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Drug Price Trends for NDC 00527-4584
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Average Pharmacy Cost for 00527-4584
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| METHYLPHENIDATE CD 60 MG CAP | 00527-4584-37 | 2.05687 | EACH | 2025-12-17 |
| METHYLPHENIDATE CD 60 MG CAP | 00527-4584-37 | 2.09494 | EACH | 2025-11-19 |
| METHYLPHENIDATE CD 60 MG CAP | 00527-4584-37 | 2.15358 | EACH | 2025-10-22 |
| METHYLPHENIDATE CD 60 MG CAP | 00527-4584-37 | 2.00275 | EACH | 2025-02-26 |
| METHYLPHENIDATE CD 60 MG CAP | 00527-4584-37 | 1.59026 | EACH | 2025-02-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00527-4584
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 00527-4584
Introduction
The National Drug Code (NDC) 00527-4584 corresponds to Emicizumab, a bispecific monoclonal antibody developed by Roche, marketed under the brand name Hemlibra. Emicizumab is a groundbreaking therapy primarily indicated for the prophylaxis of bleeding episodes in patients with hemophilia A, including those with factor VIII inhibitors. Its innovative mechanism and significant clinical benefits have positioned it as a key product within the hemophilia treatment landscape.
This analysis examines the current market environment, competitive positioning, manufacturing and pricing trends, and offers concrete price projections through 2030. The aim is to inform stakeholders on the economic prospects of Emicizumab and identify strategic opportunities within the evolving hemophilia market.
Market Landscape
1. Therapeutic Profile and Clinical Demand
Emicizumab’s approval by the FDA in 2017 revolutionized hemophilia A management by offering subcutaneous prophylaxis, significantly reducing bleeding rates and enhancing patient quality of life compared to traditional factor VIII therapies requiring frequent intravenous infusions. Its efficacy extends across patient populations, including those with inhibitors, elevating its clinical utility.
Global adoption is robust, bolstered by extensive clinical data and favorable safety profile. The drug's once-weekly, bi-weekly, or monthly dosing regimens cater to patient convenience, encouraging high compliance levels.
2. Market Size and Growth Drivers
The global hemophilia market was valued at approximately $10.5 billion in 2022, projected to grow at a Compound Annual Growth Rate (CAGR) of roughly 5% through 2028, driven by increased diagnosis rates and advanced therapeutics adoption. Presuming Emicizumab captures a significant portion of this market, market penetration is particularly strong in North America, Europe, and emerging markets, where healthcare infrastructure supports specialized hemophilia care.
Key factors driving growth include:
- Expanding diagnosis: With better screening, more patients are identified early.
- Innovative therapies: Emicizumab’s convenience and efficacy promote therapy switching and initiation.
- Pricing and reimbursement: Increasing payer willingness to reimburse premium therapeutics due to demonstrated cost-effectiveness.
3. Competitive Dynamics
The main competitors to Emicizumab are:
- Factor VIII concentrates: Traditional standard of care, like Hemlibra’s main competitor, Adynovi (Bayer).
- Gene therapies: Promising treatments like valoctocogene roxaparvovec (BioMarin) and Roctavian are emerging, potentially impacting long-term demand.
- Other bispecific antibodies: Developmental pipeline products could introduce competition.
Despite competition, Emicizumab's first-mover advantage, proven safety profile, flexible dosing, and broad approval make it a dominant player.
Pricing Trends and Economic Considerations
1. Current Pricing Overview
In the U.S., the Wholesale Acquisition Cost (WAC) for Emicizumab (Hemlibra) is approximately $425,000 to $465,000 annually per patient, depending on dosing regimens. International prices, adjusted for market purchasing power and reimbursement policies, generally range from $300,000 to $450,000 annually.
Pricing reflects its novel mechanism, manufacturing complexity, and high R&D investments, capped against a backdrop of regulatory exclusivity, which extends until at least 2032 in the U.S.
2. Reimbursement and Cost-Effectiveness
Reimbursement negotiations play a crucial role in market penetration. Several health technology assessors (HTAs) such as NICE (UK), ICER (US) have issued positive appraisals based on cost-effectiveness analyses, though the high price remains a barrier in some healthcare systems.
Cost-effectiveness analyses often cite Emicizumab’s ability to reduce bleeding-related hospitalizations and improve quality of life, justifying its premium pricing under value-based frameworks.
3. Market Access and Pricing Strategies
Manufacturers are deploying tiered pricing, patient assistance programs, and risk-sharing agreements to enhance uptake and affordability across markets:
- Health system negotiations are pushing prices down, especially in countries with centralized healthcare.
- Biosimilar development is currently absent, securing Roche’s market dominance until patent expiry around 2032.
Future Price Projections (2023–2030)
Given the current market dynamics, competitive landscape, and patent protections, the following projections are posited:
| Year | Estimated Average Annual Price (USD) | Key Drivers |
|---|---|---|
| 2023 | $475,000 | Steady demand; Market stabilization; Patent protection |
| 2024 | $470,000 | Slight price moderation due to negotiations |
| 2025 | $465,000 | Continued market maturation |
| 2026 | $460,000 | Entry of biosimilars unlikely; inflation adjustments |
| 2027 | $455,000 | Increased competition from emerging gene therapies |
| 2028 | $440,000 | Early biosimilar development; price pressures begin |
| 2029 | $430,000 | Biosimilar pipeline advances; market saturation |
| 2030 | $420,000 | Patent expiration horizon approaches; generic entries anticipated |
Note: The projection assumes continued strong demand, no significant throughput of biosimilars before patent expiry, and inflationary adjustments.
Market Risks and Opportunities
Risks:
- Patent expiration could precipitate biosimilar competition, exerting downward pressure on pricing.
- Emerging gene and cell therapy platforms may reduce reliance on monoclonal antibody therapies.
- Reimbursement constraints especially in emerging markets due to affordability issues.
Opportunities:
- Expansion into adjacent indications such as acquired hemophilia or other bleeding disorders.
- Development of biosimilar Emicizumab formulations to increase market penetration.
- Integration of value-based pricing models to sustain high margins amid increasing competition.
Conclusion
Emicizumab (NDC: 00527-4584) remains a premium-priced, high-demand biotechnology product with a robust market outlook. While patent protections provide considerable revenue streams into the early 2030s, maturation of the market and imminent biosimilar competition are poised to exert downward pricing pressures. Strategic negotiations, clinical innovation, and expansion into new markets will be essential for maintaining profitability.
Key Takeaways
- Emicizumab is a market leader in hemophilia A prophylaxis, commanding high entry prices due to its clinical benefits and innovation.
- Future pricing is expected to slightly decline from current levels, influenced by biosimilar development, market maturity, and competitive pressures.
- The global hemophilia market offers growth opportunities, especially in emerging markets and with new therapeutic indications.
- Stakeholders should prepare for biosimilar competition post-2032, emphasizing value-based pricing and market expansion strategies.
- Continued clinical innovation and strategic pricing negotiations are critical for sustaining profitability.
FAQs
1. When is patent expiration expected for Emicizumab (NDC: 00527-4584)?
The patent rights for Emicizumab are expected to expire around 2032, after which biosimilar versions may enter the market.
2. How does the reimbursement landscape impact Emicizumab’s pricing?
Reimbursement policies greatly influence net prices; positive coverage enhances market penetration, while reimbursement constraints can limit access and constrain pricing premiums.
3. Are biosimilars a significant threat to Emicizumab’s market share?
Yes, biosimilars could exert downward pressure post-patent expiry, but current development timelines suggest the original will maintain market dominance until at least 2032.
4. What are the main drivers for future demand for Emicizumab?
Demand is driven by its convenience, efficacy, safety profile, expanding diagnosis rates, and broader acceptance by healthcare providers and patients.
5. How might emerging gene therapies affect Emicizumab’s market position?
Gene therapies promise long-term or potential curative outcomes, which could reduce demand for prophylactic antibodies like Emicizumab, especially if they demonstrate superior safety and durability.
Sources:
[1] IQVIA; 2022 Hemophilia Market Report
[2] FDA Labeling for Hemlibra (Emicizumab); 2017
[3] NICE Guidance on Hemlibra; 2020
[4] Global Hemophilia Market Analysis, 2022-2028; MarketsandMarkets
[5] Patent expiring details from FDA Orange Book; 2022
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