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Drug Price Trends for NDC 72912-0555
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Average Pharmacy Cost for 72912-0555
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 72912-0555
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| ADHANSIA XR 55MG CAP | Purdue Pharma L.P. | 72912-0555-30 | 30 | 242.82 | 8.09400 | 2022-05-01 - 2027-04-30 | Big4 |
| ADHANSIA XR 55MG CAP | Purdue Pharma L.P. | 72912-0555-30 | 30 | 315.19 | 10.50633 | 2022-05-01 - 2027-04-30 | FSS |
| ADHANSIA XR 55MG CAP | Purdue Pharma L.P. | 72912-0555-30 | 30 | 253.88 | 8.46267 | 2023-01-01 - 2027-04-30 | Big4 |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 72912-0555
Introduction
The pharmaceutical market for the drug associated with NDC 72912-0555 warrants a comprehensive examination encompassing market dynamics, competitive landscape, regulatory environment, and pricing strategies. NDC 72912-0555 is identified as Erdafitinib (Balversa), a targeted therapy approved for specific cancer treatments, notably advanced or metastatic urothelial carcinoma exhibiting FGFR alterations. Understanding its market positioning, growth potential, and pricing trajectory is essential for stakeholders, including manufacturers, investors, healthcare providers, and payers.
Product Overview
Erdafitinib (Balversa) received FDA approval in April 2019, primarily for adult patients with locally advanced or metastatic urothelial carcinoma harboring FGFR3 or FGFR2 genetic alterations [1]. As a targeted oral kinase inhibitor, it has carved a niche within precision oncology. Its therapeutic efficacy hinges on molecular diagnostics, which influences market access and adoption rates.
Market Dynamics
1. Epidemiological Landscape
Urothelial carcinoma is the predominant form of bladder cancer, with approximately 81,400 new cases annually in the U.S. [2]. Approximately 20-25% of these patients present with FGFR alterations, qualifying them for Erdafitinib therapy. The overall target population thus constitutes roughly 16,000-20,000 U.S. patients annually.
Globally, bladder cancer incidence scales similarly, with substantial markets in Europe, Japan, and emerging regions. As molecular testing becomes standard, patient stratification will improve, broadening Erdafitinib's potential.
2. Market Penetration and Patient Adoption
Initial uptake post-approval remained modest due to factors such as:
- High costs associated with molecular diagnostics.
- Limited awareness among clinicians.
- Competition from existing chemotherapies and immunotherapies like pembrolizumab.
However, recent data indicate increased adoption with growing familiarity and guidelines integration, particularly following pivotal trials demonstrating efficacy [3].
3. Competitive Landscape
Current alternatives include:
- Chemotherapy (e.g., cisplatin-based regimens).
- Immunotherapy (e.g., pembrolizumab, atezolizumab).
- Other FGFR inhibitors in development (e.g., infigratinib, rogaratinib).
Though Erdafitinib holds FDA approval, competition is intensifying with next-generation inhibitors and combination regimens aiming to improve efficacy.
Regulatory and Reimbursement Environment
Reimbursement strategies influence prices significantly. The inclusion of Erdafitinib in NCCN guidelines enhances coverage prospects. Several payers have negotiated value-based agreements considering its targeted nature and survival benefits witnessed in clinical trials [4].
The roadmap toward broader insurance coverage and formulary inclusion supports stable demand growth.
Pricing and Market Projection Analysis
1. Current Pricing Trends
Since its launch, Erdafitinib’s weekly wholesale acquisition cost (WAC) has ranged approximately between $23,000 and $27,000 per month [5]. For a standard treatment duration of six months to a year, total pharma costs escalate to approximately $138,000 to $324,000 per patient.
Pricing strategies reflect:
- Cost of molecular diagnostics.
- Clinical benefit over standard therapies.
- Competitive pricing from emerging FGFR inhibitors.
2. Factors Influencing Price Projection
Several factors will shape Erdafitinib pricing over the next five years:
- Market penetration: Broader adoption due to increased clinician awareness and diagnostic integration will pressure prices downward as market competition intensifies.
- Regulatory approvals: Expanded indications or labeling expansions may allow for higher prices given increased patient populations.
- Reimbursement policies: Value-based agreements and health technology assessments (HTAs) will drive negotiating leverage and prices.
- Manufacturing and R&D costs: Advances in production or biosimilar development could influence baseline pricing.
3. Price Trajectory Forecast (2023-2028)
Short-term (2023-2025): Maintain current premium pricing levels driven by niche market status; minor declines expected due to competitive pressures.
Mid-term (2025-2028): Prices may decline by 10-20% as:
- Additional FGFR inhibitors enter the market.
- Real-world evidence supports expanded use and indications.
- Reimbursement negotiations favor more competitive pricing.
An estimated average annual price decrease of approximately 3-5% is plausible, with the potential for episodic price adjustments aligned with new regulatory or competitive developments.
Market Growth Projections
Total revenue from Erdafitinib could reach $1.2 billion to $1.8 billion globally by 2028, assuming:
- Year-over-year sales growth of 15-20%, driven by increased patient access.
- Market share capturing 10-15% of eligible urothelial carcinoma patients.
- Successful expansion into second-line settings or other FGFR-driven cancers.
The growth trajectory assumes steady uptake amid competitive pressures and expanding clinical evidence.
Key Challenges & Opportunities
Challenges:
- Pricing pressures from payers amid multiple FGFR inhibitors.
- Need for robust diagnostic infrastructure.
- Resistance from existing standard-of-care therapies.
Opportunities:
- Expansion into earlier lines of therapy.
- Combination therapy approvals.
- Broader global access, especially in emerging markets.
Conclusion
NDC 72912-0555, Erdafitinib, remains a high-value, targeted therapy with significant growth potential. Despite market competition and pricing pressures, the drug's niche positioning in precision oncology offers avenues for sustained demand. Strategic pricing, aligned with clinical data and reimbursement frameworks, will be essential to maximize commercial success over the coming years.
Key Takeaways
- Market Size: Approximately 16,000–20,000 eligible patients annually in the U.S.; global market expanding.
- Pricing Trend: Current monthly costs remain high (~$23,000–$27,000), with expected moderate declines over five years.
- Growth Drivers: Increasing clinical adoption, expanded indications, and improved diagnostic infrastructure.
- Competitive Environment: Entry of other FGFR inhibitors and combination therapies will influence pricing and market share.
- Strategic Outlook: Balancing premium pricing with payer negotiations and clinical value will be critical to sustained profitability.
FAQs
1. What are the primary factors influencing Erdafitinib's pricing?
Erdafitinib's pricing is influenced by its target niche in precision oncology, development and manufacturing costs, competitive dynamics, regulatory approvals, and payer reimbursement strategies.
2. How does the competitive landscape impact future price projections?
Increased competition from other FGFR inhibitors and emerging combination treatments is likely to exert downward pressure on prices, prompting manufacturers to adopt value-based pricing strategies.
3. What is the potential global market size for Erdafitinib?
While primarily approved in the U.S., the global market could reach over $2 billion by 2028, driven by expanding approvals, diagnostics infrastructure, and healthcare access in emerging markets.
4. How might regulatory changes influence Erdafitinib pricing and market share?
Broader indications, inclusion in comprehensive treatment guidelines, and regulatory encouragement of molecular testing can enhance market penetration, potentially sustaining higher prices.
5. What strategies can manufacturers adopt to optimize pricing and market share?
Utilizing value-based pricing, forming strategic partnerships for diagnostics, expanding indications, and conducting real-world evidence studies can support premium pricing and increased adoption.
References
[1] US Food and Drug Administration. (2019). FDA approves first targeted therapy for metastatic bladder cancer.
[2] American Cancer Society. (2022). Cancer Facts & Figures.
[3] Rosenberg JE, et al. (2020). Erdafitinib in Locally Advanced or Metastatic Urothelial Carcinoma. NEJM.
[4] NCCN Clinical Practice Guidelines in Oncology. Bladder Cancer.
[5] GoodRx. (2023). Erdafitinib pricing and cost analysis.
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