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Last Updated: December 26, 2024

KOATE Drug Profile


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Note on Biologic Patents

Matching patents to biologic drugs is far more complicated than for small-molecule drugs.

DrugPatentWatch employs three methods to identify biologic patents:

  1. Brand-side disclosures in response to biosimilar applications
  2. These patents were identified from disclosures by the brand-side company, in response to a potential biosimilar seeking to launch. They have a high certainty of blocking biosimilar entry. The expiration dates listed are not estimates — they're expiration dates as indicated by the brand-side company.

  3. General brand-side disclosures
  4. These patents were identified from searching drug labels and other general disclosures from the brand-side company. This list may exclude some of the patents which block biosimilar launch, and some of these patents listed may not actually block biosimilar launch. The expiration dates listed for these patents are estimates, based on the grant date of the patent.

  5. Patents from broad patent text search
  6. For completeness, these patents were identified by searching the patent literature for mentions of the branded or ingredient name of the drug. Some of these patents protect the original drug, whereas others may protect follow-on inventions or even inventions casually mentioning the drug. The expiration dates listed for these patents are estimates, based on the grant date of the patent.

1) High Certainty: US Patents for KOATE Derived from Brand-Side Litigation

No patents found based on brand-side litigation

2) High Certainty: US Patents for KOATE Derived from Company Disclosures

No patents found based on company disclosures

3) Low Certainty: US Patents for KOATE Derived from Patent Text Search

These patents were obtained by searching patent claims

KOATE Market Analysis and Financial Projection Experimental

Market Dynamics and Financial Trajectory for Biologic Drugs: A Focus on KOĀTE

Introduction

The biologics market is experiencing rapid growth, driven by several key factors including the increasing prevalence of chronic diseases, advancements in drug delivery systems, and the expanding use of biosimilars. This article will delve into the market dynamics and financial trajectory of biologic drugs, with a specific focus on KOĀTE, a biologic therapy used for the treatment of hemophilia A.

Global Biologics Market Outlook

The global biologics market is projected to grow significantly over the next few years. By 2032, the market is expected to reach USD 699.5 billion, growing at a compound annual growth rate (CAGR) of 7.8% from 2024 to 2032[1].

Key Drivers of the Biologics Market

Several factors are driving the growth of the biologics market:

Increasing Burden of Chronic Diseases

The rising prevalence of chronic diseases such as cancer, autoimmune disorders, and genetic diseases is a major driver. Biologics offer targeted and often more effective treatments for these conditions[1].

Technological Advancements

Continuous technological advancements, including the development of cell and gene therapies, are facilitating the creation of more targeted and efficient biologic drugs[3].

Growing Adoption of Biosimilars

Biosimilars, which are biologic products that are highly similar to an already approved biologic drug, are gaining traction due to their cost-effectiveness and similar efficacy profiles[1].

Improved Healthcare Infrastructure

Enhancements in healthcare infrastructure, particularly in emerging economies like China and India, are increasing access to biologic therapies[1].

KOĀTE: A Specific Biologic Therapy

Overview of KOĀTE

KOĀTE (Antihemophilic Factor (Human)) is a plasma-derived Factor VIII/VWF complex product used for the control and prevention of bleeding episodes in patients with hemophilia A. It is characterized by a mean biologic half-life of 16.1 hours and has a low risk of side effects, with only 0.7% of infusions associated with adverse reactions[2].

Clinical Efficacy

In clinical studies, KOĀTE has demonstrated high efficacy in managing bleeding episodes, with 82% of bleeds effectively managed with a single infusion. The product also undergoes two independent viral inactivation steps, ensuring no documented cases of viral transmission[2].

Safety Profile

While KOĀTE is generally well-tolerated, it carries risks such as the development of inhibitors (antibodies that neutralize Factor VIII) and the potential for transmitting infectious agents, although the current manufacturing process has shown no cases of viral transmission[2].

Market Segmentation and Regional Analysis

Market Segmentation

The biologics market is segmented by source (microbial, mammalian, others), product type (therapeutic proteins, monoclonal antibodies, vaccines), and application (cancer, autoimmune diseases, genetic disorders)[3].

Regional Analysis

  • Asia-Pacific: This region is a significant contributor to the biologics market due to its large patient population and growing healthcare infrastructure. Countries like China and India are investing heavily in biotechnology and R&D, driving market growth[1].
  • Latin America: Increased healthcare access and expenditures in countries such as Brazil and Mexico are expanding the market for biologic therapies in this region[1].
  • Middle East and Africa: Growing healthcare investments and international collaborations are driving the demand for biologics in this region[1].

Financial Trajectory of the Biologics Market

Current Market Size

The global biologics market was valued at USD 349.6 billion in 2023 and is expected to reach USD 699.5 billion by 2032[1].

Growth Projections

The market is forecasted to grow at a CAGR of 7.8% from 2024 to 2032. Another report predicts a higher CAGR of 12.7% from 2023 to 2028, with the market expected to reach USD 823.4 billion by the end of 2028[1][3].

Impact of KOĀTE on the Market

Market Share

While specific financial data for KOĀTE is not provided, its efficacy and safety profile contribute to its market share within the hemophilia A treatment segment. The overall growth of the biologics market benefits products like KOĀTE, which are part of the larger therapeutic protein segment[2].

Competitive Landscape

The biologics market is highly competitive, with several major players. KOĀTE competes with other Factor VIII products, both recombinant and plasma-derived, and its market position is influenced by factors such as pricing, reimbursement policies, and clinical outcomes[4].

Key Takeaways

  • The global biologics market is expected to grow significantly, driven by chronic diseases, technological advancements, and the adoption of biosimilars.
  • KOĀTE is a plasma-derived biologic therapy with a strong clinical efficacy and safety profile, used for treating hemophilia A.
  • The market is segmented by source, product type, and application, with regional growth driven by improving healthcare infrastructure and increasing awareness of biologic therapies.
  • The financial trajectory of the biologics market indicates substantial growth, with KOĀTE contributing to this trend within its specific therapeutic segment.

FAQs

What is the projected growth rate of the global biologics market?

The global biologics market is expected to grow at a CAGR of 7.8% from 2024 to 2032, reaching USD 699.5 billion by 2032[1].

What are the key drivers of the biologics market?

Key drivers include the increasing prevalence of chronic diseases, technological advancements, growing adoption of biosimilars, and improvements in healthcare infrastructure[1].

What is KOĀTE used for?

KOĀTE is used for the control and prevention of bleeding episodes in patients with hemophilia A[2].

What is the safety profile of KOĀTE?

KOĀTE has a low risk of side effects, with 0.7% of infusions associated with adverse reactions. However, it carries risks such as the development of inhibitors and potential transmission of infectious agents, although no cases have been documented with the current manufacturing process[2].

How does KOĀTE compare to other biologic therapies in terms of market share?

KOĀTE competes within the therapeutic protein segment, particularly for hemophilia A treatments. Its market share is influenced by factors such as clinical outcomes, pricing, and reimbursement policies[4].

What regions are driving the growth of the biologics market?

The Asia-Pacific, Latin America, and Middle East and Africa regions are significant contributors to the growth of the biologics market due to their large patient populations and improving healthcare infrastructures[1].

Sources

  1. Biologics Market Size to Reach USD 699.5 Billion by 2032, Impelled by Emergence of Advanced Drug Delivery Systems - Biospace
  2. POWERED BY PLASMA - koāte - Mykoate
  3. Big Growth Ahead Biologic Drugs Market to Hit 823.4 Billion by 2028 - BCC Research
  4. Biologic Therapeutic Drugs: Technologies and Global Markets - BCC Research

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.