(Clarification: This post analyzes patent reexaminations of a subject patent that claims the benefit of an earlier filed CIP and/or provisional application for priority purposes.  In such circumstances, intervening art presenting a Substantial New Question of patentability (SNQ) may be applied calling into question these priorty dates.  In such unique circumstances, enablement and written description issues pertaining to the originally issued patent claims will be considered by the USPTO for the purpose of detemining whether or not the priority claim is properly supported.  Of course, such an analysis of original patent claims is not performed outside of these limited circumstances). 

According the MPEP §§ 2258 and 2658, the USPTO during a reexamination proceeding will not consider 35 U.S.C. § 112, 1st paragraph issues with respect to the reexamination of original patent claims. It will, however, consider such issues where new or amended claims are presented or where any part of the disclosure is amended.

Nevertheless, where the patent subject to reexamination has claimed the benefit of the filing date of an earlier filed U.S. or foreign patent application, reexamination proceedings may be based on intervening patents or printed publications where the patent claims under reexamination may be entitled only to the actual filing date of the patent.

But can this strategy be used as a “back door” attack on the original patent claims’ compliance with 35 U.S.C. § 112, 1st paragraph where the patent for which reexamination is sought is a continuation or divisional patent?

Do the examiners in the Central Reexamination Unit have to make a determination of original continuation or divisional patent claims’ compliance with 35 U.S.C. § 112, 1st paragraph when assessing whether the parent application or patent complies with 35 U.S.C. § 112, 1st paragraph?

Suppose that the original patent’s prosecution history includes no intervening prior art. In such circumstance, the original examiner presumably made no affirmative determination as to the right of priority. Further assume that the patents or printed publications included in the reexamination request are non-cumulative with respect to the prior art of record in the original patent’s file history and raise a substantial new question of patentability against the original patent claims, if these claims are not entitled to the filing date of the earlier filed applications.

In accordance with the MPEP §2258 (I)(C), reexamination can be ordered under these facts, even though the effect will be to assess whether the original patent claims have adequate written description support and are full enabled.

The patent owner will likely presents arguments and evidence during reexamination that the parent applications provide adequate support for the original patent claims rather than amending or cancelling claims, or that the right to priority was determined in the original prosecution. (For an example of this issue where priority was assessed in the original prosecution see Reexamination Control No. 95/000,312 (discussing the Aotake reference)).

Advisedly, a third party requester should consider using inter partes reexamination rather than ex parte reexamination in order to fully participate in the proceedings. It is highly likely that the third party will need to rely on expert declaration evidence to rebut the patent owner’s showings as to why the original patent claims are entitled to an earlier filing date to antedate the intervening prior patents or printed publications.
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Singulair is Merck's best-selling drug, with sales of nearly $1.1 billion in the third quarter of 2009.  However, Merck' patent covering Singulair has also been hotly contested in court, at the FDA, and, most recently, at the USPTO. The Singulair patent, U.S. Patent No. 5,565,473, issued in 1996, covers the basic compound as well as a method of treating asthma.  The ‘473 patent has been the subject of ongoing litigation between Merck and generic manufacturer Teva Pharmaceuticals.  Merck filed three suits against Teva in April of 2007, May of 2007, and January of 2009, all in the U.S. District Court for the District of New Jersey, claiming that Teva infringed the ‘473 patent by filing an ANDA for generic Singulair. Because the suits all asserted infringement of the ‘473 patent, the later two suits were stayed pending a final decision on the merits in the first suit. On August 19, 2009, Judge Garrett E. Brown of the U.S. District Court for the District of New Jersey ruled that Teva’s generic drug would infringe Merck’s ‘473 patent, and ordered the FDA to stay market approval of the generic version of Singulair pending expiration of the ‘473 patent in 2012. Unfortunately for Merck, the success in the District Court represents only one front of battle for defending the validity of the ‘473 patent.  On April 27, 2009, four months prior to Judge Brown’s ruling, an ex parte reexamination request was filed for the ‘473 patent by Article One Partners LLC, a global research community which rewards Advisors for finding prior art to invalidate patents. The ex parte examination request was submitted with eight prior art documents in which Article One set forth over 276 pages of obviousness arguments.  The request was granted by the USPTO on May 28, 2009. Despite the painstaking efforts by Article One in their Request for Ex Parte Reexamination, on September 3, 2009, the USPTO issued a single obvious-type double patenting rejection over lapsed U.S. Patent No. 5,428,033 in view of U.S. Patent No. 5,104,882.  Despite vehement arguments that the claims of the ‘473 patent are patentably distinct over the claims of the ‘033 patent, Merck filed a terminal disclaimer on November 2, 2009 to obviate the obvious-type double patenting rejection. The terminal disclaimer would seemingly result in the ‘473 patent expiring on June 27, 2012, which is the expiration date of the ‘033 patent as defined under 35 U.S.C. 154 and 173.  There being no further issues unresolved in the reexamination of the ‘473 patent, it appears that a Notice of Intent to issue a Reexamination Certificate (NIRC) will be issued by the USPTO to Merck. At $1.1 billion per quarter, at first glance the filing of the terminal disclaimer over the ‘033 patent would appear to be good news for Teva.  However, the newly filed terminal disclaimer will not affect the expiration date of the ‘473 patent.  The terminal disclaimer filed in the reexamination proceedings disclaimed the patent term beyond June 27, 2012, but the statutory patent term of ‘473 will have already expired well prior to this date in view of a terminal disclaimer filed over U.S. Patent No. 5,266,568 during the original prosecution of the ‘473 patent resulting in an already shortened patent term to November 30, 2010. It is worth noting that the terminal disclaimer will also have no affect on the ultimate expiration of the ‘473 patent on February 3, 2012, which takes into account a 430-day extension granted under § 156 for delays in FDA regulatory review.  In March 2007 the Court of Appeals for the Federal Circuit held that if a patent is subject to a terminal disclaimer, the term extensions for regulatory review granted by section § 156 of the Patent Law are added on after the terminal disclaimer date.  Merck & Co. v. Hi-Tech Pharmacal Co., 82 USPQ2d 1203, 1208 (Fed. Cir. 2007).
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Where does a Patent Owner go for judicial review after losing an ex parte reexamination appeal at the Board of Patent Appeals and Interferences (BPAI)? Prior to 2001, Patent Owners had a clear choice of filing suit against the USPTO in the U.S. District Court for the District of Columbia, or appealing adverse BPAI decisions to the Court of Appeals for the Federal Circuit (CAFC). In 2001, amendments to the patent statutes ( 35 U.S.C. §§ 141 and 145 ) in the American Inventor Protection Act (AIPA) appeared to eliminate the District Court option, providing only for appeal to the CAFC. However, a recent case filed in the Eastern District of Virginia questions the USPTO’s interpretation of the statutory changes set forth in MPEP § 2279. In Sigram Schindler Beteilungsgesellschaft mbH v. Kappos, No. 1:09-cv-935-TSE-IDD (E.D. Va.) the patent owner (Sigram Schindler) seeks a right to a trial de novo under 35 U.S.C. § 145 after an adverse decision of the BPAI in an ex parte reexamination (requested by Cisco Systems Inc.) of Sigram Schindler's 2005 patent for a telecommunications network data transmission method and related network switch. Sigram Schindler is challenging the USPTO's interpretation of Section 13202(d) of Public Law 107-273 regarding judicial review of BPAI ex parte reexamination decisions. At the heart of Sigram Schindler’s law suit is a desire to obtain a de novo review of the BPAI’s decision in a federal district court that will provide discovery power over Cisco to obtain code utilized in Cisco’s products. Sigram Schindler appears to be advancing the theory that Cisco’s code will demonstrate that Sigram Schindler’s declaration evidence presented during the reexamination proceedings as to secondary considerations of non-obviousness is more significant than the BPAI gave it credit. (i.e., evidence of use of the invention by others is an objective indicator of non-obviousness).  Sigram Schindler is seeking the Eastern District of Virginia to nullify the USPTO 's interpretation of Public Law 107-273, section 13202(d) as "unlawful and legally void." In Sigram Schindler's August 19, 2009 filed complaint, they aver that "those rules are unlawful and should be set aside as having been adopted in excess of the PTO's statutory authority." They say the USPTO's efforts to regulate proceedings outside the USPTO is ultra vires. On October 21, 2009 the USPTO filed a motion for summary judgment seeking to dismiss the case. The USPTO says that Sigram Schindler lacks standing to bring the "premature" case because it's not clear how the BPAI will ultimately rule and whether they will even need to file an appeal to the courts. According to the USPTO's memo supporting its motion for summary judgment, "the challenged regulation -- whatever its import -- does not apply to [Sigram Schindler] now and may never apply to [Sigram Schindler] at all." The USPTO's position on the merits is that Sigram Schindler's case should fail because of the statutory language Congress specifically placed into the Patent Act in sections 141 and 145 regarding patent owners recourse to appeal only to the Federal Circuit. The USPTO argues that Congressional amendments in Public Law 107-273 that spurred the USPTO interpretation set forth in MPEP § 2279 in question supercede the prior versions of sections 141 and 145, and are controlling. Sigram Schindler’s strategy seems to be seeking a second chance in court to persuade the fact finder than its claims are non-obvious by gaining access to third party information that was not in its possession and that it could not obtain during the ex parte reexamination proceedings. As can be appreciated, if Sigram Schindler is successful, Patent Owner’s can emerge from the USPTO’s adverse decision by the BPAI and through a federal district court action obtain discovery from third parties that would be advantageous to its position in seeking reversal of an adverse decision by the USPTO’s BPAI in ex parte reexamination proceedings. For this reason, this case is an interesting one to watch unfold.
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In the summer of 2005, responding to industry criticism on the efficacy of patent reexamination, the USPTO created the Central Reexamination Unit (CRU).  The CRU is formed of highly skilled primary patent examiners that have been specially selected from the Patent Examining Corps.  These examiners average more than 15 years of experience and have technical backgrounds that reflect the broad spectrum of technologies encountered in patent reexamination.  Many of the primary examiners chosen to work in the CRU have advanced technical and law degrees.

The mission of the CRU is to ensure high quality, objective and timely processing of reexamined patents.  The CRU endeavors to comply with the “special dispatch” requirements of the reexamination statutes.  Reexamined patents are assigned to examiners in the CRU who were not previously involved in the examination of the original patents or in prior reexamination proceedings of the patents.  The examiners work in teams of three including a Special Program Examiner (SPE).  Patentability review conferences are conducted at each point in the reexamination decision making process in order to reach a consensus in decision making on claim patentability.

Currently, the CRU has 48 primary examiners working in 3 Units.  Gregory Morse, who was appointed the Director of the CRU on June 23, 2008 has 5 SPEs and fourteen technical support staff.  Mr. Morse, in turn reports to Technology Center Director Irem Yucel.

The CRU will only reexamine patent claims for which reexamination has been requested for which a substantial new question of patentability has been established. MPEP § 2240 (citing Sony v. Dudas)  The CRU makes the determination as to whether the new or previously presented patents and printed publications would have been important to a reasonable examiner in deciding whether to allow the patents claims.  The new or previously presented patents and printed publications must be noncumulative to the information previously considered during the original patent examination.

The CRU works closely with the Office of Patent Legal Administration (OPLA) directed by Brian Hanlon to address issues associated with, intra alia, petitions, merger of proceedings, and return of improperly submitted papers.

For fiscal year 2009 ending September 30, 2009, 658 ex parte reexamination and 258 inter partes reexamination requests were filed.  92% of ex parte reexamination requests and 95% of inter partes reexamination requests were granted.  Of the patents that were subject to reexamination recent trends show that more than 60% of these patents are involved in concurrent litigation.  Average pendencies to reexamination certificate for these proceedings were 25.2 and 35.8 months, respectively.  For ex parte reexamination concluded proceedings, 25% had all claims confirmed, 11% had all claims canceled and 64% had claim changes.  For inter partes reexamination concluded proceedings, 6% had all claims confirmed, 54% had all claims canceled or disclaimed and 40% had claim changes.

These USPTO reexamination statistics demonstrate that reexamination proceedings conducted by the CRU quite often result in patents having their scope of protection narrowed; accounting for the increased popularity of third parties filing reexamination requests, especially where the reexamined patents are in concurrent litigation.
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In the case of concurrent post grant proceedings at the USPTO, 37 CFR §§ 1.565(d) and 1.991 provide for a discretionary merger of reissue application examination with either ex parte or inter partes reexamination proceedings.  These rules provide that such merged proceedings will be conducted using the rules set forth for reissue application examination that are normally less restrictive than those applicable to reexamination.  As can be appreciated, such a merger would provide the patentee greater flexibility after final rejection and, in most situations, RCE practice and extensions of time as a matter of right; important procedural advantages.  But note that the USPTO may undo the merged proceedings if an RCE is filed in the reissue application (See MPEP §1452) and modify the response period/extension of time practice for reissue applications involved in a concurrent litigation (See MPEP §1442.03).

Moreover, although amendments to claims in reexamination can only be narrowing amendments, if the patent for which reissue is two years or less old, a broadened reissue application can be filed.  In this way, use of patent reissue together with merged reexamination proceedings may provide useful procedural and tactical advantages to a patent owner.

However, whether to merge such proceedings or to suspend action on one of them is a decision that is made by the USPTO sua sponte based on the relative timing of the filings of the reissue application and the reexamination requests, the stage of the respective proceedings, whether a continuation or RCE of the reissue application has been filed, whether the reexamination proceeding is ex parte or inter partes, and whether the patent owner will consent to a stay of the examination of the reissue application pending the outcome of the reexamination proceeding.  Normally, the USPTO favors merger to prevent inconsistency in the handling of the proceedings, if conducted separately.

A merger order issued by the USPTO in merged proceedings sets forth the conditions for how the merged proceedings will be conducted.  If the merged proceedings involve inter partes reexamination, the third party’s participation will be limited to the issues applicable to reexamination.  This permits the patent owner to have other issues such as those applicable to broadened reissue claims dealt with on an ex parte basis.  Moreover, the merged proceedings may be assigned to an examiner in the Technology Center handling the reissue application rather than to examiners in the Central Reexamination Unit (CRU).  This could be advantageous to the patent owner, especially when considering the fate of the patents subjected to inter partes reexamination by the CRU where for completed inter partes reexamination proceedings only 6% have survived with all claims confirmed.  Currently, the Office appears to disfavor merger of inter partes reexamination proceedings and may instead choose to stay the reissue application proceeding in favor of such reexamination proceedings.

However, there are also significant disadvantages to the rules of reissue examination practice.  Patent reissue permits the correction of defects relating to subject matter eligibility, utility, written description, enablement, and clarity of the original claims.  During reexamination, these same defects may only be considered in claims which are amended or added by the reexamination, and not in the originally patented claims. See MPEP §2258.  Thus, a patentee should seriously consider filing a reissue application where the issued patent, for example,  issued prior to In re Bilski, 545 F.3d 943, 88 USPQ2d 1385 (Fed. Cir. 2008), as a significant risk of invalidation may exist for certain method claims if litigated.

Additionally, in reexamination, it is Office practice to examine only those claims specifically identified in the reexamination request.  On the other hand, patent reissue will typically include a comprehensive examination of all claims. 37 C.F.R. §1.176 (See MPEP §1440)

Merger provides interesting opportunities for patent owners and third party requesters alike, (via serial patent reexamination requests).  However, the question of whether or not concurrent USPTO proceedings should be initiated in any given case, requires a close analysis of the facts.

Further information regarding the advantages and disadvantages of merger will be presented at the Patent Law Institute Reissue and Reexamination Strategies and Tactics with Concurrent Litigation 2010.
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