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The Future of the U.S. Biologics and Biosimilars Treatment Market for Psoriasis

October 2017 | 104 pages | ID: F37ECDE89F7EN
MP Advisors

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The U.S. psoriasis treatment market for Biologics and Biosimilars was estimated at $6.6bn in 2016 is projected to almost double during the forecast period to reach $12.9bn in 2021 driven by safety and efficacy improvements of the new generation biologics.

The psoriasis treatment market is dominated by topical agents and photo therapy for the non-severe forms (mainly corticosteroids), but mild to severe forms are treated with systemic agents. The psoriasis treatment market is dominated by topical agents and photo therapy for the non-severe forms (mainly corticosteroids), but mild to severe forms are treated with systemic agents.

Driven by improved efficacy, the first group of anti TNF treatments led by Enbrel, Humira and Remicade made strong penetration into the psoriasis market. However the emergence of the IL-17 inhibitor class driven by Novartis’ Cosentyx and Eli Lilly’s Talz have set a new benchmark for efficacy in moderate to severe psoriasis treatment with potential for safety improvement in comparison to the anti TNF drugs given their greater specificity in immune Suppression. MP Advisors expect the TNF class of drugs to lose share to the newer brands with improved clinical profiles in Psoriasis.

The market growth in psoriasis is driven by an upsurge in demand from new therapies in moderate to severe patient population which overshadows reduced pricing of branded TNF-α inhibitor and recent biosimilar launches. The psoriasis treatment market is facing increasing competitive pressure from a wave of biosimilar launches such as biosimilars of Janssen’s Remicade, and Amgen’s Enbrel with the impact of the headwinds expected to be more pronounced in the next few years.

Stelara has been an important growth driver of Janssen’s immunology franchise in recent years, with overall global sales doubling from $1.5bn in 2013 to more than $3.2bn in 2016. However Stelara has started to face steeper competition from the IL-17 drug class. A new head-to-head study report IL-17 products to demonstrate superior efficacy to Stelara for psoriasis.
1. PSORIASIS MARKET OVERVIEW

1.1. Disease background
1.2. Types of psoriasis
  1.2.1. Plaque psoriasis
  1.2.2. Guttate psoriasis
  1.2.3. Inverse (flexural) psoriasis
  1.2.4. Pustular psoriasis
  1.2.5. Erythrodermic psoriasis
1.3. Pathophysiology
1.4. Etiology
  1.4.1. Environmental factors
  1.4.2. Genetic factors
  1.4.3. Immunologic factors
1.5. Risk factors and co-morbidities
1.6. Epidemiology
1.7. Treatment options
  1.7.1. Phototherapy
  1.7.2. Topical treatments
  1.7.3. Conventional systemic agents
  1.7.4. Other systemic drugs
  1.7.5. Biologics
1.8. Treatment Guidelines
  1.8.1. Mild to moderate Psoriasis
  1.8.2. Moderate Psoriasis
  1.8.3. Moderate –to–severe psoriasis
  1.8.4. Severe psoriasis

2. PSORIASIS TREATMENT MARKET FOR BIOLOGICS

2.1. Introduction and Market Overview
2.2. Revenue Analysis for Biologics in the U.S.
2.3. Key marketed products for psoriasis treatment
  2.3.1. Remicade (infliximab; Janssen)
  2.3.2. Humira (adalimumab; AbbVie)
  2.3.3. Stelara (ustekinumab; Janssen)
  2.3.4. Cosentyx (secukinumab; Novartis)
  2.3.5. Taltz (ixekizumab; Lilly)
  2.3.6. Siliq (brodalumab; Valeant)
  2.3.7. Tremfya (guselkumab; Janssen)
2.4. Key pipeline products for psoriasis treatment
  2.4.1. Tildrakizumab; Merck / Sun Pharma
  2.4.2. Cimzia (certolizumab pegol; UCB/Dermira Pharmaceuticals)
  2.4.3. Risankizumab; AbbVie/Boehringer Ingelheim
2.5. Growth Drivers and Resistors for Biologics
  2.5.1. Growth Drivers:
  2.5.2. Resistors
2.6. Competitive Landscape ‒ Approved Products
2.7. Competitive Landscape ‒ Pipeline Products

3. PSORIASIS MARKET FOR BIOSIMILARS

3.1. Introduction and Market Overview
3.2. Approved biosimilars
  3.2.1. Approved biosimilars in the U.S.
  3.2.2. Revenue Analysis for Biosimilars in U.S.
  3.2.3. Approved biosimilars in the EU
3.3. Pipeline Analysis
  3.3.1. Clinical development ‒ Humira (adalimumab) biosimilars
  3.3.2. Clinical development ‒ Enbrel (etanercept) biosimilars
  3.3.3. Clinical development ‒ Remicade (infliximab) biosimilars
3.4. Biosimilars deals and partnerships
3.5. Growth Drivers and Resistors for Biosimilars
  3.5.1. Growth Drivers
  3.5.2. Resistors
3.6. Competitive Landscape ‒ Approved Biosimilars in the U.S. and EU
3.7. Competitive Landscape – TNF α Inhibitors Biosimilars Pipeline
References:


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