Overview of Pharma Patent Landscape in India

Report
Summit on Vistas in Structural Chemistry
28-30 April 2014, Karachi, Pakistan
Overview of Pharma Patent
Landscape in India
Ashwini Nangia
University of Hyderabad
http://chemistry.uohyd.ernet.in/~an/
http://www.crystalin.co.in/
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History of Indian Patents act
• Patents and Designs Act, 1911. Provisions both for Product and Process
patents
• Modified to the Act XXXII of 1950. Inventions, Compulsory licensing,
revocation of patents, and then Act LXX of 1952 to provide for compulsory
license for food and medicines
• Patents Act 1970. Process patent regime.
• Between 1970 to 1994 the Indian Pharmaceutical industry became selfsufficient and an exporter of medicines
• GATT and WTO regime in 1995 made India part of Int. IPR regime and
TRIPS compliant. Now again both Product and Process patent for Drugs,
Pharma, Food, Cosmetics, etc. 2005 onwards after 35 years
• Art. 65 of TRIPS allowed for a 10 year transition period to developing
countries, i.e. 2005
• Product patents for inventions on pharma, agro, foods, and chemical
reactions since 01.01.2005. Patent period of 20 years
• Pharma patents are of utmost concern not only to India, but also ROW as
India has emerged as "the pharmacy of the world".
• Today’s IPR regime of India Patents Act 1970 and Amendments 2005
Sections relevant to Pharma
• Section 2 (1) (j): Novelty, inventive step & industrial
applicability of products or processes
• Section 3 (d): Mere discovery of new form of known
substance which does not result in enhancement of known
(therapeutic) efficacy or mere discovery of any new property
or new use for a known substance
– New forms of known substance such as: Salts, Ethers and Esters;
Polymorphs; Solvates, including Hydrates, Clathrates;
Stereoisomers; Enantiomers; Metabolites and pro-drugs;
Conjugates; Pure forms; Particle size; Isomers and mixtures
thereof; Complexes; Derivatives of known substances
• Section 3 (e): Mere admixture resulting only in aggregation of the
properties of the components thereof or a process for producing
such admixture
• Section 3 (p): An invention which in effect is traditional knowledge or
which is an aggregation or duplication of known properties of
traditionally known component or components
Gleevec case – Novartis AG vs. UoI
• Imatinib is a protein-tyrosine kinase inhibitor
• Imatinib mesylate has 2 main forms,  and 
• α crystals needle morphology and hygroscopic. Pose difficulties in
manufacturing and tableing
• β crystals are of uniform morphology and easy to handle and also
thermodynamically stable
• The free base imatinib is protected by US patent 5,521,184, Granted
on May 1996, Priority April 1992 (Zimmermann Patent )
• Subsequently US patent 6,894,051, Granted May 2005, Priority July
1997 for the β crystalline form
• The drug was submitted for approval (in India) taking priority of
Zimmerman patent, the marketed crystalline form of Gleevec (also
Glivec) is the latter patent on the β form
• The 1993 patent disclosed imatinib and a list of pharmaceutically
acceptable salts including the mesylate
Novartis vs. Union of India
• Novartis argued that Gleevec was claimed in the Zimmerman patent
(imatinib molecule), but it was not fully disclosed in an enabling manner
(the β polymorph), thus making a differentiation between “claims” and
“disclosure”
• This wonderful legalese was eloquently rejected by the Indian Supreme
Court. 1 April 2013
• “We certainly do not wish the law of patent in this country to develop
on lines where there may be a vast gap between the coverage and the
disclosure under the patent; where the scope of the patent is
determined not on the intrinsic worth of the invention but by the artful
drafting of its claims by skilful lawyers, and where patents are traded as
a commodity not for production and marketing of the patented
products but to search for someone who may be sued for infringement.
• The Supreme Court heralds Section 3(d) as a “second tier of qualifying
standards for chemical substances/ pharmaceutical products in order to
leave the door open for true and genuine inventions but, to check any
attempt at repetitive patenting or extension of the patent term on
spurious grounds.” NO to Ever-greening/ Incremental innovation
Glenmark vs. Merck
• Januvia – Sitagliptin phosphate hydrate
• Plaintiff contends that it has invented the innovator salt sitagliptin
phosphate hydrate
• Merck has separate patents in USA for drug molecule (Markush) and
PO4 salt (specific claim). US 6,699,871, Mar 2004 (broad class of DPIV inhibitors, incl. many salts, reported HCl salt) and US 7,326,708,
Feb 2008 (phosphate salt hydrate)
• They abandoned the phosphate salt patent in India after filing appln.
• The free drug patent IN 209816 discloses all salts of Sita (‘871)
• IN ‘871 describes preparation of HCl salt but not phosphate
• The compound that is marketed is not patented (in India), and the
one that is patent covered (HCl salt, Sita base) is not marketed
• Case is under litigation in Indian Courts
• Delhi High Court refused to restrain Defendant Glenmark from
marketing its Zita/ Zitamet version for type II diabetes, 5 April 2013
Tarceva – Erlotinib HCl
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Roche vs. Cipla
Verdict by Delhi High Court in Sept. 2012
Roche and Pfizer were granted IN 196774 in Feb. 2007 (US 5,747,498 of May 1996)
Two main issues by Defendant Cipla
– Obviousness: Bioisosterism (ethynyl vs. methyl) and lack of inventive step (close relative of
Gefitinib, AZ drug). Ruling rejected Obviousness under Sect. 64(1)(f)
– Sect. 3(d): ‘774 patent (filed in 1996, granted 2006) claims polymorphs A and B of erlotinib HCl.
Marketed Tarceva is polymorph B. IN ‘507 on B polymorph filed by Roche in 2006 was rejected
by Patent controller in 2008 due to pre grant oppositions
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US ‘221 of Roche is the prior art patent for IN ’507 appln.
Sect. 8 of Indian Patents Act: submission of information of corresponding Foreign
applications (Form 3) on “same or substantially the same” inventions relating to the
Indian application during the pendency of the Indian Application
Plaintiffs did not furnish form 3, stating that US ‘221 is a different compound and
not part of polymorph B (IN ‘507 appln.)
Justice Manmohan Singh concluded that US‘221 patent relates to the same or
substantially the same invention being polymorphic form B of erlotonib HCl claimed
in IN ‘774.
Non compliance of Sect. 8 was the only major ground on which this case was
revoked in favor of Cipla
Not really the technical analysis but more to do with proper paper trail
Compulsory licensing
• Baeyer obtained patent in India for Nexavar, anticancer drug,
in 2008
• In Mar 2012 the Patents Controller granted Compulsory
license to Natco for manufacture and marketing of sorofenib
tosylate (INN)
• Bayer tablet cost Rs. 2500. Natco Rs. 75
• Reason for invoking CL was that Bayer did not market the
drug for 4 years after taking the license
• Lack of availability of life saving cancer drugs to patients
• Bayer appealed to the CL decision of Controller but IPAB
upheld the verdict
• Rare case of CL but a precedent in Indian patent legalese
World opinion – March 2014 news
• USTR assessing India’s IP and patents system
• Pharma Cos. opposed to granting of product
patents by invoking Sect. 3(d)
• Sectors supporting India’s IPR regime are
Honeywell and Boeing
• US Profs. And academics are in support of India’s
IPR regime as practiced
• Whereas US is critical of India’s patenting
protection for generic Pharma, the USTR blatantly
favored Apple over Samsung in “Smartphone
patent wars”

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