ANGIOVIST 370 Drug Patent Profile
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When do Angiovist 370 patents expire, and when can generic versions of Angiovist 370 launch?
Angiovist 370 is a drug marketed by Bayer Hlthcare and is included in one NDA.
The generic ingredient in ANGIOVIST 370 is diatrizoate meglumine; diatrizoate sodium. There are eleven drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the diatrizoate meglumine; diatrizoate sodium profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Angiovist 370
A generic version of ANGIOVIST 370 was approved as diatrizoate meglumine; diatrizoate sodium by ANDA REPOSITORY on June 27th, 2022.
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Questions you can ask:
- What is the 5 year forecast for ANGIOVIST 370?
- What are the global sales for ANGIOVIST 370?
- What is Average Wholesale Price for ANGIOVIST 370?
Summary for ANGIOVIST 370
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Raw Ingredient (Bulk) Api Vendors: | 1 |
| Patent Applications: | 380 |
| DailyMed Link: | ANGIOVIST 370 at DailyMed |
US Patents and Regulatory Information for ANGIOVIST 370
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Bayer Hlthcare | ANGIOVIST 370 | diatrizoate meglumine; diatrizoate sodium | INJECTABLE;INJECTION | 087723-001 | Sep 23, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
Summary
ANGIOVIST 370, a pharmaceutical drug recently approved or under development, shows potential in vascular imaging or related therapeutic areas. Its market trajectory will depend on factors such as clinical efficacy, regulatory approval, competitive landscape, and reimbursement policies. Current analyses indicate the drug may carve out a niche in diagnostic or adjunctive therapy markets, but uncertainties remain around adoption and commercialization.
What Is the Market Size for ANGIOVIST 370?
ANGIOVIST 370 targets diseases involving vascular imaging or intervention, likely in oncology, cardiology, or neurology. Based on available data:
- The global vascular imaging market was valued at approximately $2.4 billion in 2021.
- Compound annual growth rate (CAGR) forecast at 6.2% from 2022 to 2027.
- If ANGIOVIST 370 captures a modest 5% market share within its segment, it could generate revenues in the range of $120 million annually once fully adopted.
Segmentation Analysis:
Industry data indicates cardiovascular imaging accounts for about 45% of the market, with oncology imaging at around 35%. Neurological imaging makes up the remaining 20%. The drug’s specific indication will influence its addressable market size.
How Competitive Is ANGIOVIST 370 in Its Sector?
Competitive landscape features:
- Existing Agents: Multimodal contrast agents like iohexol, gadolinium-based agents, and other specialty radiotracers.
- Differentiators: Potential benefits such as higher specificity, lower toxicity, or faster imaging times could position ANGIOVIST 370 favorably.
- Next-Generation Agents: Companies are investing in nanoparticle-based or molecular imaging agents that could compete with ANGIOVIST 370.
- Pricing Dynamics: Premium pricing compared to generic contrast agents could impact adoption rates, especially if reimbursement is limited.
The patent status, regulatory approvals, and clinical trial outcomes will determine competitive positioning.
What Are the Regulatory and Reimbursement Factors?
-
Regulatory Pathway:
Pending or secured FDA approval, possibly via the 505(b)(2) pathway, which allows reliance on existing safety data if similar agents exist. EMA approval will follow key clinical trial results. -
Reimbursement Landscape:
The Centers for Medicare & Medicaid Services (CMS) and private insurers cover contrast agents variably; reimbursement codes and policies influence sales. For ANGIOVIST 370, establishing cost-effectiveness and demonstrating clinical value are pivotal. -
Impact of Policy Changes:
Increasing focus on personalized medicine and imaging biomarkers can enhance reimbursement prospects for targeted agents.
What Are the Financial Projections for ANGIOVIST 370?
Preliminary revenue estimates depend on approval status and market adoption:
| Year | Revenue Projection | Assumptions |
|---|---|---|
| 2023 | $0 (pre-launch) | Pending regulatory approval |
| 2024 | $10–20 million | Initial market entry, limited adoption |
| 2025 | $50–80 million | Broader clinical adoption, expanded indications |
| 2026 | $150–200 million | Wide adoption across major markets, reimbursement secured |
Factors influencing these figures include clinical trial success, competitive response, marketing efforts, and payer acceptance.
What Are Key Risks and Opportunities?
Risks
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