You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 25, 2024

~ Buy the LICART (diclofenac epolamine) Drug Profile, 2024 PDF Report in the Report Store ~

LICART Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


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

Licart is a drug marketed by Ibsa Inst Bio and is included in one NDA. There are two patents protecting this drug.

The generic ingredient in LICART is diclofenac epolamine. There are forty-seven drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the diclofenac epolamine profile page.

DrugPatentWatch® Generic Entry Outlook for Licart

By analyzing the patents and regulatory protections it appears that the earliest date for generic entry will be February 20, 2035. This may change due to patent challenges or generic licensing.

Indicators of Generic Entry

< Available with Subscription >

  Subscribe

AI Research Assistant
Questions you can ask:
  • What is the 5 year forecast for LICART?
  • What are the global sales for LICART?
  • What is Average Wholesale Price for LICART?
Summary for LICART
Drug patent expirations by year for LICART
Drug Prices for LICART

See drug prices for LICART

DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for LICART
Generic Entry Date for LICART*:
Constraining patent/regulatory exclusivity:
NDA:
Dosage:
SYSTEM;TOPICAL

*The generic entry opportunity date is the latter of the last compound-claiming patent and the last regulatory exclusivity protection. Many factors can influence early or later generic entry. This date is provided as a rough estimate of generic entry potential and should not be used as an independent source.

Recent Clinical Trials for LICART

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
IBSA Institut Biochimique SAPhase 3

See all LICART clinical trials

Pharmacology for LICART

US Patents and Regulatory Information for LICART

LICART is protected by two US patents.

Based on analysis by DrugPatentWatch, the earliest date for a generic version of LICART is ⤷  Subscribe.

This potential generic entry date is based on patent ⤷  Subscribe.

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ibsa Inst Bio LICART diclofenac epolamine SYSTEM;TOPICAL 206976-001 Dec 19, 2018 RX Yes Yes ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Ibsa Inst Bio LICART diclofenac epolamine SYSTEM;TOPICAL 206976-001 Dec 19, 2018 RX Yes Yes ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

LICART Market Analysis and Financial Projection Experimental

Market Dynamics and Financial Trajectory for LICART

Introduction to LICART

LICART, a topical nonsteroidal anti-inflammatory drug (NSAID) containing diclofenac epolamine, has been launched in the US market for the treatment of acute pain due to minor strains, sprains, and contusions. It is the first and only once-a-day topical NSAID therapy approved by the FDA, leveraging patented next-generation patch technology for fast onset and sustained pain relief[1].

Market Overview

Global Diclofenac Market

The diclofenac market, which includes LICART, is projected to grow significantly. By 2027, the market is expected to reach $6.1 billion, growing at a CAGR of 3.9% from 2022 to 2027. This growth is driven by the increasing prevalence of inflammation-related conditions, particularly among the geriatric population[2].

Geographic Segmentation

North America holds a dominant market share, primarily due to robust medical infrastructure and high disease literacy. However, the Asia-Pacific region is expected to offer lucrative growth opportunities due to increasing medical investments and a growing geriatric population[2][3].

Key Drivers of the Market

Geriatric Population

The growing number of geriatric individuals globally is a significant driver for the diclofenac market. This population is highly susceptible to inflammation-related problems, thereby increasing the demand for diclofenac-based treatments[2].

Sports and Trauma Injuries

The rise in sports-related injuries, especially with increased government support for sporting events, is another key driver. For instance, the approval for the USA to host a significant portion of the ICC T20 World Cup is expected to increase sports-related injuries, thus boosting the demand for diclofenac products[2].

Technological Advancements

The introduction of new formulations, such as LICART's once-a-day topical patch, enhances patient compliance and satisfaction. This innovation is expected to drive market growth as it offers faster onset and sustained pain relief compared to traditional NSAIDs[1].

Financial Trajectory

Revenue Projections

The diclofenac market, including LICART, is expected to see steady growth. The market size is projected to reach $6.1 billion by 2027, with a CAGR of 3.9% from 2022 to 2027. This growth is supported by increasing regulatory approvals and the launch of new diclofenac generics and formulations[2].

Segmental Growth

  • Oral Segment: While the oral segment currently accounts for a significant proportion of the diclofenac market, the topical segment, where LICART belongs, is expected to grow significantly. Topical diclofenac medications, such as gels, creams, sprays, and patches, are gaining popularity due to their ease of application and higher patient acceptance[3].

  • Parenteral Segment: The parenteral segment also holds a considerable market share, driven by the continuity of drug delivery and lower systemic side effects. However, the topical segment is anticipated to grow at a faster rate due to innovations like LICART[3].

Market Impact of LICART

Unique Selling Proposition

LICART's once-a-day dosing and patented next-generation patch technology set it apart from other topical NSAIDs. This unique selling proposition is expected to attract more patients and healthcare providers, thereby increasing its market share[1].

Competitive Landscape

The launch of LICART has introduced a new competitor in the topical NSAID market. Its approval and availability through participating mail order and retail pharmacies are expected to capture a significant portion of the market, especially in the treatment of acute pain due to minor strains, sprains, and contusions[1].

Challenges and Opportunities

Side Effects and Regulatory Considerations

Despite the growth potential, the diclofenac market faces challenges related to side effects. Cases of unwanted side effects have hampered market growth in the past. However, regulatory approvals and the development of safer formulations like LICART are mitigating these risks[2].

Emerging Markets

The Asia-Pacific region offers significant growth opportunities due to robust medical advertisements, government support for medicinal developments, and increasing foreign direct investment (FDI) in the healthcare sector. This region is expected to drive the future growth of the diclofenac market, including LICART[2].

Impact of COVID-19

The COVID-19 pandemic had a slightly negative impact on the diclofenac market in 2020 due to decreased demand and supply chain disruptions. However, with the relaxation of government restrictions and the normalization of drug supply chains in 2021 and 2022, the market has recovered and is expected to grow steadily over the forecast period[3].

Key Takeaways

  • Market Growth: The diclofenac market, including LICART, is projected to reach $6.1 billion by 2027, growing at a CAGR of 3.9%.
  • Geographic Dominance: North America currently dominates the market, but the Asia-Pacific region is expected to offer significant growth opportunities.
  • Geriatric Population: The growing geriatric population is a key driver for the market.
  • Technological Advancements: Innovations like LICART's once-a-day topical patch are driving market growth.
  • Segmental Growth: The topical segment is expected to grow significantly due to ease of application and higher patient acceptance.

FAQs

What is LICART used for?

LICART is used for the treatment of acute pain due to minor strains, sprains, and contusions. It is a topical nonsteroidal anti-inflammatory drug (NSAID) containing diclofenac epolamine[1].

How does LICART differ from other NSAIDs?

LICART is the first and only once-a-day topical NSAID therapy approved by the FDA, featuring patented next-generation patch technology for fast onset and sustained pain relief[1].

What are the key drivers of the diclofenac market?

The key drivers include the growing geriatric population, sports and trauma injuries, and technological advancements in formulations like LICART[2].

How has the COVID-19 pandemic affected the diclofenac market?

The pandemic had a slightly negative impact in 2020 but the market has recovered with the normalization of supply chains and is expected to grow steadily over the forecast period[3].

What is the projected market size of the diclofenac market by 2027?

The diclofenac market is projected to reach $6.1 billion by 2027, growing at a CAGR of 3.9% from 2022 to 2027[2].

Sources

  1. IBSA Pharma Inc. - "Licartâ„¢ Now Available to Treat Acute Pain Due to Minor Strains, Sprains, and Contusions" - PR Newswire, October 30, 2020.
  2. IndustryARC - "Diclofenac Market Size Report, 2022-2027".
  3. Fortune Business Insights - "Diclofenac Market Size, Trends, Growth, 2032".
  4. Markets Business Insider - "Global Acute Pain Market Insights, Epidemiology and Market Forecast to 2028".

More… ↓

⤷  Subscribe

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. 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.