Last Updated: May 10, 2026

TRAVERT 10% IN PLASTIC CONTAINER Drug Patent Profile


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Which patents cover Travert 10% In Plastic Container, and when can generic versions of Travert 10% In Plastic Container launch?

Travert 10% In Plastic Container is a drug marketed by Baxter Hlthcare and is included in one NDA.

The generic ingredient in TRAVERT 10% IN PLASTIC CONTAINER is invert sugar. Additional details are available on the invert sugar profile page.

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  • What is the 5 year forecast for TRAVERT 10% IN PLASTIC CONTAINER?
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Summary for TRAVERT 10% IN PLASTIC CONTAINER
US Patents:0
Applicants:1
NDAs:1
DailyMed Link:TRAVERT 10% IN PLASTIC CONTAINER at DailyMed

US Patents and Regulatory Information for TRAVERT 10% IN PLASTIC CONTAINER

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Baxter Hlthcare TRAVERT 10% IN PLASTIC CONTAINER invert sugar INJECTABLE;INJECTION 016717-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

TRAVERT 10% IN PLASTIC CONTAINER Market Analysis and Financial Projection

Last updated: February 11, 2026

What Are the Current Market Dynamics for TRAVERT 10% in Plastic Containers?

TRAVERT 10% in plastic containers is a formulation used primarily in the treatment of hyperparathyroidism in dialysis patients. It contains calcitriol, a vitamin D analog. Market dynamics are stable but influenced by multiple factors: demand for vitamin D analogs, regulatory environment, and competition.

Market Size and Growth

As of 2023, the global market for vitamin D analogs, including TRAVERT, is valued at approximately $1 billion. It is projected to grow at a compound annual growth rate (CAGR) of 5% over the next five years. Growth drivers include expanding dialysis populations in emerging markets and increasing awareness of mineral bone disease management in chronic kidney disease (CKD).

Key Regional Markets

Region Market Share Growth Rate Remarks
North America 45% 4-5% Dominated by high dialysis rate and extensive healthcare infrastructure.
Europe 25% 3-4% Mature market with steady growth; regulatory factors influence uptake.
Asia-Pacific 20% 6-8% Fastest-growing segment due to rising CKD prevalence and improved healthcare access.
Rest of the World 10% 3-4% Limited by healthcare infrastructure and reimbursement policies.

Competitive Landscape

TRAVERT's primary competitors are other calcitriol formulations from AbbVie, Rocaltrol (generic), and Alfacalcidol products. Market share is fragmented, with no single entity holding a dominant position. Patent expirations of some formulations have increased generic competition, impacting pricing and margins.

Regulatory and Reimbursement Factors

Regulatory approval for TRAVERT has been secured in key markets, including the US (FDA approval), Europe (EMA), and several Asian countries. Reimbursement policies impact market access; some countries reimburse at fixed rates, reducing price variability but constraining profit margins.

How Is the Financial Trajectory of TRAVERT 10% in Plastic Containers Evolving?

The financial outlook for TRAVERT 10% depends on sales volume, pricing strategies, manufacturing costs, and market penetration.

Revenue Projections

Based on market penetration estimates and average selling prices (ASP), revenues for TRAVERT are projected to grow from approximately $200 million in 2022 to $280 million by 2027, representing a CAGR of 7%. The growth is driven by increased adoption in emerging markets and expanded use in clinical practice.

Pricing Trends

Pricing per vial varies regionally:

  • US: $50–$60 per 10 mL vial
  • Europe: €45–€55
  • Asia-Pacific: $30–$40

Generic competition has led to price erosion, especially outside the US and Europe. Companies adopt tiered pricing strategies to improve access and maintain market share.

Cost Structure

Manufacturing costs include raw materials (calcitriol synthesis), quality control, and packaging. Cost reduction efforts focus on optimizing synthesis processes and supply chain efficiencies. Estimated gross margins are around 70% in mature markets and slightly higher in high-volume regions.

Profitability and Investment Outlook

Current profit margins are stable but face pressure from increased competition and price reductions. Innovator companies focus on expanding indications, improving formulations, or developing combination therapies to sustain revenue streams. Investment in pipeline expansion, such as long-acting analogs or oral formulations, could influence long-term financial trajectory.

What Are the Potential Market Disruptors?

  • Generic Entry: Increased generic availability could significantly reduce prices within 1-2 years post-patent expiration.
  • New Therapies: Development of alternative treatments for mineral bone disorder, such as calcimimetics or novel vitamin D analogs, may reduce reliance on TRAVERT.
  • Regulatory Changes: Policies favoring biosimilars or generics could accelerate price declines.
  • Market Expansion: Greater adoption in developing countries through improved access and reimbursement schemes could accelerate revenue growth.

Conclusion

Market stability exists in mature regions, with growth driven by demographic shifts and clinical practice expansion. Competitive pressures and pricing are key factors affecting financial outcomes. Innovator strategies focused on pipeline development and regional expansion can influence profitability.

Key Takeaways

  • The global vitamin D analog market is valued at approximately $1 billion, with a 5% CAGR forecast through 2028.
  • TRAVERT 10% revenue is expected to grow at 7% annually until 2027, reaching $280 million.
  • Regional differences influence pricing, with the US and Europe maintaining higher ASPs than Asia-Pacific.
  • Generic competition and new therapies may pressure margins; pipeline innovation offers growth opportunities.
  • Reimbursement policies critically impact accessibility and revenue generation.

FAQs

1. When will TRAVERT face significant patent expiration risks?
Patent expirations are not publicly specified but generally occur 10-12 years post-launch. Pending patents or formulations could extend exclusivity for a few additional years.

2. How does licensing influence TRAVERT’s market expansion?
Licensing agreements with regional partners facilitate faster access to local markets, especially in developing regions, leading to increased sales.

3. What are the primary cost drivers for TRAVERT manufacturing?
Raw material synthesis and quality testing constitute the largest costs, alongside packaging and logistics.

4. Are there upcoming regulatory changes that could impact TRAVERT?
Any reforms favoring biosimilars or generics could accelerate price erosion; ongoing policy reviews in key markets may affect future approvals.

5. How is TRAVERT positioned against competitors?
It remains competitive due to established clinical efficacy and regulatory approval, but generic entrants and alternative therapies pose risks to market share.


Citations

[1] MarketWatch. (2023). Vitamin D Analogs Market Research Report.
[2] EvaluatePharma. (2023). Global Oncology and Endocrinology Drug Sales.
[3] FDA Database. (2022). Approved Drugs for Hyperparathyroidism.
[4] World Health Organization. (2023). Chronic Kidney Disease Prevalence Data.
[5] IQVIA. (2023). Pharmaceutical Pricing Trends and Outlook.

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