`
`IN THE UNITED STATES DISTRICT COURT
`FOR THE DISTRICT OF NEW JERSEY
`CAMDEN VICINAGE
`
`Wan—“fl
`
`ASTRAZENECA PHARMACEUTICALS,
`LP, et al.,
`
`Plaintiffs/Counterclaim—
`Defendants,
`
`v.
`
`SANDOZ INC.,
`
`Defendant/Counterclaim~
`Plaintiff.
`
`ASTRAZENECA PHARMACEUTICALS,
`LP, et al.,
`
`Plaintiffs/Counterclaim—
`
`Defendants,
`
`V.
`
`SAGENT PHARMACEUTICALS,
`
`INC.,
`
`Defendant/Counterclaim—
`Plaintiff.
`
`
`ASTRAZENECA PHARMACEUTICALS,
`LP, et al.,
`
`Plaintiffs/Counterclaim—
`
`Defendants,
`
`V.
`
`GLENMARK GENERICS INC., USA,
`
`Defendant/Counterclaim—
`Plaintiff.
`
`
`iiiiiiiiiiiiiiiiiiiiiii
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`iiiiiiiiiiiiiiiiiii| iiiiiiiiii iiiiiiiiiiiiiii
`
`.1
`
`Consolidated Civil Action No.
`i1:14—cv—03547
`
`(RMB/KMW)
`
`ORDER
`
`InnoPharma Exhibit 1010.0001
`
`
`
`Case 1:14-cv-03547-RMB-KMW Document 102 Filed 07/29/15 Page 2 of 4 PageID: 3213
`
`The Court having reviewed the parties’ submissions and
`
`having conducted a Markman hearing,
`
`IT IS ON THIS 29th day of July 2015, ORDERED that the Court
`
`construes the disputed claims as follows:
`
`1.
`
`“[AJdministration to a human in need of such treatment,"
`
`as it appears in the claims of the ’122 and '160 Patents,
`
`and “a human in need of such treatment," as it appears in
`
`the claims of the ’680 and ’139 Patents, require no
`
`construction.
`
`2.
`
`“[F]ulvestrant,” as it appears in the claims of the ’122,
`
`’160,
`
`’680, and ’139 Patents, means “7d—[9—(4,4,5,5,5—
`
`pentafluoropentylsulphinyl)nonyl]oestra—l,3,5(10)—triene~
`
`3,17B—diol,
`
`including pharmaceutically acceptable salts
`
`thereof, and any possible solvates of either thereof ”
`
`3.
`
`“[E]thanol,” as it appears in the claims of the ’122,
`
`’160,
`
`'680, and ’139 Patents, requires no construction.
`
`4.
`
`“[SJufficient amount of a castor oil vehicle,” as it
`
`appears in the claims of the ’122 and '160 Patents, and
`
`“sufficient amount of castor oil vehicle,” as it appears
`
`in the claims of the ’680 and ’139 Patents, will be
`
`reserved for construction until additional expert evidence
`
`is available in the record.
`
`5.
`
`“[WJhereby a therapeutically significant blood plasma
`
`fulvestrant concentration of at least 2.5 ngmld~is
`
`InnoPharma Exhibit 1010.0002
`
`
`
`Case 1:14-cv-03547-RMB-KMW Document 102 Filed 07/29/15 Page 3 of 4 PageID: 3214
`
`attained for at least 2 weeks after injection,” as it
`
`appears in the claims of the ’122 and '160 Patents, means
`
`“the blood plasma fulvestrant concentration of at least
`
`2.5 ngmlfl is achieved and maintained for at least 2
`
`weeks."
`
`6.
`
`“[WJherein the blood plasma fulvestrant concentration is
`
`attained for at least 4 weeks after injection,” as it
`
`appears in the claims of the ’122 Patent, means “the blood
`
`plasma fulvestrant concentration of at least 2.5 ngml4 is
`
`achieved and maintained for at least 4 weeks.”
`
`7.
`
`“[W]herein the blood plasma fulvestrant concentration is
`
`attained for 2 to 5 weeks after injection,” as it appears
`
`in the claims of the '122 Patent, means “the blood plasma
`
`fulvestrant concentration of at least 2.5 ngmld is
`
`achieved and maintained for 2 to 5 weeks.”
`
`8.
`
`“[F]ormulation,” as it appears in the Claims of the ’680
`
`and ’139 Patents, means “pharmaceutical formulation.”
`
`9.
`
`“[W]herein the method achieves a therapeutically
`
`significant blood plasma fulvestrant concentration of at
`
`least 2.5 ngmld-for at least four weeks,” as it appears in
`
`the claims of the ’680 Patent, means “the blood plasma
`
`fulvestrant concentration of at least 2.5 ngmlfl is
`
`achieved and maintained for at least 4 weeks ”
`
`InnoPharma Exhibit 1010.0003
`
`
`
`Case 1:14-cv-03547-RMB-KMW Document 102 Filed 07/29/15 Page 4 of 4 PageID: 3215
`
`10. “[W]herein the therapeutically significant blood plasma
`
`fulvestrant concentration is at least 8.5 ngmlfl,” as it
`
`appears in the claims of the ’680 Patent, means “the blood
`
`plasma fulvestrant concentration of at least 8.5 ngmlq is
`
`achieved and maintained for at least 4 weeks."
`
`11. “[W]herein the method achieves a blood plasma fulvestrant
`
`concentration of at least 2.5 ngmlq for at least two
`
`weeks,” as it appears in the claims of the '139 Patent,
`
`means “the blood plasma fulvestrant concentration of at
`
`least 2.5 ngml4 is achieved and maintained for at least 2
`
`weeks.”
`
`12. “[W]herein .
`
`.
`
`.
`
`the blood plasma fuvlestrant
`
`concentration is attained for at least 4 weeks," as it
`
`appears in the claims of the ’139 Patent, means “the blood
`
`plasma fulvestrant concentration of at least 2.5 ngmld is
`
`achieved and maintained for at least 4 weeks.”
`
`The Court will set forth the bases for the foregoing
`
`construction if such an explanation becomes necessary as the
`
`case progresses.
`
`W
`
`RENEE MARIE BUMB
`UNITED STATES DISTRICT JUDGE
`
`InnoPharma Exhibit 1010.0004
`
`