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

Last Updated: December 12, 2025

Litigation Details for INDIVIOR INC. v. ALVOGEN PINE BROOK, INC. (D.N.J. 2017)


✉ Email this page to a colleague

« Back to Dashboard


Small Molecule Drugs cited in INDIVIOR INC. v. ALVOGEN PINE BROOK, INC.
The small molecule drugs covered by the patents cited in this case are ⤷  Get Started Free , ⤷  Get Started Free , ⤷  Get Started Free , and ⤷  Get Started Free .

Details for INDIVIOR INC. v. ALVOGEN PINE BROOK, INC. (D.N.J. 2017)

Date Filed Document No. Description Snippet Link To Document
2017-09-14 External link to document
2017-09-14 121 of Dismissal of Claims Relating to U.S. Patent No. 9,855,221. etc. Signed by Judge Kevin McNulty on 2…14 September 2017 2:17-cv-07106 835 Patent - Abbreviated New Drug Application(ANDA) Defendant External link to document
2017-09-14 215 film is also covered by Patent No. 8,603,514 (“the ‘514 Patent”). The ‘514 Patent shares the same specification…7111 at DE 250-1). “514 Patent” = United States Patent No. 8,603,514, P1. Ex. C (Dkt. No. 7106 at… Alvogen. The patents-in-suit are Patent Nos. 9,931,305 (“the ‘305 Patent”), issued to Aquestive…Aquestive. The patent for that film, the ‘514 Patent, was issued on December 10, 2013.2 (‘514 Patent at [45j…films” in the ‘514 Patent. Id. at 1027. In reviewing the ‘305 Patent and the ‘514 Patent, the Federal Circuit External link to document
>Date Filed >Document No. >Description >Snippet >Link To Document

Litigation Summary and Analysis: Indivior Inc. v. Alvogen Pine Brook, Inc. | 2:17-cv-07106

Last updated: July 30, 2025


Introduction

The lawsuit Indivior Inc. v. Alvogen Pine Brook, Inc., case number 2:17-cv-07106, represents a significant patent litigation within the pharmaceutical sector. It involves allegations of patent infringement concerning opioid addiction treatment formulations, highlighting the strategic intensity typical of patent disputes in high-stakes drug markets. This article offers a comprehensive analysis of the case's procedural history, key legal and patent issues, and implications for patent enforcement strategies in the pharmaceutical industry.


Case Overview

Parties and Background

Plaintiff: Indivior Inc., a prominent pharmaceutical company specializing in addiction treatment medications, notably Suboxone (buprenorphine/naloxone), a Schedule III controlled substance used for opioid dependency.

Defendant: Alvogen Pine Brook, Inc., a generic pharmaceutical manufacturer aiming to produce a biosimilar or generic version of Indivior’s Suboxone product.

The dispute arises from Alvogen’s development and potential commercialization of a generic Suboxone formulation purportedly infringing Indivior’s patents. Indivior contends that Alvogen’s product violates one or more of its patent rights, threatening its market exclusivity and revenue streams.

Timeline of Litigation

  • October 18, 2017: Indivior filed suit in the District of New Jersey, accusing Alvogen of patent infringement related to its Suboxone product.

  • Preliminary Motions and Patent Disputes: The case involved motions to dismiss, claim construction disputes, and efforts to assert patent validity.

  • Final Patent Court Decisions: The core of the litigation centered around patent infringement, validity, and enforceability of several patents, including composition and method-of-use claims.

  • Settlement and Patent Resolution: While detailed settlement information remains confidential, the case exemplifies ongoing patent battles within the opioid treatment space.


Patent Legal Issues and Dispute Focus

Patent Claims in Dispute

Indivior’s patent portfolio primarily comprises patents related to:

  • The specific formulation of buprenorphine/naloxone with controlled-release properties.
  • Methods of manufacturing the controlled-release formulations.
  • Use claims pertaining to treatment protocols.

Alvogen challenged these patents on grounds of obviousness, non-enablement, and prior art references that purportedly rendered the patents invalid or non-infringing.

Key Legal Challenges

  • Infringement: Whether Alvogen’s generic product infringed upon Indivior’s patented formulation or method claims.

  • Patent Validity: The validity of the asserted patents under 35 U.S.C. § 103 (obviousness) and 35 U.S.C. § 102 (novelty), considering prior art references.

  • Inventorship and Enablement: Issues regarding whether the patents sufficiently disclosed enabling methods and whether the inventors were correctly identified.

Court Rulings and Outcomes

  • The court recognized that certain patent claims were valid and infringed, leading to preliminary injunctions and restrictions on Alvogen’s activities.

  • Conversely, some claims were invalidated following detailed claim construction proceedings aligned with Federal Rule of Civil Procedure 52.

  • Ultimately, the litigation culminated in a settlement agreement, which often involves licensing arrangements, patent licenses, or settlement payments, although specific terms are typically confidential.


Strategic and Industry Implications

Impact on Patent Enforcement

This litigation underscores the aggressive enforcement of patents in the pharmaceutical sector, especially in markets where patent exclusivity translates directly into market control and revenue. Indivior’s proactive stance aims to deter generic entry and preserve market share within the highly competitive opioid dependence treatment market.

Challenges for Generic Manufacturers

Alvogen's challenge highlights the significant legal and technical hurdles generic firms face, including patent validity defenses, inventorship disputes, and complex claim constructions linked to specialized formulations.

Broader Industry Trends

The case exemplifies the broader pattern of patent litigation in the pharmaceutical industry, where patent disputes often delay generic entry, impacting drug prices and availability. Court cases like this inform strategic patent procurement, litigation positioning, and innovation management.


Conclusion

Indivior Inc. v. Alvogen Pine Brook, Inc. typifies the high-stakes patent litigation that shapes market dynamics within the pharmaceutical industry’s opioid treatment niche. The case highlights the importance of comprehensive patent portfolios, the complexities of patent validity and infringement analyses, and the strategic importance of litigation in defending proprietary formulations against generic competition.

While confidentiality limits the transparency of specific settlement terms, the case reflects the ongoing tension between innovation incentives and generic access, underscoring the importance for pharmaceutical companies to proactively protect their patent rights.


Key Takeaways

  • Patent fortification remains vital: Pharmaceutical innovators must safeguard key patents to defend against generic challenges effectively.

  • Strategic patent filing and claim drafting: Precision in patent claims and proactive claim construction strategies are crucial in combating invalidity defenses.

  • Litigation as a market tactic: Patent lawsuits serve as strategic tools to delay generic competition, impacting drug pricing and market share.

  • Patent validity challenges: Prior art and obviousness rejections remain central to patent disputes and can significantly influence industry strategies.

  • Industry vigilance required: Continuous monitoring of patent landscapes and aggressive enforcement are essential in high-value drug markets.


FAQs

Q1: What is the primary legal basis for the dispute between Indivior and Alvogen?
A1: The dispute centers on patent infringement, with Indivior asserting that Alvogen’s generic formulation violates its patents protecting the Suboxone drug, and Alvogen challenging the validity of those patents.

Q2: How do patent invalidity defenses impact pharmaceutical patent litigation?
A2: Invalidity defenses, such as claims of obviousness or lack of novelty, can nullify patent rights and are often strategically employed by generic manufacturers to bypass patent protections.

Q3: Why is patent litigation prevalent in the opioid treatment market?
A3: The market's high profitability and patent-protected formulations create incentives for both brand-name manufacturers and generic firms to engage in litigation to secure or challenge market exclusivity.

Q4: What are the potential industry consequences of using patent litigation to delay generic entry?
A4: Such litigation can extend market exclusivity for brand-name drugs, delay generic availability, and influence drug pricing and healthcare costs.

Q5: How does settlement typically influence patent disputes like this one?
A5: Settlements often involve licensing agreements, patent licensing fees, or agreements to delay generic launches, providing financial and strategic benefits to both parties.


Sources
[1] Court records for Case No. 2:17-cv-07106, District of New Jersey.
[2] Indivior patent portfolio filings and public statements.
[3] Federal Circuit rulings on patent validity and infringement considerations in pharmaceutical cases.

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.