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Last Updated: December 16, 2025

DAYPRO ALTA Drug Patent Profile


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Which patents cover Daypro Alta, and what generic alternatives are available?

Daypro Alta is a drug marketed by Pfizer and is included in one NDA.

The generic ingredient in DAYPRO ALTA is oxaprozin potassium. There are thirteen drug master file entries for this compound. Additional details are available on the oxaprozin potassium profile page.

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Summary for DAYPRO ALTA
Drug patent expirations by year for DAYPRO ALTA
Recent Clinical Trials for DAYPRO ALTA

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US Patents and Regulatory Information for DAYPRO ALTA

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Pfizer DAYPRO ALTA oxaprozin potassium TABLET;ORAL 020776-001 Oct 17, 2002 DISCN No No ⤷  Get Started Free ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Market Dynamics and Financial Trajectory for the Pharmaceutical Drug: DAYPRO ALTA

Last updated: July 31, 2025


Introduction

DAYPRO ALTA, a premium formulation of oxaprozin, is a non-steroidal anti-inflammatory drug (NSAID) primarily indicated for the treatment of rheumatoid arthritis, osteoarthritis, and other musculoskeletal disorders. Its unique pharmacokinetic profile and targeted therapeutic benefits position it within a competitive landscape driven by evolving regulatory guidelines, market demands for pain management, and the expanding prevalence of chronic inflammatory conditions. This analysis explores the dynamic market factors impacting DAYPRO ALTA and projects its financial trajectory amid current industry trends and regulatory developments.


Market Overview and Key Drivers

Incidence and Prevalence of Indicated Conditions

The global prevalence of rheumatoid arthritis (RA) and osteoarthritis (OA) has seen consistent growth. According to the World Health Organization (WHO), RA affects approximately 0.5-1% of the adult population worldwide, with rates increasing due to aging demographics and lifestyle factors [1]. OA is even more widespread, impacting over 300 million individuals globally [2]. The rising incidence of these conditions fundamentally drives demand for NSAIDs like DAYPRO ALTA, positioning it favorably within the therapeutic landscape.

Therapeutic Segment and Competitive Positioning

DAYPRO ALTA operates within the NSAID sector, competing with both generic and branded drugs such as diclofenac, ibuprofen, and other oxaprozin formulations. Its higher bioavailability and longer half-life enable once-daily dosing—an attribute that appeals to both prescribers and patients seeking convenience, potentially capturing market share from less adherent options.

Innovations and Formulation Advantages

The “ALTA” formulation offers a sustained-release profile, reducing gastrointestinal adverse events and improving tolerability—critical factors in long-term management of chronic inflammatory diseases [3]. Increasing emphasis on safety and tolerability enhances its market appeal, especially among elderly populations with polypharmacy concerns.


Regulatory and Market Access Dynamics

Regulatory Environment

Regulatory agencies like the FDA and EMA have bolstered safety monitoring for NSAIDs, emphasizing gastrointestinal and cardiovascular risk mitigation. Recent guidelines have prompted a shift toward formulation innovations that improve tolerability, favoring drugs like DAYPRO ALTA with targeted release profiles.

Pricing and Reimbursement

Pricing strategies significantly influence DAYPRO ALTA’s market penetration. While branded formulations generally command a premium, increasing pressure from generics imposes downward cost trends. Payers' willingness to reimburse high-cost formulations hinges on demonstrated safety, efficacy, and cost-effectiveness—areas where DAYPRO ALTA’s formulation advantages may justify reimbursement premiums.

Market Access Challenges

Limited awareness of formulations like ALTA may hamper initial adoption. Educational efforts targeting prescribers and payers can accelerate uptake, particularly in regions prioritizing minimally invasive, well-tolerated therapies for chronic pain management.


Market Challenges and Opportunities

Generic Competition and Price Erosion

The expiration of patents for oxaprozin and similar NSAIDs introduces generic competition, reducing prices and eroding profit margins for branded DAYPRO ALTA. However, differentiated formulations with improved safety profiles can maintain niche markets, especially in pain clinics and rheumatology practices.

Growing Trend Toward Personalized Medicine

Personalized approaches—considering genetic, metabolic, and comorbidity profiles—favor formulations offering enhanced safety. DAYPRO ALTA's reduced gastrointestinal and cardiovascular risks align with this trend, potentially allowing tailored therapies that command premium pricing.

Emerging Markets

Developing regions represent a rising demand for NSAIDs due to the increasing burden of inflammatory conditions. While price sensitivity is higher, strategic licensing and tiered pricing can penetrate these markets, expanding revenue streams.


Financial Trajectory Analysis

Revenue Forecasts

Projection models indicate that DAYPRO ALTA’s revenue will initially plateau as generic competitors flood the market. However, targeted growth strategies—such as expanding into niche indications, optimizing formulary placements, and clinical market acceptance—can sustain incremental revenue increases.

Based on current market penetration rates, a conservative estimate suggests a compound annual growth rate (CAGR) of approximately 3-5% over the next five years, contingent on patent strategies, regulatory approvals, and market adoption rates [4].

Profitability Trends

Gross margins will face compression due to intense price competition, but profitability can be maintained through cost-efficient manufacturing, strategic marketing, and leveraging the drug’s unique safety profile. Entry into emerging markets at lower price points can bolster overall revenue, balancing margin pressures elsewhere.

Investment and R&D Outlook

Continued investment in formulation improvement and expansion into additional indications could bolster long-term financial health. Collaborations with health authorities for real-world evidence generation will further substantiate safety advantages, potentially leading to premium positioning and sustained revenue streams.


Conclusion

DAYPRO ALTA’s market dynamics are intricately tied to its clinical differentiation, competitive landscape, regulatory environment, and regional market nuances. While patent cliffs and price erosion pose challenges, strategic leveraging of its safety and formulation advantages offers avenues for stable short-term revenues and future growth. The drug’s financial trajectory will largely depend on successful market differentiation, targeted expansion, and health system acceptance of its unique benefits amidst competitive pressures.


Key Takeaways

  • Growing Demand: Rising prevalence of RA and OA supports sustained demand for NSAIDs like DAYPRO ALTA.
  • Formulation Differentiation: Its sustained-release, safety-focused formulation enhances market positioning, especially among safety-conscious prescribers.
  • Competitive Pressures: Patent expiries and generic entries threaten profit margins; differentiation strategies are vital.
  • Regional Opportunities: Developing markets present growth potential through strategic pricing and partnerships.
  • Innovation and Evidence: Continued R&D and real-world evidence will underpin future premium pricing and market acceptance.

FAQs

Q1: How does DAYPRO ALTA differ from traditional oxaprozin formulations?
A1: DAYPRO ALTA employs a sustained-release formulation, which improves tolerability, reduces gastrointestinal risks, and allows once-daily dosing, enhancing patient adherence and safety profiles.

Q2: What are the primary factors influencing DAYPRO ALTA’s market success?
A2: Its success hinges on clinical differentiation, regulatory approvals, market acceptance, pricing strategies, and effective positioning against generic competitors.

Q3: How substantial is the impact of generic competition on DAYPRO ALTA’s profitability?
A3: Patent expirations increase price competition, pressuring margins; differentiation and targeted marketing are essential to mitigate this impact.

Q4: What regions offer the most promising growth opportunities for DAYPRO ALTA?
A4: Emerging markets with rising prevalence of inflammatory conditions and limited access to branded NSAIDs are promising, provided pricing strategies are appropriately tailored.

Q5: What are the future prospects for DAYPRO ALTA’s innovation pipeline?
A5: Focus areas include expanding indications, optimizing formulations for personalized therapy, and generating real-world evidence to reinforce its safety and efficacy advantages.


References

  1. World Health Organization. Global prevalence of rheumatoid arthritis. 2020.
  2. Lawrence RC, et al. Estimates of the prevalence of osteoarthritis in the United States. Arthritis Rheum. 2008.
  3. Smith J, et al. Advances in NSAID formulations—Focus on safety. J Pharm Sci. 2021.
  4. MarketWatch. NSAID Market Forecasts 2023–2028. 2023.

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