Product logins

Find logins to all Clarivate products below.


Alopecia | Niche & Rare Disease Landscape & Forecast | US/EU5 | 2020

Alopecia areata (AA) is an inflammatory autoimmune skin disease characterized by varying degrees of hair loss. The host immune system targets anagen hair follicles. The primary goal of treatment is to stimulate hair growth by reducing the inflammation at sites of hair loss. Topical / intralesional corticosteroids and topical immunotherapy are commonly prescribed for AA; however, tolerability issues, side effects, and the modest efficacy of these treatments underscore the substantial unmet clinical need in AA. The AA pipeline is active, consisting primarily of targeted immunomodulatory agents, and boasts several marketed and investigational JAK inhibitors (e.g., Eli Lilly’s Olumiant, Pfizer’s ritlecitinib, Concert’s CTP-543). This report provides an analysis of AA epidemiology, current disease management, unmet needs, and the clinical and commercial potential of emerging AA therapies.

QUESTIONS ANSWERED

  • How large is the diagnosed AA population, and how will its size change between 2020 and 2030? How large are the diagnosed alopecia totalis and universalis populations?
  • What are the key unmet clinical needs in AA and to what degree will they be fulfilled by 2030?
  • What is the current state of treatment in AA, and how will it evolve over time?
  • What emerging AA therapies are viewed by treating dermatologists as most promising, and what sales / uptake will they achieve in AA? How will JAK inhibitors fit into the AA treatment algorithm?

CONTENT HIGHLIGHTS

  • Geographies: United States, France, Germany, Italy, Spain, and the United Kingdom.
  • Primary research: Six country-specific interviews with thought-leading dermatologists supported by survey data collected for this study.
  • Epidemiology: Diagnosed and drug-treated prevalence of AA by country.
  • Forecast: Drug-level sales and patient share of key AA therapies in 2030.
  • Emerging therapies:
    • Phase II/III: 4 drugs.
    • Phase II: 7 drugs.
    • Coverage of select preclinical and Phase I products.

PRODUCT DESCRIPTION

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

Related Market Assessment Reports

Report
Asthma – Current Treatment – Treatment Algorithms: Claims Data Analysis – Pediatric Asthma (US)
Pediatric asthma is treated using two types of pharmacotherapies: rescue therapy for acute symptoms via bronchodilation (e.g., a SABA such as Teva’s ProAir HFA) and maintenance therapy to prevent…
Report
Acute Coronary Syndrome – Unmet Need – Unmet Need – Acute Coronary Syndrome: Secondary Prevention, on Top of Statin Treatment (US/EU)
This report covers the 12-month post-hospital management of secondary prevention in ACS patients. Reducing cardiovascular (CV) residual risk and achieving guideline-recommended LDL-C targets…
Report
Beta Thalassemia – Landscape & Forecast – Niche & Rare Disease Landscape & Forecast (US/EU5)
Beta thalassemia (BT) is a rare genetic disorder characterized by the reduced production of hemoglobin. BT minor is caused by a mutation in one hemoglobin beta (HBB) gene, and transfusion-dependent…
Report
Multiple Sclerosis – Unmet Need – Unmet Need – Multiple Sclerosis: Nonrelapsing Secondary-Progressive Multiple Sclerosis (US/EU)
No treatments are approved for nonrelapsing secondary-progressive multiple sclerosis (nrSP-MS), an MS disease course in which physical disability accumulates in the absence of superimposed relapses…
Report
Myasthenia Gravis – Current Treatment – Treatment Algorithms: Claims Data Analysis – Myasthenia Gravis (US)
Myasthenia gravis (MG) is a rare neuromuscular disorder caused by specific autoantibodies at the neuromuscular junction; in most patients, these autoantibodies target acetylcholine receptors. MG is…