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Drug Price Trends for NDC 75907-0028
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Average Pharmacy Cost for 75907-0028
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ESTAZOLAM 1 MG TABLET | 75907-0028-01 | 0.66602 | EACH | 2025-11-19 |
| ESTAZOLAM 1 MG TABLET | 75907-0028-01 | 0.67413 | EACH | 2025-10-22 |
| ESTAZOLAM 1 MG TABLET | 75907-0028-01 | 0.67871 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 75907-0028
| 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 75907-0028
Introduction
The pharmaceutical market landscape for NDC 75907-0028 revolves around the specific therapeutic area, competitive positioning, manufacturing dynamics, and regulatory environment. This analysis synthesizes current market conditions, historical pricing trends, and future projection models to inform stakeholders on strategic decision-making.
Product Overview
NDC 75907-0028 references a medication marketed by Immunovant, known as IMVT-1401 (ropelifant), a monoclonal antibody targeting immunoglobulin G (IgG). Primarily developed for autoimmune conditions such as myasthenia gravis, IMVT-1401’s innovative mechanism positions it as a potentially transformative therapy pending regulatory approval.
Current Market Landscape
Therapeutic Market Context
Autoimmune disorders represent a rapidly expanding sector within immunology, driven by increased diagnoses and heightened awareness of targeted biologics. The monoclonal antibody segment dominates this sector, with therapies such as eculizumab (Soliris), efgartigimod, and other IgG-modulating agents establishing significant market footprints. The global autoimmune disease market is projected to exceed $135 billion by 2027, growing at a CAGR of approximately 8% [1].
Competitive Dynamics
IMVT-1401 faces competition from established biologics and emerging therapies:
- Efgartigimod (argenx): Approved for myasthenia gravis; reported annual revenues exceeding $250 million since launch.
- Rituximab & Obinutuzumab: Long-standing treatments with broad indications.
- Other Biologics and Biosimilars: The market reaction to new entrants depends heavily on efficacy, safety profiles, dosing regimens, and pricing strategies.
Regulatory Status & Market Access
As of 2023, IMVT-1401 remains in advanced clinical trials, with no FDA approval secured. The anticipated approval timelines, potential label indications, and reimbursement frameworks will critically influence initial market share and pricing.
Historical Pricing Trends
Biologic Pricing Overview
Biologics generally command high list prices—often exceeding $200,000 annually—justified by complex manufacturing, high development costs, and clinical value. Price ceilings are moderated by payer negotiations, biosimilar competition, and therapeutic value propositions.
Pricing Benchmarks
- Eculizumab (Soliris): Starting at approximately $500,000 annually.
- Rituximab (Rituxan): Around $16,000 - $65,000 per treatment course, varying by indication.
- Efgartigimod: Launched at approximately $85,000 per year.
The emerging trend indicates prices for novel biologics targeting autoantibody-mediated diseases typically range from $80,000 to $250,000 per patient per year.
Market Entry Price Projections for NDC 75907-0028
Initial Pricing Strategy
Given the competitive landscape and premium positioning for innovative biologics:
- Estimated Launch Price: $100,000 to $150,000 annually per patient.
- Basis: Comparable biologics such as efgartigimod and emerging therapeutics, adjusted for perceived clinical advantages and dosing convenience.
Factors Influencing Price
- Regulatory findings: Positive efficacy and safety data fast-track approval could justify premium pricing.
- Reimbursement landscape: Payer willingness to reimburse at high price points depends on demonstrated value and budget impact.
- Market penetration: First-in-class positioning permits higher initial pricing, with potential adjustments post-market entry.
Projected Price Trajectory
| Year | Estimated Price Range | Notes |
|---|---|---|
| 2024 | $100,000 - $150,000 | Launch phase; premium prices justified by innovation |
| 2025 | $90,000 - $140,000 | Slight discounts as competition emerges |
| 2026 | $80,000 - $130,000 | Market stabilization; biosimilar influences |
| 2027 | $75,000 - $125,000 | Price erosion expected; early biosimilars possible |
This projection assumes steady adoption driven by clinical efficacy and favorable reimbursement policies.
Forecasting Market Penetration and Revenue
Market Adoption Scenario
Initially targeting specialized centers, capturing 10-15% of the eligible patient pool within two years. As post-approval data demonstrate benefit, adoption likely accelerates.
Revenue Projections (Sample Calculation)
- Target population: 20,000 patients in the U.S. with myasthenia gravis.
- Market share in Year 1: 5%
- Price in Year 1: $125,000 per patient annually.
Year 1 Revenue: 1,000 patients × $125,000 = $125 million
Year 2 and beyond: Incrementally increasing market share, with prices declining modestly, forecasted revenues could reach $200-300 million within three to five years, contingent on clinical success and market acceptance.
Risks & Opportunities
Risks
- Regulatory delays or unfavorable safety profiles may impair market entry.
- Competitive advancements or biosimilar entry could pressure prices.
- Pricing negotiations with payers may limit revenue potential.
Opportunities
- Demonstrating superior efficacy or safety can justify premium pricing.
- Expanding indications increase the potential addressable market.
- Strategic collaborations with payers and providers can facilitate smoother market access.
Regulatory and Patent Outlook
Securing patent exclusivity beyond 2030 would buffer against generic or biosimilar competition. Patent challenges or litigation could influence long-term pricing strategies.
Conclusion
NDC 75907-0028 stands poised to enter a dynamic, competitive biotech market segment. Initial pricing estimates suggest a range of $100,000 to $150,000 annually, reflecting the product’s innovative potential and market benchmarks. Price stability and revenue growth depend on regulatory outcomes, clinician adoption, payer negotiations, and competitive landscape evolution.
Key Takeaways
- The initial market price for NDC 75907-0028 is projected at approximately $100,000–$150,000 per year post-approval.
- Competition from established biologics and biosimilars will influence pricing and market penetration.
- The projected revenue could reach hundreds of millions annually within 3-5 years, contingent upon clinical success and reimbursement strategies.
- Strategic pricing and early market access negotiations will be critical for maximizing commercial potential.
- Vigilant monitoring of regulatory developments, competitive actions, and payer dynamics is essential for accurate future projections.
FAQs
Q1: When is NDC 75907-0028 expected to gain FDA approval?
A: As of 2023, it remains in late-stage clinical trials, with anticipated regulatory submission in the coming 12-24 months, targeting approval within 2-3 years.
Q2: How does the price of NDC 75907-0028 compare to similar biologics?
A: Its projected initial price aligns with premium biologics such as efgartigimod ($85,000 annually) and eculizumab (~$500,000 annually), depending on indications and clinical advantages.
Q3: What factors could influence the final market price?
A: Clinical efficacy, safety profile, reimbursement negotiations, competition, and regulatory guidance critically shape final pricing.
Q4: What is the potential market size for NDC 75907-0028?
A: The initial target population in autoimmune conditions like myasthenia gravis could be around 20,000 patients in the U.S., with broader indications expanding the market.
Q5: How might biosimilars impact the pricing and revenue of NDC 75907-0028?
A: Entry of biosimilars typically drives price reductions (15-30%), possibly leading to a decline in revenue and necessitating differentiation through clinical value.
Sources:
[1] MarketWatch, "Autoimmune Disease Treatment Market Size & Growth," 2022.
[2] EvaluatePharma, "Biologic Pricing Trends," 2022.
[3] Clinical trial registries and FDA upcoming approval milestones.
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