MarketVue®: Dupixent-refractory atopic dermatitis (AD)
The MarketVue®: Dupixent-refractory atopic dermatitis 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®: Dupixent-refractory atopic dermatitis report is supported by 4 qualitative interviews with key opinion leaders (U.S. Dermatologists), a quantitative survey with 27 U.S. physicians and secondary research.
Geographies covered:United States plus epidemiology for EU5 (France, Germany, Italy, Spain, United Kingdom)
Key companies mentioned:• Eli Lilly
• Galderma
• Amgen
• Sanofi
• Keymed Biosciences
• Kyowa Kirin
• Ichnos Sciences
• Akesobio Australia
• Jiangsu Hengrui Pharmaceuticals
• Sunshine Guojian Pharmaceutical
• Oneness Biotech Co
• Allakos Therapeutics
Key drugs mentioned:• Topical corticosteroids
• Dupilumab (Dupixent)
• Abrocitnib (Cibinqo)
• Upadacitinib (Rinvoq)
• Tralokinumab (Adbry)
• Methotrexate
• Cyclosporine
• Azathioprine
• Mycophenolate (Cellcept)
• Ruxolitinib (Jakafi, Jakavi, Opzelura)
• Crisaborole (Eucrisa)
• Lebrikizumab (Ebglyss)
• Nemolizumab (Nemluvio)
• Rocatinlimab
• Amlitelimab
• CM310
• Telazorlimab / ISB 830
• AK120
• SHR-1819
• CM326
• FB825
• Lirentelimab / AK002
Key takeaways from the report:
Atopic dermatitis (AD) is a chronic, inflammatory skin disease characterized by skin lesions and severe itching.
Dermatologists typically begin AD treatment with topical corticosteroids (TCS), then progress to Dupixent for uncontrolled, moderate-severe cases. For patients who are refractory to Dupixent (9% of moderate cases and 16% of severe cases), physicians turn to oral JAK inhibitors despite associated black box warnings, according to REACH Market Research. Adbry, an IL-13 with a similar mechanism of action to Dupixent, was recently approved, however, interviewed dermatologists report that in their experience Adbry is not as effective as Dupixent.
These post-Dupixent AD therapy options include:
• LEO Pharma’s IL-13 inhibitor Adbry (Tralokinumab)
• Pfizer’s JAK inhibitor Cibinqo (Abrocitinib)
• AbbVie’s JAK inhibitor Rinvoq (Upadacitinib)
The AD pipeline is full of promising new biologics in development, including:
• Eli Lilly & Co.’s IL-13 inhibitor – lebrikizumab
• Keymed Biosciences Co. Ltd.’s IL-4Rα inhibitor – CM310
• Galderma’s IL-31R inhibitor – nemolizumab
• Amgen/Kyowa’s OX40 inhibitor – rocatinlimab
Most therapies in development for AD target patients with inadequate response to topicals rather than Dupixent-refractory patients, however, Eli Lilly and Co.’s lebrikizumab is one of the few investigational therapies specifically being studied in Dupixent-refractory patients.
Dermatologist, U.S.: “If a patient had suboptimal response to Dupixent, I would explain that the tralokinumab has a similar mechanism, and people might not be against injection, but it’s not their favorite thing to do, putting all those factors together. Some patients may say, ‘I’d rather try a different medication with a different mechanism,’ and also, you know, it’s a pill. It’s kind of appealing to them, but then others will say, you know, ‘No problem, I’d rather stay with a biologic because that’s what the FDA recommends.’”
Please note: the online download version of this report is for a global site license.