The period spanning April to June 2026 has witnessed a series of significant judicial pronouncements and regulatory developments that continue to shape the intellectual property landscape in India’s pharmaceutical and life sciences sector. Courts have engaged with pressing questions around patent evergreening, procedural fairness in patent examination, trademark similarity in the healthcare space, and the growing challenge of protecting well-known pharmaceutical brands against imitation.
Overview: Key Developments at a Glance
This newsletter provides a structured overview of the most consequential IP and regulatory developments across patents, trademarks, and drug quality standards — and analyses their implications for innovator companies, generic manufacturers, and healthcare brands operating in or entering the Indian market.

AbbVie’s Venetoclax Patent Rejected by the Indian Patent Office
Key Patent Development
Background
The Indian Patent Office (IPO) rejected a patent application filed by AbbVie for Venetoclax, a drug used in the treatment of chronic lymphocytic leukaemia and acute myeloid leukaemia, marketed in India under the brand name Venclyxto. The application attracted seven pre-grant oppositions filed between 2018 and 2025. The IPO’s Delhi office ultimately declined to grant the patent on two grounds:
- The claimed invention was obvious and lacked an inventive step
- It constituted a violation of Section 3(d) of the Indian Patents Act, 1970
Legal Framework: Section 3(d)
Section 3(d) restricts the grant of patents on new forms or derivatives of known substances unless the applicant demonstrates a significant enhancement in therapeutic efficacy. This provision is a legislative tool specifically designed to prevent the evergreening of pharmaceutical patents — the practice of seeking extended patent protection through minor modifications that do not deliver meaningful therapeutic improvements.
IPO’s Core Finding
The applicant had completely failed to establish pharmacological activity or therapeutic efficacy across the millions of compounds claimed in the application. The Office concluded this was a textbook instance of evergreening.
What’s at Stake
If AbbVie does not challenge this decision, it could pave the way for affordable generic versions of Venetoclax entering the Indian market — significantly benefiting patients requiring treatment for blood cancers.
‘Cannot Launch a Drug Without a Basic Trademark Search’: PLAVIX vs. CLAVIX
Sanofi v. Intas Pharmaceuticals Ltd. & Anr. | CS(COMM) 120/2016 | 2026:DHC:3574 | Delhi High Court

Court’s Analysis
The Delhi High Court held that ‘PLAVIX’ is a coined word with no direct meaning in any language, making it highly distinctive and entitled to strong protection. The Court observed that ‘PLAVIX’ and ‘CLAVIX’ differ by only a single letter — the substitution of ‘P’ for ‘C’ — while being used for identical therapeutic products (anti-thrombotic medicinal preparations).
The adoption of ‘CLAVIX’ was held to be dishonest. Intas’s defence under Section 34 of the Trade Marks Act — which protects continued use of a mark used in good faith prior to the plaintiff’s mark — was rejected as being unavailable to parties whose adoption was tainted by bad faith.
Outcome
- Permanent injunction restraining Intas from manufacturing, selling, or dealing in any medicinal preparations under ‘CLAVIX’ or any deceptively similar mark
- Nominal damages of ₹20 lakhs awarded to Sanofi
- Litigation costs also awarded
Court’s Sharp Observation
“A company cannot launch a drug into the market without conducting even a basic trademark search.”
Practical Takeaway:
Section 34 defence cannot be relied upon where adoption is dishonest. Comprehensive trademark clearance searches covering phonetic, visual, and structural similarity must be conducted before any pharmaceutical product is launched. A one-letter difference between marks in the same therapeutic class will not save a defendant from infringement liability.
Delhi High Court Declares ‘MULTANI’ a Well-Known Trademark
Multani Pharmaceuticals Limited v. Mayuri Bhupal Bhamare | CS(COMM) 934/2024 | 2026 LLBiz HC (DEL) 436
Background
Multani Pharmaceuticals Limited, a company with roots tracing back to a clinic established in Lahore in 1905 and the formal establishment of Multani Pharmacy in 1938, approached the Delhi High Court seeking a permanent injunction and a declaration that its mark ‘MULTANI’ be recognised as a well-known trademark under the Trade Marks Act, 1999.
The dispute arose when the company became aware that Mayuri Bhupal Bhamare had filed a trademark application incorporating the word ‘MULTANI’ and was allegedly using it for identical skincare and hair care products, creating a likelihood of consumer confusion.
Statutory Criteria Applied
Justice Jyoti Singh examined the factors prescribed under Sections 11(6) and 11(7) of the Trade Marks Act, 1999:
Extent of public knowledge and recognition of the mark
Duration, geographical reach, and extent of use and promotion
History of registration and successful enforcement of trademark rights
Recognition among consumers, distributors, and business circles
The ‘MULTANI’ mark enjoyed substantial goodwill and recognition among consumers of Ayurvedic and pharmaceutical products, supported by its extensive commercial presence, long-standing market reputation, and continuous use over several decades.
The Court declared ‘MULTANI’ a well-known trademark and granted a permanent injunction restraining the defendant from using the mark in relation to identical or related goods.
Significance:
A well-known trademark declaration affords the highest tier of protection under Indian trademark law — extending across all classes of goods and services, regardless of whether the proprietor is active in a particular market segment. For heritage pharmaceutical and Ayurvedic brands, this ruling illustrates the value of building and documenting a sustained commercial track record.
Practical Takeaway:
Companies with long-established pharmaceutical or Ayurvedic brands should consider proactively seeking a well-known trademark declaration. Maintaining comprehensive documentation of sales, marketing expenditure, market reach, and judicial recognition is essential to support such an application.
India Tightens Drug Quality Standards Under Indian Pharmacopoeia 2026
India’s pharmaceutical regulatory framework has taken a decisive step toward higher quality and compliance standards following a series of scientific conclaves held in April 2026, organised jointly by the Indian Pharmacopoeia Commission (IPC) and the Council of Scientific and Industrial Research (CSIR). The discussions centred on proposed revisions under the Indian Pharmacopoeia (IP) 2026, which, once formally notified, will carry binding regulatory force.
Enhanced Impurity Profiling
Stricter requirements for identifying and quantifying impurities in pharmaceutical formulations, raising the bar for what is considered analytically acceptable.
Advanced Analytical Testing
Updated testing procedures aligned with contemporary scientific standards to ensure reliability and reproducibility of quality assessments.
Strengthened Microbiological Standards
Revised microbiological requirements to reduce the risk of contamination and improve product safety across the manufacturing chain.
Biologics & Phytopharmaceuticals
Clearer regulatory guidance on biologics and plant-derived medicines — two rapidly growing categories historically addressed less comprehensively under the pharmacopoeia.
Global Alignment
Revisions designed to align Indian standards with the United States Pharmacopeia (USP) and the European Pharmacopoeia, improving international acceptance of Indian-manufactured medicines.
IP 2026: Implications for the Pharmaceutical Industry
Once formally notified, the IP 2026 revisions will increase compliance obligations for manufacturers and testing laboratories across India. Companies with existing quality systems will need to assess the gap between current practices and the revised standards, and invest in appropriate upgrades to testing infrastructure and documentation.
Compliance Challenges
- Gap assessment between current practices and revised IP 2026 standards
- Investment in upgraded testing infrastructure and equipment
- Documentation overhaul to meet enhanced analytical requirements
- Staff training on new microbiological and impurity profiling protocols
- Revised SOPs for biologics and phytopharmaceutical product lines
Strategic Opportunities
- Alignment with USP and European Pharmacopoeia strengthens India’s credibility as a reliable pharmaceutical manufacturing hub
- Early preparation reduces risk of compliance disruption once standards become enforceable
- May provide a competitive advantage in regulated export markets
- Reinforces public health through stronger safety safeguards
- Positions export-oriented manufacturers ahead of international regulatory expectations
Indian pharmaceutical manufacturers, particularly those with export-oriented operations, should treat the IP 2026 revisions as an opportunity to benchmark their quality systems against international standards. Early preparation will reduce the risk of compliance disruption once the revised standards become enforceable.
Key Takeaways & Strategic Guidance
The April–June 2026 period has delivered a series of consequential developments that collectively reinforce India’s robust and evolving IP framework for the pharmaceutical and life sciences sector. Here is a consolidated view of the strategic imperatives for industry stakeholders.
India’s IP and regulatory landscape continues to mature — rewarding well-prepared innovators and generic manufacturers alike, while raising the bar for quality, transparency, and good faith conduct across the pharmaceutical sector.
“GLIMET” vs “GLYZET / GLYNET”
Laboratories Griffon Pvt Ltd And Anr vs Rajiv Mukul Proprietor Of Zee. | INTERIM APPLICATION NO. 3540 OF 2022 IN COMM IP SUIT NO. 213 OF 2022 | Bombay High Court – 13th January 2026
In a significant ruling reaffirming the heightened scrutiny applicable to pharmaceutical trademarks, the Hon’ble Bombay High Court granted an injunction in favour of the plaintiff’s mark “GLIMET”, restraining the defendants from using the deceptively similar marks “GLYZET” and “GLYNET.”
Factual Background: The dispute arose in the context of anti-diabetic pharmaceutical products, a therapeutic segment where precision in drug identification is critical. The plaintiff, proprietor of the mark “GLIMET,” had been using the mark in relation to medicines for the treatment of diabetes and had built a degree of recognition in the market. The defendants had earlier given undertakings to the Court agreeing not to use marks that were deceptively similar to the plaintiff’s mark. Despite such undertakings, the defendants adopted and continued to use the marks “GLYZET” and “GLYNET,” prompting the plaintiff to initiate contempt and infringement proceedings.
Court’s Analysis: The Court undertook a phonetic, visual, and structural comparison of the marks and observed that:
- All marks shared the common prefix “GLY”, which is commonly associated with glucose-related medications.
- The suffixes “MET,” “ZET,” and “NET” were found to be phonetically similar, especially in the context of prescriptions, where handwriting or verbal communication may be unclear.
- The overall structure and cadence of the marks created a real likelihood of confusion, particularly among patients, pharmacists, and medical practitioners.
The Court placed strong reliance on established jurisprudence (including principles from Cadila Healthcare Ltd. v. Cadila Pharmaceuticals Ltd.) which mandates a stricter test in pharmaceutical trademark disputes due to the direct impact on public health.
Aggravating Factors: What made this case particularly serious was the conduct of the defendants:
- Deliberate breach of prior undertakings given to the Court;
- Evidence suggesting dishonest adoption rather than coincidental similarity;
- Continued use of the impugned marks despite being on notice.
Relief and Penalties: In light of these factors, the Hon’ble Court:
- Granted a permanent injunction restraining use of the impugned marks;
- Imposed exemplary costs of ₹50 lakhs, signalling strong judicial disapproval;
- Directed initiation of perjury proceedings, highlighting the seriousness of misleading the Court.
Legal Significance: This decision reinforces several key principles:
- Pharmaceutical trademark disputes are subject to a public interest overlay, where even minimal confusion is unacceptable;
- Courts are willing to impose punitive costs and sanctions where parties act in bad faith;
- Prior undertakings, once breached, significantly weaken a defendant’s case and invite stricter scrutiny.
Practical Takeaway: This decision highlights that courts take a very strict approach in pharmaceutical trademark disputes, where even minor similarities can lead to injunctions due to public health concerns. It also underscores that dishonest conduct, especially breach of court undertakings, can result in heavy penalties and adverse orders, making it important for companies to adopt distinct marks and act in good faith.
Further Trademark Developments
“GLIMET” vs “GLYZET / GLYNET”
Laboratories Griffon Pvt Ltd And Anr vs Rajiv Mukul Proprietor Of Zee. | INTERIM APPLICATION NO. 3540 OF 2022 IN COMM IP SUIT NO. 213 OF 2022 | Bombay High Court – 13th January 2026
In a significant ruling reaffirming the heightened scrutiny applicable to pharmaceutical trademarks, the Hon’ble Bombay High Court granted an injunction in favour of the plaintiff’s mark “GLIMET”, restraining the defendants from using the deceptively similar marks “GLYZET” and “GLYNET.”
Factual Background: The dispute arose in the context of anti-diabetic pharmaceutical products, a therapeutic segment where precision in drug identification is critical. The plaintiff, proprietor of the mark “GLIMET,” had been using the mark in relation to medicines for the treatment of diabetes and had built a degree of recognition in the market. The defendants had earlier given undertakings to the Court agreeing not to use marks that were deceptively similar to the plaintiff’s mark. Despite such undertakings, the defendants adopted and continued to use the marks “GLYZET” and “GLYNET,” prompting the plaintiff to initiate contempt and infringement proceedings.
Court’s Analysis: The Court undertook a phonetic, visual, and structural comparison of the marks and observed that:
- All marks shared the common prefix “GLY”, which is commonly associated with glucose-related medications.
- The suffixes “MET,” “ZET,” and “NET” were found to be phonetically similar, especially in the context of prescriptions, where handwriting or verbal communication may be unclear.
- The overall structure and cadence of the marks created a real likelihood of confusion, particularly among patients, pharmacists, and medical practitioners.
The Court placed strong reliance on established jurisprudence (including principles from Cadila Healthcare Ltd. v. Cadila Pharmaceuticals Ltd.) which mandates a stricter test in pharmaceutical trademark disputes due to the direct impact on public health.
Aggravating Factors: What made this case particularly serious was the conduct of the defendants:
- Deliberate breach of prior undertakings given to the Court;
- Evidence suggesting dishonest adoption rather than coincidental similarity;
- Continued use of the impugned marks despite being on notice.
Relief and Penalties: In light of these factors, the Hon’ble Court:
- Granted a permanent injunction restraining use of the impugned marks;
- Imposed exemplary costs of ₹50 lakhs, signalling strong judicial disapproval;
- Directed initiation of perjury proceedings, highlighting the seriousness of misleading the Court.
Legal Significance: This decision reinforces several key principles:
- Pharmaceutical trademark disputes are subject to a public interest overlay, where even minimal confusion is unacceptable;
- Courts are willing to impose punitive costs and sanctions where parties act in bad faith;
- Prior undertakings, once breached, significantly weaken a defendant’s case and invite stricter scrutiny.
Practical Takeaway: This decision highlights that courts take a very strict approach in pharmaceutical trademark disputes, where even minor similarities can lead to injunctions due to public health concerns. It also underscores that dishonest conduct, especially breach of court undertakings, can result in heavy penalties and adverse orders, making it important for companies to adopt distinct marks and act in good faith.




