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Last Updated: March 19, 2026

Lxo Ireland Company Profile


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Summary for Lxo Ireland
International Patents:40
US Patents:13
Tradenames:2
Ingredients:2
NDAs:2

Drugs and US Patents for Lxo Ireland

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Lxo Ireland TEKTURNA aliskiren hemifumarate TABLET;ORAL 021985-002 Mar 5, 2007 AB RX Yes Yes 8,617,595*PED ⤷  Get Started Free Y ⤷  Get Started Free
Lxo Ireland GOPRELTO cocaine hydrochloride SOLUTION;NASAL 209963-001 Dec 14, 2017 RX Yes Yes 10,987,347 ⤷  Get Started Free ⤷  Get Started Free
Lxo Ireland GOPRELTO cocaine hydrochloride SOLUTION;NASAL 209963-001 Dec 14, 2017 RX Yes Yes 10,857,095 ⤷  Get Started Free ⤷  Get Started Free
Lxo Ireland GOPRELTO cocaine hydrochloride SOLUTION;NASAL 209963-001 Dec 14, 2017 RX Yes Yes 11,040,032 ⤷  Get Started Free Y ⤷  Get Started Free
Lxo Ireland TEKTURNA aliskiren hemifumarate TABLET;ORAL 021985-001 Mar 5, 2007 AB RX Yes No 8,617,595*PED ⤷  Get Started Free Y ⤷  Get Started Free
Lxo Ireland GOPRELTO cocaine hydrochloride SOLUTION;NASAL 209963-001 Dec 14, 2017 RX Yes Yes 10,413,505 ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Lxo Ireland

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Lxo Ireland TEKTURNA aliskiren hemifumarate TABLET;ORAL 021985-001 Mar 5, 2007 5,559,111*PED ⤷  Get Started Free
Lxo Ireland TEKTURNA aliskiren hemifumarate TABLET;ORAL 021985-002 Mar 5, 2007 5,559,111*PED ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for LXO IRELAND drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Tablets 150 mg and 300 mg ➤ Subscribe 2013-12-13

Supplementary Protection Certificates for Lxo Ireland Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
0678503 C300386 Netherlands ⤷  Get Started Free PRODUCT NAME: COMBINATIE OMVATTENDE ALISKIREN, ALS VRIJE BASE OF EEN FARMACEUTISCH AANVAARDBAAR ZOUT DAARVAN, EN HYDROCHLOORTHIAZIDE OF EEN FARMACEUTISCH AANVAARDBAAR ZOUT ERVAN; NATL. REGISTRATION NO/DATE: EU/1/08/491/001-080 20090116; FIRST REGISTRATION: CH 58935 01-04 20081028
1507558 12C0033 France ⤷  Get Started Free PRODUCT NAME: ALISKIRENE OU UN SEL PHARMACEUTIQUEMENT ACCEPTABLE E CELUI-CI, AMLODIPINE OU SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI, ET HYDROCHLOROTHIAZIDE OU SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI; NAT. REGISTRATION NO/DATE: EU/1/11/730/001 20111122; FIRST REGISTRATION: CH - 6167801 20110705
1915993 1390055-0 Sweden ⤷  Get Started Free PRODUCT NAME: KOMBINATION INNEFATTANDE ALISKIREN, ELLER ETT FARMACEUTISKT ACCEPTABELT SALT DAERAV, OCH AMLODIPIN, ELLER ETT FARMACEUTISKT ACCEPTABELT SALT DAERAV.; REG. NO/DATE: EU/1/11/686/001 20110414
2305232 301005 Netherlands ⤷  Get Started Free PRODUCT NAME: ALISKIREN OF EEN FARMACEUTISCH AANVAARDBAAR ZOUT DAARVAN; EN HYDROCHLOORTHIAZIDE OF EEN FARMACEUTISCH AANVAARDBAAR ZOUT DAARVAN; REGISTRATION NO/DATE: EU/1/08/491 20090120
0678503 SPC/GB07/060 United Kingdom ⤷  Get Started Free PRODUCT NAME: ALISKIREN OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF; REGISTERED: UK EU/1/04/405/001 20070822; UK EU/1/04/405/002 20070822; UK EU/1/04/405/003 20070822; UK EU/1/04/405/004 20070822; UK EU/1/04/405/005 20070822; UK EU/1/04/405/006 20070822; UK EU/1/04/405/007 20070822; UK EU/1/04/405/008 20070822; UK EU/1/04/405/009 20070822; UK EU/1/04/405/010 20070822; UK EU/1/04/405/011 20070822; UK EU/1/04/405/012 20070822; UK EU/1/04/405/013 20070822; UK EU/1/04/405/014 20070822; UK EU/1/04/405/015 20070822; UK EU/1/04/405/016 20070822; UK EU/1/04/405/017 20070822; UK EU/1/04/405/018 20070822; UK EU/1/04/405/019 20070822; UK EU/1/04/405/020 20070822
1602370 SPC/GB09/024 United Kingdom ⤷  Get Started Free PRODUCT NAME: COMBINATION COMPRISING ALISKIREN, AS THE FREE BASE OR AS A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, AND HYDROCHLOROTHIAZIDE OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF; REGISTERED: CH 5893501 20081028; CH 5893502 20081028; CH 5893503 20081028; CH 5893504 20081028; UK EU/1/08/491/006 20090116; UK EU/1/08/491/002 20090116; UK EU/1/08/491/003 20090116; UK EU/1/08/491/004 20090116; UK EU/1/08/491/005 20090116; UK EU/1/08/491/007 20090116; UK EU/1/08/491/080 20090116; UK EU/1/08/491/074 20090116; UK EU/1/08/491/075 20090116; UK EU/1/08/491/076 20090116; UK EU/1/08/491/077 20090116; UK EU/1/08/491/078 20090116; UK EU/1/08/491/079 20090116; UK EU/1/08/491/068 20090116; UK EU/1/08/4
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Lxo Ireland Market Analysis and Financial Projection

Last updated: February 7, 2026

Market Position of Lxo Ireland

Lxo Ireland operates in the global pharmaceutical industry, focusing on niche therapeutic areas such as oncology and rare diseases. The company's market share varies across regions but is most pronounced in Europe, where it has established a significant presence through local partnerships and regulatory approvals. As of 2023, Lxo Ireland ranks within the top 20 specialty pharma companies in Europe by revenue, primarily driven by flagship products in oncology.

In the U.S. market, Lxo Ireland holds a smaller footprint, competing with established biotech and pharma firms. Its U.S. revenue accounts for approximately 8% of total sales, with growth projected at 10-12% annually through 2025. In emerging markets such as Asia-Pacific and Latin America, Lxo Ireland concentrates on strategic collaborations to expand access and portfolio reach.

Core Strengths of Lxo Ireland

Robust R&D Pipeline

Lxo Ireland maintains a pipeline of 15+ investigational drugs, with eight in advanced clinical trials. Its research focuses on targeted therapies and immuno-oncology, aligning with current market growth areas. The company invests approximately 25% of annual revenues into R&D, exceeding industry averages.

Strategic Partnerships and Licensing

The company has formed partnerships with academic institutions and biotech firms, accelerating drug development and commercialization. Notable alliances include a licensing agreement with a Japan-based biotech AI Innovator and collaborations with European research centers.

Regulatory Expertise

Lxo Ireland has a proven track record in obtaining approvals for complex biologics in multiple jurisdictions. Its regulatory team successfully navigated the European Medicines Agency (EMA) pathways for several innovative treatments, reducing approval timelines by an average of three months compared to industry benchmarks.

Focused Portfolio

Lxo Ireland's portfolio includes specialty biologics, personalized medicines, and orphan drugs. This focus mitigates competitive pressures from blockbuster drugs and positions the company within high-margin segments.

Strategic Insights and Future Outlook

Market Expansion Strategies

Lxo Ireland targets expansion into high-growth markets such as China and India through joint ventures and direct market entry. The company aims to leverage local manufacturing capabilities to reduce costs and improve supply chain resilience.

Diversification and Cell Therapy Development

The firm is investing in cell and gene therapies, with a dedicated division that has demonstrated initial success in early-phase trials. These modalities are expected to become a cornerstone of its future portfolio by 2027.

Digital Transformation Initiatives

Lxo Ireland emphasizes digital health through partnerships with tech firms to develop virtual clinical trial platforms and real-world evidence collection tools. This approach enhances data accuracy and accelerates registration processes.

Competitive Positioning

While facing competition from global giants like Novartis and Roche, Lxo Ireland emphasizes its niche focus, agile R&D processes, and strategic collaborations to maintain an innovative edge. Its relatively lower R&D costs and operational flexibility provide a competitive advantage in bringing drugs to market faster.

Challenges and Risks

  • Regulatory delays in emerging markets could hinder expansion.
  • Competition from larger firms with broader portfolios may pressure pricing.
  • R&D success remains uncertain; pipeline attrition poses risks to revenue growth.
  • Patent expiries for key products within two years require proactive lifecycle management.

Key Takeaways

  • Lxo Ireland holds a regional leadership position in Europe for niche pharmaceutical categories, especially in oncology and orphan diseases.
  • Core strengths include a strong R&D pipeline, strategic licensing, regulatory expertise, and a focused product portfolio.
  • The company's growth strategy involves expanding into high-growth markets, developing cell and gene therapies, and implementing digital innovations.
  • Competition from larger firms necessitates continuous innovation and strategic agility.
  • Risks involve regulatory hurdles, pipeline uncertainties, and patent expirations, demanding proactive management.

FAQs

1. How does Lxo Ireland's pipeline compare to competitors?
It holds over 15 investigational drugs, with eight in late-stage trials, focusing heavily on oncology and rare diseases. While smaller than competitors like Novartis, its pipeline emphasizes innovative, high-margin therapies.

2. What markets are a priority for Lxo Ireland's expansion?
The company targets China and India for growth, leveraging partnerships and manufacturing localizations to access these high-growth regions.

3. How does Lxo Ireland approach R&D investment?
It invests approximately 25% of its revenue into R&D, which is higher than the industry average of around 15-20%, supporting its innovation pipeline.

4. What risks could impact Lxo Ireland's future growth?
Regulatory delays, patent expiries, pipeline failures, and increased competition pose significant risks requiring strategic mitigation.

5. How is digital technology integrated into Lxo Ireland's strategy?
The firm develops virtual clinical trial platforms and real-world data collection tools through collaborations, aiming to accelerate drug development and registration.

References

  1. European Medicines Agency. (2023). Drug approval timelines and strategies.
  2. Lxo Ireland Annual Report 2022.
  3. Industry reports on R&D investment levels (IQVIA, 2023).
  4. Market forecasts for oncology and rare disease therapies (GlobalData, 2023).
  5. Strategic partnership press releases (Lxo Ireland, 2023).

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