Product logins

Find logins to all Clarivate products below.


Sickle Cell Disease | Niche & Rare Disease Landscape & Forecast | US/EU5 | 2018

MARKET OUTLOOK

Sickle cell disease (SCD) is a rare genetic blood disorder characterized by a polymerization of hemoglobin in red blood cells (RBCs) that causes the cells to become distorted into a sickle shape. The distorted RBCs lead to several complications such as vaso-occlusion (VOC) associated with pain attacks, acute chest syndrome, and anemia. No curative therapy exists for SCD other than an allogenic hematopoietic stem cell transplantation with a matched (most often sibling) donor. Prophylactic penicillin to prevent commonly occurring infections, analgesics for pain episodes, hydroxyurea to increase the expression of an alternative form of hemoglobin, and blood transfusions are the cornerstones of SCD management, but a high unmet need remains for improved therapies. Drug developers have recognized the commercial opportunity in SCD, developing agents with novel mechanisms of action that target the underlying genetic defect and reduce VOC. A robust and diverse late-stage pipeline will be a key driver for substantial expansion of the SCD market by 2027 while patients await potentially curative options in early-stage development.

QUESTIONS ANSWERED

  • How large is the diagnosed prevalent SCD population in the United States and EU5? How will the population change through 2027?
  • What is the current treatment landscape for SCD patients and how will it change in the next ten years? What clinical needs remain unfulfilled?
  • What pipeline products are most promising, and what sales/uptake could they secure in SCD? How will new therapies impact medical practice?

PRODUCT DESCRIPTION

Niche & Rare Disease Landscape & Forecast: Comprehensive market intelligence providing world-class epidemiology, keen insight into current treatment paradigms, in-depth pipeline assessments, and drug forecasts supported by detailed primary and secondary research.

RELEASE DATE

October 2018

GEOGRAPHIES

United States and EU5

PRIMARY RESEARCH:

  • Six country-specific interviews with thought-leading hematologists
  • Supported by survey data collected for this study

EPIDEMIOLOGY:

Diagnosed prevalent and drug-treatable cases of sickle cell disease by country, segmented by clinical subtypes.

FORECAST

Drug-level sales and patient shares of key sickle cell disease therapies in 2027.

EMERGING THERAPIES

Phase III: 5 drugs. Phase II: 4 drugs. Coverage of select preclinical and Phase I and Phase I/II products.

Related Market Assessment Reports

Report
Atopic Dermatitis / Atopic Eczema – Current Treatment – Current Treatment: Physician Insights – Atopic Dermatitis / Atopic Eczema – Moderate to Severe (US)
AD is a chronic inflammatory skin condition characterized by recurrent flares and persistent itch, significantly impacting patient quality of life. Moderate to severe AD continues to undergo rapid…
Report
Renal Anemia – Current Treatment – Treatment Algorithms: Claims Data Analysis – Renal Anemia (US)
Renal anemia is a common complication of chronic kidney disease (CKD) resulting from insufficient erythropoietin production by impaired kidneys. The primary goal of renal anemia treatment is to…
Report
Myasthenia Gravis – Current Treatment – Treatment Algorithms: Claims Data Analysis – Myasthenia Gravis (US)
Myasthenia gravis (MG) is a rare neuromuscular disorder caused by autoantibodies at the neuromuscular junction. It leads to fluctuating muscle weakness and fatigue. Standard treatments include…
Report
Squamous Cell Carcinoma of the Head and Neck – Landscape & Forecast – Disease Landscape & Forecast (G7)
Squamous cell carcinoma of the head and neck (SCCHN) is the seventh most commonly diagnosed cancer. It encompasses a spectrum of heterogeneous tumors originating at multiple sites in the head and…
Report
Hemophilia A – Current Treatment – Current Treatment: Physician Insights – Hemophilia A with Inhibitors (US)
Development of neutralizing antibodies against factor VIII replacement is the most significant clinical complication in hemophilia A, necessitating specialized and often high-cost management…