Delhi High Court
Sun Pharma Laboratories Limited vs Intas Pharmaceuticals Limited on 28 March, 2026
* IN THE HIGH COURT OF DELHI AT NEW DELHI
% Judgment delivered on: 28.03.2026
+ CS(COMM) 39/2023
SUN PHARMA LABORATORIES LIMITED .....Plaintiff
versus
INTAS PHARMACEUTICALS LIMITED .....Defendant
Advocates who appeared in this case
For the Plaintiff : Mr. Sachin Gupta, Ms. Mahima
Chanchalani, Ms. Prashansa, Mr. Rohit
Pradhan, Ms. Diksha, Mr. Ajay & Mr.
Aadarsh, Advocates.
For the Defendant : Ms. Bitika Sharma, Mr. George Vithayathil,
Ms. Ahaana Singh Rana & Mr. Aditya P.
Mishra, Advocates.
CORAM:
HON'BLE MR. JUSTICE TEJAS KARIA
JUDGMENT
TEJAS KARIA, J
1. The present Suit has been filed seeking a permanent injunction against
infringement of the Trade Mark ‘BEVETEX’ (“Plaintiff’s Mark”), passing
off, unfair competition, dilution, rendition of accounts and damages.
2. The drug under the Plaintiff’s Mark (“Plaintiff’s Drug”) is a
scheduled drug used for treatment of breast cancer, non-small cell lung
cancer and pancreatic cancer. The Defendant is using the Mark ‘BEVATAS’
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 1 of 34
Signing Date:28.03.2026
18:57:27
(“Impugned Mark”) for manufacturing and selling drugs for treatment of
colorectal cancer, ovarian cancer, cervical cancer, lung cancer and recurrent
glioblastoma (“Defendant’s Drug”).
PROCEDURAL HISTORY:
3. The present Suit was listed before the Court of the District Judge,
Saket Courts, Delhi (“Trial Court”) on 02.01.2018, wherein the learned
Trial Court refused to grant an ex-parte ad-interim injunction on the ground
that the Defendant’s Drug is a cancer drug and it would not be in the interest
of the public to grant an injunction against the Defendant’s Drug without
granting the Defendant an opportunity of being heard. Accordingly, the
Defendant was granted a period of one week to file its reply to the
Application filed by the Plaintiff under Order XXXIX Rules 1 and 2 of the
Code of Civil Procedure, 1908 (“CPC“).
4. After completion of arguments with respect to the Application under
Order XXXIX Rules 1 and 2 of the CPC, the learned Trial Court vide Order
dated 17.09.2018, dismissed the Application of the Plaintiff for grant of
interim injunction on the ground that the Plaintiff had failed to establish a
prima facie case for grant of an interim injunction.
5. On 17.12.2018, the learned Trial Court framed the following issues:
1. Whether the plaintiff is registered owner of the Trademark
‘BEVETEX’ in relation to medical and pharmaceutical preparations?
OPP
2. Whether the plaintiff is the prior and continuous user of the
trade mark ‘BEVETEX’ in comparison to the defendant’s use of the
mark ‘BEVATAS’ in relation to medical and pharmaceutical
preparations? OPPSignature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 2 of 34
Signing Date:28.03.2026
18:57:27
3. Whether the use of the impugned mark ‘BEVATAS’ by the
defendant in respect to medical and pharmaceutical preparations
amounts to infringement of plaintiffs registered trade mark
‘BEVETEX’? OPP
4. Whether there is any similarity or likelihood of
confusion/deception between the marks ‘BEVETEX’ and
‘BEVATAS’? OPParties
5. Whether the plaintiff is guilty of hoarding its mark
‘BEVETEX’? OPD
6. Whether the present suit has been instituted by the plaintiff
without any authorization? OPD
7. Whether the present suit suffers from delay, laches and
acquiescence? OPD
8. Whether the plaintiff has failed to disclose any cause of action
to file the present suit? OPD
9. Whether the defendant is the proprietor of the trade mark
‘BEVATAS’? OPD
10. Whether the defendant is the honest adopter and prior user of
the mark ‘BEVATAS’? OPD
11. Relief.
6. Aggrieved by the dismissal of the Application for interim injunction
against the use of the Impugned Mark by the learned Trial Court, the
Plaintiff filed an appeal before this Court bearing No. FAO 447 of 2018
(“Appeal”). The Appeal filed by the Plaintiff came to be dismissed vide
order dated 09.01.2020. The Plaintiff preferred Special Leave Petition No.
3385 of 2020 (“SLP”) against the order of dismissal of the Appeal. The SLP
filed by the Plaintiff was also dismissed vide order dated 14.02.2020 with
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 3 of 34
Signing Date:28.03.2026
18:57:27
the direction that the learned Trial Court shall decide the Suit being
uninfluenced by any observation by the High Court.
7. Thereafter, the Plaintiff revalued the Suit and, accordingly, the Suit
was transferred before this Court for adjudication. After completion of final
arguments on behalf of the Parties, the Judgment in the Suit was reserved on
01.12.2025.
SUBMISSIONS ON BEHALF OF THE PLAINTIFF:
8. The learned Counsel for the Plaintiff made the following submissions:
8.1 The Plaintiff is a wholly owned subsidiary of Sun
Pharmaceuticals Industries Limited, which started the business
of marketing pharmaceutical products in the year 1978. The
Plaintiff markets drugs and formulations in more than 150
countries of the world under its extensive range of distinctive
Trade Marks and Trade Names and has been referred to in trade
circles as ‘SUN’ and ‘SUN PHARMA’. The Plaintiff has a
consolidated annual turnover of over ₹3,00,00,00,00,000
globally. The Plaintiff is now ranked as No. 1 Pharma Company
in India in a total of 11 specialties and is the world’s 4th largest
Generic Pharmaceutical Company.
8.2 The Plaintiff’s manufacturing operations are focused on
producing generics, branded generics, specialty, over-the-
counter products, anti-retrovirals, Active Pharmaceutical
Ingredients (“APIs”) and intermediates in the full range of
dosage forms, including tablets, capsules, injectables,
ointments, creams and liquids. The Plaintiff also manufactures
specialty APIs, including controlled substances, steroids,
peptides and anti-cancers. The Plaintiff has a highly skilled
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 4 of 34
Signing Date:28.03.2026
18:57:27
team of regulatory affairs specialists who are well versed with
regulatory, policies and procedures around the world. The
Plaintiff has a wealth of experience in the timely filing of
dossiers as well as handling regulatory queries from both
authorities and customers.
8.3 The Plaintiff’s predecessor, Sun Pharmaceutical Industries Ltd.,
coined the Plaintiff’s Mark in the year 1983 and accordingly
obtained a Trade Mark registration for the same, the details of
which are as follows:
Trade Mark Cl. Registration no. Goods
& Date
BEVETEX 5 410744 dated Medicinal & Pharmaceutical
16.09.1983 preparations for human use
8.4 The Plaintiff’s Mark is entitled to maximum protection as the
same is an invented mark containing Molecule / Salt
‘PACLITAXEL’. The Plaintiff on account of registration has a
statutory right to the exclusive use of the Plaintiff’s Mark and
the use of the same or a deceptively similar Trade Mark by an
unauthorised person or trader in relation to the similar kind of
goods will constitute infringement of the Plaintiff’s right of the
exclusive use and the registered Trade Mark under the
provisions of the Trade Marks Act, 1999 (“Act”).
8.5 The Plaintiff has been selling the Plaintiff’s Drug since the year
2015. The Plaintiff has taken efforts to popularize Plaintiff’s
Drug and has expended substantial sums of money on sales
promotion and publicity of the Plaintiff’s Drug bearing the
Plaintiff’s Mark. Due to superior quality and high efficacy of
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 5 of 34
Signing Date:28.03.2026
18:57:27
the Plaintiff’s Drug bearing the Plaintiff’s Mark, continuous
and extensive use of the Plaintiff’s Mark and large sales of the
Plaintiff’s Drug as also wide publicity given to the Plaintiff’s
Drug bearing the Plaintiff’s Mark, the Plaintiff has acquired
immense reputation and goodwill in the Plaintiff’s Mark and
the goods sold thereunder. Consequently, the members of the
trade, public as also the doctors and chemists exclusively
associate the Plaintiff’s Mark with the Plaintiff and the
Plaintiff’s Drug and with none else. The statement of sales and
promotional expenses qua the Plaintiff’s Drug under the
Plaintiff’s Mark is as under:
Year Expenses Sales
Rs. In Lac (Approx) Rs. In Lac (Approx)
2015-16 18.99 379.97
2016-17 34.80 696.09
Total 53.79 1076.06
8.6 The Plaintiff came across the publication of the Application for
registration of the Impugned Mark under Trade Mark
Application No. 3254683 dated 09.05.2016 filed by the
Defendant on a proposed to be used basis. The Plaintiff
immediately filed its notice of Opposition (“Opposition”)
before the Trade Marks Registry on 27.12.2016. The
Opposition proceedings are currently pending. Sometime in the
third week of December 2017, the Plaintiff came across the
Defendant’s Drug under the Impugned Mark selling in Delhi.
The Plaintiff upon enquiry came to know that the Defendant
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 6 of 34
Signing Date:28.03.2026
18:57:27
has launched the Defendant’s Drug under the Impugned Mark
sometime in October 2017.
8.7 The Defendant’s Drug although a cancer drug contains a
different salt namely ‘BEVACIZUMAB’ and is used for the
treatment of colorectal cancer, ovarian cancer, cervical cancer,
lung cancer and recurrent glioblastoma. Wrong administration
of drugs can prove fatal. A comparison between the competing
drugs is enumerated below:
Product Bevetex Bevatas Remarks
features
Company Sun Pharma Intas
What is the This is Paclitaxel Monoclonal antibody, Very different
product Injection used as anti-angiogenic class of drugs with
Concentrate for agent to treat various different
Nanodispersion cancer indications indications &
mode of action
Presentation Vials of 100mg & Vials 100mg & 400mg Almost same
300mg
Dosage 260 mg / m2 to 10 to 15 mg / kg
approved 295 mg / m2 every repeated every 2 or 3
21 days weeks
Route of IV Infusion IV Infusion Same
administration
Effective dose 400 mg 700 - 900 mg (2 vials 400mg Bevetex &
based on BSA or more of 400mg Bevetas can be
used). confused at the
100mg for titration pharmacy / para
medical level
Broadly Metastatic breast 1) Metastatic colorectal Non overlapping
recommended cancer cancer, indications.
for 2) Unresectable, Patient may get
locally advanced, wrong drug for the
recurrent or metastatic given indication.
non-squamous NSCLC This may cause
3) Recurrent severe / life
glioblastoma threatening
4) Metastatic renal cell complications
carcinoma, with no tumour
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 7 of 34
Signing Date:28.03.2026
18:57:27
5) Recurrent or kill effect
metastatic cervical
cancer
6) Recurrent epithelial
ovarian, fallopian tube,
or primary peritoneal
cancer that is:
platinum-resistant or
platinum-sensitive
Most common Pain, peripheral Gastrointestinal Very different
side effects neuropathy, perforation, surgery & toxicity profile.
neutropenia, wound healing Life threatening
leucopenia, complications, severe toxicities observed
alopecia, mucosal & fatal Hemorrhage with Bevacizumab
inflammation,
asthenia, pyrexia,
nausea, vomiting
8.8 The Defendant has unlawfully adopted the Impugned Mark.
Being in pharmaceutical business, the Defendant is well aware
of the Plaintiff’s adoption and use of the Plaintiff’s Mark. The
Impugned Mark is structurally, visually and phonetically
similar to the Plaintiff’s Mark. The competing medicines are
sold in the same dosage form, i.e., injections and are sold at
similar prices. Such adoption also amounts to unfair trade
practice, unfair competition and dilution. Such act also amounts
to misrepresentation and misappropriation of the Plaintiff’s
goodwill in the Plaintiff’s Mark.
8.9 Both the Plaintiff’s Drug and the Impugned Drug are used for
treatment of cancer. Both of the competing drugs are Schedule-
H drugs and also come in a single pack injection vials of 100
mg dosage. The Defendant’s Drug is also sold for a price nearly
identical to the price of the Plaintiff’s Drug. If the wrong drug
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 8 of 34
Signing Date:28.03.2026
18:57:27
is given to the cancer patient undergoing treatment it can lead
to disastrous consequences, hence, it is in public interest that
the use of the Impugned Mark is restrained and therefore the
Plaintiff has also given up its claim for damages and limited the
relief to restrain the use of the Impugned Mark so as to avoid
disastrous results.
8.10 In a case like the present where the molecule/ salt contained in
the competing drugs, i.e., ‘PACLITEXEL’ and
‘BEVACIZUMAB’, cannot be easily pronounced, can one
expect the patients / their attendants / chemist and their staff /
nurses to know the finer difference between chemical
compounds and biological compounds. Courts have repeatedly
held that courts are not to speculate if there shall be confusion
or not as the test of deceptive similarity is stringent and the
threshold of confusion is low. Judicial notice has been taken in
the judgment of Cadila Healthcare v. Cadila Pharmaceuticals,
AIR 2001 SC 1952, that prescription drugs are sold even
without prescription.
8.11 Prescription does not contain name of the salt or the Trade
Dress / packaging of the drug. The competing Marks are not to
be compared side by side. The test of confusion is to see if an
average person with imperfect recollection would get confused
as has been held in Corn Products. v. Shangrila Food, AIR
1960 SC 142. The consumer / patient does not know the
difference between the salts. One cannot even pronounce the
competing salts / molecules therefore, to be able to distinguish
between the two is not possible.
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 9 of 34
Signing Date:28.03.2026
18:57:27
8.12 Section 29(3) of the Act also contains a presumption that when
there is identity between two competing Marks and goods, the
Courts shall presume that the Impugned Mark is likely to cause
confusion. It has been held in the decisions of Novartis v. Crest
Pharma, 2009 (41) PTC 57 (Del), Charak Pharma. v.
Glenmark, 2014 (57) PTC 538 (Bom) and Sun Pharma v.
Glenmark, (2023) SCC Online Del 3786, that it is more
dangerous when identical or deceptively similar Marks are used
for drugs for different ailments.
8.13 It is the likelihood of confusion, which needs to be seen and not
the actual confusion. The Impugned Mark has close
resemblance to the Plaintiff’s Mark. The first and last syllable
are almost identical in the competing Marks and therefore the
Impugned Mark is deceptively similar to the Plaintiff’s Mark
which is likely to cause confusion which will have dangerous
consequences which can prove to be fatal. The Plaintiff’s Drug
and the Defendant’s Drug are used for overlapping cancers,
namely Lung and Breast cancer, in the background of medical
negligence cases and medicines are sold without prescription or
with prescriptions with illegible handwriting, Courts are not to
speculate as to whether there is a probability of confusion
between similar names as has been held in Cadila Healthcare
v. Cadila Pharmaceuticals (supra) judgment.
8.14 The present Suit has been instituted by the Plaintiff with
authorisation. Power of Attorney in favour of Mr. Amit
Aggarwal issued by the Plaintiff was filed on record on
17.02.2018 after serving advance copy to the Defendant’s
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 10 of 34
Signing Date:28.03.2026
18:57:27
Counsel, Ms. Isha Tyagi, Advocate, through email of the same
date. The original Power of Attorney was shown during trial at
the time of exhibiting documents and was exhibited as Ex. PW
1/1.
8.15 Accordingly, the Plaintiff is entitled to a relief of permanent
injunction against the use of the Impugned Mark by the
Defendant.
SUBMISSIONS ON BEHALF OF THE DEFENDANT:
9. The learned Counsel for the Defendant made the following
submissions:
9.1 It is fundamental to Trade Mark law that the competing Marks
are to be compared as a whole to ascertain similarity and
likelihood of confusion. The Plaintiff’s Mark and the Impugned
Mark are entirely different and there can be no likelihood of
confusion or deception and / or similarity between the two
Marks. The Plaintiff’s Mark and the Impugned Mark are totally
different, dissimilar and distinct. The competing Marks are
visually and phonetically dissimilar and there cannot be
likelihood of confusion at any level. Even the Drugs sold under
these marks are administered under the supervision of
specialists in different ways. The Marks are visually,
structurally and phonetically different as compared below:
PLAINTIFF'S MARK IMPUGNED MARK
BEVETEX BEVATAS
Phonetics of the mark starts with phonics Phonetics of the mark starts with
BEVE phonics BEVA
Phonetics of the mark ends with phonics Phonetics of the mark ends with
TEX phonics TAS
No visual similarity as the labels are No visual similarity as the labels areSignature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 11 of 34
Signing Date:28.03.2026
18:57:27
completely different. completely different.
The Trade Mark is qualified by the name The Trade Mark is qualified by the
of its chemical compound being name of its chemical compound being
“PACLITAXEL” “BEVACIZUMAB”
9.2 The Defendant had also applied for the registration of the
Impugned Mark. When the Impugned Mark was examined by
the Examiner of Trade Marks, he did not cite any conflicting
Marks and the Application for registration of the Impugned
Mark was accepted for advertisement. Even the Trade Marks
Registry did not find any similarity between the Plaintiff’s
Mark and the Impugned Mark.
9.3 The Defendant’s Drug contains the compound
‘BEVACIZUMAB’ under the Impugned Mark. The Defendant
has been manufacturing and selling the Defendant’s Drug at
least since 2016 and has obtained all required permissions from
the concerned authorities. The Defendant has coined / invented
the Impugned Mark by amalgamating the words ‘BEVA’
derived from or referable to the active ingredient
‘BEVACIZUMAB’ and ‘TAS’ from the Defendant’s Trade
Name, INTAS, a pharmaceutical company of trade repute and
standing since the last several decades. Various clinical trials
were conducted by the Defendant and said trials were approved
by the appropriate authorities. The said permission was granted
by Drug Controller General of India, Directorate General of
Health Services on 23.06.2016 and 27.06.2016 respectively and
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 12 of 34
Signing Date:28.03.2026
18:57:27
thereafter by the Deputy Commissioner, Food and Drugs
Control Administration, Gujarat State, Gandhinagar on
30.07.2016.
9.4 The Plaintiff’s Drug contains Molecule / Salt ‘PACLITAXEL’
under the Plaintiff’s Mark as a scheduled drug for treatment of
breast cancer, non-small lung cancer and pancreatic cancer.
Admittedly the Plaintiff avers to have started selling the
Plaintiff’s Drug only since the year 2015 even though the
Plaintiff has claimed to have invented the Plaintiff’s Mark in
the year 1983. Thus, the Plaintiff has mala fidely hoarded the
Plaintiff’s Mark. The Plaintiff has no goodwill or recognition
with the mark owing to non-use until 2015. The Plaintiff’s
Witness in his cross-examination has admitted that the Plaintiff
was not using the Plaintiff’s Mark from 1983 until 2015.
Further, the Supreme Court in the judgment of Neon
Laboratories Ltd. v. Medical Technologies Ltd., 2016 (2) SCJ
260, held that Section 47 of the Act is in the same vein and
statutory strain inasmuch as it postulates the possibility of a
registered mark being taken off the register on an application
being made by any aggrieved person, inter alia, on the ground
that for a continuous period of five years and three months from
the date on which the trade mark was registered, there was no
bona fide use thereof.
9.5 The turnover of the Defendant’s Drug is more than that of the
Plaintiff’s Drug. It cannot therefore be said that the Defendant
is trying to encash upon the reputation and goodwill of the
Plaintiff’s Mark.
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 13 of 34
Signing Date:28.03.2026
18:57:27
9.6 The Plaintiff’s Drug and the Defendant’s Drug are Schedule H,
IV Injection drugs and cannot be self-administered. They are
also not ‘Over The Counter’ drugs or for that matter easily /
readily available for self-medication. Indications and effect of
both the drugs are different and is well known to the experts
and medical practitioners who prescribe these drugs. Moreover,
these drugs are available only on prescriptions and can be
administered to patients only by or under the supervision of
highly specialized super specialist oncologists. Thus, there
cannot be any likelihood of confusion. The modes of
administration and the drug formulations of the competing
marks are completely different. The Plaintiff has itself admitted
that the Plaintiff’s Mark and the Impugned Mark themselves
point out their main molecule which belong to different
pharmacological groups. Further, due to the distinct and
different nature of the main molecules, the modes of
administration of the two products also become different. A
chart comparing the 4 modes of administration of the
Defendant’s Drug and the Plaintiff’s Drug is as below:
PARTICULARS BEVATAS BEVETEX
Reconstitution It should be diluted with It should be diluted with
0.9% sodium chloride 5% w/v dextrose
solution for injection. injection in 1:20 ratio.
The concentration of the Each ml of reconstituted
final Bevacizumab nanodispersion contains 5
solution should be kept mg paclitaxel (Drug
within the range of 1.4 to concentration will be 5
16.5 mg/ml. mg/ml).
Administration The initial dose should be It has to be administered
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 14 of 34
Signing Date:28.03.2026
18:57:27
delivered over 90 as intravenous infusion
minutes as an IV over 30 minutes every 3
infusion. If the first weeks.
infusion is well tolerated,
the second infusion may
be administered over 60
minutes. If the 60-minute
infusion is well tolerated,
all subsequent infusions
may be administered over
30 minutes.
Bevacizumab infusion
frequency varies from 2
weekly to 3 weekly
depending on the
indication.
9.7 The process of infusion is a half or full day process, depending
upon the medical condition of the patient. It is an ‘Intravenous
Product’ and cannot be self-administered. Entire process of
infusion is done under constant monitoring, guidance and
supervision of super specialists. Medical practitioners
prescribing or administering the drug are super specialists like
oncologists and radiologists and the drugs can be administered
only under their supervision by trained and skilled personnel
within oncology centres. The Plaintiff’s Witness admitted the
fact that the Plaintiff’s Drug cannot be administered by the
Patient on his own. This Court in Kalindi Medicure Pvt. Ltd. v.
Intas Pharmaceuticals Ltd., 2007 (34) PTC 18 (Del) held that
the method of intake of the drug is not to be ignored.
9.8 Admittedly, both the Plaintiff’s Drug and the Defendant’s Drug
contain totally different molecules / salt. The Plaintiff’s Drug is
a product of chemical formulation ‘PACLITAXEL’ which is a
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 15 of 34
Signing Date:28.03.2026
18:57:27
synthetic chemical compound. Whereas the Defendant’s Drug
is a biosimilar product ‘BEVACIZUMAB’ which is a DNA in
nature. Though both the drugs are cancer drugs, there is a
remarkable difference in the products. The name of the salts is
predominantly reflected on packaging of the two products,
further, the use of the prefix ‘BEVA’ is common to trade and the
Defendant has several products with the suffix ‘TAS’.
9.9 The Defendant’s Drug costs three times more than the
Plaintiff’s Drug. The Defendant’s Drug is a biological /
biosimilar drug which involves extremely expensive clinical
trials. There are also technical differences between the
Plaintiff’s Drug and the Defendant’s Drug which is
demonstrated as under:
BRAND NAME: BEVATAS BRAND NAME: BEVETEX
Defendant's drug Plaintiff's drug
Molecule: Molecule:
Bevacizumab for injection Paclitaxel injection concentration for
Nano dispersion
Type of Drug: Type of Drug:
rDNA Drug Synthetic Chemical Drug
Dosage form: Dosage form:
100mg and 400mg for injection 100mg and 300mg for injection
Route of Administration: Route of Administration:
Intra venous injection and need to be Intra venous injection and need to
administered by trained oncology administered by trained oncology
nurses at a multi-speciality hospital nurses at a multi-speciality hospital
under supervision of medical or surgical under supervision of medical or surgical
oncologists. Unlike other injectable oncologists. Unlike other injectable
medicines it cannot be administered at medicines it cannot be administered at
any common hospital or clinic. Bevatas any common hospital or clinic.
cannot be sold without prescription of
an oncologist.
Therapy: Therapy:
For the treatment purpose For the treatment purpose
IMS category: IMS category:
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 16 of 34
Signing Date:28.03.2026
18:57:27
Monoclonal antibody (Anti Vascular Cytotoxic agent or microtubule
endothelial growth factor) inhibitor
Prescribed by: Prescribed by:
Medical / Surgical and Radiation Medical / Surgical and Radiation
Oncologist Oncologist
Product appearance: Product appearance:
Vial for injection in a single pack Vial for injection in a single pack
Indication: Indication:
First-line treatment of non-squamous After failure of combination
NSCLC in combination with chemotherapy for Metastatic breast
platinumbased chemotherapy. cancer (mBC) or relapse within 6
Metastatic carcinoma of the colon or months of adjuvant chemotherapy.
rectum (mCRC). Advanced and/or
metastatic renal cell cancer (mRCC).
Epithelial ovarian, fallopian tube and
primary peritoneal cancer. Cervical
Cancer. Glioblastoma. Metastatic breast
cancer (mBC).
Type of medicine: Type of medicine:
Hospital based medicine, need to supply Hospital based medicine, need to supply
against prescription of registered against prescription of registered
medical practitioner or oncologist only. medical practitioner or oncologist only.
Need to be administered as an intra Need to be administered as an intra
venous injection by trained oncology venous injection by trained oncology
nurses under the supervision of nurses under the supervision of
registered medical practitioner (90 registered medical practitioner (30
minutes infusion) minutes infusion)
MRP: MRP:
Bevatas: Rs. 39995/- for 400mg and Rs. Bevetex: Rs. 37000/- for 300mg and Rs.
25990/- for 100mg 12500/- for 100mg
Dose: Dose:
The recommended dose of bevacizumab 260 mg/m2 and Bevetex 295 mg/m2
is 7.5 mg/kg or 15 mg/kg of body every 3 weeks as IV infusion over 30
weight given once every 3 weeks as an minutes.
IV infusion in non-small cell lung
cancer. Advanced and/or metastatic
renal cell cancer (mRCC) : The
recommended dose of bevacizumab is
10 mg/kg of body weight given once
every 2 weeks as an IV infusion.
Epithelial ovarian, fallopian tube and
primary peritoneal cancer: The
recommended dose of bevacizumab is
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 17 of 34
Signing Date:28.03.2026
18:57:27
15mg/kg of body weight given once
every 3 weeks as an IV infusion.
9.10 No case of infringement or passing off has been made out and
the Plaintiff has failed to establish sufficient grounds for grant
of an injunction in its favour. There is no evidence to show that
the Plaintiff has acquired goodwill and reputation in the
Plaintiff’s Mark. The Impugned Mark, on the contrary, has
acquired considerable reputation and goodwill in a short span
of time. The motive of the Plaintiff is to curb healthy
competition in the market. The launch of the Defendant’s Drug
was aimed at making the compound ‘BEVACIZUMAB’
accessible for Indian patients. Before the launch of the
Defendant’s Drug, only approximately 200 patients per month
could afford the ‘BEVACIZUMAB’ therapy. However, now
there has been a phenomenal increase and roughly 700 patients
get benefited, of which the Defendant’s Product is the most
preferred product.
9.11 The drug formulations of the Plaintiff’s Drug and the
Defendant’s Drug are completely different along with their
modes of administration. There cannot be any likelihood of
confusion as these drugs are Schedule H drugs and cannot be
sold off the shelf. Indications and effects of both the drugs are
different and are known to the experts and medical practitioners
who prescribe and administer these drugs. The Plaintiff had
contented in the Plaint that there is likelihood of confusion
between the competing marks. However, the Plaintiff suddenly
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 18 of 34
Signing Date:28.03.2026
18:57:27
shifted its stand making a bald misleading averment that actual
confusion had taken place. However, the Plaintiff has failed to
file any documentary proof establishing an instance of actual
confusion.
9.12 The view that the competing drugs are Schedule-H drugs which
are available only through prescription will also have a material
bearing while deciding the question of infringement, has also
been upheld in the judgment of Astrazeneca UK Limited v.
Orchid Chemicals and Pharmaceuticals Limited, 2007 (34)
PTC 469 (Del). In Gufic Ltd. & Anr. v. Clinique Laboratories,
LLC & Anr., 2010 (43) PTC 788 (Del), it was held that the
price differential between the two products being so vast that no
consumer of products of either the appellant or the respondent
would confuse one for the other is also a relevant factor while
deciding the question of infringement.
9.13 In the judgment of Sun Pharmaceutical Industries Ltd. v.
Anglo French Drugs & Industries Ltd., 2015 (63) PTC 580
(Del), it was held that the judgment in Cadila Healthcare v.
Cadila Pharmaceuticals (supra) cannot lead to the conclusion
that any slight resemblance of phonetic similarity between two
marks would automatically satisfy the test of confusion to a
man of average intelligence having imperfect recollection. Both
marks have to be seen as a whole. In the judgment of Schering
Corporation v. Alkem Laboratories, 2010 (42) PTC 772 (Del),
it was held that the appellants cannot appropriate to themselves
the exclusive use of a generic term which is publici juris and
descriptive, the fact that the drugs in question are Schedule-H
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 19 of 34
Signing Date:28.03.2026
18:57:27
drugs and that there are vast price differences also have a
bearing while deciding the question of infringement of trade
mark.
9.14 The Plaintiff has approached this Court with unclean hands and
has suppressed relevant information. The Plaintiff filed
Opposition against the Application for registration of the
Impugned Mark. The Defendant filed the detailed response to
the Opposition on 28.03.2017. The Defendant had launched the
Defendant’s Drug in October 2016, the launch was extensively
covered in the media. Therefore, the Plaintiff has been well
aware of the Defendant’s Drug since 2016. However, the
Plaintiff blatantly misrepresented facts and had filed the present
Suit on frivolous cause of action with ulterior motive to deprive
the Defendant of its lawful right.
9.15 The alleged cause of action that there could be confusion
leading to false administration of drug and the sale of
Defendant’s Drug is thus not in public interest is completely
unreal, far stretched and frivolous. The allegation of chances of
confusion are premised on mere assumption that the Plaintiff’s
Mark and the Impugned Mark are deceptively similar which is
not the case. Further, the Plaintiff’s Drug and the Impugned
Drug are not off the shelf products and are prescribed and
administered by experts in oncology and the chances of
confusion and wrong administration are only hypothetical
arguments. There is also gross impropriety on the part of the
Plaintiff for claiming that the cause of action only arose in the
third week of December, 2017, since the Plaintiff had opposed
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 20 of 34
Signing Date:28.03.2026
18:57:27
the Defendant’s Application for registration of the Impugned
Mark in 2016 and further the launch of the Defendant’s Drug
was also in 2016. Thus, the cause of action of the present Suit is
clearly manufactured and the Plaintiff has approached the Court
with unclean hands.
REJOINDER SUBMISSIONS ON BEHALF OF THE PLAINTIFF
10. The learned Counsel for the Plaintiff made the following rejoinder
submissions:
10.1 The Defendant has submitted that the competing drugs have
different drug formulations and effects. The Defendant has
alleged that there shall be no confusion because the competing
drugs are scheduled drugs and are administered under the
supervision, control, administration of specialized doctors. This
defence has been rejected in the judgment of Cadila
Healthcare v. Cadila Pharmaceuticals (supra).
10.2 Examination Report issued by the Trade Marks Registry is an
e-report obtained by a mechanical process without application
of mind. It is result thrown electronically within the internal
data base. If search report is held to be conclusive then there is
no need for the Trade Marks Registrar to publish a Mark and
invite opposition. Therefore, if that is so, once there are no
conflicting marks shown in the examination report, the mark
should be automatically registered. Which is never the case.
The Application for registration of the Defendant’s Mark has
been opposed by the Plaintiff and the same is pending disposal.
10.3 Trade Marks are not to be dissected for the purposes of
comparison, which is against the Anti-Dissection Rule. The
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 21 of 34
Signing Date:28.03.2026
18:57:27
Marks are to be compared as a whole. The Plaintiff is not
claiming any right in the suffix ‘BEV’. In the judgment of
United Biotech v. Orchid Chemicals, 2012 (50) PTC4 33 (Del)
(DB), it was held that the overall impression of the product
created in the minds of an ordinary shopper should be looked at
while deciding on the aspect of infringement, and the rival
marks should not be dissected into two words. It was further
held that minor differences are not to be found very technically
in case of conflicting marks. Further, common to register does
not prove common to trade. Various marks containing prefix
‘BEV’ have been applied for / pending before Trade Marks
Registry does not prove that they are in use as has been held in
Century Traders v. Roshan Lal Duggar, AIR 1978 Delhi 250.
The defence of prefix having been derived from salt, and
common to trade, have been rejected by this Court in Cadila
Healthcare v. Aureate Healthcare, 2012 (51) PTC 585 (Del).
Further, plea of common use shall fail unless substantial usage
by others persons proven as has been held in Pankaj Goel v.
Dabur India Ltd. 2008 (38) PTC 49 (Del).
10.4 The Defendant lead evidence through its sole witness Sh.
Mehul Pathak (“DW1”) by filing his Affidavit in evidence,
which was exhibited as DW 1/A. The evidence given by DW1
cannot be relied upon by this Court as he had been evasive and
deposed falsely. He also chose not to answer whenever he felt
that his answer would expose his false deposition. The evidence
of DW1 is not credible as he contradicted himself several times
and was continuously changing his stand. On most of the
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 22 of 34
Signing Date:28.03.2026
18:57:27
occasions when a question was put to DW1, he simply evaded
the questions by answering that ‘it is a matter of record’ or that
‘I am not aware’. Such answers by DW1 suggests an admission
on his behalf and also consolidates the evasive conduct of the
DW1.
10.5 There is no delay in filing the present Suit. The Suit was filed
immediately in December 2017 on acquiring knowledge of the
use of the Impugned Mark for the Defendant’s Drug in the
same month. As has been held in Midas Hygiene Industries
(P.) Ltd. v. Sudhir Bhatia & Ors., (2004) 3 SCC 90, delay
cannot be a ground for refusing injunction. The Plaintiff in
December 2016 opposed the Defendant’s Application for the
registration of the Impugned Mark immediately upon its
publication in 24.10.2016.
10.6 There is no hoarding of the Plaintiff’s Mark by the Plaintiff.
There is a concept of deemed user under the Act and use is not
required to be shown in an infringement suit as has been held in
Gujarat Bottling Co. Ltd. & Ors. v. Coca Cola Co. & Ors.,
(1995) 5 SCC 545 and Wockhardt Ltd. v. Eden Healthcare,
2014 SCC OnLine Bom 163. The Plaintiff is admittedly the
prior user of the Plaintiff’s Mark. The statutory defenses
provided in Section 30, 34 and 35 of the Act are not available to
the Defendant. Hoarding of Trade Marks is no statutory defense
and hence has no bearing.
10.7 Honest and concurrent use is a ground for obtaining registration
under Section 12 of the Act but not a defence to an injunction
action. Neither the use is honest nor it is concurrent. The
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 23 of 34
Signing Date:28.03.2026
18:57:27
Defendant’s Application for registration of the Impugned Mark
is opposed and the Defendant has no registration. Dishonest
adoption and use run the risk of being challenged for
infringement.
10.8 The judgment in Sun Pharmaceutical Industries Ltd. v. Anglo
French Drugs & Industries Ltd. (supra) has been set aside by
the Supreme Court by the consent of the parties. It has been
held in the judgment of Saregama India Limited v. Balaji
Motion Pictures, 2019 SCC OnLine Del 10036, that even if a
judgment has been set aside by the appellate court at the
consent of the parties, or for whatever reason it maybe, the
judgment cannot be cited as a precedent.
10.9 The Plaintiff has, in Paragraph No. 23 of the Plaint, stated that
the cause of action arose in favour of the Plaintiff when the
Plaintiff’s representative came across the Defendant’s Drug
under the Impugned Mark selling in Delhi. The present Suit is
filed for relief against infringement of Plaintiff’s statutory
rights, apart from common law rights, and therefore it cannot be
said that there is no cause of action.
ANALYSIS AND FINDINGS:
Issue Nos. 1 and 2
WHETHER THE PLAINTIFF IS THE REGISTERED PROPRIETOR AND
PRIOR USER OF THE TRADE MARK ‘BEVETEX’
11. Admittedly, the Plaintiff is engaged in manufacture, distribution and
sale of Schedule-H Drug used for treatment of breast cancer, non-small cell
lung cancer and pancreatic cancer under the Mark ‘BEVETEX’ and has
registration for the following Trade Mark:
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 24 of 34
Signing Date:28.03.2026
18:57:27
Trade Mark Cl. Registration no. Goods
& Date
BEVETEX 5 410744 dated Medicinal &
16.09.1983 Pharmaceutical
preparations for human
use
12. The Plaintiff has registered the Plaintiff’s Mark in Class 05 in 1983
and has been using it since 2015. The Defendant has claimed the use of the
Impugned Mark since 2016, subsequent to the registration and use of the
Plaintiff’s Mark. The Plaintiff has produced documentary and oral evidence
in support of its registration and use of the Plaintiff’s Mark. The Plaintiff has
also established that the Plaintiff’s Mark is a uniquely coined term and that it
is inherently distinctive. Admittedly, the Plaintiff was the prior user and the
proprietor of the registered Mark, ‘BEVETEX’.
13. Accordingly, the Plaintiff is the proprietor of the Plaintiff’s Mark. The
Plaintiff’s Mark is entitled to the highest degree of protection, restraining
infringement based on the registration since the year 1983.
14. Accordingly, Issue Nos. 1 and 2 are decided in favour of the Plaintiff
and against the Defendant.
Issue Nos. 9 and 10
WHETHER THE DEFENDANT IS THE PROPRIETOR, HONEST AND
PRIOR USER OF THE MARK ‘BEVATAS’
15. The Defendant has coined and adopted the Impugned Mark in 2016,
while the Plaintiff had obtained registration for the Plaintiff’s Mark in 1983
and started manufacturing the Plaintiff’s Drug under the Plaintiff’s Mark in
2015 which is also prior to the claimed use of the Defendant’s Drug.
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 25 of 34
Signing Date:28.03.2026
18:57:27
16. There is nothing on record to show that the adoption of the Impugned
Mark by the Defendant was dishonest, nonetheless, honest subsequent use is
not a valid defence in a suit for infringement of Trade Mark. The Plaintiff
has obtained the registration for the Plaintiff’s Mark in 1983 while the
Defendant filed the Application for the registration of the Impugned Mark in
2016, which has been opposed by the Plaintiff. The Opposition proceedings
against registration of the Impugned Mark are pending.
17. Even if the Defendant’s reasoning behind the adoption of the
Impugned Mark, i.e., the Impugned Mark was coined by amalgamating the
words ‘BEVA’ derived from or referable to the active ingredient
‘BEVACIZUMAB’ and ‘TAS’ from the Defendant’s Trade Name, INTAS is
accepted, the Defendant is not the prior user of the Impugned Mark.
18. Accordingly, Issue Nos. 9 and 10 are decided in favour of the Plaintiff
and against the Defendant.
Issue Nos. 3 and 4
WHETHER THE USE OF THE MARK ‘BEVATAS’ BY THE
DEFENDANT AMOUNTS TO INFRINGEMENT OF THE PLAINTIFF’S
MARK ‘BEVETEX’
19. The Impugned Mark, ‘BEVATAS’, is structurally and phonetically
similar to the Plaintiff’s Mark, ‘BEVETEX’. An average consumer of
average intelligence and imperfect recollection is likely to get confused
between the competing Marks. The first and last syllable are almost identical
in the competing Marks and, therefore, the Impugned Mark is structurally
and phonetically similar to the Plaintiff’s Mark, which is likely to cause
confusion.
20. The two competing Marks are to be compared as a whole and as per
the anti-dissection rule, if the Plaintiff’s Mark and the Impugned Mark are
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 26 of 34
Signing Date:28.03.2026
18:57:27
compared as a whole, they are deceptively similar and likely to cause
confusion in the minds of the consumers with average intelligence and
imperfect recollection.
21. Although the Plaintiff has not claimed exclusive right over the use of
the suffix ‘BEV’, it has claimed exclusive right over the Plaintiff’s Mark as
a whole and as has been held in the judgment of United Biotech v. Orchid
Chemicals (supra), the overall impression of the product created in the
minds of an ordinary person should be looked at while deciding on the
aspect of infringement, and the rival marks should not be dissected into two
words.
22. Further, common to register does not prove common to trade. Various
marks containing prefix ‘BEV’ have been applied for / pending before the
Trade Marks Registry does not prove that they are in use as has been held in
Century Traders v. Roshan Lal Duggar (supra). Further, plea of common
use shall fail unless substantial usage by other persons proven as has been
held in Pankaj Goel v. Dabur India Ltd. (supra).
23. Trade Mark law seeks to prevent consumer confusion regarding the
source or sponsorship of goods and services. In assessing likelihood of
confusion between Trade Marks, it is necessary to keep in mind that
consumers generally rely on the overall impressions or prominent details of
a mark, rather than retaining a photographic memory of the entire Trade
Mark. Thus, similarity between two Trade Marks is not assessed in isolation,
but in the context of their market use. It is also essential to consider whether
the goods or services offered under the competing Marks are identical or
similar.
24. A consumer of a drug is likely not aware of the compound or salt
behind the drug and is not expected to check the salt or compound of the
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 27 of 34
Signing Date:28.03.2026
18:57:27
drug that he is purchasing. The likelihood of confusion also increases with
the fact that both the Plaintiff’s Drug and the Defendant’s Drug are used for
the treatment of different kinds of cancer. In order to succeed in a claim of
infringement, and to be entitled to an injunction on that basis, the Plaintiff is
not required to prove actual confusion, all that has to be proved is likelihood
of confusion. Confusion between drugs treating different ailments is even
more dangerous and, therefore, a strict approach shall be applied while
comparing the marks as has been held in the decisions of Novartis v. Crest
Pharma (supra), Charak Pharma. v. Glenmark (supra) and Sun Pharma v.
Glenmark (supra).
25. The judgment of the Supreme Court in Cadila Healthcare v. Cadila
Pharmaceuticals (supra) holds that in pharmaceutical cases, a stricter
approach has to be applied and the court has to ensure that there is no
likelihood of confusion between two drugs and the mere fact that the
products may be Schedule-H Drugs, or may be differently priced, does not
mitigate the possibility or likelihood of confusion. Public health is of
paramount importance and there could be no leniency whatsoever with
respect to subject matters concerning public health and any likelihood of
confusion between two drugs has to be avoided.
26. Schedule-H drugs differ from Schedule-L drugs in their availability
and handling. Schedule-L drugs are accessible exclusively to physicians,
whose expertise reduces the likelihood of confusion from their perspective.
In contrast, Schedule-H drugs are dispensed by prescription and involve not
only doctors, but also pharmacists, who supply these medicines to patients
upon receipt of a valid prescription.
27. The probability of confusion significantly increases when
prescriptions are managed by pharmacists and patients or individuals
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 28 of 34
Signing Date:28.03.2026
18:57:27
purchasing medication on their behalf. Moreover, first-time buyers may lack
knowledge regarding drug pricing, rendering price distinctions less relevant.
Thus, the risk of confusion in dealing with pharmaceutical products arises
not only at the prescribing stage but also during dispensing and purchase.
Any potential for confusion at any point, particularly concerning
pharmaceutical preparations, is sufficient to justify the issuance of an
injunction.
28. In view of the structural and phonetic similarity of the Plaintiff’s
Mark and the Impugned Mark, the competing Marks being used for similar
products, i.e., medicinal and pharmaceutical preparations for human use,
more particularly targeting different kinds of cancers, the prior use of the
Plaintiff’s Mark, and the likelihood of confusion, the use of the Impugned
Mark by the Defendant amounts to infringement of the Plaintiff’s Mark.
29. Accordingly, Issue Nos. 3 and 4 are decided in favour of the Plaintiff
and against the Defendant.
Issue No. 5
WHETHER THE PLAINTIFF IS GUILTY OF HOARDING ITS MARK
‘BEVETEX’?
30. Section 47 of the Act governs the right of a person to approach the
Registrar of Trade Marks seeking removal of a registered Trade Mark from
the Register of Trade Marks. Under Section 47(1)(b) of the Act, continuous
non-use of a registered Trade Mark, extending up to a period of three
months preceding the filing of the application, constitutes a valid ground
upon which the applicant may seek cancellation of the registered Trade
Mark from the Register of Trade Marks.
31. Section 47 of the Act is not an exception either to Section 29 of the
Act, or to Section 28(1) read with Section 135 of the Act, which entitles the
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 29 of 34
Signing Date:28.03.2026
18:57:27
proprietor of a registered Trade Mark to an injunction against an infringer of
such a registered Trade Mark. Any interested party can apply to the Registrar
of Trade Marks for rectification of the Trade Mark from the Register of
Trade Marks on the ground of five years of non-use of the registered Trade
Mark. However, if no such application is made to the Registrar and it is not
adjudicated upon, the registered Trade Mark remains on the Register of
Trade Marks, and infringement of the registered Trade Marks is
impermissible and, if infringement takes place, the proprietor of a registered
Trade Mark is well within its right to seek reliefs against the infringement of
its registered Trade Mark. The reliance of the Defendant on the decision in
Neon Laboratories Ltd. v. Medical Technologies Ltd. (supra) is misplaced
and does not help the case of the Defendant.
32. As long as a Trade Mark is validly subsisting on the register of Trade
Marks, the rights of the registered proprietor of Trade Mark under Section
28(1) of the Act are protected. The registration by itself grants the Plaintiff
the right to protect its Trade Mark and seek remedies against infringement of
the Mark. Only registration of a Trade Mark is required to be shown in a suit
for infringement of Trade Mark and actual use is not required to be shown in
an infringement suit as has been held in the judgments of Gujarat Bottling
Co. Ltd. & Ors. v. Coca Cola Co. & Ors. (supra) and Wockhardt Limited v.
Torrent Pharmaceuticals Ltd (supra).
33. Considering the facts and circumstances of the present case, the
Defendant has not applied for rectification of the Plaintiff’s Mark from the
Register of Trade Marks and instead adopted the Impugned Mark which is
deceptively similar to the Plaintiff’s Mark. The Plaintiff is admittedly the
prior user and prior registrant of the Plaintiff’s Mark and has successfully
made out a case for infringement of the Plaintiff’s Mark and therefore, the
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 30 of 34
Signing Date:28.03.2026
18:57:27
defence of non-use and hoarding of Trade Mark is not available to the
Defendant. The Plaintiff has statutory remedies to protect the Plaintiff’s
Mark from infringement as long as the Plaintiff’s Mark is validly subsisting
on the Register of Trade Marks.
34. Accordingly, Issue No. 5 is decided in favour of the Plaintiff and
against the Defendant.
Issue No. 6
WHETHER THE PRESENT SUIT HAS BEEN INSTITUTED BY THE
PLAINTIFF WITHOUT ANY AUTHORIZATION?
35. The fact that the Suit was instituted by an authorised and competent
individual, with the knowledge and approval of the Plaintiff, and that the
actions of the constituted attorney have been duly ratified, is clear from
express authority in favour of the constituted attorney viz. the Power of
Attorney filed in the present proceedings. This Court also takes note of the
fact that the prosecution of the suit has been done continuously by the
Plaintiff for the last eight years. Requisite court fees have been duly paid in
support of the Plaint.
36. The present Suit has been instituted by the Plaintiff with due
authorisation. Power of Attorney in favour of Mr. Amit Aggarwal issued by
the Plaintiff was filed on record on 17.02.2018 after serving advance copy to
the Defendant’s Counsel, Ms. Isha Tyagi, Advocate, through email of same
date. The original Power of Attorney was shown during trial at the time of
exhibition of documents and was exhibited as Ex. PW 1/1. The said Exhibit
also stands proven during the course of the Trial. The Defendant has not met
its burden to prove otherwise and has not let any evidence in its favour.
37. Accordingly, Issue No. 6 is decided in favour of the Plaintiff and
against the Defendant.
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 31 of 34
Signing Date:28.03.2026
18:57:27
Issue No. 7
WHETHER THE PRESENT SUIT SUFFERS FROM DELAY, LACHES
AND ACQUIESCENCE?
38. The burden of proving delay, laches and acquiescence, lay upon the
Defendant. However, there is nothing on record to show that the Suit by the
Plaintiff is delayed in any manner or there is acquiescence on the part of the
Plaintiff to the use of the Impugned Mark by the Defendant. Acquiescence is
a positive act. It must involve active facilitation, whether by action or
omission, of continued infringement by the respondent. Mere inaction, even
any, would not amount to acquiescence.
39. The Plaintiff as soon as becoming aware of the Application for
registration of the Impugned Mark filed the Opposition against the same and
upon finding actual use of the Impugned Mark, the Plaintiff filed the present
Suit for infringement of the Plaintiff’s Mark. Therefore, there has been no
delay on behalf of the Plaintiff in filing of the present Suit.
40. Even otherwise, the law with respect to delay while filing a suit
against infringement of Trade Mark has been settled in a plethora of cases by
the Supreme Court and this Court. This Court in Pankaj Goel v. Dabur
India Ltd. (supra) clearly states that mere delay if any does not amount to
acquiescence, unless accompanied by an act that indicates acceptance or
encouragement of the infringing activities further, it is also settled that delay
cannot be a ground for refusing injunction in cases of Trade Mark
infringement as has been held in Hindustan Pencils v. India Stationery, 38
(1989) DLT 54 SJ and in Midas Hygiene Industries (P.) Ltd. v. Sudhir
Bhatia & Ors. (supra).
41. Accordingly, Issue No. 7 is decided in favour of the Plaintiff and
against the Defendant.
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 32 of 34
Signing Date:28.03.2026
18:57:27
Issue No. 8
WHETHER THE PLAINTIFF HAS FAILED TO DISCLOSE ANY CAUSE
OF ACTION TO FILE THE PRESENT SUIT?
42. In Paragraph 23 of the Plaint, the Plaintiff asserts that the cause of
action arose when the Plaintiff’s representative observed the Defendant’s
drug being sold in Delhi under the Impugned Mark. The present suit seeks
relief for infringement of both statutory and common law rights; therefore, it
cannot be concluded that there is no cause of action.
43. The Defendant’s argument that a cause of action arises only upon
actual confusion is not persuasive.
44. Accordingly, Issue No. 8 is resolved in favour of the Plaintiff and
against the Defendant.
Issue No. 11
RELIEF
45. In view of the above findings, the Plaintiff is entitled to a relief of
permanent injunction against the use of the Mark ‘BEVATAS’ with respect
to pharmaceutical drugs. As the Plaintiff has submitted that the present Suit
is in Public Interest, the Plaintiff has given up its claim for damages and
rendition of accounts against the Defendant as stated in Paragraph No. 22 of
the Plaintiff’s Replication to the Defendant’s Reply to the Application under
Order XXXIX Rules 1 and 2 of the CPC, which is referred in Paragraph No.
10 of the Written Submissions dated 29.05.2025. Accordingly, no direction
is required to be passed regarding damages and rendition of accounts.
46. In view of the above, it is declared that:
i. The Plaintiff is the registered proprietor and continuous as well
as prior user of the Plaintiff’s Mark, ‘BEVETEX’;
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 33 of 34
Signing Date:28.03.2026
18:57:27
ii. The Plaintiff is not guilty of hoarding the Plaintiff’s Mark,
‘BEVETEX’; and
iii. The Defendant’s use of the Impugned Mark, ‘BEVATAS’
amounts to infringement of the Plaintiff’s Mark, ‘BEVETEX’.
47. In view of the above, the Defendant or anyone acting on its behalf are
permanently injuncted and restrained from manufacturing, selling, or
offering for sale, marketing, advertising, or in any other manner dealing with
medicinal and pharmaceutical preparations for human use using the
Impugned Mark, ‘BEVATAS’ or any other Mark identical and / or
deceptively similar to the Plaintiff’s Mark, ‘BEVETEX’.
48. As the Plaintiff has stated that this Suit is in Public Interest, there shall
be no order as to costs.
49. Accordingly, the Suit is decreed in terms of the above directions. Let
the Decree Sheet be drawn up accordingly. The Suit stands disposed of.
TEJAS KARIA, J
MARCH 28, 2026/’AK’
50. After the pronouncement, at this stage, Mr. George Vithayathil, the
learned Counsel for the Defendant makes a request for passing directions
with regard to the existing stock containing the Impugned Mark
‘BEVATAS’.
51. The Defendant is granted liberty to move an appropriate Application
with regard to the same.
TEJAS KARIA, J
MARCH 28, 2026/’A’
Signature Not Verified
Signed By:NEELAM
SHARMA CS(COMM) 39/2023 Page 34 of 34
Signing Date:28.03.2026
18:57:27
