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Doc Code: TRACK1.REQ
`Document Description: TrackOne Request
`
`PTO/AlA/424 (04-14)
`
`CERTIFICATION AND REQUEST FOR PRIORITIZED EXAMINATION
`
`UNDER 37 CFR 1.102(e) (Page 1 of 1)
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`APPLICANT HEREBY CERTIFIES THE FOLLOWING AND REQUESTS PRIORITIZED EXAMINATION FOR
`THE ABOVE-IDENTIFIED APPLICATION.
`
`
`
`1. The processing fee set forth in 37 CFR 1.17(i)(1) and the prioritized examination fee set forth in
`37 CFR 1.17(c) have been filed with the request. The publication fee requirement is met
`because that fee, set forth in 37 CFR 1.18(d), is currently $0. The basic filing fee, search fee,
`and examination fee are filed with the request or have been already been paid.
`I understand
`that any required excess claims fees or application size fee must be paid for the application.
`
`I understand that the application may not contain, or be amended to contain, more than four
`independent claims, more than thirty total claims, or any multiple dependent claims, and that
`any request for an extension of time will cause an outstanding Track I request to be dismissed.
`
`3. The applicable box is checked below:
`
`Ori
`
`inal Ao olication Track One - Prioritized Examination under ~
`
`i.
`
`(a) The application is an original nonprovisional utility application filed under 35 U.S.C. 111(a).
`This certification and request is being filed with the utility application via EFS—Web.
`___OR___
`
`(b) The application is an original nonprovisional plant application filed under 35 U.S.C. 111(a).
`This certification and request is being filed with the plant application in paper.
`
`ii. An executed inventor’s oath or declaration under 37 CFR 1.63 or 37 CFR 1.64 for each
`
`inventor, g the application data sheet meeting the conditions specified in 37 CFR 1.53(f)(3)(i) is
`filed with the application.
`
`Re uest for Continued Examination - Prioritized Examination under
`
`.
`
`'
`
`A request for continued examination has been filed with, or prior to, this form.
`If the application is a utility application, this certification and request is being filed via EFS-Web.
`The application is an original nonprovisional utility application filed under 35 U.S.C. 111(a), or is
`a national stage entry under 35 U.S.C. 371.
`. This certification and request is being filed prior to the mailing of a first Office action responsive
`to the request for continued examination.
`No prior request for continued examination has been granted prioritized examination status
`under 37 CFR 1.102(e)(2).
`
`
`3,9na,,,,e /Yueien Zhou/
`Date2017.1 1 -21
`
`Name
`(Print/Typed)
`
`Yuefen ZhOU
`
`Practitioner
`Registration Number
`
`73398
`
`This form must be signed in accordance with 37 CFR 1.33. See 37 CFR 1.4(d) for signature requirements and certifications.
`Note:
`Submit multile forms if more than one sinature is re-uired. *
`
`*Total of
`
`1
`
`forms are submitted.
`
`Griin. Exh. 1037
`
`PGR for U.S. Patent No. 10,052,338
`
`1
`
`Grün. Exh. 1037
`PGR for U.S. Patent No. 10,052,338
`
`

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`EECLARATEQN {3? CFR 133} FQR UTiLiTY QR EESiGi‘é APPLECATEGN US’EENQ AN
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`-
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`-
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`Application Data Sheet 37 CFR 1.76
`Application Number
`
`
`
`Title of Invention
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`The application data sheet is part of the provisional or nonprovisional application for which it is being submitted. The following form contains the
`bibliographic data arranged in a format specified by the United States Patent and Trademark Office as outlined in 37 CFR 1.78.
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`Middle Name
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`Non US Residency
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`I5 Broadway, 9th Floor
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`Email Address
`IDocket@mabr.com
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`Application Information:
`
`
`Title of the Invention
`
`eridronic Acid for Treating Complex Regional Pain Syndrome
`
`Attorney Docket Number
`
`‘ 3226.10005US49
`
`Small Entity Status Claimed
`
`
`
`
`
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`PTOIAIAI14 (11-15)
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`Attorney Docket Number
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`Application Data Sheet 37 CFR 1.76
`Application Number
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`Title of Invention
`
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`
`
`Attorney Docket Number
`A3226.10005US49
`Application Data Sheet 37 CFR 1.76
`Application Number
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`Title of Invention
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`Neridronic Acid for Treating Complex Regional Pain Syndrome
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`PTO/AlA11 4 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`US. Patent and Trademark Office; US. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`Attorney Docket Number A3226.10005US49
`
`Application Data Sheet 37 CFR 1.76
`Application Number
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`
`
`Title of Invention
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`Neridronic Acid for Treating Complex Regional Pain Syndrome
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`Application Number
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`Continuity Type
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`I 41063979
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`I ontinuation in part of
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`I 13/894274
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`Application Number
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`Continuity Type
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`I 31894274
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`I laims benefit of provisional
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`Application Number
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`Continuity Type
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`I 61/764563
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`Prior Application Number
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`I 611762225
`'013—02—07
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`Filing or 371(c) Date
`(YYYY-MM-DD)
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`I 61/655541
`'012—06—05
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`Prior Application Number
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`Filing or 371(c) Date
`(YYYY-MM-DD)
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`I012—06_—05
`I 611655527
`I laimsbeneftofprovisional
`'—31894274
`Fil-in-gor 371(c) Date
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`(YYYY-MM-DD)
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`'012—06—01
`
`Application Number
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`Continuity Type
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`Prior Application Number
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`I 31894274
`
`EFS Web 2.2.12
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`I laims benefit of provisional
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`I 611654383
`
`7
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`

`

`PTOIAIAI14 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`US. Patent and Trademark Office; US. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`Attorney Docket Number A3226.10005US49
`
`Application Data Sheet 37 CFR 1.76
`Application Number
`
`
`
`Title of Invention
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`Remove
`
`
`
`
`Filing or 371(c) Date
`
`
`
`Prior Application Number
`
`(YYYY-MM-DD)
`
`
`'012—06—01
`
`
`Filing or 371(c) Date
`(yvyy-M|\/|-DD)
`
`Prior Application Number
`
`I 61/654292
`
`Application Number
`
`Continuity Type
`
`I 3/894274
`
`I laims benefit of provisional
`
`Application Number
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`Continuity Type
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`Application Number
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`Continuity Type
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`I 61/647478
`I laims benefit of provisional
`I 31894274
`'012—05—15
`
`
`
`
`Prior Application Status Im:
`Remove
`
`
`
`Filing or 371(c) Date
`
`
`
`
` Prior Application Number
`(YYYY-MM-DD)
`
`I012—0514
`I 61/646538
`I laims beneft of prOVISIonal
`I 31894274
`
`
`_emove
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`_riorApplication Status—Iml
`Fil-in_gor 371(c) Date
`
`
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`Prior Application Number
`(YYYY-MM-DD)
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`' 01 5—05—27
`I PCT/US2015I032739
`
`
`Remove
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`
`Filing or 371(c) Date
`
`
`
` Prior Application Number
`(YYYY-MM-DD)
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`
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`014—08—08
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`Filing or 371(c) Date
`(YYYY-MM-DD)
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`Application Number
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`Continuity Type
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`I 5/360886
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`I ontinuationIn part of
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`Application Number
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`Continuity Type
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`I - CTIU820151032739 _I PCT/US2014/050427
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`Application Number
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`Continuity Type
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`Prior Application Number
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`I - CTIU820141050427 _I 14/279241
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`1114—05—15
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`
`Issue Date
`Filing Date
`Prior Application
`.
`.
`Application
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`Continuity Type
`(YYYY—MM—DD)
`(YYYY-MM—DD)
`Patent Number
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`0'1—707—11
`'01-711-21
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`Application Number
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`Continuity Type
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`Fil-in_gor 371(c) Date
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`Prior Application Number
`(YYYY-MM-DD)
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`
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`201 6-08-22
`
`I 62/378140
`I laims benefit of provisional
`I 51647140
`
`
`
`Additional Domestic Benefit/National Stage Data may be generated within this form
` Add
`
`
`by selecting the Add button.
`
`
`
`
`
`Foreign Priority Information:
`EFS Web 2.2.12
`
`8
`
`

`

`PTOIAIAI14 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`US. Patent and Trademark Office; US. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`
`_
`_
`Application Data Sheet 37 CFR 1.76
`
`A3226.10005US49
`Attorney Docket Number
`
`
`Application Number
`
`Title of Invention
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`Add button.
`
`This section allows for the applicant to claim priority to a foreign application. Providing this information in the application data sheet
`
`constitutes the claim for priority as required by 35 U.S.C. 119(b) and 37 CFR 1.5_5. When priority is claimed to a foreign application
`that is eligible for retrieval under the priority document exchange program (PDX)l the information will be used by the Office to
`automatically attempt retrieval pursuant to 37 CFR 1.55(i)(1) and (2). Under the PDX program, applicant bears the ultimate
`responsibility for ensuring that a copy of the foreign application is received by the Office from the participating foreign intellectual
`property office, or a certified copy of the foreign priority application is filed, within the time period specified in 37 CFR 1.55(g)(1)_
`
`Remove
`
`Application Number
`
`I
`
`Access Codei (if applicable)
`
`
`
`Additional Foreign Priority Data may be generated within this form by selecting the
`
`
`
`Statement under 37 CFR 1.55 or 1.78 for AIA (First Inventor to File) Transition
`
`Applications
`
`
`This application (1) claims priority to or the benefit of an application filed before March 16, 2013 and (2) also
`contains, or contained at any time, a claim to a claimed invention that has an effective filing date on or after March
`D 16, 2013.
`NOTE: By providing this statement under 37 CFR 1.55 or 1.78, this application, with a filing date on or after March
`16, 2013, will be examined under the first inventor to file provisions of the AIA.
`
`EFS Web 2.2.12
`
`9
`
`

`

`PTOIAIAI14 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`U.S. Patent and Trademark Office; U.S. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`
`
`Attorney Docket Number A3226.10005US49
`Application Data Sheet 37 CFR 1.76
`Application Number
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`Title of Invention
`
`Authorization or Opt-Out of Authorization to Permit Access:
`
`When this Application Data Sheet is properly signed and filed with the application, applicant has provided written
`authority to permit a participating foreign intellectual property (IP) office access to the instant application—as-filed (see
`paragraph A in subsection 1 below) and the European Patent Office (EPO) access to any search results from the instant
`application (see paragraph B in subsection 1 below).
`
`Should applicant choose not to provide an authorization identified in subsection 1 below, applicant must opt-out of the
`authorization by checking the corresponding box A or B or both in subsection 2 below.
`
`NOTE: This section of the Application Data Sheet is ONLY reviewed and processed with the INITIAL filing of an
`application. After the initial filing of an application, an Application Data Sheet cannot be used to provide or rescind
`authorization for access by a foreign lP office(s). Instead, Form PTO/SB/39 or PTO/SB/69 must be used as appropriate.
`
`
`
`1. Authorization to Permit Access by a Foreign Intellectual Property Office(s)
`
`
`A. Priority Document Exchange (PDX) - Unless box A in subsection 2 (opt-out of authorization) is checked, the
`undersigned hereby grants the USPTO authority to provide the European Patent Office (EPO), the Japan Patent Office
`(JPO), the Korean Intellectual Property Office (KIPO), the State Intellectual Property Office of the People’s Republic of
`China (SIPO), the World Intellectual Property Organization (WIPO), and any other foreign intellectual property office
`participating with the USPTO in a bilateral or multilateral priority document exchange agreement in which a foreign
`application claiming priority to the instant patent application is filed, access to: (1) the instant patent application-as-filed
`and its related bibliographic data, (2) any foreign or domestic application to which priority or benefit is claimed by the
`instant application and its related bibliographic data, and (3) the date of filing of this Authorization. See 37 CFR 1.14(h)
`(1)-
`
`
`B. Search Results from U.S. Application to EPO - Unless box B in subsection 2 (opt—out of authorization) is checked,
`the undersigned hereby grants the USPTO authority to provide the EPO access to the bibliographic data and search
`results from the instant patent application when a European patent application claiming priority to the instant patent
`application is filed. See 37 CFR 1.14(h)(2).
`
`The applicant is reminded that the EPO’s Rule 141(1) EPC (European Patent Convention) requires applicants to submit a
`copy of search results from the instant application without delay in a European patent application that claims priority to
`the instant application.
`
`2. Opt-Out of Authorizations to Permit Access by a Foreign Intellectual Property Office(s)
`
`A. Applicant DOES NOT authorize the USPTO to permit a participating foreign IP office access to the instant
`D application-as—filed.
`If this box is checked, the USPTO will not be providing a participating foreign IP office with
`any documents and information identified in subsection 1A above.
`
`|:|
`
`B. Applicant DOES NOT authorize the USPTO to transmit to the EPO any search results from the instant patent
`application. If this box is checked, the USPTO will not be providing the EPO with search results from the instant
`application.
`NOTE: Once the application has published or is othenNise publicly available, the USPTO may provide access to the
`application in accordance with 37 CFR 1.14.
`
`EFS Web 2.2.12
`
`10
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`10
`
`

`

`PTOIAIAI14 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`U.S. Patent and Trademark Office; US. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`
`Application Data Sheet 37 CFR 1.76
`Application Number
`
`
`Attorney Docket Number
`A3226.10005US49
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`Title of Invention
`
`Applicant Information:
`
`
`Providing assignment information in this section does not substitute for compliance with any requirement of part 3 of Title 37 of CFR
`to have an assignment recorded by the Office.
`
`
`1
`Applicant
`If the applicant is the inventor (or the remaining joint inventor or inventors under 37 CFR 1.45), this section should not be completed.
`The information to be provided in this section is the name and address of the legal representative who is the applicant under 37 CFR
`1.43; or the name and address of the assignee, person to whom the inventor is under an obligation to assign the invention, or person
`who otherwise shows sufficient proprietary interest in the matter who is the applicant under 37 CFR 1.46. If the applicant is an
`applicant under 37 CFR 1.46 (assignee, person to whom the inventor is obligated to assign, or person who otherwise shows sufficient
`proprietary interest) together with one or more joint inventors, then the joint inventor or inventors who are also the applicant should be
`identified in this section.
`
`Legal Representative under 35 U.S.C. 117
`
`Joint Inventor
`
`Person to whom the inventor is obligated to assign.
`
`Person who shows sufficient proprietary interest
`
`If applicant is the legal representative, indicate the authority to file the patent application, the inventor is:
`
`
`
`
`
`
`Name of the Deceased or Legally lncapacitated Inventor:
`
`If the Applicant is an Organization check here.
`
`IX
`
`Mailing Address Information For Applicant:
`
`Address 1-30 FIFTH AVENUE, SUITE 2000
`
`AddressZ
`
`
`
`Email Address
`
`Additional Applicant Data may be generated within this form by selecting the Add button.
`
`Assignee Information including Non-Applicant Assignee Information:
`
`
`Providing assignment information in this section does not substitute for compliance with any requirement of part 3 of Title
`37 of CFR to have an assignment recorded by the Office.
`
`
`EFS Web 2.2.12
`
`11
`
`11
`
`

`

`PTOIAIAI14 (11-15)
`Approved for use through 0413012017. OMB 0651-0032
`US. Patent and Trademark Office; US. DEPARTMENT OF COMMERCE
`Under the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it contains a valid OMB control number.
`
`Attorney Docket Number A3226.10005US49
`Application Data Sheet 37 CFR 1.76
`Application Number
`
`
`
`Title of Invention
`
`Neridronic Acid for Treating Complex Regional Pain Syndrome
`
`
`
`Assignee 1
`Complete this section if assignee information, including non—applicant assignee information, is desired to be included on the patent
`application publication. An assignee—applicant identified in the "Applicant Information" section will appear on the patent application
`publication as an applicant. For an assignee—applicant, complete this section only if identification as an assignee is also desired on the
`patent application publication.
`Remove
`
`
`
`
`If the Assignee or Non-Applicant Assignee is an Organization check here.
`|:|
`
`Given Name
`
`Middle Name
`
`Family Name
`
`
`
`selecting the Add button.
`
`
`Mailing Address Information For Assignee including Non-Applicant Assignee:
`
`
`
`Phone Number
`
`Fax Number
`
`Email Addre

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