`
`(12) United States Patent
`Evans et al.
`
`(10) Patent No.:
`
`(45) Date of Patent:
`
`US 8,466,139 B2
`*Jun. 18, 2013
`
`(54) FORMULATION
`
`(56)
`
`References Cited
`
`(75)
`
`Inventors: John R Evans, Macclesfield (GB);
`Rosalind U Grundy, Macclesfield (GB)
`
`(73) Assignee: AstraZenecaAB (SE)
`
`( * ) Notice:
`
`Subject to any disclaimer, the term of this
`patent is extended or adjusted under 35
`U.S.C. l54(b) by 0 days.
`
`This patent is subject to a terminal dis-
`claimer.
`
`(21) Appl.No.: 13/602,667
`
`(22)
`
`Filed:
`
`Sep. 4, 2012
`
`(65)
`
`Prior Publication Data
`
`US 2012/0329766 A1
`
`Dec. 27, 2012
`
`U.S. PATENT DOCUMENTS
`
`2,822,316 A
`2,983,649 A
`3,164,520 A
`3,541,209 A
`RE28,690 E
`4,048,309 A
`4,048,310 A
`4,212,863 A
`4,388,307 A
`4,659,516 A
`4,888,331 A
`5,095,129 A
`5,183,814 A
`
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`
`(Continued)
`FOREIGN PATENT DOCUMENTS
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`4/1985
`0310542 A1
`4/1989
`
`EP
`EP
`
`(Continued)
`OTHER PUBLICATIONS
`
`Related U.S. Application Data
`
`U.S. Appl. No. 13/387,584, filed Jan. 27, 2012, Dimery et al.
`
`(63) Continuation of application No. 12/285,887, filed on
`Oct. 15, 2008, now Pat. No. 8,329,680, which is a
`continuation of application No. 10/872,784, filed on
`Jun. 22, 2004, which is a continuation of application
`No. 09/756,291, filed on Jan. 9, 2001.
`
`(30)
`
`Foreign Application Priority Data
`
`Jan. 10, 2000
`Apr. 12, 2000
`
`(GB) ................................. .. 0000313.7
`(GB) ................................. .. 0008837.7
`
`(51)
`
`(2006.01)
`
`Int. Cl.
`A61K 31/56
`(52) U.S. Cl.
`USPC ......................................... .. 514/177; 514/178
`(58) Field of Classification Search
`USPC ................................................ .. 514/177,178
`See application file for complete search history.
`
`(Continued)
`
`Primary Examiner — San-Ming Hui
`(74) Attorney, Agent, or Firm — Finnegan, Henderson,
`Farabow, Garrett & Dunner LLP
`
`ABSTRACT
`(57)
`The invention relates to a novel sustained release pharmaceu-
`tical formulation adapted for administration by injection con-
`taining the compound 70L-[9-(4,4,5,5,5-pentafluoropentyl-
`sulphinyl)nonyl]oestra-1 ,3 ,5 (1 0)-triene-3 , 1 7 [3-diol,
`more
`particularly to a formulation adapted for administration by
`injection containing the compound 70L-[9-(4,4,5,5,5-pen-
`tafluoropentyl sulphinyl)nonyl] oestra-1 ,3 ,5 (1 0)-triene-3,
`l7[3-diol in solution in a ricinoleate vehicle which addition-
`ally comprises at least one alcohol and a non-aqueous ester
`solvent which is miscible in the ricinoleate vehicle.
`
`20 Claims, 2 Drawing Sheets
`
`
`
`Fulvosu-am(ngplrrnlplain-Ia)
`
`—O—F1Fmmul|lionF(CutoroI)
`-A-r2uwa1z4a
`--0--r:cmuvsuumoI1.1
`
`
`
`|nnoPharma Exhibit 1001.0001
`
`
`
`US 8,466,139 B2
`Page 2
`
`U.S. PATENT DOCUMENTS
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`7/1959
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`1126892
`9/1968
`GB
`1207571
`10/1970
`GB
`1569286
`6/1980
`GB
`43-27327
`11/1992
`JP
`09-208496
`12/1997
`JP
`10-203982
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`JP
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`7/1979
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`5/1995
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`3/1998
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`6/1999
`W0
`W0 03/006064
`1/2003
`W0
`W0 W0 2011/012885
`2/2011
`ZA
`681014
`2/1968
`ZA
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`.
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`|nnoPharma Exhibit 10010002
`
`
`
`US 8,466,139 B2
`Page 3
`
`Lavy, et al., “Pharmacokinetics of clindamycin HCI administered
`intravenously, intramuscularly and subcutaneously to dogs”, J. Vet.
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`
`|nnoPharma Exhibit 10010003
`
`
`
`U.S. Patent
`
`Jun. 18,2013
`
`Sheet 1 012
`
`US 8,466,139 B2
`
`—O—F1 Fonnulation F (Castor oil)
`- -A - F2 Miglyol 312-N
`- - O - -F3 Caslsorlsesame oil 1:1
`
`A
`
`Fulvestrant(ngpermlplasma)
`
`Figure 1
`
`|nnoPharma Exhibit 1001.0004
`
`
`
`U.S. Patent
`
`Jun. 18,2013
`
`Sheet 2 of2
`
`US 8,466,139 B2
`
`FLOW DIAGRAM OF MANUFACTURING
`
`Ingredients/Components
`
`process
`
`Fulvestrant
`Alcohol
`
`
`BeuzylAlcohol
`
`STAGE 1; DISSOLUTION OF
`——> ACTIVE AGENT
`
`¢
`
`Benzyl Benzoate
`
`A} STAGE 22 MIX
`
`,
`
`_._> STAGE 3: MAKE TO
`
`I
`
`STAGE 4: STERILE FILTRATION
`
`(0.2 pm)
`INTO BULK RECEIVING VESSEL
`
`I
`
`STAGE 5: STERILE (0.2p.m)
`IN-LINE FILTRATION
`
`STAGt6: ASEPTICFILLING,
`
`AND STOPPERING
`
`STAG?7: VISUAL
`
`INSPECTION
`
`Figure 2
`
`|nnoPharma Exhibit 1001.0005
`
`
`
`1
`FORMULATION
`
`CROSS-REFERENCE TO RELATED
`APPLICATIONS
`
`This application is a Continuation application of U.S.
`patent application No. 12/285,887, filed on Oct. 15, 2008,
`which claimed benefit of U.S. patent application Ser. No.
`10/872,784, filed Jun. 22, 2004, now U.S. Pat. No. 6,774,122
`which claims benefit of U.S. patent application Ser. No.
`09/756,291, filed Jan. 9, 2001 now U.S. Pat. No. 7,456,160
`which claims the benefit of Great Britain Application No.
`0008837.7 filed Apr. 12, 2000 and Great Britain Application
`No. 0000313.7 filed Jan. 10, 2000, all five applications are
`incorporated herein by reference in their entireties.
`
`BACKGROUND OF THE INVENTION
`
`1. Field of the Invention
`
`The invention relates to a novel sustained release pharma-
`ceutical formulation adapted for administration by injection
`containing the compound 70¢-[9-(4,4,5,5,5-pentafluoropen-
`tylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17[3-diol.
`2. Description of the Related Art
`Oestrogen deprivation is fundamental to the treatment of
`many benign and malignant diseases of the breast and repro-
`ductive tract. In premenopausal women, this is achieved by
`the ablation of ovarian function through surgical, radiothera-
`peutic, or medical means, and, in postmenopausal women, by
`the use of aromatase inhibitors.
`
`An alternative approach to oestrogen withdrawal is to
`antagonise oestrogens with antioestrogens. These are drugs
`that bind to and compete for oestrogen receptors (ER) present
`in the nuclei of oestrogen-responsive tissue. Conventional
`nonsteroidal antioestrogens, such as tamoxifen, compete effi-
`ciently for ER binding but their effectiveness is often limited
`by the partial agonism they display, which results in an
`incomplete blockade of oestrogen-mediated activity (Furr
`and Jordan 1984, May and Westley 1987).
`The potential for nonsteroidal antioestrogens to display
`agonistic properties prompted the search for novel com-
`pounds that would bind ER with high afiinity without acti-
`vating any of the normal transcriptional hormone responses
`and consequent manifestations of oestrogens. Such mol-
`ecules would be “pure” antioestrogens, clearly distinguished
`from tamoxifen-like ligands and capable of eliciting com-
`plete ablation of the trophic effects of oestrogens. Such com-
`pounds are referred to as Estrogen Receptor-Downregulators
`(E.R.D.). The rationale for the design and testing of novel,
`pure antioestrogens has been described in: Bowler et al 1989,
`Wakeling 1990a, 1990b, 1990c. Wakeli11g and Bowler 1987,
`1 988.
`
`Steroidal analogues of oestradiol, with an alkylsulphinyl
`side chain in the 70. position, provided the first examples of
`compounds devoid of oestrogenic activity (Bowler et al
`1989). One of these, 70L-[9-(4,4,5,5,5-pentafluoropentyl sul-
`phinyl)nonyl]oestra-1,3,5-(10)triene-3,17[3-diol
`was
`selected for intensive study on the basis of its pure oestrogen
`antagonist activity and significantly increased antioestro-
`genic potency over other available antioestrogens. In vitro
`findings and early clinical experience with 7(X-[9-(4,4,5,5,5-
`pentafluoropentylsulphinyl)nonyl]oestra-1 ,3 -5(10)-triene-3,
`17[3-diol have promoted interest in the development of the
`drug as a therapeutic agent for oestrogen-dependent indica-
`tions such as breast cancer and certain benign gynaecological
`conditions.
`
`10
`
`15
`
`20
`
`25
`
`30
`
`35
`
`40
`
`45
`
`50
`
`55
`
`60
`
`US 8,466,139 B2
`
`2
`
`70L-[9-(4,4,5,5,5-Pentafluoropentylsulphinyl)nonyl]
`oestra-1,3-5(10)-triene-3,17[3-diol, or ICI 182,780, has been
`allocated the international non-proprietary name fulvestrant,
`which is used hereinafter. When referring to fulvestrant we
`include pharmaceutically-acceptable salts thereof and any
`possible solvates of either thereof.
`Fulvestrant binds to ER with an afiinity similar to that of
`oestradiol and completely blocks the growth stimulatory
`action of oestradiol on human breast cancer cells in vitro; it is
`more potent and more effective than tamoxifen in this respect.
`Fulvestrant blocks completely the uterotrophic action of
`oestradiol in rats, mice and monkeys, and also blocks the
`uterotrophic activity of tamoxifen.
`Because fulvestrant has none of the oestrogen-like stimu-
`latory activity that is characteristic of clinically available
`antioestrogens such as tamoxifen or toremifene, it may offer
`improved therapeutic activity characterised by more rapid,
`complete, or longer-lasting tumour regression; a lower inci-
`dence or rate of development of resistance to treatment; and a
`reduction of tumour invasiveness.
`
`In intact adult rats, fulvestrant achieves maximum regres-
`sion of the uterus at a dose which does not adversely affect
`bor1e density or lead to increased gor1adotropl1ir1 secretion. If
`also true in humans, these findings could be ofextreme impor-
`tance clinically. Reduced bone density limits the duration of
`oestrogen-ablative treatment for endometriosis. Fulvestrant
`does not block hypothalamic ER. Oestrogen ablation also
`causes or exacerbates hot flushes and other menopausal
`symptoms; fulvestrant will not cause such effects because it
`does not cross the blood-brain barrier.
`
`European Patent Application No. 0 138 504 discloses that
`certain steroid derivatives are effective antioestrogenic
`agents. The disclosure includes information relating to the
`preparation ofthe steroid derivatives. In particular there is the
`disclosure within Example 35 of the compound 70.-[9-(4,4,
`5 ,5 ,5 -pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-
`triene-3,17[3-diol, which compound is specifically named in
`claim 4. It is also disclosed that the compounds of that inven-
`tion may be provided for use in the form of a pharmaceutical
`composition comprising a steroid derivative of the invention
`together with a pharrnaceutically-acceptable diluent or car-
`rier. It is stated therein that the composition can be in a form
`suitable for oral or parenteral administration.
`Fulvestrant shows, along with other steroidal based com-
`pounds, certain physical properties which make formulation
`of these compounds difficult. Fulvestrant is a particularly
`lipophilic molecule, even when compared with other steroi-
`dal compounds, and its aqueous solubility is extremely low at
`around 10 ngml‘1 (this is an estimate from a water/solvent
`mixture solute since measurements this low could not be
`
`achieved in a water only solute).
`Currently there are a number of sustained release inj ectable
`steroidal formulations which have been commercialised.
`
`Commonly these formulations use oil as a solvent and
`wherein additional excipients may be present. Below in Table
`1 are described a few commercialised sustained release
`
`injectable formulations.
`In the formulations within Table 1 a number of different
`
`oils are used to solubilise the compound and additional
`excipients such as benzyl benzoate, benzyl alcohol and etha-
`nol have been used. Volumes of oil needed to solubilise the
`
`steroid active ingredient are low. Extended release is achiev-
`able for periods from 1 to 8 weeks.
`
`|nnoPharma Exhibit 1001.0006
`
`
`
`US 8,466,139 B2
`
`TABLE 1
`
`OIL BASED LONG-ACTING INTRAMUSCULAR INJECTIONS
`
`PRODUCT NAME
`
`STEROID
`
`DOSE
`
`TYPE
`
`COMP’.
`
`SOURCE
`
`OIL
`
`30 mg
`60 mg
`
`Androgen
`
`Organon
`
`Arachis
`
`ABPI Data
`Sheet
`Comp. 1999
`
`60 mg
`100 mg
`250 mgml’1 Progestogen
`
`200 mg
`
`Progestogen
`
`Schering
`HC
`
`AB ’I Data
`Sheet
`Comp. 1999
`Theramax Dic .Vidal
`1999
`
`Castor
`
`Ethyl
`oleate
`
`50 mg
`250 mg
`1.3 mg
`50 mg
`80 mg
`
`Mixed
`
`Theramax Dic . Vidal
`1997
`
`Olive
`
`SUSTANON 100
`
`PROLUTON
`DEPOT
`
`TOCOGESTAN
`
`TROPHOBOLENE
`
`NORISTERAT
`
`BENZO-
`GYNOESTRYL
`PROGESTERONE-
`RETARD
`GRAVIBINAN
`
`PARABOLAN
`
`DELESTROGEN
`
`DELALUTIN
`
`Testosterone proprionate
`Testosterone
`3henylproprionate
`Testosterone isocaproate
`Testosterone decanoate
`Iydroxy progesterone
`iexanoate
`
`Iydroxy progesterone
`enantate
`’rogesterone
`OL-TOCOphC1‘Ol
`istrapronicate
`Nandrolone undecanoate
`Iydroxyprogesterone
`ieptanoate
`Norethisterone
`oenanthoate
`
`Estradiol
`iexahydrobenzoate
`Iydroxy progesterone
`caproate
`Estradiol17-[5-valerate
`Iydroxyprogesterone
`caproate
`Trenbolone
`
`:stradiol
`valerate
`
`7-Hydroxy
`3rogesterone
`
`200 mg
`
`Contraceptive
`
`Schering
`HC
`
`5 mg
`
`Estradiol
`
`Roussel
`
`250 mgml’1 Progestogen
`
`Pharlon
`
`5 mgml" Mixed
`250 mgml’1
`
`Schering
`HC
`
`AB ’I Data
`Sheet
`Comp. 1999
`Dic .Vidal
`199 8
`Dic .Vidal
`1 999
`Dic .Vidal
`1995
`
`76 mg
`
`Androgen
`
`Negma
`
`20 mgml’1 Estradiol
`40 mgml’1
`
`BMS
`
`250 mgml’1 Progestrogen
`
`DMS
`
`Castor
`
`Arachis
`
`Castor
`
`Castor
`
`Arachis
`
`Castor
`
`Castor
`
`Dic .Vidal
`1997
`J. P13Il'H.
`Sci (1964)
`53(8) 891
`J. P13Il'H.
`Sci. (1964)
`53(8) 891
`DOSE
`
`’ {OD JCT NAVIE
`
`BZBZ
`
`BZOH
`
`EtOH
`
`SJSTANON 100
`’ {OL JTON
`DEPOT
`TOCOGESTAN
`T{OP IOBOLENE
`NORISTERAT
`33NZO-
`GYNOESTRYL
`’ {OG ESTERONE—
`{ETA {D
`GKAV BINAN
`’ARA 3OLAN
`3 ELESTROGEN
`
`D ELA 3UTIN
`
`up to
`46%
`*40%
`45%
`YES
`
`YES
`
`YES
`
`78%
`58%
`YES
`
`0.1 ml
`
`75 mg
`20%
`40%
`YES
`
`45 mg
`2%
`2%
`up to
`2%
`
`DOSING
`
`1 ml
`1 or 2 ml
`2 ml
`1 ml
`1 ml
`1 ml
`
`1 or 2 ml
`
`1 or 2 ml
`1.5 ml
`
`3 weeks
`1 week
`<1 week
`15 to 30 days
`8 weeks
`1 week
`
`1 week
`
`1-2 weeks
`2 weeks
`
`BZBZ = benzylbenzoate
`BZOH = benzylalcohol
`EtOH = ethanol
`Dict. Vidal = Dictionnaire Vidal
`% are w/v and
`*approximate as measured directly from a single sample
`
`described which comprises 50 mg of fulvestrant, 400 mg of
`benzyl alcohol and sufficient castor oil to bring the solution to
`a volume of 1 ml. Manufacture at a commercial scale of a
`formulation as described in U.S. Pat. No. 5,183,814 will be
`complicated by the high alcohol concentration. Therefore,
`there is a need to lower the alcohol concentration in fulves-
`trant formulations whilst preventing precipitation of fulves-
`trant from the formulation.
`
`SUMMARY OF THE INVENTION
`
`55
`
`60
`
`65
`
`containing the compound 70¢-[9-(4,4,5,5,5-pentafluoropen-
`tylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17[3-diol, more
`particularly to a formulation adapted for administration by
`injection containing the compound 70t-[9-(4,4,5,5,5-pen-
`tafluoropentyl sulphinyl)nonyl] oestra-1 ,3 ,5 (1 0)-triene-3,
`17[3-diol in solution in a ricinoleate vehicle which addition-
`ally comprises at least one alcohol and a non-aqueous ester
`solvent which is miscible in the ricinoleate vehicle.
`
`BRIEF DESCRIPTION OF THE DRAWING
`
`The invention relates to a novel sustained release pharma-
`ceutical formulation adapted for administration by injection
`
`FIG. 1 shows the release profile in vivo of the four formu-
`lations from the second part of Table 4 below, and shows the
`
`|nnoPharma Exhibit 10010007
`
`
`
`US 8,466,139 B2
`
`5
`effect ofthe fixed oil component on fulvestrant plasma profile
`over five days following intramuscular administration in rab-
`bits.
`
`FIG. 2 shows a process flow diagram associated with the
`Formulation Example.
`
`5
`
`DETAILED DESCRIPTION OF THE INVENTION
`
`Table 2 shows the solubility of fulvestrant in a number of
`different solvents.
`
`10
`
`6
`Therefore, we present as a feature of the invention a phar-
`maceutical formulation comprising fulvestrant (preferably
`fulvestrant is present at 3-10% w/v, 4-9% w/v, 4-8% w/v,
`4-7% w/v, 4-6% w/v and most preferably at about 5% w/v) in
`a ricinoleate vehicle, a pharmaceutically acceptable non-
`aqueous ester solvent, and a pharmaceutically acceptable
`alcohol wherein the formulation is adapted for intramuscular
`administration and attaining a therapeutically significant
`blood plasma fulvestrant concentration for at least 2 weeks.
`Another feature of the invention is a pharmaceutical for-
`mulation comprising fulvestrant in which the formulation is
`adapted for intra-muscular injection into a human and which
`is capable after injection of attaining a therapeutically signifi-
`cant blood plasma fulvestrant concentration for at least 2
`weeks.
`
`Further features of the invention include a pharmaceutical
`formulation adapted for intra-muscular injection comprising
`fulvestrant, 30% or less weight of a pharmaceutically-accept-
`able alcohol per volume of formulation, at least 1% weight of
`a pharrnaceutically-acceptable non-aqueous ester solvent
`miscible in a ricinoleate vehicle per volume of formulation
`and a sufficient amount of a ricinoleate vehicle so as to pre-
`pare a formulation which is capable after injection of attain-
`ing a therapeutically significant blood plasma fulvestrant
`concentration for at least 2 weeks.
`
`Further features of the invention include a pharmaceutical
`formulation adapted for intra-muscular injection comprising
`fulvestrant; 35% (preferably 30% and ideally 25%) or less
`weight of a pharmaceutically-acceptable alcohol per volume
`of formulation, at least 1% (preferably at least 5% or ideally
`10%) weight of a pharmaceutically-acceptable non-aqueous
`ester solvent miscible within a ricinoleate vehicle per volume
`offormulation and a sufiicient amount of a ricinoleate vehicle
`
`15
`
`20
`
`25
`
`30
`
`TABLE 2
`
`SOLUBILITY OF FULVESTRANT
`
`SOLVENT
`Water
`Arachis oil
`Sesame oil
`Castor oil
`Miglyol 810
`Miglyol 812
`Ethyl oleate
`Benzyl benzoate
`Isopropyl myristate
`Span 85 (surfactant)
`Ethanol
`Benzyl Alcohol
`
`SOLUBILITY
`(mgml’1 at 25° C.)
`0.001
`0.45
`0.58
`20
`3.06
`2.72
`1.25
`6.15
`0.80
`3.79
`>200
`>200
`
`As can be seen fulvestrant is significantly more soluble in
`castor oil than any of the other oils tested. The greater solvat-
`ing ability of castor oil for steroidal compounds is known and
`is attributed to the high number of hydroxy groups of ricino-
`leic acid, which is the major constituent of the fatty acids
`within the triglycerides present in castor oil—see (Riffkin et.
`al. J. Pharm. Sci., (1964), 53, 891).
`However, even when using the best oil based solvent, cas-
`tor oil, we have found that it is not possible to dissolve
`fulvestrant in an oil based solvent alone so as to achieve a high
`enough concentration to dose a patient in a low volume injec-
`tion and achieve a therapeutically significant release rate. To
`achieve a therapeutically significant release rate the amount
`of fulvestrant needed would require the formulation volume
`to be large, at least 10 ml. This requires the doctor to inject an
`excessively large volume of formulation to administer a dose
`significantly high enough for human therapy.
`Currently guidelines recommend that no more than 5 mls
`of liquid is injected intramuscularly iii a single injection.
`Pharmacologically active doses required for a 1 month long
`acting depot formulation of fulvestrant is around 250 mg.
`Therefore, when dissolved injust castor oil, fulvestrant would
`need to be administered in at least 10 ml of castor oil.
`
`The addition of organic solvents in which fulvestrant is
`freely soluble, and which are miscible with castor oil, may be
`used, such as an alcohol. With the addition of high concen-
`trations of an alcohol concentrations of >50 mgml‘1 of ful-
`vestrant in a castor oil formulation is achievable, thereby
`giving an injection volumes of <5 ml—see Table 3 below. We
`have surprisingly found that the introduction of a non-aque-
`ous ester solvent which is miscible in the castor oil and an
`
`alcohol surprisingly eases the solubilisation of fulvestrant
`into a concentration of at least 50 mgml‘1—see Table 3
`below. The finding is surprising since the solubility of fulves-
`trant in non-aqueous ester solvents—see Table 2 above—is
`significantly lower than the solubility of fulvestrant in an
`alcohol. The solubility of fulvestrant is also lower in non-
`aqueous ester solvents than is the solubility of fulvestrant in
`castor oil.
`
`35
`
`so as to prepare a formulation of at least 45 mgml‘1 of ful-
`vestrant.
`
`For the avoidance of any doubt when using the term %
`weight per volume of formulation for the constituents of the
`formulation we mean that within a unit volume of the formu-
`
`lation a certain percentage ofthe constituent by weight will be
`present, for example a 1% weight per volume formulation
`will contain within a 100 ml volume of formulation 1 g ofthe
`constituent. By way of further illustration
`
`% ofx by weight per
`volume of formulation
`
`weight of x in
`1 ml of formulation
`
`30%
`20%
`10%
`5%
`1%
`
`300 mg
`200 mg
`100 mg
`50 mg
`10 mg
`
`Preferred pharmaceutical formulations ofthe invention are
`as described above wherein:
`1. The total volume ofthe formulation is 6 ml, or less, and the
`concentration of fulvestrant is at least 45 mgml‘1.
`2. The total amount of fulvestrant in the formulation is 250
`
`mg, or more, and the total volume of the formulation is 6
`ml, or less.
`3. The total amount offulvestrant in the formulation is 250 mg
`and the total volume of the formulation is 5-5.25 ml.
`
`It is appreciated that in the formulation an excess of for-
`mulation may be included to allow the attendant physician or
`care giver to be able to deliver the required dose. Therefore,
`when a 5 ml dose is required it would be appreciated that an
`excess of up to 0.25 ml, preferably up to 0.15 ml will also be
`
`40
`
`45
`
`50
`
`55
`
`60
`
`65
`
`|nnoPharma Exhibit 1001.0008
`
`
`
`US 8,466,139 B2
`
`8
`It will be understood by the skilled person that the phar-
`maceutically-acceptable non-aqueous ester solvent will be of
`a quality that it will meet pharmacopoeial standards (such as
`described in the US, British, European and Japanese pharma-
`copoeias).
`Preferred combinations of pharmaceutically-acceptable
`alcohol and pharmaceutically-acceptable non-aqueous ester
`solvent in the formulation are set out below:
`
`10
`
`Pha.1rnaceutically-acceptable
`alcohol(% w/v)
`
`Pharmaceutically-acceptable non-aqueous
`ester (% w/v)
`
`7
`present in the formulation. Typically the formulation will be
`presented in a vial or a prefilled syringe, preferably a prefilled
`syringe, contaimng a unit dosage of the formulation as
`described herein, these being further features ofthe invention.
`Preferred concentrations of a pharmaceutically-acceptable
`alcohol present in any of the above formulations are; at least
`3% w/v, at least 5% w/v, at least 7% w/v, at least 10% w/v, at
`least 11% w/v, at least 12% w/v, at least 13% w/v, at least 14%
`w/v, at least 15% w/v and, preferably, at least 16% w/v.
`Preferred maximal concentrations of pharmaceutically-ac-
`ceptable alcohol present in the formulation are; 28% w/v or
`less, 22% w/v or less and 20% w/v or less. Preferred ranges of
`pharmaceutically-acceptable alcohol present in any of the
`above formulations are selected from any minimum or maxi-
`mum value described above and preferably are; 3-35% w/v,
`4-35% w/v, 5-35% w/v, 5-32% w/v, 7-32% w/v, 10-30% w/v,
`12-28% w/v, 15-25% w/v, 17-23% w/v, 18-22% w/v and
`ideally 19-21% w/v.
`The pharmaceutically-acceptable alcohol may consist of
`one alcohol or a mixture of two or more alcohols, preferably
`a mixture of two alcohols. Preferred pharmaceutically-ac-
`ceptable alcohols for parenteral administration are ethanol,
`benzyl alcohol or a mixture of both ethanol and benzyl alco-
`hol, prcfcrably thc cthanol and bcnzyl alcohol are prcscnt in
`the formulation in the same w/v amounts. Preferably the
`formulation alcohol contains 10% w/v ethanol and 10% w/v
`
`benzyl alcohol.
`The pharmaceutically-acceptable non-aqueous ester sol-
`vent may consist of one or a mixture of two or more pharma-
`ceutically-acceptable non-aqueous ester solvents, preferably
`just one. A preferred pharrnaceutically-acceptable non-aque-
`ous ester solvent for parenteral administration is selected
`from benzyl benzoate, ethyl oleate, isopropyl myristate, iso-
`propyl palmitate or a mixture of any thereof.
`The ricinoleate vehicle should preferably be present in the
`formulation in a proportion ofat least 30% weight per volume
`ofthe formulation, ideally at least 40% or at least 50% weight
`per volume of formulation.
`It will be understood by the skilled person that the phar-
`maceutically-acceptable alcohol will be of a quality such that
`it will meet pharmacopoeial standards (such as are described
`in the US, British, European and Japanese pharmacopoeias)
`and as such will contain some water and possibly other
`organic solvents, for example ethanol in the US Pharma-
`copeia contains not less than 94.9% by volume and not more
`than 96.0% by volume ofethanol when measured at 15 .56° C.
`Dehydrated alcohol in the US Pharmacopeia contains not less
`than 99.5% ethanol by volume when measured at 15.56° C.
`Preferred concentrations of the pharmaceutically-accept-
`able non-aqueous ester solvent present in any of the above
`formulations are; at least 5% w/v, at least 8% w/v, at least 10%
`w/v, at least 11% w/v, at least 12% w/v, at least 13% w/v, at
`least 15% w/v, at least 16% w/v, at least 17% w/v, at least 18%
`w/v, at least 19% w/v and at least 20% w/v. Preferred maximal
`concentrations ofthe pharrnaceuti