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Last Updated: December 22, 2024

PIPOBROMAN - Generic Drug Details


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What are the generic sources for pipobroman and what is the scope of patent protection?

Pipobroman is the generic ingredient in one branded drug marketed by Abbott and is included in one NDA. Additional information is available in the individual branded drug profile pages.

Summary for PIPOBROMAN
US Patents:0
Tradenames:1
Applicants:1
NDAs:1
Raw Ingredient (Bulk) Api Vendors: 68
Clinical Trials: 3
Patent Applications: 7,316
DailyMed Link:PIPOBROMAN at DailyMed
Recent Clinical Trials for PIPOBROMAN

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
NovartisPhase 2
RWTH Aachen UniversityPhase 2
Novartis PharmaceuticalsPhase 2

See all PIPOBROMAN clinical trials

Medical Subject Heading (MeSH) Categories for PIPOBROMAN

US Patents and Regulatory Information for PIPOBROMAN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Abbott VERCYTE pipobroman TABLET;ORAL 016245-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Abbott VERCYTE pipobroman TABLET;ORAL 016245-002 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

PIPOBROMAN Market Analysis and Financial Projection Experimental

Market Dynamics and Financial Trajectory for Pipobroman

Introduction

Pipobroman is a chemotherapeutic agent used primarily in the treatment of myeloproliferative disorders, such as polycythemia vera (PV) and essential thrombocythemia (ET). Understanding the market dynamics and financial trajectory of pipobroman involves analyzing various factors, including its efficacy, market demand, competition, and regulatory environment.

Efficacy and Clinical Use

Pipobroman has been shown to be effective in the long-term control of PV. A study published on PubMed demonstrated that pipobroman achieved hematologic remission in 94% of patients, with a median overall survival of 215 months[4].

Treatment Outcomes

  • Hematologic Remission: Achieved in a median time of 13 weeks.
  • Survival Rates: Median overall survival of 215 months.
  • Complications: The study noted risks of thrombotic events, acute leukemia, myelofibrosis, and solid tumors, but these were not significantly correlated with the duration of pipobroman treatment.

Market Demand

The demand for pipobroman is influenced by the prevalence of myeloproliferative disorders and the availability of alternative treatments.

Prevalence of Myeloproliferative Disorders

  • Myeloproliferative disorders such as PV and ET have a relatively low prevalence but a significant impact on patient quality of life. This niche market ensures a steady demand for effective treatments like pipobroman.

Alternative Treatments

  • Other treatments like hydroxyurea and interferon-alpha are also used, but pipobroman remains a viable option due to its efficacy and long-term control of the disease[5].

Competitive Landscape

The competitive landscape for pipobroman includes other cytoreductive agents and emerging therapies.

Existing Competitors

  • Hydroxyurea: A commonly used cytoreductive agent, but it has been suggested to increase the progression of myeloproliferative disorders[5].
  • Interferon-alpha: Another treatment option, but it may have different side effect profiles and efficacy rates compared to pipobroman.

Emerging Therapies

  • The market for myeloproliferative disorders is seeing the development of novel therapies, including JAK inhibitors and other targeted treatments. These emerging therapies could potentially impact the market share of pipobroman[1].

Regulatory Environment

The regulatory environment plays a crucial role in the financial trajectory of pipobroman.

Approval and Licensing

  • Pipobroman has been approved for use in various countries, but regulatory approvals and licensing agreements can affect its market availability and pricing.

Reimbursement Scenario

  • The reimbursement scenario for pipobroman is critical. In many regions, the increasing awareness of myeloproliferative disorders and incremental healthcare spending are expected to expand the market size, enabling drug manufacturers to penetrate the market more effectively[1].

Financial Trajectory

The financial trajectory of pipobroman is influenced by several factors, including market size, pricing, and development costs.

Market Size

  • The market size for myeloproliferative disorder treatments is expected to grow due to rising awareness and healthcare spending. For example, the Essential Thrombocythemia (ET) market is projected to see significant growth from 2017 to 2030[1].

Pricing Strategies

  • The pricing of pipobroman is influenced by its efficacy, the size of the patient population, and the presence of alternative treatments. Given the small patient population for myeloproliferative disorders, prices for treatments like pipobroman can be higher to justify the research and development investments[3].

Development Costs

  • The development costs for pipobroman and similar drugs are high due to the complexity of myeloproliferative disorders and the need for long-term clinical trials. Public and private funding play a significant role in supporting these costs, with public-private partnerships becoming increasingly common[2].

Public and Private Funding

Funding for drug development, including for pipobroman, comes from both public and private sources.

Public Funding

  • Public sector funding for cancer and related drug research is substantial. For instance, in the EU and the USA, significant investments are made annually, with the EU collectively spending around €2.79 billion and the USA spending around €5.8 billion[2].

Private Funding

  • Private sector investment is also crucial, with top pharmaceutical companies contributing significantly to R&D. Public-private partnerships are becoming more prevalent, facilitating the development of new therapies[2].

Key Takeaways

  • Efficacy: Pipobroman is effective in the long-term control of PV and ET.
  • Market Demand: Steady demand due to the prevalence of myeloproliferative disorders.
  • Competitive Landscape: Faces competition from other cytoreductive agents and emerging therapies.
  • Regulatory Environment: Regulatory approvals and reimbursement scenarios significantly impact market availability and pricing.
  • Financial Trajectory: Market size growth, pricing strategies, and development costs are key factors.

FAQs

What is pipobroman used for?

Pipobroman is used primarily in the treatment of myeloproliferative disorders such as polycythemia vera (PV) and essential thrombocythemia (ET).

How effective is pipobroman in treating PV?

Pipobroman has been shown to achieve hematologic remission in 94% of patients with PV, with a median overall survival of 215 months[4].

What are the potential risks associated with pipobroman treatment?

The treatment is associated with risks of thrombotic events, acute leukemia, myelofibrosis, and solid tumors, although these risks are not significantly correlated with the duration of treatment[4].

How does the competitive landscape affect pipobroman?

Pipobroman faces competition from other cytoreductive agents like hydroxyurea and emerging therapies such as JAK inhibitors, which could impact its market share[1][5].

What role does public and private funding play in the development of pipobroman?

Public and private funding are crucial for the development of pipobroman, with significant investments from both sectors and the increasing importance of public-private partnerships[2].

Sources

  1. Global Essential Thrombocythemia (ET) Market Overview 2017-2030 - ResearchAndMarkets.com
  2. The role of funding and policies on innovation in cancer drug development - LSE
  3. The Economics of Drug Development: Pricing and Innovation in a Changing Market - NBER
  4. Efficacy of pipobroman in the treatment of polycythemia vera - PubMed
  5. Insights into the Potential Mechanisms of JAK2V617F Somatic Mutation - MDPI

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