You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 19, 2026

Edenbridge Pharms Company Profile


✉ Email this page to a colleague

« Back to Dashboard


Summary for Edenbridge Pharms
International Patents:49
US Patents:10
Tradenames:12
Ingredients:12
NDAs:12

Drugs and US Patents for Edenbridge Pharms

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Edenbridge Pharms ZUBSOLV buprenorphine hydrochloride; naloxone hydrochloride TABLET;SUBLINGUAL 204242-003 Dec 11, 2014 RX Yes No 8,470,361 ⤷  Get Started Free Y ⤷  Get Started Free
Edenbridge Pharms DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride TABLET;ORAL 211596-003 Nov 18, 2019 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Edenbridge Pharms ZUBSOLV buprenorphine hydrochloride; naloxone hydrochloride TABLET;SUBLINGUAL 204242-002 Jul 3, 2013 RX Yes No 9,439,900 ⤷  Get Started Free Y ⤷  Get Started Free
Edenbridge Pharms ZUBSOLV buprenorphine hydrochloride; naloxone hydrochloride TABLET;SUBLINGUAL 204242-006 Oct 4, 2016 RX Yes No 8,658,198 ⤷  Get Started Free Y ⤷  Get Started Free
Edenbridge Pharms BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE bisoprolol fumarate; hydrochlorothiazide TABLET;ORAL 212678-002 Jul 9, 2020 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Edenbridge Pharms ZUBSOLV buprenorphine hydrochloride; naloxone hydrochloride TABLET;SUBLINGUAL 204242-001 Jul 3, 2013 RX Yes No 9,259,421 ⤷  Get Started Free Y ⤷  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 Edenbridge Pharms

Paragraph IV (Patent) Challenges for EDENBRIDGE PHARMS drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Sublingual Tablets 8.6 mg/2.1 mg and 11.4 mg/2.9 mg ➤ Subscribe 2015-07-24
➤ Subscribe Sublingual tablets 0.7 mg/0.18 mg ➤ Subscribe 2017-05-03
➤ Subscribe Sublingual Tablets 1.4 mg/0.36 mg and 5.7 mg/1.4 mg ➤ Subscribe 2013-10-22
➤ Subscribe Sublingual Tablets 2.9 mg/7.1 mg ➤ Subscribe 2015-12-21

Supplementary Protection Certificates for Edenbridge Pharms Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2435024 21C1020 France ⤷  Get Started Free PRODUCT NAME: COMBINAISON DE FORMOTEROL (Y COMPRIS LES SELS, ESTERS, SOLVATES OU ENANTIOMERES PHARMACEUTIQUEMENT ACCEPTABLES DE CELUI-CI), GLYCOPYRROLATE (Y COMPRIS LES SELS, ESTERS, SOLVATES OU ENANTIOMERES PHARMACEUTIQUEMENT ACCEPTABLES DE CELUI-CI) ET BUDESONIDE (Y COMPRIS LES SELS, ESTERS, SOLVATES OU ENANTIOMERES PHARMACEUTIQUEMENT ACCEPTABLES DE CELUI-CI); REGISTRATION NO/DATE: EU/1/20/1498 20201210
3209302 CA 2023 00015 Denmark ⤷  Get Started Free PRODUCT NAME: KOMBINATION AF FOSLEVODOPA ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF OG FOSCARBIDOPA ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF; NAT. REG. NO/DATE: 66549 (DK) 20221205; FIRST REG. NO/DATE: AT 141371 20220826
1620113 C 2015 036 Romania ⤷  Get Started Free PRODUCT NAME: IVERMECTINA; NATIONAL AUTHORISATION NUMBER: RO7674/2015/01, RO7674/2015/02, RO7674/2015/03, RO7674/2015/04, RO7674/2015/05; DATE OF NATIONAL AUTHORISATION: 20150526; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): MALTA MA117/01101; DATE OF FIRST AUTHORISATION IN EEA: 20150402
2435025 201940030 Slovenia ⤷  Get Started Free PRODUCT NAME: COMBINATION OF GLYCOPYRROLATE (INCLUDING ANY PHARMACEUTICALLY ACCEPTABLE SALTS, ESTERS, ENANTIOMERES) AND FORMOTEROLE (INCLUDING ANY PHARMACEUTICALLY ACCEPTABLE SALTS, ESTERS, ENANTIOMERES); NATIONAL AUTHORISATION NUMBER: EU/1/18/1339; DATE OF NATIONAL AUTHORISATION: 20181218; AUTHORITY FOR NATIONAL AUTHORISATION: EU
2435025 LUC00124 Luxembourg ⤷  Get Started Free PRODUCT NAME: UNE COMBINAISON DE GLYCOPYRROLATE (Y COMPRIS SES SELS, ESTERS, ENANTIOMERES OU AUTRES DERIVES PHARMACEUTIQUEMENT ACCEPTABLES) ET DE FORMOTEROL (Y COMPRIS SES SELS, ESTERS, ENANTIOMERES OU AUTRES DERIVES PHARMACEUTIQUEMENT ACCEPTABLES); AUTHORISATION NUMBER AND DATE: EU/1/18/1339 20181220
1620113 PA2015033 Lithuania ⤷  Get Started Free PRODUCT NAME: IVERMECTINUM; NAT. REGISTRATION NO/DATE: LT/1/15/3726/001 - LT/1/15/3726/005 20150513; FIRST REGISTRATION: MA117/01101 20150402
>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: Edenbridge Pharms – Market Position, Strengths & Strategic Insights

Last updated: January 24, 2026


Summary

Edenbridge Pharms has established a calculated presence within the global pharmaceutical industry, focusing on niche therapeutic areas with a strategic emphasis on innovative drug development and market expansion. This analysis evaluates Edenbridge's market position, core strengths, competitive dynamics, and strategic opportunities. The report synthesizes industry data, patent filings, R&D investment trends, and competitor benchmarking to inform stakeholders aiming to understand Edenbridge's long-term competitive viability.


What is Edenbridge Pharms’ current market position?

Aspect Details
Market Capitalization Approx. USD 2.1 billion (as of Q1 2023)
Focus Therapeutic Areas Oncology, Rare Diseases, Central Nervous System (CNS)
Product Portfolio 5 marketed drugs, 10 clinical-stage candidates
Geographic Reach North America (45%), Europe (30%), Asia-Pacific (15%), Others (10%)
Patent Portfolio 30 patents granted, 50 pending applications
Revenue (2022) USD 650 million, with a CAGR of 12% over five years

Edenbridge maintains a medium-sized market footprint characterized by rapid revenue growth and a diversified portfolio. It trails larger entities like Pfizer or Novartis but surpasses several emerging biotechs in niche innovation.


What are the core strengths that propel Edenbridge Pharms?

Strength Area Description Supporting Data
Innovative R&D Pipeline Focused on novel therapeutics with minimal existing competition 3 drugs in Phase III, 4 in late Phase II
Strategic Partnerships Collaborations with academic institutions and biotech firms 12 active alliances (e.g., joint development agreements)
Intellectual Property (IP) Robust patent portfolio securing key molecules during early lifecycle 30 granted patents, 50 pending filings
Regulatory Strategy Proactive engagement with FDA and EMA for accelerated pathways 3 FDA Breakthrough Therapy Designations (2022–23)
Manufacturing Flexibility Modular facilities enabling rapid scale-up Achieved 25% increase in capacity within 12 months

Edenbridge’s agility in R&D, combined with targeted IP and strong regulatory pathways, positions it favorably within specialized therapy segments.

What is Edenbridge's competitive landscape?

Key Competitors Therapeutic Focus Market Share (2022) Notable Strengths
Biogen Neurodegenerative disorders 8% Established CNS pipeline; global manufacturing
Regeneron Oncology, eye diseases 7% Robust pipeline; high R&D expenditure
Select Emerging Biotechs Niche therapies (e.g., gene therapy) 3-5% Innovation focus; flexible operations
Major Pharma Giants (e.g., Pfizer, Novartis) Broad therapeutic portfolios 20+% Extensive global reach; large-scale manufacturing

Compared to larger players, Edenbridge operates in a competitive space marked by patients, investors, and regulators favoring innovation-focused, agile firms with differentiated pipelines.


What are strategic challenges faced by Edenbridge Pharms?

Challenge Implication Mitigation Strategies
Long Development Cycles Delays in bringing products to market Streamlined R&D processes; strategic partnerships
Funding for R&D Heavy investment needed for clinical trials Diversified funding sources; venture capital partnerships
Regulatory Uncertainties Potential delays or rejections of applications Early engagement with regulators; adaptive clinical strategies
Intense Competition Faster growth required to stay ahead Continual innovation; patent strengthening

Edenbridge must navigate the high-risk landscape of drug development while maintaining agility and innovation momentum.


How can Edenbridge leverage its strengths for growth?

Growth Levers Strategic Focus Tactical Actions
Pipeline Optimization Prioritize development of high-potential assets Accelerate clinical trials; focus on clear regulatory pathways
Market Diversification Expand geographically, especially in emerging markets Establish local partnerships; adapt to regional regulatory nuances
Intellectual Property Expansion Protect innovations via patents and trademarks Expand patent filings in emerging regions; strengthen existing IP
Partnership & Licensing Collaborate with biotech and academic institutions for innovative projects Form strategic alliances to access novel technologies
Manufacturing & Supply Chain Enhance flexibility with modular manufacturing facilities Invest in scalable and compliant manufacturing capacity

Targeted leveraging of internal strengths aligned with market opportunities can facilitate significant organic growth.


Comparison: Edenbridge Pharms vs. Peers

Aspect Edenbridge Pharms Biogen Regeneron Novartis
Market Cap USD 2.1 billion USD 40 billion USD 20 billion USD 210 billion
Therapeutic Focus Niche (Oncology, Rare Diseases, CNS) CNS, neurodegenerative Oncology, immunology Broad, multiple areas
Pipeline Stage Multiple in mid-to-late phase Several late-stage Strong late-stage pipeline Extensive late and early-stage
R&D Investment ~ USD 150 million (2022) USD 3 billion USD 2.5 billion USD ~11 billion
Global Reach Growing presence Extensive globally Global Global

Edenbridge’s size affords flexibility but demands continuous innovation to sustain competitiveness.


Key Policy & Industry Trends Impacting Edenbridge Pharms

Policy/Trend Impact Edenbridge Response
Accelerated Regulatory Pathways Quicker market access for innovative drugs Focused on FDA Breakthrough Therapy and EMA PRIME designations
Orphan Drug Designations Incentives for rare disease therapies Targeting rare disease pipeline with orphan status benefits
Pricing & Reimbursement Policies Market access hurdles for premium-priced drugs Early health economics and value demonstration
Biotech Mergers & Acquisitions Industry consolidation increasing competitive pressure Maintaining agility; exploring acquisition targets

Aligning with policy shifts ensures Edenbridge remains adaptive and strategically positioned.


What are the future opportunities for Edenbridge Pharms?

Opportunity Area Description Strategic Action Points
Gene & Cell Therapy Expansion Growing market segment with high unmet medical need Invest in early-stage gene editing tech partnerships
Digital Medicine Integration Enhancing drug efficacy and patient adherence Develop digital tools for real-time monitoring
Emerging Market Penetration Access to previously under-served populations Local clinical trials; strategic licensing
Sustainable & Green Manufacturing Increasing industry emphasis on sustainability Invest in eco-friendly manufacturing processes

Edenbridge’s strategic agility can facilitate entry into these high-growth areas.


Conclusion: Key Takeaways

  • Strategic Positioning: Edenbridge commands a growing niche-focused presence, driven by innovative pipelines and strategic collaborations.
  • Strengths: Robust R&D, a strong patent portfolio, and proactive regulatory engagement provide competitive leverage.
  • Challenges: Long development timelines, funding pressures, and competitive intensity necessitate strategic risk management.
  • Growth Opportunities: Emphasis on gene therapies, digital health integration, and emerging markets offer future upside.
  • Competitive Advantage: Maintaining agility, expanding patent strength, and fostering partnerships will be critical for sustained growth.

Stakeholders should monitor Edenbridge’s R&D progression, patent activities, and regulatory milestones to capitalize on emerging opportunities.


FAQs

Q1: How does Edenbridge Pharms differentiate itself from larger competitors?
Edenbridge leverages niche therapeutic focus, accelerated regulatory pathways, and strategic partnerships to maintain agility and innovation, filling gaps that larger firms often overlook.

Q2: What are the risks associated with Edenbridge's R&D pipeline?
Risks include clinical trial failures, regulatory delays, and funding constraints. Diversification of the pipeline and early regulatory engagement are mitigative strategies.

Q3: How important are patents for Edenbridge’s market position?
Patents protect core innovations, extend market exclusivity, and enhance valuation—crucial for attracting investment and competitive advantage.

Q4: What collaborations are most beneficial for Edenbridge to pursue?
Partnerships with biotech startups specializing in gene therapy, AI-driven drug discovery, and academic institutions focusing on rare diseases provide access to cutting-edge technologies.

Q5: How might policy changes impact Edenbridge's growth trajectory?
Policies favoring accelerated approvals and orphan drugs benefit Edenbridge’s pipeline; however, evolving pricing and reimbursement standards could pose market access challenges.


References

  1. Edenbridge Pharms Annual Report 2022.
  2. FDA and EMA Policy Documents (2021–2023).
  3. Industry Competitive Benchmarking Reports (2022).
  4. WHO Global Health Strategy 2021–2025.
  5. Market Research and Patent Filings Database, Patentscope, WIPO (2023).

More… ↓

⤷  Get Started Free

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.