Sickle Cell Disease (SCD) – Market outlook, Epidemiology, Competitive Landscape and Market Forecast Report – 2020 To 2030
Sickle cell disease (SCD) is a group of inherited red blood cell disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disease have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.
Etiology-
Mutations in the HBB gene
cause sickle cell disease. The HBB gene provides instructions for making
beta-globin. Various versions of beta-globin result from different mutations in
the HBB gene. One HBB gene mutation produces an abnormal version of beta-globin
known as hemoglobin S (HbS). Other mutations in the HBB gene lead to different bizarre
versions of beta-globin, such as hemoglobin C (HbC) and hemoglobin E (HbE). HBB
gene mutations can also result in a shallow level of beta-globin; this
abnormality is called beta-thalassemia.
Epidemiology-
Sickle
cell disease is the most common inherited blood disorder in the United States,
affecting 100,000 Americans. The disease is estimated to occur in 1 in 500
African Americans and 1 in 1,000 to 1,400 Hispanic Americans.
The competitive
landscape of Sickle Cell Disease (SCD) includes country-specific approved and
pipeline therapies. Any asset/product-specific designation or review and
Accelerated Approval are tracked and supplemented with analyst commentary.
KOLs insights of Sickle
Cell Disease (SCD) across 8 MM market from the center of Excellence/ Public/
Private hospitals participated in the study. Insights around current treatment
landscape, epidemiology, clinical characteristics, future treatment paradigm,
and Unmet needs.
Sickle
Cell Disease (SCD) Market
Forecast: Patient Based Forecast Model (MS. Excel Based Automated
Dashboard) which Data Inputs with sourcing, Market Event, and Product Event,
Country specific Forecast Model, Market uptake and patient share uptake,
Attribute Analysis, Analog Analysis, Disease burden, and pricing scenario,
Summary, and Insights.
S. No Asset Company Stage
1 VIT-2763 Vifor
(International) Inc. Phase 2
2 SHP655 Shire Phase 1
3 CTX001 Vertex
Pharmaceuticals Incorporated Phase 1/2
4 Rivipansel GlycoMimetics
Incorporated Phase 3
5 GPH101 Graphite
Bio, Inc. Phase 1/2
6 FT-4202 Forma
Therapeutics, Inc. Phase 2/3
7 Mitapivat Agios
Pharmaceuticals, Inc. Phase 2/3
8 IMR-687 Bioverativ,
a Sanofi company Phase 2
9 SANGUINATE Prolong
Pharmaceuticals Phase 2
10 Hydroxyurea Nova
Laboratories Limited Phase 2
Comments
Post a Comment