here.
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