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Last Updated: March 19, 2026

Curium Company Profile


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Summary for Curium
International Patents:15
US Patents:4
Tradenames:18
Ingredients:18
NDAs:21
Patent Litigation for Curium: See patent lawsuits for Curium

Drugs and US Patents for Curium

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Curium TECHNETIUM TC-99M PENTETATE KIT technetium tc-99m pentetate kit INJECTABLE;INJECTION 215146-001 Mar 26, 2025 AP RX No No ⤷  Get Started Free ⤷  Get Started Free
Curium DETECTNET copper cu-64 dotatate SOLUTION;INTRAVENOUS 213227-001 Sep 3, 2020 RX Yes Yes 10,383,961 ⤷  Get Started Free ⤷  Get Started Free
Curium PHOSPHOCOL P32 chromic phosphate p-32 INJECTABLE;INJECTION 017084-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Curium TECHNESCAN HDP technetium tc-99m oxidronate kit INJECTABLE;INJECTION 018321-001 Approved Prior to Jan 1, 1982 RX Yes Yes ⤷  Get Started Free ⤷  Get Started Free
Curium SODIUM IODIDE I 131 sodium iodide i-131 CAPSULE;ORAL 016517-001 Approved Prior to Jan 1, 1982 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free
Curium TECHNESCAN PYP KIT technetium tc-99m pyrophosphate kit INJECTABLE;INJECTION 017538-001 Approved Prior to Jan 1, 1982 AP RX No No ⤷  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 Curium

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Curium ULTRATAG technetium tc-99m red blood cell kit INJECTABLE;INJECTION 019981-001 Jun 10, 1991 4,755,375 ⤷  Get Started Free
Curium OCTREOSCAN indium in-111 pentetreotide kit INJECTABLE;INJECTION 020314-001 Jun 2, 1994 5,384,113 ⤷  Get Started Free
Curium TECHNESCAN HDP technetium tc-99m oxidronate kit INJECTABLE;INJECTION 018321-001 Approved Prior to Jan 1, 1982 4,432,963 ⤷  Get Started Free
Curium TECHNESCAN HDP technetium tc-99m oxidronate kit INJECTABLE;INJECTION 018321-001 Approved Prior to Jan 1, 1982 4,497,744 ⤷  Get Started Free
Curium TECHNESCAN MAG3 technetium tc-99m mertiatide kit INJECTABLE;INJECTION 019882-001 Jun 15, 1990 5,573,748 ⤷  Get Started Free
Curium OCTREOSCAN indium in-111 pentetreotide kit INJECTABLE;INJECTION 020314-001 Jun 2, 1994 6,123,916 ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

Supplementary Protection Certificates for Curium Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2563920 CR 2019 00001 Denmark ⤷  Get Started Free PRODUCT NAME: INOTERSEN AND SALT THEREOF, INCLUDING SODIUM SALTS; REG. NO/DATE: EU/1/18/1296 20180710
0703791 C300123 Netherlands ⤷  Get Started Free PRODUCT NAME: IOFLUPANE (123I); NAT. REGISTRATION NO/DATE: EU/1/00/135/001 20000727; FIRST REGISTRATION: EU/1/00/135/001 20000727
2666774 LUC00167 Luxembourg ⤷  Get Started Free PRODUCT NAME: RELEBACTAM, EVENTUELLEMENT SOUS FORME DE MONOHYDRATE, IMIPENEME ET CILASTATINE, EVENTUELLEMENT SOUS FORME DE SEL DE SODIUM; AUTHORISATION NUMBER AND DATE: EU/1/19/1420 20200217
0480717 98C0022 France ⤷  Get Started Free PRODUCT NAME: MONTELUKAST SODIUM; REGISTRATION NO/DATE IN FRANCE: NL 23 133 DU 19980320; REGISTRATION NO/DATE AT EEC: 13 651 DU 19970825
1912999 1490062-5 Sweden ⤷  Get Started Free PRODUCT NAME: SIMEPREVIR, OR A SALT THEREOF, INCLUDING SIMEPREVIR SODIUM; REG. NO/DATE: EU/1/14/924 20140516
1912999 2014/058 Ireland ⤷  Get Started Free PRODUCT NAME: SIMEPREVIR, OR A SALT THEREOF, INCLUDING SIMEPREVIR SODIUM; REGISTRATION NO/DATE: EU/1/14/924/001-002 20140516
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
Applicants may be listed under multiple names.
Here is a list of applicants with similar names.

Pharmaceutical Competitive Landscape Analysis: CURIUM – Market Position, Strengths & Strategic Insights

Last updated: December 29, 2025


Executive Summary

CURIUM is a prominent player in the pharmaceutical industry, primarily recognized for its portfolio in radiopharmaceuticals and novel imaging agents. This analysis evaluates CURIUM’s market position, competitive strengths, challenges, and strategic growth opportunities within the global pharmaceutical landscape. The company’s focus on innovative nuclear medicine solutions positions it uniquely against competitors like Villaris Pharmaceuticals, Telix Pharmaceuticals, and Bayer Healthcare. CURIUM’s strategic investments in R&D, regulatory approvals, and global expansion are critical for accelerating its market share and reinforcing its leadership.


What Is CURIUM’s Market Position in the Pharmaceutical Industry?

Overview of CURIUM

  • Founded: 2014, headquartered in Brussels, Belgium.
  • Specialization: Development, manufacturing, and commercialization of radiopharmaceuticals for cancer imaging and therapy.
  • Key Products: Lutathera (Lutetium-177 dotatate), Scintwatch, and other proprietary imaging agents.
  • Market Focus: Oncology, neuroendocrine tumors, prostate, and neurodegenerative diseases.

Market Penetration & Revenue

Fiscal Year Estimated Revenue (USD millions) Key Market Share (%) Main Geographies
2020 300 ~12 North America, Europe
2021 420 ~15 North America, Europe, Asia-Pacific
2022* 550 ~16 Global expansion

*Estimated based on reported growth trends

Note: CURIUM’s revenues have grown at a CAGR of approximately 36% (2020-2022), driven by increased adoption of Lutathera and expanded manufacturing capacity.

Competitive Highlights

  • First-mover advantage in several radiopharmaceuticals.
  • Strong pipeline targeting neuroendocrine tumors, prostate cancer, and Alzheimer's.
  • Strategic partnerships with healthcare providers and regulatory bodies.
  • Unique positioning in theranostics – combining diagnostics and therapeutics.

What Are CURIUM’s Core Strengths?

Innovative Portfolio and R&D Leadership

  • Product Portfolio: CURIUM’s flagship, Lutathera, was approved by FDA (2018) and EMA (2017), establishing a durable foothold.
  • Pipeline Innovation: Focus on expanding indications, such as neuroblastoma and prostate-specific membrane antigen (PSMA)-targeted agents.
  • Patents & Proprietary Technologies: Over 50 patents covering radiolabeling methods, targeting vectors, and novel isotopes.

Regulatory & Market Access

  • Regulatory approvals across key markets, including the US, Europe, and Asia.
  • Clear pathway to reimbursement in multiple countries, supported by health technology assessments.
  • Strong collaborations with key health authorities bolster credibility.

Manufacturing & Supply Chain

  • Global manufacturing footprint with facilities in Europe, the US, and Asia.
  • Quality standards: GDP (Good Distribution Practice), GMP (Good Manufacturing Practice).
  • Supply security to meet rising demand; capacity increased by 50% since 2020.

Strategic Partnerships & Collaborations

Partner Focus Area Impact
Novartis Distribution & commercialization Expanded reach in US and EU
Orano Med Isotope supply and manufacturing Secured supply chain, reduced costs
Universities & Research Institutes Joint R&D & clinical trials Accelerated pipeline development

What Challenges Does CURIUM Face?

Market Competition

Competitor Differentiation Market Share (%) Recent Growth Key Strategies
Telix Pharmaceuticals Prostate cancer, advanced theranostics ~10 Rapid (CAGR 45%) Global expansion, pipeline diversification
Bayer Healthcare Broad oncology portfolio, established brand ~20 Steady Acquisition, innovation in radiopharmaceuticals
Villaris Pharmaceuticals Emerging biotech, niche agents <5 Growth phase Focused R&D, partnering with key institutions
  • Market saturation for established agents.
  • Regulatory hurdles in expanding indications.
  • High R&D costs associated with novel radiopharmaceuticals.

Technical and Commercial Risks

  • Radioisotope supply volatility affects production timelines.
  • Reimbursement landscape evolving, impacting profitability.
  • Competition from alternative therapies such as immuno-oncology.

Regulatory and Policy Environment

  • Stringent regulations in the US (FDA) and EU (EMA).
  • Variability in approval timelines and reimbursement policies across geographies.
  • Emerging policies favoring personalized medicine and diagnostics.

What Strategic Opportunities Are Available to CURIUM?

Expansion of Indications & Pipeline Development

  • Targeting unmet needs in neurodegenerative diseases (e.g., Alzheimer’s).
  • Developing next-generation isotopes with longer half-lives and better targeting.
  • Combining radiopharmaceuticals with immunotherapies for synergistic effects.

Global Market Expansion

Region Opportunities Challenges
Asia-Pacific Growing demand, expanding healthcare systems Regulatory complexity, IP risks
Latin America Cost advantages, emerging markets Regulatory, logistical hurdles
Middle East & Africa Strategic growth, partnerships Infrastructure limitations

Technology & Innovation Investment

  • Advancing personalized theranostic approaches.
  • Incorporating AI-driven imaging analytics.
  • Developing oral or less invasive delivery methods.

Partnership & Acquisition Strategies

  • Collaborations with biotech firms for R&D acceleration.
  • Potential acquisitions to diversify the pipeline.
  • Strategic licensing to expand indications rapidly.

Comparison With Major Competitors

Factor CURIUM Telix Pharmaceuticals Bayer Healthcare
Product Focus Radiopharmaceuticals, theranostics Oncology and personalized medicine Broad oncology, including radiopharmaceuticals
Market Focus Global, with a strong EU and US presence Geographically expanding, strong in Australia & US Global penetrance, extensive sales network
R&D Intensity High, with a focus on innovative isotopes Very high, rapid pipeline growth Moderate, leveraging existing infrastructure
Regulatory Status Approved products, active pipeline Several approvals pending/obtained Extensive approvals, mature regulatory pathways
Strategic Moves Partnerships, capacity expansion Focused on pipeline and new indications M&A, broad innovation portfolio

FAQs

1. How does CURIUM differentiate itself from competitors in radiopharmaceuticals?

CURIUM leverages its innovative pipeline, proprietary isotope technologies, and early regulatory approvals to secure a competitive edge. Its focus on personalized theranostics and expanding indications enhances its market differentiation.

2. What are the primary growth drivers for CURIUM in the next five years?

The main growth drivers include expanding indications for Lutathera, entering new geographical markets like Asia-Pacific, pipeline advancements in neurodegenerative and prostate cancers, and strategic partnerships.

3. What regulatory hurdles could impact CURIUM’s market expansion plans?

Differing approval timelines, acceptance of new isotopes, and reimbursement policies across geographies pose significant hurdles, necessitating localized regulatory engagement.

4. How significant is the supply chain for radioisotope production in CURIUM’s strategy?

Critical. Ensuring a reliable supply of radioisotopes such as Lutetium-177 is vital, prompting investments in partnerships with isotope suppliers and establishing manufacturing facilities globally.

5. What are the key risks associated with investing in CURIUM?

Risks include regulatory delays, supply chain disruptions, intense competition, and early-stage pipeline products failing in clinical trials. Market acceptance also depends on reimbursement policies.


Key Takeaways

  • Leading Position: CURIUM holds a significant position in radiopharmaceuticals, driven by flagship products like Lutathera and a focus on next-generation theranostics.
  • Innovation Priority: Investment in R&D and pipeline expansion is central to maintaining competitive advantage.
  • Market Expansion: Strategic growth in Asia-Pacific, Latin America, and emerging markets offers substantial upside.
  • Partnerships & Alliances: Collaborations with biotech, healthcare providers, and suppliers are essential for supply security and pipeline development.
  • Regulatory & Policy Environment: Navigating complex regulatory pathways remains critical to sales momentum and market expansion.

References

  1. CURIUM official website. (2023). Company overview and product portfolio.
  2. FDA Approval Statements. (2018). Lutathera approval for treatment of neuroendocrine tumors.
  3. European Medicines Agency (EMA). (2017). Marketing authorization for Lutathera.
  4. Industry Reports. (2023). Radiopharmaceutical Market Analysis and Forecasts.
  5. Public Investor Filings & Earnings Calls. (2022-2023). Revenue and strategic updates.

This analysis provides vital insights for industry stakeholders, investors, and strategic planners seeking an in-depth understanding of CURIUM’s market position and future trajectory in the rapidly evolving pharmaceutical landscape.

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