Doxycycline - USA

On Oct 04, 2019 (unsealed opinion), Delaware court found infringement of formulation patents & rejected Sun’s argument that the patents were obvious.

Galderma sued Sun pharma over Oracea® Capsules patents, US 8,206,740; US 8,394,405; US 8,470,364 and US 7,749,532. Sun seeks to bring to market a new drug (NDA) which is bioequivalent to Galderma's Oracea Capsules, a once-daily 40mg administration of doxycycline for the treatment of the papules and pustules of acne rosacea. In December 2018, the Court held a three-day bench trial. At trial, Galderma asserted infringement of claim 1 of the '740 patent, claims 1 and 3 of the '405 patent, and claims 1 and 2 of the '364 patent.

Claim 1 of the '740 patent recites:

An oral pharmaceutical composition of doxycycline, which at a once-daily dosage will give steady state blood levels of doxycycline of a minimum ofO.l ~g/ml and a maximum of 1.0 ~g/ml, the composition consisting of (i) an immediate release (IR) portion comprising 30 mg doxycycline; (ii) a delayed release (DR) portion comprising 10 mg doxycycline; and optionally, (iii) one or more pharmaceutically acceptable excipients.

Claim 1 of the '405 patent recites:

An oral pharmaceutical composition comprising about 40 mg of total doxycycline, which at a once-daily dosage will give steady state blood levels of doxycycline of a minimum of 0.1 J.Lg/ml and a maximum of 1.0 J.Lg/ml, wherein the composition consists of 70 to 80 percent of the doxycycline formulated as an immediate release (IR) formulation and 20 to 30 percent of the doxycycline formulated as a delayed release (DR) formulation.

Claim 1 of the '364 patent recites:

An oral pharmaceutical composition consisting of (i) an immediate release formulation (IR) comprising about 30 mg doxycycline; a delayed release formulation (DR) comprising about 10 mg doxycycline; and optionally, (iii) one or more pharmaceutically acceptable excipients.

Claim 2 of the '3 64 patent recites:

An oral pharmaceutical composition comprising doxycycline, which at a once-daily dosage will give blood levels of the doxycycline of a minimum of 0.1 J.Lg/ml and a maximum of 1.0 J.Lg/ml, the composition consisting of (i) an immediate release formulation (IR) comprising about 30 mg doxycycline; as [sic] a delayed release formulation (DR) comprising about 10 mg doxycycline; and optionally, (iii) one or more pharmaceutically acceptable excipients.

Sun's NDA Product is a once-daily doxycycline bilayer tablet consisting of two distinct layers as an immediate release ("IR") layer and a modified release ("MR") layer, each of which contains doxycycline. IR layer contains 26.4 mg of doxycycline & releases all 26.4 mg of its doxycycline immediately upon administration without any enhanced, delayed, or extended effect. MR layer contains 13.6 mg of doxycycline out of which 3.6 mg doxycycline get released in the first 30 minutes after administration, and remaining 10 mg doxycycline releases later than 30 minutes after administration. This dual release from MR layer is because of use of two hypromellose polymers.

Main dispute was regarding "IR Portion" and "DR Portion". The parties agreed at trial that "immediate release" (IR ), as defined in the patents, is "a dosage form that is intended to release substantially all of the active ingredient on administration with no enhanced, delayed, or extended release effect." Court construed "delayed release" (DR) to mean "release of a drug at a time other than immediately following oral administration." The case was tried without any specific construction of "portion" as the parties agreed throughout trial (and even for some time after trial) that the term would be given its "plain and ordinary meaning."

Galderma contends that the "immediate release portion" limitations are met by the combination of: (1) the Sun NDA Product's IR layer; and (2) the part of the Sun NDA Product's MR layer that dissolves in the first 30 minutes after administration. Under Galderma's theory, the Sun NDA Product's IR portion, therefore, has about 30 mg of doxycycline, consisting of: (1) the entire 26.4 mg of doxycycline in the IR layer, and (2) the about 3.6 mg of doxycycline that is released from the MR layer in the first 30 minutes after administration. Similarly, on Galderma's view, the "delayed release" portion of Sun's NDA Product is the remaining 10 mg of doxycycline- all from the MR layer- which is released following the first 30 minutes after administration.

Sun counters that its NDA Product's "immediate release portion" includes only the 26.4 mg of doxycycline in the IR layer. Thus, because the IR layer has less than the about 30 mg of doxycycline claimed by the patents, Sun's view is that its NDA Product does not meet the IR portion limitations. Sun contends that its NDA Product also does not meet the "delayed release portion" limitations, for two reasons: (1) the MR layer is not "delayed release" because it releases doxycycline starting immediately after administration and the amount of doxycycline released "continuously increases over time, with no plateau or stoppage of release" and (2) even if the MR layer were a "delayed release portion," the MR layer has 13.6 mg of doxycycline, which is greater than the about 10 mg of doxycycline required by the claims.

After careful review, the Court concluded that the parties' dispute over whether the IR portion and DR portion limitations are met by Sun's NDA Product turns on the meaning of "portion." If "portion" is a functional term - such that the "IR portion" limitation is satisfied if a formulation dissolves in a manner in which 30 mg (or about 30 mg) of doxycycline is released immediately after oral administration, regardless of where in the product that doxycycline comes from- then the Sun NDA Product infringes. If, alternatively, "portion" is a structural term - such that each part of an accused product must be analyzed for its structure and then characterized as either an IR or DR structure - then the Sun NDA Product does not infringe.

In this case parties never asked the Court to construe the disputed claim term, “potion”. This is because in previous Amneal case, court issued claim construction where "portion" had its "plain and ordinary meaning”.  In present case it became apparent when Court reviewed the parties' post-trial briefs.  It was only during closing argument, which the Court heard on the last day of trial, that it began to appear as if Sun was, in fact, seeking additional claim construction. Throughout the case the understanding of portion was like plain and ordinary meaning.  Court said that it is now clear, has always been Sun- that has desired for the Court to modify its understanding of what constitutes a DR portion (as well as an IR portion). Therefore, it was incumbent on Sun somehow to have asked the Court to alter its understanding of the scope of the asserted claims by construing the portion terms. Sun has now done so, but it is far too late.

Nevertheless, court said that it will,  address the claim construction dispute and apply this construction to the evidence presented at trial. With respect to claim language, court said that it supports Galderma’s position. The absence of an explicit structural requirement in the asserted claims suggests that the inventors intended "portion" by itself not to impose a structural requirement. With respect to specification, court said that it too does not provide strong support for either side's proposed construction. The term "portion" is used four times in the specification and none of those uses indicates that the term is being used in a restrictive or narrowing manner. Nothing in this usage of "portion" indicates that the patent is using the term to refer to a physically or structurally discrete part of the composition. Prosecution History and Amneal IPR supports Sun's proposed construction. But court said that for purposes of determining the proper construction of the "portion" terms to apply in the instant litigation, the IPR provides some limited- but not dispositive, and, ultimately, not sufficiently persuasive- support for Sun's proposed construction. Court also looked into extrinsic evidences & said that the definitions provide support for Galderma's proposed constructions and none for Sun's, as they do not suggest that "portion," in general usage, is narrowly limited to structurally discrete parts. Hence, court concluded that that a POSA would understand the "portion" terms to have a broad, functional meaning, rather than a narrow, structural meaning.

Court therefore held that under this construction Sun's NDA Product satisfies immediate release & delayed release portion limitations of claim. Moreover, Sun has not proven by clear and convincing evidence that the asserted claims of the patents are invalid due to obviousness.

Erlotinib - USA

On Oct 04, 2019, Federal Circuit reversed PTAB’s decision & found method of treatment claims valid in Tarceva® case.

This appeal concerns OSI’s patents, U.S6,900,221. Specifically Claims 44–46 and 53 are at issue.

44. A method for the treatment of NSCLC (non small cell lung cancer), pediatric malignancies, cervical and other tumors caused or promoted by human papilloma virus (H[P]V), Barrett's esophagus (pre-malignant syndrome), or neoplastic cutaneous diseases in a mammal comprising administering to said mammal a therapeutically effective amount of a pharmaceutical composition comprised of at least one of N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine, or pharmaceutically acceptable salts thereof in anhydrous or hydrate forms, and a carrier.

45. The method of claim 44, wherein the treatment further comprises a palliative or neo-adjuvant/adjuvant monotherapy.

46. The method of claim 44, wherein the treatment further comprises blocking epidermal growth factor receptors (EGFR).

53. The method of claim 44 for the treatment of non-small cell lung cancer (NSCLC).

PTAB determined that  these claims would have been obvious over Schnur in view of Gibbs or OSI’s 10-K.

Schnur – relates to compound family where erlotinib is listed as preferred compound. It also discloses that these compounds inhibits EGFR receptors & therefore useful for treatment of various cancers including lung cancer.

Gibbs  - is review article & discusse s various signaling mechanisms in the cell and how they are associated with tumor malignancy. This article discusses generally EGFR as one of the target & erlotinib is one of those compounds. Cross reference 13 refers to Moyer, which discloses how erlotinib inhibits EGFR in mouse liver tumors and in human HN5 tumors. Moyer however, does not discuss NSCLC.

OSI’s 10-K  - states that erlotinib has entered phase II trials & is potent inhibitor of EGFR receptor. OSI’s 10-K discloses no data regarding erlotinib’s effect on NSCLC.

The Board found that the disclosures in OSI’s 10-K that erlotinib targeted a variety of cancers including NSCLC, and that erlotinib had entered Phase II clinical trials, would have provided a person of ordinary skill with a reasonable expectation of success in light of Schnur’s teachings. Although nothing in the record indicated that any preclinical data related to NSCLC existed, the Board concluded that an ordinary artisan would understand from the commencement of Phase I studies that “preclinical animal efficacy data” had been submitted to the FDA. It found similarly with regard to Gibbs, focusing on Gibbs’s disclosure that “[ZD-1839 and erlotinib] appear to have good anti-cancer activity in preclinical models, with an acceptable therapeutic index particularly in patients with non-small cell lung cancer.”

Federal Circuit on appeal said that as an initial matter, in reaching its conclusion, the Board misinterpreted the asserted references to teach more than substantial evidence supports. When the references are properly read, the Board’s finding that the asserted references provide a reasonable expectation of success also is not supported by substantial evidence. To be clear, the claims require only treatment of a mammal with erlotinib—efficacy in humans is not required. But the asserted references do not disclose any data or other information about erlotinib’s efficacy in treating NSCLC. The record does not contain any clinical (human) data or preclinical (animal) data. It does not even include in vitro (test tube) data regarding erlotinib’s effect on NSCLC. At the same time, it is undisputed that NSCLC treatment was highly unpredictable with an over 99.5% rate of failure for drugs entering Phase II clinical studies. On this record, we are not persuaded that a reasonable factfinder could conclude that a person of ordinary skill would have reasonably expected success based on the combination of Schnur and Gibbs or Schnur and OSI’s 10-K.

PTAB’s reading of Gibbs is erroneous because cross reference, Moyer discloses erlotinib but it does not disclose NSCLC. Instead other cross reference, Woodburn mentions NSCLC but it does not mention erlotinib at all. Thus, Board’s finding that there is a “clear inference” in Gibbs that “erlotinib has anti-cancer activity against non-small cell lung cancer” is thus not supported by substantial evidence.

With respect to reasonable expectation of success,CAFC concluded that, properly read, these combinations do not provide substantial evidence supporting the Board’s findings of reasonable expectation of success. Schnur in view of Gibbs, the asserted references do not disclose any information about erlotinib’s efficacy in treating NSCLC in a mammal. There is no dispute that Schnur fails to disclose any in vitro or in vivo efficacy data for erlotinib for NSCLC. The lack of erlotinib-NSCLC efficacy data or other indication of success here is significant because of the highly unpredictable nature of treating NSCLC, which is illustrated by the over 99.5% failure rate of drugs entering Phase II. Moreover, EGFR is involved in many types of cancers & therefore drug’s success in treating one type of cancer does not necessarily translate to success in treating a different type of cancer.

Federal Circuit, however cautioned & said that-

“To be clear, we do not hold today that efficacy data is always required for a reasonable expectation of success. Nor are we requiring “absolute predictability of success.” We conclude only that, on these particular facts, a reasonable fact finder could not find a reasonable expectation of success. The Board’s finding is thus not supported by substantial evidence, and accordingly we reverse its obviousness determination.”

Dolutegravir - USA

Claim Construction (District of Delaware): Sep 26, 2019

This patent litigation dispute involves seven consolidated patent infringement and invalidity lawsuits, all arising under the Hatch-Waxman Act. Plaintiffs [Viiv/Shinogi] filed each of these actions for patent infringement of US 9,246,986 alleging violation of 35 U.S.C. § 271, based upon Defendants’ [Lupin; Apotex; Cipla ; Sandoz; Lek Pharmaceuticals and Laurus Labs] submissions of Abbreviated New Drug Applications (“ANDAs”) with the Federal Drug Administration (“FDA”). Those ANDAs seek FDA approval of generic versions of one or both of two brand-name drugs, “TIVICAY®” and “TRIUMEQ®.” Defendants responded with counterclaims for noninfringement and invalidity.

Plaintiffs and Defendants dispute the appropriate construction of two claim terms:

(1) “A crystal form of a sodium salt of a compound of formula AA,” contained in Claims 1 through 6 of the ’986 Patent.

Claim 1: A crystal form of a sodium salt of a compound of formula AA having characteristic diffraction peaks at 6.4°±0.2°, 9.2°±0.2°, 13.8°±0.2°, 19.2°±0.2°, and 21.8°±0.2° degrees two-theta in an X-ray powder diffraction pattern.

(2) “A crystal form of a hydrate of a sodium salt of a compound of formula AA,” contained in Claims 7 through 12 of the ’986 Patent.

Claim 7: A crystal form of a hydrate of a sodium salt of a compound of formula AA having characteristic diffraction peaks at 8.0°±0.2°, 9.3°±0.2°, 11.3°±0.2°, 16.0°±0.2°, and 22.8°±0.2° degrees two-theta in an X-ray powder diffraction pattern.

What the parties dispute is whether the term “crystal form” in each of the claims should be further construed to identify the particular hydration state of the claimed crystal forms—in light of the specific measurement data set out in both of the claims and the specification. Thus, for Claims 1 through 6, Defendants contend that the term “a crystal form” of dolutegravir sodium should be construed as “an anhydrate crystalline form of dolutegravir sodium”—because the measurement data shows that the crystal form is an anhydrate. Likewise, for Claims 7 through 12, Defendants argue that the term “a crystal form of a hydrate of” dolutegravir sodium should be further construed as “a monohydrate crystalline form of dolutegravir sodium".

Defendants’ position relies on the specification, which identifies, as examples of the invention, two crystal forms of dolutegravir sodium: Compound 13, which is an anhydrate, and Compound 13b, which is a monohydrate. Defendants contend that these two crystal forms of dolutegravir sodium are, in fact, the entirety of the invention, because—as the specification itself reveals—these two crystal forms yield the same measurement data that is listed in the twelve claims. Specifically, Compound 13 yields the same measurement data listed in Claims 1 thorough 6; and Compound 13b yields the same measurement data listed in Claims 7 through 12.

Court, however, sided with Plaintiff & said that Defendants’ proposed construction impermissibly imports limitations from the specification into the claims. Court said that the appropriate inquiry is whether the claim language, the specification, and the prosecution history of the ’986 Patent “clearly indicate that the invention encompasses no more” than Compounds 13 and 13b. Court further said that while it is true that the ’986 Patent claims specific crystal forms by way of certain measurement data, and that Compounds 13 and 13b exhibit that exact same data, it does not follow that Plaintiffs intended Compounds 13 and 13b to constitute the entirety of the invention. As Plaintiffs note, a crystalline form of dolutegravir sodium may exist that exhibits the same crystal structure as Compound 13 or Compounds 13b—and thus exhibits the measurement data set out in the ’986 Patent’s claims—but yet differs in hydration state. Specifically, Plaintiffs point out that non-stoichiometric crystalline compound can lose water (thus changing hydration state) without changing the crystal structure. It therefore makes sense that a patent applicant—like Plaintiffs here—seeking to claim a particular crystalline structure as the invention, would define the invention by reference to the measurement data, rather than by reference to the hydration state.

Court therefore, denied Defendants claim construction because claim language, specification, and prosecution history of the ’986 Patent are not ambiguous& they do not clearly indicate that Compounds 13 and 13b are the entirety of the invention.

Cyclosporine - USA

IPR decision: Sep 27, 2019

AIA Review #	Filing Date	Institution Date	Petitioner	Patent	Respondent	Status
IPR2016-01127	06/03/2016	12/08/2016	Mylan	8685930	Allergan, Inc.	Terminated-Dismissed
IPR2016-01128	06/03/2016	12/08/2016	Mylan	8629111	Allergan, Inc.	Terminated-Dismissed
IPR2016-01129	06/03/2016	12/08/2016	Mylan	8642556	Allergan, Inc.	Claims are unpatentable
IPR2016-01130	06/03/2016	12/08/2016	Mylan	8633162	Allergan, Inc.	Claims are unpatentable
IPR2016-01131	06/03/2016	12/08/2016	Mylan	8648048	Allergan, Inc.	Terminated-Dismissed
IPR2016-01132	06/03/2016	12/08/2016	Mylan	9248191	Allergan, Inc.	Terminated-Dismissed

On US’930 patent, Apotex, Famy Care, Teva & Akorn filed IPR petitions which were denied, terminated, terminated & instituted respectively.

On US’111 patent, Apotex, Argentum, Famy Care, Teva & Akorn filed IPR petitions which were denied, terminated, terminated, terminated & instituted respectively.

On US’556 patent, Apotex, Famy Care, Teva & Akorn filed IPR petitions which were denied, terminated, terminated & instituted respectively.

On US’162 patent, Apotex, Famy Care, Teva & Akorn filed IPR petitions which were denied, terminated, instituted & terminated respectively.

On US’048 patent, Apotex, Famy Care, Teva & Akorn filed IPR petitions which were denied, terminated, instituted & terminated respectively.

On US’191 patent, Famy Care, Teva & Akorn filed IPR petitions which were terminated, instituted & terminated respectively.

US 8,685,930 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a topical ophthalmic emulsion for treating an eye of a human having keratoconjunctivitis sicca, dry eye & or increasing tear production.

US 8,629,111 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a topical ophthalmic emulsion for treating an eye comprising cyclosporin A with certain excipients.

US 8,642,556 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a first topical ophthalmic emulsion for treating an eye comprising cyclosporin A with certain excipients.

US 8,633,162 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a method of treating dry eye disease comprising cyclosporin A with certain excipients.

US 8,648,048 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a method of increasing tear production in the eye comprising cyclosporin A with certain excipients.

US 9,248,191 (Allergan, Inc.; Exp: Aug 27, 2024) – OB listed

Claims a method of treating dry eye disease comprising cyclosporin A with certain excipients.

Weekly Patent Litigation Round-up

CJEU refuses UK High Court’s request for preliminary ruling on SPC applications based on third-party MAs, on account of referred question being “hypothetical” (C-239/19 Eli Lilly v Genentech)

On 5 September 2019, the Ninth Chamber of the CJEU refused a request for referral in relation to the interpretation of Article 3(b) of Regulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (‘SPC Regulation‘). In its order, the CJEU held that this request for a preliminary ruling was manifestly inadmissible a under Article 52(3) of the Rules of Procedure of the Court of Justice, as the question referred was hypothetical for the purposes of the dispute in the main proceedings…

https://hsfnotes.com/ip/2019/09/18/cjeu-refuses-uk-high-courts-request-for-preliminary-ruling-on-spc-applications-based-on-third-party-mas-on-account-of-referred-question-being-hypothetical-c-239-19-eli-lilly-v-genentech/

Article 3(a) just keeps on giving: AG Opinion in SPC referrals C-650/17 and C-114/18

The Advocate General (AG) has issued his opinion in SPC Referrals C-650/17 (Royalty Pharma) and C‑114/18 (Sandoz). Both referrals seek clarification over whether an SPC may be granted to a specific, individualized, embodiment of the product claimed by the basic patent.  The referrals particularly relate to the correct interpretation of Article 3(a) of the SPC Regulation (Regulation (EC) No. 469/2009). Article 3(a) states that an SPC shall be granted for a product “protected by a basic patent in force”. C-650/17 asks how Article 3(a) should be applied to functional claims, and C‑114/18 asks how Article 3(a) should be applied to claims specifying a Markush formula. In his opinion, the AG is clear that Article 3(a) should be interpreted for these types of claims according to the test provided in the CJEU decision C-121/17 (Teva)….

http://ipkitten.blogspot.com/2019/09/article-3a-just-keeps-on-giving-ag.html

CJEU preliminary ruling judgment in C-688/17 (Bayer) provides interpretation on Art. 9 (7) of the Directive 48/2004/EC (Enforcement Directive) based on a referral from the Hungarian court

On September 12, 2019 the Court of Justice laid down its decision in C-688/17 (Bayer) in a preliminary ruling proceeding coming from the Metropolitan Court, Budapest, about the interpretation of Art. 9 (7) of the Enforcement Directive, particularly regarding the term “appropriate compensation” that is due to defendants in the event a preliminary injunction is subsequently lifted.

In the decision the CJEU ruled that the term “appropriate compensation” is a sui generis notion of EU law and shall be interpreted in a uniform manner throughout the EU. Also the court highlighted that the subsequent revocation of the patent in suit does not as such render the earlier granted preliminary injunction unfounded.…

http://eplaw.org/cjeu-bayer-art-9-7-enforcement-directive/

Vectura wins additional $10m patent damages against GSK

A district court has upped Vectura’s award of $89.7 million in damages by $10m, after a jury trial earlier this year found that GlaxoSmithKline (GSK) has willfully infringed one of its patents. In a press release on Friday, September 13, Vectura announced that the US District Court for the District of Delaware had granted its motion for a 3% royalty rate on all future US sales of the infringing products until Vectura’s patent expires in 2021. It was also granted royalties on previous sales of the products from January 1, 2019 to May 16, 2019.…

https://www.lifesciencesipreview.com/news/vectura-wins-additional-10m-patent-damages-against-gsk-3686

Allergan, Lupin Must Face Payer Class in Loestrin Antitrust Suit

A group of pension and benefit funds won class action status Sept. 17 in a lawsuit accusing Allergan PLC, Lupin Ltd. and their affiliates of divvying up the birth control market, but a District of Rhode Island judge rejected a parallel bid by consumers. The multidistrict suit also targets several formerly independent companies owned by Allergan. It concerns patent infringement settlements that Warner Chilcott Co., now an Allergan subsidiary, reached with other drugmakers looking to roll out generic versions of its contraceptive pill Loestrin 24 FE…

https://news.bloomberglaw.com/health-law-and-business/allergan-lupin-must-face-payer-class-in-loestrin-antitrust-suit?utm_source=rss&utm_medium=HLNW&utm_campaign=0000016d-4125-d00c-afff-7dfd74160001

Cabaret Biotech Files Lawsuit Against Gilead Over Yescarta Drug

Closely held Cabaret Biotech said it had filed a preemptive lawsuit against Gilead Sciences Inc. and its Kite unit “to end a needless dispute about patent royalties” over the cancer treatment Yescarta (axicabtagene ciloleucel). Gilead, which exclusively licenses a patent from Cabaret for Yescarta in the field of oncology, has protested its royalty payment obligations since October 2018, according to complaint filed Monday in federal court in Wilmington, Delaware. Cabaret is seeking a judgment that the patent isn’t invalid and that but for the license agreement, Yescarta infringes the patent, complaint says…

https://news.bloomberglaw.com/ip-law/cabaret-biotech-files-lawsuit-against-gilead-over-yescarta-drug?utm_source=rss&utm_medium=IPNW&utm_campaign=0000016d-3be5-d433-a3ef-fff564b70000

Cinacalcet – USA

On Sep 18, 2019, Delaware court judge rejected Sun Pharma’s contention that its settlement with Amgen entitles Sun to launch its generic version.

Amgen sued Sun in Sep. 2016 for filing ANDA to market generic version of Sensipar®. The Parties settled & entered into Settlement Agreement on Oct. 24, 2017. On Aug. 24, 2018, Court entered a judgment of non-infringement in favor of Piramal, Amneal and Watson (Teva). On Dec 27, 2018, FDA approved Watson / Teva’s ANDA & on Dec. 28, Teva launched generic product in US market. Shortly thereafter, on Jan 2, 2019, Amgen and Teva reached a settlement agreement whereby Teva acknowledged that its generic product infringed the US 9,375,405 patent and agreed that it would immediately cease sales of this product. Also, on Jan 2, 2019, in order to comply with its notification duties outlined in section 5.3 of the Agreement, Amgen notified Sun of Teva’s launch and of their subsequent settlement.

Main dispute in this case was related to the part of Agreement which relates to Amgen’s obligations if other manufacturers of generic Cinacalcet entered the market at risk. Sun argued that it is entitled to a license under Section 5 of the Agreement. Specifically, Section 5.2(b) states that the “Entry Date” could be the earlier of “the Launch of a Generic Cinacalcet Product by a Third Party, Amgen, or an Amgen Affiliate, except as provided under Section 5.5.” Section 5.5 outlines Amgen’s obligations if a Third Party engages in an “At-Risk Launch.  According to it, Amgen need to enter into an agreement with each such Third Party selling such Generic Cinacalcet Product requiring each such Third Party to cease and desist from selling such Generic Cinacalcet Product form the market within 30 days of such agreement, then Amgen will not seek a temporary restraining order or preliminary injunction against Sun.

Sun urges that, based on Amgen’s deficient response to Teva’s market entry, it is entitled to a license to sell its generic Cinacalcet. Sun’s argument rests primarily on its claim that despite Teva’s launch and downstream sales, Amgen did not contract with each downstream distributor to effectuate a cease and desist regarding the selling of the Teva product. Per Sun’s reading of the Agreement, such authorized downstream sales trigger application of section 5.2 of the Agreement, thus granting Sun a license to enter the market.

Court however, disagreed & said that Amgen complied with Section 5.5(a)(ii) as it did in fact enter into a cease and desist agreement with Teva five days after Teva entered the market. Sun reads this language differently, urging that it obligates Amgen to effectuate “any further sale of such Generic Cinacalcet Product” by both Teva and all Third-Party distributors. In short, relying on language that simply does not exist, Sun insists that Amgen must have “policed the market,” – that is, policed both Teva and Third-Party distributors. Court disagreed with Sun’s interpretation for several reasons.

First and foremost, Amgen’s cease and desist obligations under the Agreement refers to Third Parties who engaged in at risk launch. It is undisputed that distributors and resalers did not engage in at-risk launch – only Teva did. Thus, reading the agreement as a whole, Court concluded that a “Third Party” does not include distributors. The Agreement is absolutely silent that this obligation also includes distributor resales and downstream purchasers.

Second, there simply is no language in the Agreement to support Sun’s contention that Amgen agreed to remove all generic products from the market, or that Amgen had a duty to police the entire market after such a launch. Reading section 5.5 as a whole, “each such Third Party” can only refer to Teva because only the generic manufacturer has the ability to be the first to sell the specific generic Cinacalcet product in the United States. And Teva was the only third party to have “Launched” a generic Cinacalcet.

Therefore, under this construction, Sun is not granted a license to market its Generic Cinacalcet Product at this time.

Oxycodone - USA

Claim Construction (District of Delaware): Sep 11, 2019

In these consolidated Hatch-Waxman patent litigation matters filed by Plaintiff Collegium Pharmaceutical, Inc. ("Plaintiff') against Defendant Teva Pharmaceuticals USA, Inc. ("Defendant"), Plaintiff alleges infringement of 13 patents: United States Patent Nos. 7,771,707, 8,449,909, 8,557,291, 8,758,813, 8,840,928, 9,044,398, 9,248,195, 9,592,200, 9,682,075, 9,737,530, 9,763,883, 9,968,598 and 10,004,729. Defendant filed ANDA to market generic version of XTAMPZA ER.

According to Plaintiff, the patented inventions "make attempts to abuse powerful pain medications more difficult or less rewarding, generally by protecting against unintended exposure of drugs such as opiates." The claims of the asserted patents purport to "involve new ways to dissolve [such drugs] in very small beads of wax that will release the drug over time when administered as intended, but that make it difficult to manipulate the formulation for purposes of abuse and misuse."

A. "homogeneous single phase"

Plaintiff                : "Drug is dissolved in the excipient matrix and uniformly and molecularly dispersed"

Defendant            :  Plain and ordinary meaning.

Court                   : "Drug is dissolved in the excipient matrix and uniformly dispersed."

B. "solidified solution"

Plaintiff                : "a system in a solid wherein the drug is molecularly dispersed throughout a matrix such that the system is chemically and physically uniform or homogeneous throughout"

Defendant            : Plain and ordinary meaning.

Court                   : "a solution that has transitioned to a solid form."

Esomeprazole & Naproxen

IPR decision: Sep 06, 2019

AIA Review #	Filing Date	Institution Decision Date	Petitioner	Patent	Respondent	Status
IPR2018-00272	12/04/2017	06/14/2018	Mylan Pharmaceuticals Inc.*/ DRL	9,393,208	Horizon Pharma	Claims 1–7 unpatentable

* PTAB terminated the proceeding between Petitioner Mylan  Pharmaceuticals Inc. and Patent Owners by Order on August 12, 2019. Petitioner Dr. Reddy’s Laboratories, Inc. (“Dr. Reddy’s”) from IPR2018-1341 was joined as Petitioner to this proceeding on April 1, 2019. Dr. Reddy’s remains as a Petitioner in this case.

US 9,393,208 (Pozen Inc./ Horizon Pharma USA, Inc.; Exp: 09/03/2029) – OB listed

1. A method for delivering a pharmaceutical composition to a patient in need thereof, comprising: orally administering to the patient an AM unit dose form and, 10 hours (.+-.20%) later, a PM unit dose form, wherein: the AM and PM unit dose forms each comprises: i) naproxen, or a pharmaceutically acceptable salt thereof, in an amount to provide 500 mg of naproxen, and ii) esomeprazole, or a pharmaceutically acceptable salt thereof, in an amount to provide 20 mg of esomeprazole; said esomeprazole, or pharmaceutically acceptable salt thereof, is released from said AM and PM unit dose forms at a pH of 0 or greater, the AM and PM unit dose forms target: i) a pharmacokinetic (pk) profile for naproxen where: a) for the AM dose of naproxen, the mean C.sub.max is 86.2 .mu.g/mL (.+-.20%) and the median T.sub.max is 3.0 hours (.+-.20%); and b) for the PM dose of naproxen, the mean C.sub.max is 76.8 .mu.g/mL (.+-.20%) and the median T.sub.max is 10 hours (.+-.20%); and ii) a pharmacokinetic (pk) profile for esomeprazole where: a) for the AM dose of esomeprazole, the mean area under the plasma concentration-time curve from when the AM dose is administered to 10 hours (.+-.20%) after the AM dose is administered (AUC0-10,am) is 1216 hr*ng/mL (.+-.20%), b) for the PM dose of esomeprazole, the mean area under the plasma concentration-time curve from when the PM dose is administered to 14 hours (.+-.20%) after the PM dose is administered (AUC0-14,pm) is 919 hr*ng/mL (.+-.20%), and c) the total mean area under the plasma concentration-time curve for esomeprazole from when the AM dose is administered to 24 hours (.+-.20%) after the AM dose is administered (AUC0-24) is 2000 hr*ng/mL (.+-.20%); and the AM and PM unit dose forms further target a mean % time at which intragastric pH remains at about 4.0 or greater for about a 24 hour period after reaching steady state that is at least about 60%.

Sucroferric oxyhydroxide - USA

Claim Construction (District of Delaware): Sep 05, 2019

Plaintiffs Vifor Fresenius Medical Care Renal Pharma Ltd. and Vifor Fresenius Medical Care Renal Pharma France S.A.S. ("Plaintiffs") filed suit against Defendants Lupin Atlantis Holdings SA, Lupin Pharmaceuticals, Inc., and Teva Pharmaceuticals USA, Inc. ("Defendants") on March 12, 2018, alleging infringement of U.S. Patent No. 9,561 ,251 (the '"251 Patent").  The patent-in-suit relates to pharmaceutical compositions of iron oxy-hydroxide in high loading.

II. CONSTRUCTION OF DISPUTED TERMS:

A. "essentially non-bioabsorbable"

Plaintiff: Plain and ordinary meaning, otherwise: upon oral administration, the iron oxyhydroxide is not absorbed by the human body in a clinically significant amount

Defendant: Indefinite

Court: Upon oral administration, the iron oxyhydroxide is not absorbed by the human body in a clinically significant amount

B. "iron release rate below 2.5% w/w"

Plaintiff: The iron release measured in water at a pH of 3 according to European Pharmacopeia chapter 2.9.3 using standard dissolution equipment and parameters as described in the monograph, where iron content is analyzed by titration after 2 hours, wherein the quantity of iron dissolved after 2 hours is less than 2.5% w/w

Defendant: Indefinite

Court: The iron release measured in water at a pH of 3 according to European Pharmacopeia chapter 2.9.3 using standard dissolution equipment and parameters as described in the monograph, where iron content is analyzed by titration after 2 hours, wherein the quantity of iron dissolved after 2 hours is less than 2.5% w/w

C. "not bound as a complex compound"

Plaintiff: Plain and ordinary meaning, otherwise: not forming any intramolecular bonds such that a water-soluble stabilization agent can be removed by washing the stabilized iron oxy-hydroxide with water

Defendant: Indefinite

Court: Not forming any intramolecular bonds such that a water-soluble stabilization agent can be removed by washing the stabilized iron oxy-hydroxide with water

D. "rapid disintegration"

Plaintiff: Plain and ordinary meaning

Defendant: Indefinite

Court: Disintegration that begins upon administration and, on average, takes no longer than 3 minutes to complete

Weekly Patent Litigation Roundup:

Amgen patents on Repatha invalid, judge rules in reversal

A federal judge on Wednesday ruled two patents held by Amgen on its cholesterol drug Repatha are invalid, reversing a February jury verdict that had upheld the California biotech's claims in its legal battle with rivals Sanofi and Regeneron. Judge Richard Andrews' decision will not remove Repatha from market, and Amgen said it plans to appeal. Still, it's a setback that strengthens the position of Sanofi and Regeneron, which sell the competing drug Praluent. Both Repatha and Praluent are antibodies that lower cholesterol by binding to a protein called PCSK9..…

https://www.biopharmadive.com/news/amgen-patents-on-repatha-invalid-judge-rules-in-reversal/561882/

Delhi High Court Revoked the Patent on Novartis’ Ceritinib

The Court suspended the earlier interim relief granted to Novartis, which had restrained the manufacture and sale of the generic version of the cancer drug by Natco Pharma. It was only end-May the Delhi High Court had restrained Natco from carrying out any fresh manufacture of drugs comprising the API ceritinib, a non-small cell lung cancer (NSCLC) treatment. The Court’s May decision came on a plea filed by Novartis seeking an order restraining Natco from manufacturing and selling ceritinib. The Swiss company submitted that, in March 2019, it came across Natco’s product under the trademark Noxalk at a pharmaceutical conference in Kolkata.…

https://gmpnews.net/2019/08/delhi-high-court-revoked-the-patent-on-novartis-ceritinib/

Del HC Vacates Interim Orders Restraining Dr. Reddy’s & Ors. from Selling AstraZeneca’s Ticagrelor

On 8th August, the Single Bench of the Delhi High Court vacated the interim orders granted in favour of AstraZeneca (‘plaintiff’) preventing Micro Labs, Natco Pharma and Dr. Reddy’s Laboratories (‘defendants’) from selling, marketing or dealing with TICAGRELOR (an effective platelet aggregation inhibitor) or any other product violating the plaintiff’s registered patents- IN 907, IN 984 and IN 674. The case relates to two important issues, namely, selection patents and the difference between coverage and disclosure in a patent. The interim applications dealt with in the instant case were IA 3986/2018 in CS (Comm.) 749/2018, IA 4771/2018 in CS (Comm.) 792/2018, IA 9332/2018 filed in CS (Comm.) 1023/2018 filed by the plaintiffs, and IA 5096/2018 in CS (Comm.) 749/2018 filed by the defendants seeking vacation of the interim orders..…

https://spicyip.com/2019/08/del-hc-refuses-astra-zenecas-interim-injunction-plea-to-restrain-dr-reddys-ors-from-selling-ticagrelor.html

Parties Agree That Mylan's Pegfilgrastim Biosimilar Does Not Infringe Amgen's Patent

Amgen, maker of the brand-name pegfilgrastim (Neulasta), and Mylan, which partnered with Biocon to develop a biosimilar (Fulphila), have entered a joint status report in the District Court for the Western District of Pennsylvania. In the status report, they agree that Amgen cannot maintain a claim of infringement against Mylan with respect to US Patent Number 8,273,707, which covers a process for purifying proteins by mixing a protein preparation with a solution involving 2 salts. This latest development stems from an earlier decision in another case related to the same patent; in March 2018, a Delaware court dismissed a lawsuit brought by Amgen over a different biosimilar developer’s alleged infringement of this same patent; in that case, Amgen alleged that Coherus BioSciences infringed on its patent because Coherus’ biosimilar pegfilgrastim, later approved as Udenyca, mixed salts that, in combinations, were equivalent to Amgen’s patented combinations. According to the court, Amgen had previously acknowledged that Coherus did not literally infringe on the patent..

https://www.centerforbiosimilars.com/news/parties-agree-that-mylans-pegfilgrastim-biosimilar-does-not-infringe-amgens-patent

Baxalta Loses Motion for Patent Infringement Retrial Against Bayer

A federal court in Delaware has denied Baxalta’s request for a new trial in a suit brought by Bayer over patent infringement by Baxalta’s hemophilia A drug Adynovate.  The Takeda subsidiary sought a new trial on the grounds that its clotting factor VIII drug could not infringe on Bayer’s patent for factor VIII because the patent was invalid.  Bayer sued Baxalta and Nektar Pharmaceuticals in 2016 alleging that they infringed on its patent by making, selling and importing Adynovate. Nektar had worked with Bayer on its version of the drug, but also helped Baxalta develop Adynovate, according to Bayer’s complaint.  The FDA approved Jivi, Bayer’s factor VIII hemophilia A treatment, in August 2018. In a trial held earlier this year, a jury found that Baxalta did infringe on Bayer’s patent, and the company was ordered to pay $872 million in royalties and $155 million in damages.…

https://pharmajobs.co/baxalta-loses-motion-for-patent-infringement-retrial-against-bayer/

Purdue Pharma proposes $12B settlement to clean up opioid mess — report

After months of negotiations with states and federal plaintiffs accusing it of instigating the opioid crisis through aggressive and deceptive marketing tactics, Purdue Pharma is ready to pay $10 to $12 billion to settle it all. The potential deal would cover hundreds of lawsuits being waged against the company by states, cities, towns and tribes, which is being overseen by United States district judge Dan Polster in Cleveland, alongside cases involving other prescription opioid makers. As part of the deal, the Sackler family — who had been charged with building a “multibillion-dollar drug empire based on addiction” — will give up ownership in Purdue..

https://endpts.com/purdue-pharma-proposes-12b-settlement-to-clean-up-opioid-mess-report/