MarketVue®: Bullous Pemphigoid
The MarketVue®: Bullous Pemphigoid market landscape report combines primary (KOL interviews and survey data) and secondary market research to empower strategic decision-making and provide a complete view of the market.
Every MarketVue® includes a disease overview, epidemiology (US and EU5), current treatment, unmet needs, pipeline and access and reimbursement chapter.
Topics covered in this report:• Disease overview: Review the disease pathophysiology and potential druggable targets
• Epidemiology: Understand prevalence, diagnosed and drug-treated prevalence of the population and key market segments
• Current treatment: Understand the treatment decision tree and strengths and weaknesses of current on-label and off-label treatment
• Unmet needs: Identify opportunities to address treatment or disease management gaps
• Pipeline analysis: Compare current and emerging therapy clinical development strategy; their performance on efficacy, safety, and delivery metrics; and their potential to address unmet needs
• Value and access: Review the evidence needed to assess and communicate value to key stakeholders (e.g., providers, payers, regulators) and learn what competitors have done or are doing
Methodology:Research for the MarketVue®: Bullous Pemphigoid report is supported by 4 qualitative interviews with key opinion leaders, a quantitative survey with 25 U.S. physicians and secondary research.
Geographies covered:United States plus epidemiology for EU5 (France, Germany, Italy, Spain, United Kingdom)
Key companies mentioned:• Regeneron
• Sanofi
• AstraZeneca
• argenx
• AKARI Therapeutics
• Immune Pharmaceuticals
Key drugs mentioned:• Corticosteroids
• Tetracycline
• Rituximab (Rituxan)
• Omalizumab (Xolair)
• Dupilumab (Dupixent)
• Benralizumab (Fasenra)
• Doxycycline
• Dapsone+J17
• Niacinamide
• Minocycline
• Azathioprine
• Cyclophosphamide
• Methotrexate
• Cyclosporine
• IVIg (Panzyga)
• Efgartigimod
• Nomacopan
• Prednisone
• Bertilimumab
• Mycophenolate mofetil
Key takeaways from the report:
Bullous pemphigoid (BP) is a rare, autoimmune, blistering disease for which there are no approved therapies. BP is associated with significant morbidities such as:
• Subepidermal blistering
• Severe pruritis
• Infection
• Diminished quality of life
In the absence of approved treatments, physicians utilize oral corticosteroids as first-line treatment to quickly eliminate pruritus and stop further blistering in the acute phase of BP. However, chronic use of corticosteroids can lead to life-threatening side effects; therefore, physicians assert that improving the time between relapses without long-term reliance on corticosteroids is a significant unmet need in the treatment of BP. Furthermore, nearly three-quarters of surveyed dermatologists rated therapies that can minimize corticosteroid exposure in the acute setting as an “important” unmet need in the treatment landscape, according to REACH Market Research’s MarketVue® assessment.
Dermatologist, U.S.: I’m most optimistic for the biologics. I think there’s enough in the pipeline that something will hopefully get an on-label indication, and that’ll improve accessibility for patients to these treatments. Being able to give somebody something that’s not increasing their risk of infection and death, but rather helping their symptoms without increasing those risks would be nice and seems attainable.
The BP pipeline contains a number of biologics, including:
• argenx’s FcRn inhibitor - efgartigimod
• Regeneron/Sanofi’s IL-4/IL-13 inhibitor - dupilumab
• AstraZeneca’s IL-5 inhibitor - benralizumab
Dermatologists report that preliminary results from clinical trials of biologics such as FcRn and IL-4 inhibitors look promising, although some express doubts that they would be efficacious enough to eliminate the need for corticosteroids.
Tyler Jakab, Analyst at REACH: ""Physicians seem to agree that emerging therapies like FcRn inhibitors hold promise in reducing the circulating autoantibodies that drive autoimmune diseases like bullous pemphigoid. However, BP is also characterized by complement and eosinophil activity, so we’ll have to await clinical trial results to see if these therapies measure up to steroids in terms of efficacy and speed in controlling the inflammation found in the acute phase of the disease.""
Please note: the online download version of this report is for a global site license.