Étude de marché sur les biosimilaires

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S'engager dans une étude approfondie du marché des biosimilaires aide les entreprises à comprendre la dynamique du marché, les changements réglementaires et les préférences des consommateurs, garantissant ainsi qu'elles peuvent prendre des décisions stratégiques qui stimulent la croissance et l'innovation.

The truth about biosimilars? They’re not just cheaper alternatives—they’re healthcare game-changers that most executives still don’t fully understand. I’ve sat across from pharmaceutical CEOs who dismissed them, only to watch their market share erode months later.

Having led SIS International through decades of market evolution, I can assure you that few sectors offer the complexity and opportunity that biosimilars present today. Our specialists have uncovered patterns that separate market leaders from those struggling to adapt—and the differences might surprise you.

Pourquoi les entreprises ont-elles besoin d’une étude de marché sur les biosimilaires ?

Biosimilar market research is crucial for developing effective market entry and growth strategies. It identifies the market size, growth potential, and key drivers of demand. Companies can tailor their products and marketing strategies to meet the specific needs of different market segments by analyzing trends in patient adoption, healthcare provider preferences, and regional market variations.

De plus, the biosimilar market is heavily regulated, with stringent requirements for approval and ongoing compliance. Therefore, biosimilar market research enables businesses to stay updated on regulatory changes, understand the approval processes in different regions, and anticipate potential regulatory hurdles. This knowledge helps companies develop regulatory strategies that ensure timely approval and compliance, reducing the risk of delays and additional costs.

En plus, market research provides detailed competitive analysis, helping businesses understand their competitors’ strategies, strengths, and weaknesses. It is essential to identify market gaps, develop unique value propositions, and effectively position biosimilar products to gain a competitive advantage.

The Evolving Landscape of Biosimilars

The truth about biosimilars? They’re not just cheaper alternatives—they’re healthcare game-changers that most executives still don’t fully understand.

Market disruption is the daily reality reshaping pharmaceutical economics worldwide. The biosimilar market research we’ve conducted over the past five years reveals a startling truth: manufacturers who initially scoffed at biosimilar competition now scramble to develop their portfolios. You’re witnessing a fundamental shift in how biological therapies reach patients, with ripple effects touching everything from pricing strategies to R&D priorities.

… And what’s driving this transformation? It’s not just cost savings, though they’re substantial. Our latest biosimilar market research indicates that successful market entrants are those who understand the complex interplay between regulatory pathways, physician acceptance, and patient education. The barriers to entry remain high—developing a biosimilar isn’t like producing a simple generic pill—but the rewards for getting it right have never been greater.

The most successful organizations we’ve worked with approach biosimilar market research as an ongoing commitment rather than a one-time investment. They’re constantly testing assumptions, tracking evolving prescriber behaviors, and adjusting their commercialization strategies based on real-world evidence.

Notre analyse actuelle du marché et nos recommandations

Chez SIS International, nous considérons que le marché des biosimilaires connaît une croissance significative, tirée par la demande croissante de traitements biologiques rentables, l'expiration des brevets des principaux produits biologiques et un environnement réglementaire favorable. Nos recherches indiquent que le marché devrait continuer à se développer, avec un nombre croissant de produits biosimilaires entrant sur le marché dans divers domaines thérapeutiques.

Additionally, healthcare providers’ and patients’ acceptance and adoption of biosimilars are on the rise, supported by increased education and awareness efforts. However, challenges such as regulatory complexities, competitive pressures, and the need for robust pharmacovigilance remain.

Recommandations pour les entreprises

1. Tirer parti des opportunités du marché : Nous recommandons aux entreprises de tirer parti de la demande croissante de biosimilaires en élargissant leur portefeuille de produits et en se lançant dans de nouveaux domaines thérapeutiques. En identifiant les marchés à fort potentiel et les besoins non satisfaits, les entreprises peuvent développer des produits biosimilaires destinés à des populations de patients spécifiques et acquérir un avantage concurrentiel.
2. Renforcer les stratégies réglementaires : Il est essentiel de naviguer dans le paysage réglementaire pour réussir le lancement et la commercialisation de biosimilaires. Nous pensons que les entreprises devraient investir dans l’élaboration de stratégies réglementaires solides qui garantissent le respect des exigences régionales et facilitent les approbations en temps opportun. 
3. Améliorer l’engagement des parties prenantes : Instaurer la confiance entre les prestataires de soins de santé, les payeurs et les patients est essentiel pour l’adoption généralisée des biosimilaires. Nous considérons qu'il est important que les entreprises se concentrent sur des stratégies globales d'éducation et de communication mettant en avant la sécurité, l'efficacité et la rentabilité des biosimilaires. 

Regional Variations in Biosimilar Adoption

Geographic differences in biosimilar uptake tell a fascinating story about healthcare systems and cultural attitudes toward innovation.

Dans L'Europe, where biosimilar market research shows impressive adoption rates, centralized purchasing decisions and physician incentives have created a flourishing ecosystem. Meanwhile, the U.S. market presents a more fragmented picture, with biosimilar market research revealing pockets of rapid adoption alongside areas of persistent resistance.

I’ve walked hospital corridors in Germany, where biosimilar utilization exceeds 90% for certain molecules, and contrasted this with facilities in parts of the U.S. where that figure struggles to reach 20%. Our biosimilar market research teams have identified key inflection points that predict when and how quickly adoption accelerates in different regions. It’s not simply about price—though that matters enormously—but about confidence in the regulatory framework and educational outreach.

Asian markets present perhaps the most dynamic picture of all. Our biosimilar market research in South Korea, India, and China reveals aggressive government policies promoting domestic development alongside unique physician education needs. We’ve helped multinational clients navigate these complexities, identifying partnership opportunities that leverage local knowledge while maintaining global quality standards.

Acteurs de premier plan dans les études de marché sur les biosimilaires

Sur le marché des biosimilaires, plusieurs acteurs de premier plan stimulent l’innovation, le développement et la commercialisation de produits biosimilaires. Ces entreprises s'appuient sur des études de marché complètes pour naviguer dans les paysages réglementaires, comprendre la dynamique du marché et se positionner de manière compétitive. Voici quelques-uns des principaux acteurs des études de marché sur les biosimilaires :

Amgen

• Amgen est un leader mondial en biotechnologie et l'un des pionniers dans le développement de biosimilaires. En mettant fortement l'accent sur la recherche et le développement, Amgen utilise des études de marché approfondies pour identifier les opportunités et optimiser son portefeuille de produits. 

Sandoz (une division de Novartis)

• Sandoz, une division de Novartis, est un acteur majeur sur le marché des biosimilaires, avec un large portefeuille de produits biosimilaires. La société utilise des études de marché approfondies pour comprendre les préférences des prestataires de soins de santé, les exigences réglementaires et le paysage concurrentiel. 

Biocon

• Biocon est un leader émergent du marché des biosimilaires, connu pour son approche innovante et sa portée mondiale. La société exploite les études de marché pour étendre sa présence sur les marchés clés et améliorer son positionnement concurrentiel. 

Pfizer

• Pfizer est un acteur majeur sur le marché des biosimilaires, mettant fortement l'accent sur la recherche et le développement. La société utilise des études de marché complètes pour guider ses stratégies biosimilaires, du développement du produit à la commercialisation. 

Celltrion

• Celltrion est une société de biotechnologie spécialisée dans le développement et la fabrication de biosimilaires. La société mène des études de marché approfondies pour identifier les besoins du marché, les défis réglementaires et les opportunités concurrentielles. 

Samsung Bioépis

• Samsung Bioepis est une coentreprise entre Samsung Biologics et Biogen, dédiée au développement de biosimilaires de haute qualité. La société exploite les études de marché pour naviguer dans des paysages réglementaires complexes et comprendre la dynamique du marché. 

Produits pharmaceutiques Teva

• Teva Pharmaceuticals est un leader mondial des médicaments génériques et spécialisés, y compris les biosimilaires. La société utilise des études de marché pour orienter ses stratégies de développement et de commercialisation de biosimilaires. L'accent mis par Teva sur l'accès des patients et la maîtrise des coûts motive ses efforts visant à commercialiser des biosimilaires de haute qualité, offrant ainsi des options de traitement plus abordables aux patients du monde entier.

Merck & Co. (MSD)

• Merck & Co., connue sous le nom de MSD en dehors des États-Unis et du Canada, est un acteur majeur sur le marché des biosimilaires. La société mène des études de marché approfondies pour comprendre les préférences des prestataires de soins de santé, les défis réglementaires et les opportunités de marché. L'engagement de Merck en faveur de l'innovation et de la qualité garantit que ses produits biosimilaires répondent aux normes de sécurité et d'efficacité les plus élevées.

Future Trends in Biosimilar Development

The next wave of biosimilars will transform therapeutic areas that have remained relatively untouched by this revolution. Our biosimilar market research forecasts indicate that ophthalmology, dermatology, and neurology will experience the kind of competitive reshaping that oncology and immunology have already undergone. You’re looking at a market that will nearly triple in value over the next decade, with particularly aggressive growth in emerging economies.

What makes this next phase different?

Biosimilar market research points to several key factors. Manufacturing technologies have advanced dramatically, lowering development costs. Regulatory pathways have become more predictable in major markets. And perhaps most importantly, the first generation of biosimilars has built credibility among clinicians who were initially skeptical but now have years of real-world experience with these products.

“The pioneers in biosimilar development faced headwinds that the next generation of products won’t encounter to the same degree—but they’ll face new challenges that require equally sophisticated market intelligence,” as one of our senior analysts recently noted in our global biosimilar market research report.

I’ve advised clients to pay particular attention to how digital health technologies reshape patient monitoring capabilities. Our biosimilar market research indicates that biosimilar manufacturers who can offer compelling value-added services—not just competitive pricing—will increasingly differentiate themselves in crowded therapeutic categories. We’re already seeing this play out in diabetes and growth hormone therapies, where device integration and patient support programs have become competitive battlegrounds.

Competitive Analysis in the Biosimilar Space

When we conduct biosimilar market research focused on competitive positioning, we often uncover development programs that aren’t widely publicized but could fundamentally alter market entry timing decisions. You’re operating in an environment where being third-to-market with the right strategy often outperforms being first with the wrong one.

Our biosimilar market research methodology combines traditional pharmaceutical intelligence gathering with specialized approaches developed specifically for this unique market. We track not just which molecules are in development, but also manufacturing capacity investments, clinical trial site selections, and patent litigation strategies that signal competitors’ intentions and capabilities.

What distinguishes high-value biosimilar market research is the ability to forecast product approvals and adoption curves across different customer segments. We’ve developed sophisticated models incorporating stakeholder research, analog analysis, and payer dynamics to help clients realistic volume projections at launch and throughout the product lifecycle as competitive intensity increases.

Biosimilar Market Research – Key Insights

- Market Disruption: Biosimilars are fundamentally reshaping pharmaceutical economics, with even skeptical manufacturers now developing their biosimilar portfolios.

- Success Factors: Leading companies in the biosimilar space excel through deep stakeholder insights rather than just competitive pricing, understanding the interplay between regulatory pathways, physician acceptance, and patient education.

- Regional Variations: Significant differences exist in adoption rates across regions, with Europe showing adoption rates up to 90% for certain molecules while some U.S. regions struggle to reach 20%.

- Asian Markets: Countries like South Korea, India, and China present unique opportunities with aggressive government policies promoting domestic development alongside specific education needs.

- Stakeholder Complexity: Successful biosimilar launches require orchestrating messages across multiple audiences simultaneously, including payers, hospital administrators, patient groups, and regulatory authorities.

- Value Thresholds: Different stakeholders require different cost savings to find biosimilar value propositions compelling—hospital pharmacists may demand 30% savings. In comparison, integrated health systems might change formularies at just 15% if supply reliability is high.

- Emerging Therapeutic Areas: The next wave of biosimilars will transform ophthalmology, dermatology, and neurology, with market value expected to nearly triple over the next decade.

- Regulatory Navigation: Significant differences in approval requirements across regions necessitate sophisticated intelligence to design efficient development programs meeting diverse expectations.

- Competitive Positioning: Being third-to-market with the right strategy often outperforms being first with the wrong approach—successful companies track molecules in development, manufacturing investments, and patent litigation strategies.

- Intégration numérique: Forward-thinking biosimilar manufacturers differentiate themselves through value-added services like device integration and patient support programs, particularly in diabetes and growth hormone therapies.

Comment l'étude de marché de SIS International sur le marché des biosimilaires aide les entreprises

Notre expertise en matière d'études de marché sur les biosimilaires couvre divers aspects de la dynamique du marché, des paysages réglementaires et de l'analyse concurrentielle, permettant aux entreprises de prendre des décisions éclairées et d'atteindre leurs objectifs stratégiques. Voici comment notre étude de marché sur le marché des biosimilaires aide les entreprises :

Augmentation des revenus

Our research helps companies understand which products or services resonate most with healthcare providers and patients, enabling them to focus on high-potential areas. 

Réduction de risque

Nous fournissons aux entreprises les informations nécessaires pour identifier les risques potentiels et élaborer des stratégies d’atténuation. Nos recherches aident les entreprises à prendre des décisions éclairées qui réduisent le risque d’erreurs coûteuses et assurent la résilience face aux défis.

Efficacité marketing améliorée

SIS International market research services help businesses identify the most effective marketing channels, messages, and strategies to reach their target audience. 

Croissance et innovation accélérées

Our research services provide businesses with the insights to identify emerging trends and consumer needs, fueling innovation and growth. 

Partenariat à long terme

We believe in building long-term partnerships with our clients. SIS International provides ongoing support and consultation to help businesses adapt to market changes and continuously refine their strategies. Our commitment to client success ensures you have a trusted partner to rely on as you navigate the biosimilar market. 

 

FAQ

1. What makes biosimilar market research different from traditional pharmaceutical research?

Biosimilar market research requires a more comprehensive stakeholder approach than traditional pharmaceutical research. While traditional research often focuses heavily on prescriber preferences, biosimilar research must include payers, hospital administrators, patient advocacy groups, and regulatory authorities—all of whom significantly influence adoption. Additionally, biosimilar research must account for unique considerations like interchangeability, switching studies, and reference product selection that don’t exist in other pharmaceutical categories.

2. How long do biosimilars typically take to gain significant market share after launch?

Market share acquisition varies dramatically by region, therapeutic area, and molecule. In Europe, where centralized purchasing decisions and physician incentives support adoption, biosimilars can capture 50-80% market share within 12-24 months for well-established molecules. In the U.S., adoption has historically been slower, though this is changing with improved stakeholder education and evolving payer policies. Our research shows that oncology biosimilars typically gain traction faster than those in immunology, and hospital-administered products generally see quicker uptake than self-administered ones.

3. What are the most common barriers to biosimilar market entry for entrepreneurs?

The primary barriers include:
1) High development costs and technical complexity, requiring sophisticated manufacturing capabilities;
2) Patent thickets created by reference product manufacturers;
3) Regulatory uncertainty in some regions;
4) Physician and patient education needs; 5) Reference product manufacturer defensive strategies including contracting tactics and product improvements;
6) Limited differentiation opportunities beyond price; and
7) Challenges in building credibility with key stakeholders as a new entrant. Successful entrepreneurs typically address these through strategic partnerships, focused therapeutic area selection, and innovative go-to-market approaches.

4. How important is interchangeability designation for biosimilar commercial success?

While interchangeability designation can be valuable in certain market segments, particularly retail pharmacy-dispensed products, our research shows it’s not universally necessary for commercial success. Building prescriber confidence through strong clinical data and education often proves more important than interchangeability designation in hospital and clinic settings where physicians actively prescribe products. The significance of interchangeability varies substantially by therapeutic area, product administration setting, and regional pharmacy substitution laws.

5. What role do value-added services play in biosimilar competition?

As more biosimilars enter the same therapeutic spaces, value-added services are becoming increasingly important differentiators. Our research indicates that services like patient support programs, simplified reimbursement assistance, injection training, and digital monitoring tools can significantly influence adoption decisions when multiple biosimilars offer similar pricing. For entrepreneurs entering the space, strategically designed service offerings that address specific stakeholder pain points can create competitive advantage without requiring the massive investments to compete solely on price.

6. How are biosimilar pricing strategies evolving as markets mature?

Early biosimilar entrants typically launched with modest discounts (15-30%) to reference products, but pricing strategies have become more sophisticated as competition intensifies. In mature biosimilar markets like Europe, we now see average discounts of 30-70% depending on the therapeutic area and competitive intensity. Contract structures have also evolved beyond simple percentage discounts to include volume-based tiering, outcomes guarantees, and portfolio-based contracting. Entrepreneurs should be prepared for aggressive pricing competition in established biosimilar categories while potentially finding more pricing flexibility in newly-opening therapeutic areas.

7. What capabilities are most critical for new entrants to develop when entering the biosimilar space?

Beyond the obvious technical and regulatory capabilities required for development, successful new entrants must excel at:

1) Stakeholder mapping and engagement across the entire ecosystem;
2) Health economic modeling that quantifies value beyond simple acquisition cost;
3) Educational content development tailored to different stakeholder concerns;
4) Supply chain reliability and scalability;
5) Competitive intelligence gathering;
6) Nimble commercial operations that can adapt to rapidly changing market conditions; and
7) Strategic partnership development to complement internal capabilities. Our research consistently shows that companies underinvesting in these areas struggle even with technically excellent products.

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À propos de SIS International

SIS International propose des recherches quantitatives, qualitatives et stratégiques. Nous fournissons des données, des outils, des stratégies, des rapports et des informations pour la prise de décision. Nous menons également des entretiens, des enquêtes, des groupes de discussion et d’autres méthodes et approches d’études de marché. Contactez nous pour votre prochain projet d'étude de marché.