Last Updated: May 2, 2026

CORLOPAM Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Corlopam patents expire, and when can generic versions of Corlopam launch?

Corlopam is a drug marketed by Hospira and is included in one NDA.

The generic ingredient in CORLOPAM is fenoldopam mesylate. There are five drug master file entries for this compound. Additional details are available on the fenoldopam mesylate profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for CORLOPAM?
  • What are the global sales for CORLOPAM?
  • What is Average Wholesale Price for CORLOPAM?
Summary for CORLOPAM
US Patents:0
Applicants:1
NDAs:1

US Patents and Regulatory Information for CORLOPAM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hospira CORLOPAM fenoldopam mesylate INJECTABLE;INJECTION 019922-001 Sep 23, 1997 DISCN Yes 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

CORLOPAM Investment Scenario and Fundamentals Analysis

Last updated: February 7, 2026

Overview

Corlopam (Fenoldopam mesylate) is a vasodilator indicated primarily for hypertensive crises. It acts as a dopamine D1 receptor agonist, producing vasodilation without significantly affecting heart rate, which makes it suitable for acute settings. The drug's market prospects depend on hypertensive crisis incidence, hospital adoption rates, and competitive landscape.

Market Fundamentals

  • Indications & Usage: Coronary hypertensive emergencies, perioperative hypertension. The drug is administered intravenously, limiting outpatient opportunities.
  • Market Size Estimates: The global hypertensive crisis management market was valued at approximately $2.3 billion in 2022, with an expected compound annual growth rate (CAGR) of 4.5% over five years [1].
  • Pricing & Reimbursement: In the U.S., an average dose costs around $500. Reimbursement depends on hospital formularies and insurance policies, considering the drug's intravenous administration.

Competitive Landscape

  • Key Competitors: Nitroprusside, Nicardipine, Ebrantil (Urapidil), with some off-label use of other vasodilators.
  • Market Share: Corlopam has a niche position; however, its use is limited where other vasodilators or antihypertensive agents suffice. Its IV route confines use to hospital settings.
  • Differentiators: Rapid onset (many minutes) and selectivity for D1 receptors contribute to its safety and efficacy profile, particularly avoiding tachycardia.

Regulatory & Commercial Status

  • Approval & Registrations: Approved in the U.S. by the FDA, also marketed in some other countries.
  • Sales Trends: No significant recent growth observed, partly due to generic competition and limited indication expansion.
  • Pipeline & Development: No ongoing large-scale trials or new indications committed publicly.

Financial Metrics & Investment Outlook

  • Generic Competition: Marketed as a generic or off-patent product, leading to pressure on pricing.
  • Doctor and Hospital Adoption: Adoption is cautious, mainly in specialized intensive care units rather than broad hospital settings.
  • Revenue Streams: Limited, mainly from acute care hospital sales.

Risks & Opportunities

  • Risks: Price erosion due to generics, limited ability to expand indications, competition from other IV vasodilators.
  • Opportunities: Potential for new formulations or delivery systems, combination use in hypertensive emergencies, increasing prevalence of hypertensive crises driven by aging populations.

Key Financial Indicators

Indicator Details
Estimated Market Size $2.3 billion (globally, 2022)
Growth Rate 4.5% CAGR (2023-2028)
Price per Dose ~$500 (U.S. average)
Annual Sales Volume Variable, estimates suggest under $200 million in U.S.
Market Penetration Limited, primarily hospital-based

Investment Summary

Corlopam's market is constrained by its intravenous route, limited indications, and the presence of established competitors. Its revenue potential remains moderate, with the main value drivers being hospital adoption and price optimization. Future valuation hinges on the company's ability to innovate, expand indications, or improve delivery methods.


Key Takeaways

  • Corlopam operates in a niche market with limited growth potential due to route of administration and competition.
  • The overall hypertensive crisis market is growing, but Corlopam's share remains under pressure from generics and alternative therapies.
  • No current pipeline or significant near-term developments could boost sales.
  • Investment should consider risks associated with patent expiry, pricing pressure, and market share erosion.

FAQs

  1. What factors could enhance Corlopam's market share? Adoption of new delivery systems, expansion into outpatient settings, or new indications could improve its standing.
  2. How does Corlopam compare to its main competitors? It offers rapid vasodilation with fewer cardiovascular side effects than alternatives like nitroprusside, but its IV-only route limits outpatient use.
  3. What are the primary regulatory considerations? Corlopam is FDA-approved; maintaining registration in key markets is essential for continued sales.
  4. What is the impact of generics on Corlopam? Generics place downward pressure on prices, reducing profit margins.
  5. Are there emerging markets for Corlopam? Some developing countries with hypertensive crisis management needs could present growth opportunities, contingent on regulatory approval and market entry strategies.

Sources

[1] MarketsandMarkets, "Hypertensive Crisis Management Market," 2022.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.