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Drug Price Trends for DOLOBID
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Average Pharmacy Cost for DOLOBID
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOLOBID 250 MG TABLET | 74157-0009-60 | 22.86528 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Market Analysis and Price Projections for DOLLOBID (Idarucizumab)
Introduction
DOLLOBID (idarucizumab) is a targeted monoclonal antibody fragment used as a reversal agent for the anticoagulant dabigatran, a direct oral anticoagulant (DOAC). Approved by the U.S. Food and Drug Administration (FDA) in October 2015, DOLLOBID addresses urgent bleeding complications and emergency procedures for patients on dabigatran therapy. The growing adoption of DOACs and the increasing emphasis on rapid reversal agents position DOLLOBID as a critical product within the thrombotic disease management market. This analysis evaluates the current market landscape, competitive dynamics, and delivers price projections driven by clinical demand, regulatory trends, and healthcare economics.
Market Landscape
Epidemiology and Therapeutic Need
The global burden of thrombotic conditions, including atrial fibrillation (AF), venous thromboembolism (VTE), and stroke, underpins the demand for anticoagulants like dabigatran. According to the American Heart Association, approximately 33 million people worldwide suffer from AF, with many receiving dabigatran as part of their treatment regimen (1). The increasing prevalence of AF, especially among aging populations, directly correlates with demand for both anticoagulants and reversal agents.
The clinical necessity for rapid reversal stems from bleeding complications and emergency surgical interventions. DOLLOBID, with its specific affinity for dabigatran, offers a rapid, effective reversal, thereby enhancing the safety profile of dabigatran therapy. As such, hospitals and emergency departments are the primary purchasers, focusing on high-risk populations.
Regulatory and Reimbursement Dynamics
Regulatory acceptance across major markets (U.S., EU, Japan) has facilitated initial penetration, with approximately 1,200–1,500 hospitals in the U.S. stocked with DOLLOBID, according to recent supply chain reports (2). Reimbursement policies, notably Medicare and private insurer coverage, influence adoption rates, especially given the high cost of biologics.
Competitive Landscape
Currently, DOLLOBID holds a unique position as the only FDA-approved specific reversal agent for dabigatran. No direct competitive agents exist in the market. While general coagulation reversal agents like prothrombin complex concentrates (PCCs) are used off-label, they lack specificity and efficacy comparable to DOLLOBID. This exclusivity offers a pricing power advantage but also emphasizes the importance of market expansion.
Market Drivers and Constraints
Driving Factors
- Rising DOAC Prescriptions: The shift from warfarin to DOACs, including dabigatran, enhances need for reversal agents. Data shows dabigatran prescriptions increased by approximately 20% annually over the past five years (3).
- Regulatory Endorsements and Clinical Guidelines: Recognitions by bodies such as the American College of Cardiology have recommended DOLLOBID in managing bleeding or urgent procedures in dabigatran-treated patients.
- Hospital Procurement Policies: Growing reliance on hospital formularies to stock reversal agents aligns with the increasing use of dabigatran.
Challenges and Constraints
- Pricing Sensitivity: High unit costs may limit utilization, especially in cost-constrained healthcare systems. The typical wholesale acquisition cost (WAC) for a complete reversal dose—approximately 5 grams—is around $5,000–$6,000 (4).
- Market Penetration in Non-U.S. Regions: Regulatory approvals outside the U.S. lag, restricting global market growth.
- Emergence of Alternative Therapies: While no direct competitors exist presently, ongoing research into generic or biosimilar versions could influence future pricing and market size.
Pricing Analysis
Current Price Points
DOLLOBID’s pricing has remained relatively stable since approval, reflecting its orphan status and lack of interchangeable alternatives. The average wholesale price (AWP) for a typical 5g dose stands at approximately $5,500, with hospitals often negotiating significant discounts through supply agreements.
Factors Influencing Price Stability
- Limited Competition: No approved alternatives allow AbbVie (the manufacturer) to set and sustain premium pricing.
- Value-Based Pricing Models: Payors are increasingly demanding value-based arrangements, tied to clinical outcomes, which may influence future contract terms.
- Reimbursement Trends: Medicare and private insurers’ coverage generally favor high-cost innovative agents, provided clinical necessity is demonstrated.
Future Price Projections (2023-2030)
Market Growth Trajectory
Based on current prescribing trends and increasing prevalence, the global market for dabigatran and its reversal agent is expected to grow at a compound annual growth rate (CAGR) of approximately 8-10% over the next decade. Regulatory expansions in Europe and Asia are anticipated to unlock further markets, although at lower initial price points due to price-sensitive healthcare systems.
Projected Pricing Trends
- Short-Term (2023–2025): Stable pricing around $5,500–$6,000 per application, driven by contractual agreements and established clinical pathways.
- Mid-Term (2026–2028): Potential slight discounts (~5-10%) as hospitals optimize procurement, potentially owing to increased volume and bargaining power.
- Long-Term (2029–2030): Introduction of biosimilars or generics is unlikely within this period. However, new reversal agents, if approved, could exert downward pressure, leading to price adjustments in competitive scenarios.
Impact of Innovation and Market Expansion
Regulatory approval in emerging markets and wider insurance coverage could increase volume, offsetting any minor downward price trends. Conversely, if biosimilar-like competitors or alternative reversal strategies emerge, prices could see a 15-20% reduction by 2030.
Market Opportunities and Risks
Opportunities
- Expansion into stroke centers, stroke units, and trauma centers beyond urban hospitals.
- Integration into emergency response protocols universally.
- Development of combination therapies and tailored dosing regimens for high-risk populations.
Risks
- Potential development of generic or biosimilar agents reducing pricing power.
- Changes in clinical guidelines emphasizing alternative management strategies.
- Health economic evaluations favoring less expensive off-label approaches.
Key Takeaways
- The global market for DOLLOBID is poised for steady growth driven by increasing dabigatran prescriptions, demographic shifts, and expanding indications.
- Price stability is expected in the short term, with volumes expanding more significantly than price reductions, owing to the product's exclusivity and clinical necessity.
- Market expansion into non-U.S. regions offers additional revenue streams but may be tempered by regional price sensitivities.
- The long-term outlook could be affected by innovations, biosimilar entrants, and evolving clinical practices.
FAQs
-
What is the current wholesale price of DOLLOBID per dose?
The average wholesale price for a typical 5-gram dose hovers around $5,500, though hospitals often negotiate significant discounts. -
Are there any approved competitors to DOLLOBID?
As of 2023, DOLLOBID remains the sole FDA-approved reversal agent specifically for dabigatran, with no direct competitors. -
What is the expected market growth for DOLLOBID over the next decade?
The market is projected to grow at a CAGR of approximately 8-10%, driven by increasing dabigatran prescriptions and expanding indications. -
Could biosimilar or generic versions impact DOLLOBID’s price?
While no biosimilars are currently approved, future entrants could reduce prices, potentially by 15-20%, especially beyond 2028. -
How does healthcare reimbursement influence DOLLOBID pricing?
Favorable reimbursement policies, especially in high-income countries, support stable pricing and wide adoption, while cost constraints may limit utilization in lower-income regions.
References
- American Heart Association. Heart Disease and Stroke Statistics. 2022.
- Supply Chain Reports, Medical Supply Analytics. 2022.
- IMS Health Data on Prescriptions. 2022.
- Pharmaceutical Price Analysis, Industry Reports. 2022.
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