Pharmaceutical composition for the treatment of disorders of non-human mammals

[0001] This application claims priority to U.S. Patent Application Serial No. 60/330,550 (filed Oct. 24, 2001) and to European Patent Application EP 01 123 700.5, filed Oct. 3, 2001.

[0002] The present invention relates generally to the treatment of disorders, in particular cancer, innon-human mammals, particularly to the treatment of mammary tumors in dogs.

[0003] Cancer of the mammary gland in the dog has shown to be approximately as common as it is in humans. Mammary tumors are the most common tumors of the female dog, and also the most common malignant ones (Walter et al., 1997; Walter and Schwegler, 1992; Bonnet et al., 1997).

[0004] Presently, in the treatment of canine mammary tumors, the surgical removal of the tumor is the method of choice. If surgery is done early in the course of this disease, the cancer can, in most cases, be totally eliminated in over 50% of the cases showing a malignant form of cancer.

[0005] While the effectiveness of radiation therapy for the treatment of dogs has not been thoroughly researched, several human anti-cancer drugs such as doxorubicin and actinomycin have been used in dogs. Also, some anti-hormonal drug regimens are being tested in dogs.

[0006] It was an object of the invention to provide new pharmaceutical compositions for the treatment of disorder, in particular cancers, in non-human mammals, in particular for the treatment of mammary tumors in dogs.

[0007] Modjtahedi and Dean (1994) have shown that excess EGFR (EGF receptor, Epidermal growth factor receptor) activity directly contributes to tumor cell transformation. Due to this finding, overexpressed growth factor receptors with tyrosine kinase activity, e.g. EGFR, have been recognized as promising targets for tumor therapy in humans (Woodburn, 1999; Levitzky, 1999; Klohs et al., 1997).

[0008] Consequently, chemical compounds that inhibit the tyrosine kinase activity of the growth factor receptors, antibodies directed to the extracellular domain of a growth factor receptor or the growth factors (or active fragments thereof) themselves have been suggested for the therapy of human cancers (Woodburn, 1999).

[0009] Davies and Chamberlin (1996) and Levitzky (1994), report that small molecules, which are selective for the EGFR and have the ability to inhibit the intracellular kinase domain of the EGFR, are capable of reverting the aberrant enzymatic activity of the EGFR in tumor cells. An example of a substance, which belongs to the class of pyrimido-pyrimidines, is BIBX1382: 4-((3-chloro-4-fluoro-phenyl)amino)-6-(1-methyl-4-piperidinyl-amino)-pyrimido(5,4d)pyrimidine).

[0010] It was shown that the EGFR is present in canine mammary tumors and correlates with other receptors, e.g. the estrogen receptor (Nerurkar et al., 1987). Although it was shown that mammary tumors express receptors that bind EGF the sequence of the canine EGFR was not known.

[0011] To solve the problem underlying the present invention, based on the knowledge about aberrant tyrosine kinase receptor activity in humans and the inhibition thereof in human cancer therapy, the utility of tyrosine kinase receptor inhibitors for the therapy of certain non-human mammalian cancers, in particular for the therapy of mammary tumors of the dog, was assessed.

[0012] To this end, in a first step, the canine EGF receptor was cloned and sequenced.

[0013] It was found that the human and the canine EGFR exhibit a high degree of identity. Therefore, in a next step, it was tested whether inhibitors of the human EGF receptor are capable of inhibiting the canine EGF receptor and may thus be used in the therapy of cancers with aberrant expression of this receptor.

[0014] In the experiments of the present invention, it was found that a tyrosine kinase receptor inhibitor that has been suggested for the treatment of human malignancies, is effective for inhibiting canine mammary tumors.

[0015] Therefore, the present invention relates to a pharmaceutical composition for the treatment of a disorder of a non-human mammal, which is associated with an aberrant activity of one or more tyrosine kinase receptors, wherein said pharmaceutical composition contains, as the active ingredient, one or more substances that inhibit the aberrant activity of said tyrosine kinase receptor(s).

[0016] In a preferred embodiment, the pharmaceutical composition is used for the treatment of tumors of epithelial origin, like adenocarcinoma, squamous cell carcinoma and carcinoma. Representatives of these tumor types are adenocarcinoma of the mammary gland, squamous cell carcinoma of the head and neck, trichoepithelioma of the skin, epulis fibromatosa (oral cavity), carcinoma of the bladder or urinary tract, transitional cell carcinoma of the bladder or urinary tract, Leydig cell tumors, Seminoma, Sertoli cell tumors.

[0017] Most preferably, the pharmaceutical composition is used for the treatment of mammary tumors, either of epithelial origin like adenocarcinoma of the mammary gland or of malign and benign mixed tumors of the mammary gland.

[0018] The pharmaceutical composition of the invention is also useful for the treatment of adenoma.

[0019] In a preferred embodiment, the pharmaceutical composition of the invention is used for the therapy of tumors in dogs, in particular mammary tumors, however, it is also useful for the treatment of tumors of other mammals. Since the kinase domains of the EGFRs in various mammals have shown to exhibit 100% identity on the amino acid level, the pharmaceutical composition of the invention can be applied to other animals, e.g. cats, provided there is a therapeutic need and provided the tyrosine kinase receptor that is to be inhibited, in particular the EGFR, has a high degree of identity with the corresponding human receptor. Preferably, the composition can be used for the treatment of animals whose tyrosine kinase receptor, in particular the EGFR, has an identity of 100% in the ATP binding pocket, more preferably, an identity of 100% in the entire kinase domain. The identity of the tyrosine kinase receptor domains between the animal of interest and man, or another mammal whose tyrosine kinase receptor has been cloned and sequenced, can be readily determined by cloning the receptor, as described for the canine EGFR in Example 1.

[0020] In the present invention aberrant activity of the tyrosine kinase receptor, in particular the EGFR, in tumor cells, in particular in those of epithelial origin, is defined as a) overexpression of the EGFR from the gene, b) expression of the EGFR from the amplified gene, c) expression of the EGFR from a mutated version of the gene, or d) increased sensitivity of tumor cells to the inhibition of EGFR signaling (it has been suggested that tumor cells may have an increased sensitivity to the inhibition of their major receptor tyrosine kinase's pathway).

[0021] In a preferred embodiment, the active substance is an inhibitor of a class I tyrosine kinase receptor.

[0022] In a particularly preferred embodiment, the active substance is an EGF receptor inhibitor.

[0023] Since the EGF receptor was shown to be present in the majority of canine mammary tumor samples (Nerurkar et al., 1987), it can serve as a biochemical marker for canine mammary tumors. Based on the sequence of the canine EGFR, immunohistochemistry or Northern Blot analysis can be used as diagnostic tools for detection of EGF receptor overexpression in canine tumor tissue samples. This allows for prediction and monitoring of the therapeutic benefit of an EGF receptor inhibitor therapy.

[0024] HER2 expression, besides expression of other receptor tyrosine kinases, has been shown to be causally involved in breast cancer (Baselga and Mendelsohn, 1997). Aberrant expression of HER2, like EGFR, in advanced breast cancer correlates with poor prognosis, and the anti-HER2 antibody trastuzumab (Herceptin) is being considered as one of the most promising therapeutic agents for the treatment of breast cancer.

[0025] Earp et al., 1995, have shown that members of the tyrosine kinase class I receptors can form heterodimers (e.g. between EGFR and HER2). Dimerization is the initial step in tyrosine kinase activation. Furthermore, these authors have shown that sequence homology on the amino acid level between the kinase domains of HER2, HER3 and HER4 and the kinase domain of EGFR is 82%, 59% and 79%, respectively.

[0026] For these reasons, an EGFR inhibitor has the ability not only to inhibit signaling through an EGFR homodimer, but also through EGFR/HER2 or other heterodimers.

[0027] Furthermore, specific inhibition of HER2, alone or in combination with inhibition of EGFR, provides a therapy that covers a broader spectrum of tumors.

[0028] Therefore, in another preferred embodiment, the active ingredient is an inhibitor of a tyrosine kinase receptor selected from HER2, HER3 and HER4, preferably HER2, e.g. the anti-HER2-antibody trastuzumab (Herceptin) or a specific HER2 inhibitor as described in U.S. Pat. No. 5,721,237; the active ingredient may also be a combination of any of these inhibitors with an EGFR inhibitor.

[0029] In analogy with the canine EGFR, the canine HER2, or the canine HER3 or HER4 is cloned and sequenced to confirm the homology between the human and the canine proteins.

[0030] In the preferred embodiment, compounds useful as the active ingredient in the pharmaceutical composition of the invention are inhibitors of the corresponding human tyrosine kinase receptors, e.g. the human EGFR.

[0031] Examples of EGFR low molecular weight inhibitors have been described by Strawn and Shawver, 1998, and McMahon et al., 1998. Examples of useful tyrosine kinase inhibitors are also described in, inter alia, EP 682 027, EP 564409 (4-(4-Methylpiperazin-1-ylmethyl)-N-(4-methyl-3-(4-(3-pyridyl)pyrimidin-2-ylamino)phenyl)benzamide; Glivec) WO 95/19970, WO 96/07657, WO 96/33980, e.g. N-(3-chloro-4-fluorophenyl)-7-methoxy-6-3-(4-morpholinyl)propoxy-4-chinazolinamine (ZD-1839; Iressa); WO 96/30347, e.g. N-(3-ethinylphenyl)-6,7-bis(2-methoxyethoxy)-4-chinazolinamine (CP 358774); WO 97/38983, e.g. N-(4-(3-(chloro-4-fluoro-phenylamino-7-(3-morpholine-4-yl-propoxy)-chinazoline-6-yl)-acrylamiddihydrochloride (CI 1033, PD 183805); WO 97/02266 (phenylaminopyrrolopyrimidine; PKI-166); examples of protein kinase inhibitors are also given in the article by Mc Mahon et al., 1998 and Fry, 2000.

[0032] Among the tyrosine kinase inhibitors known in the art, ATP site-directed inhibitors are particularly useful in the present invention.

[0033] Preferably, the inhibitor is a pyrimido-pyrimidine.

[0034] In a particularly preferred embodiment, the pyrimido pyrimidine is 4-((3-chloro-4-fluoro-phenyl)amino)-6-(1-methyl-4-piperidinyl-amino)-pyrimido(5,4d)pyrimidine (which is the compound BIBX1382 used in the Examples).

[0035] The tyrosine kinase inhibitor may be administered either on its own or in conjunction with one or more other active substances. For example, a compound specifically inhibiting a certain member of a class I tyrosine kinase receptor may be combined with an inhibitor of another representative of that receptor class. Alternatively, or in addition, the tyrosine kinase inhibitor(s), e.g. low molecular compounds or antibodies that interfere with receptor function, e.g. the HER2 inhibitor Herceptin, or the EGFR inhibiting antibody C225, may be used in conjunction with pharmacologically active compounds acting through other therapeutic principles, in particular with other anti-tumor therapeutic agents. Examples are combinations with inhibitors of angiogenesis, e.g. Neovastat, Thalodomid), topoisomerase inhibitors (e.g. etoposide), mitosis inhibitors (e.g. vinblastin), compounds which interact with nucleic acids (e.g. cis-platin, cyclophosphamide, adriamycin), hormone antagonists (e.g. tamoxifen), inhibitors of metabolic processes (e.g. 5-FU, gemcitabine etc.), Cox-2 inhibitors like celecoxib or rofecoxib, cytokines (e.g. interferons), antibodies, etc.

[0036] The pharmaceutical composition of the invention may be administered by the intravenous, subcutaneous, intramuscular, intrarectal, intraperitoneal or intranasal route, by inhalation or transdermally or orally.

[0037] The tyrosine kinase inhibitors are generally used in doses of 0.01-100 mg/kg of body weight, preferably 0.1-15 mg/kg. For administration, the compounds are formulated with one or more conventional inert carriers and/or diluents, e.g. with corn starch, lactose, glucose, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, water, water/ethanol, water/glycerol, water/sorbitol, water/polyethyleneglycol, propyleneglycol, stearylalcohol, carboxymethylcellulose or fatty substances such as hard fat or suitable mixtures thereof in conventional galenic preparations such as plain or coated tablets, capsules, powders, suspensions, solutions, sprays or suppositories. Application of the pharmaceutical composition of the invention, optionally containing, in addition to the tyrosine kinase receptor inhibitor, one or more other active compounds acting according to the therapeutic principles defined above, or combined with another composition containing such compound(s), may also be combined with radiation therapy.

[0038] The invention concerns a pharmaceutical composition for the treatment of a disorder of a non-human mammal, which is associated with an aberrant activity of one or more tyrosine kinase receptors, wherein said pharmaceutical composition contains, as the active ingredient, one or more substances that inhibit the aberrant activity of the tyrosine kinase receptor(s) of said non-human mammal.

[0039] The invention particularly concerns such a pharmaceutical composition for the treatment of tumors of epithelial origin.

[0040] The invention further concerns such pharmaceutical compositions for use in the treatment of tumors of the dog.

[0041] The invention further concerns all of the above such pharmaceutical compositions for use in the treatment of mammary tumors.

[0042] The invention further concerns the all of the above such pharmaceutical compositions wherein the active ingredient is an inhibitor of a class T tyrosine kinase receptor, and especially wherein the active ingredient is a compound that blocks the ATP binding site in the kinase domain of the tyrosine kinase receptor. The invention further concerns such pharmaceutical compositions wherein the active ingredient is an inhibitor of the Epidermal Growth Factor Receptor (EGFR).

[0043] The invention further concerns all such pharmaceutical compositions, wherein the active ingredient is a compound that inhibits the aberrant activity of the corresponding human receptor.

[0044] The invention further concerns all such pharmaceutical compositions, wherein the inhibitor is a pyrimido-pyrimidine, and especially wherein the inhibitor is 4-((3-chloro-4-fluoro-phenyl)amino)-6-(1-methyl-4-piperidinyl-amino)-pyrimido(5,4d)pyrimidine).

[0045] The invention further concerns all such pharmaceutical compositions, wherein the active ingredient is an inhibitor of HER2, and especially wherein the HER2 inhibitor is trastuzumab.

[0046] The invention further concerns all such pharmaceutical compositions, wherein the active ingredient is a combination of an EGFR inhibitor and a HER2 inhibitor. The invention further concerns all such pharmaceutical compositions, wherein the EGFR inhibitor is 4-((3-chloro-4-fluoro-phenyl)amino)-6-(1-methyl-4-piperidinyl-amino)-pyrimido(5,4d)pyrimidine). The invention further concerns all such pharmaceutical compositions, wherein the HER2 inhibitor is trastuzumab.

[0047] The invention further concerns the use of a compound that has the ability to inhibit the aberrant expression of a class I tyrosine kinase receptor in humans for the preparation of a pharmaceutical composition for the treatment of a disorder of a non-human mammal. The invention further concerns such use wherein the disorder is a tumor of epithelial origin. The invention further concerns such use wherein the tumor is a mammary tumor. The invention further concerns such use wherein the non-human mammal is a dog. The invention further concerns such use wherein the compound is an EGFR inhibitor (especially, wherein the EGFR inhibitor is 4-((3-chloro-4-fluoro-phenyl)amino)-6-(1-methyl-4-piperidinyl-amino)-pyrimido(5,4d)pyrimidine). The invention further concerns such use wherein the compound is a HER2 inhibitor, or a combination of an EGFR inhibitor and a HER2 inhibitor.

[0048] The invention further concerns the use of a compound that has the ability to inhibit the aberrant expression of a class I tyrosine kinase receptor in humans for the preparation of a pharmaceutical composition for the treatment of a non-human mammal (especially a dog) whose receptor has, at least in the ATP binding pocket, an identity of 100% with the corresponding human receptor on the amino acid level.

[0049] FIG. 1: Strategy for cloning the canine EGFR

[0050] FIG. 2: Expression of the EGFR in various canine cell lines (Northern Blot)

[0051] FIG. 3: Inhibition of the proliferation of cells in culture by the EGFR inhibitor BIBX1382 (³H-Thymidin proliferation assay)

[0052] FIGS. 4 and 5: Effect of the EGFR inhibitor BIBX1382 on tumor growth in nude mice

[0053] FIG. 6: Detection of the canine EGF receptor by immunohistochemical staining of paraffin sections of canine mamma-adenocarcinomas with a human EGFR-antibody

[0054] FIG. 7: Detection of EGFR on the cellular level by cytospin analysis

[0055] Having now generally described the invention, the same will be more readily understood through reference to the following examples, which are provided by way of illustration, and are not intended to be limiting of the present invention, unless specified.

[0056] For the design of the strategy to clone the canine EGF receptor the major part of the intracellular domain, the whole transmembrane and a small part of the extracellular domain of the human EGFR-sequence were used.

[0057] a) Preparation of RNA

[0058] The cell line CCL-34 was purchased from ATCC. It was derived from a kidney of an apparently normal adult female dog. It was cultured in T25, T75 or T175 tissue culture bottles (Greiner) at 37 C. and 5% CO₂. The medium was Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 10% fetal calf serum (FCS, PAA), non-essentiell amino acids (GIBCO BRL) and a standard complement of antibiotics (penicillin/streptomycin, GIBCO BRL). Cultures were split with trypsin EDTA (GIBCO BRL) when they were subconfluent. The split ration was 1:2 to 1:10.

[0059] The day before RNA preparation was performed, the cells were split with a ratio of 1:2. The next day the cells were lysed directly in the culture dish by adding TRIzol Reagent (GIBCO BRL) and the RNA was isolated using the protocol provided with the reagent. After isolation the amount of RNA was measured with a photometer and the RNA was stored at 80 C.

[0060] b) First Strand cDNA Synthesis

[0061] cDNA synthesis of lug CCL-34 RNA was done by using Superscript II Rnase H Reverse Transcriptase (GIBCO BRL) according to the standard protocol provided with the components. As a control, GAPDH and -Actin PCR were performed.

[0062] GAPDH-primer: SEQ ID NO:15(sense)

[0063] SEQ ID NO:16 (antisense)

[0064] -Actin-primer: SEQ ID NO:17 (sense)

[0065] SEQ ID NO:18(antisense)

[0066] The PCR was run for a total of 35 cycles at the following temperatures and times: 95 C. (30 seconds) and 58 C. (1 minute 30 seconds). The GAPDH PCR resulted in a 229 bp band and the -Actin in a 430 bp fragment on the agarose gel.

[0067] c) Primers and PCR Reactions

[0068] Next, three overlapping PCR primer pairs were designed to encompass the major part of the intracellular domain, the whole transmembrane and a small part of the extracellular domain of the human EGFR-sequence (the cloning strategy and the fragments are depicted in FIG. 1):

[0069] Fragment 1: SEQ ID NO:3(Fltest, sense)

[0070] SEQ ID NO:4(R1test, antisense)

[0071] Fragment 2: SEQ ID NO:5 (F2,sense)

[0072] SEQ ID NO:6 (R2, antisense)

[0073] Fragment 3: SEQ ID NO:7(F3, sense)

[0074] SEQ ID NO:8(R3, antisense)

[0075] The PCR for fragment 1 was run for a total of 35 cycles at the following temperatures and times: 95 C. (30 seconds), 56 C. (30 seconds) and 72 C. (1 minute). This PCR resulted in the fragment 1 with the length of 594 bp. To produce fragment 2 the PCR was run for a total of 40 cycles at the following temperatures and times: 95 C. (30 seconds), 58 C. (30 seconds) and 72 C. (1 minute). Fragment 2 showed a length of 800 bp on the agarose gel. Fragment 3 was amplified in a PCR reaction with a total of 35 cycles at following temperatures and times: 95 C. (30 seconds), 59 C. (30 seconds) and 72 C. (1 minute). The resulting fragment had a length of 800 bp pairs.

[0076] d) Subcloning of the PCR Fragments and Transformation

[0077] After the PCR reactions the resulting fragments were cloned into the TA-vector-system. The ligation and the transformation was done by using the protocol provided with the TA-vector system components. Blue-white selection was performed, the white colonies contain plasmids with an insert.

[0078] e) Isolation of Plasmids

[0079] The white colonies were picked from the plates and inoculated in LB-Ampicillin medium over night at 37 C. and 225 rpm. The bacteria suspension was taken and the plasmids were isolated using a standard protocol for alkaline lysis. After ethanol precipitation the plasmid-DNA was dissolved in water. Control restriction digests were performed using the restriction enzymes Spe I and Eco RV (Promega). The vectors and inserts were analysed on an agarose gel to check the length of the fragments 1, 2 and 3.

[0080] f) Sequencing Procedures

[0081] With those plasmids that contained inserts with the right length PCR for sequencing was performed. The three primer pairs Fltest/R1test, F2/R2 and F3/R3 (see c)) were again used for these PCR reactions which were run for a total of 25 cycles at the following temperatures and times: 96 C. (30 seconds), 50 C. (15 seconds) and 60 C. (4 minutes). The PCR products were precipitated with ethanol, washed, air-dried and sequenced.

[0082] g) Comparison of the Nucleotide and Amino Acid Sequences

[0083] The comparison between the achived three fragments and the human EGFR-mRNA-sequence was done by using the computer program Megalign.

[0084] h) Cloning of the 5-End of the Canine EGF-Receptor

[0085] For the cloning of the 5-end of the canine EGF-receptor the SMART (Switch mechanism at 5-end of RNA templates) cDNA synthesis technology was used. SMART cDNA synthesis started with total RNA of the cell line CCL34.

[0086] Following primers were used for this method:

[0087] SEQ ID NO:19 (oligo(dT))

[0088] SEQ ID NO:20 (cDNA-ON)

[0089] SEQ ID NO:21 (R1b)

[0090] SEQ ID NO:22 (PCR-ON)

[0091] cDNA synthesis was performed using oligo(dT) and cDNA-ON primers according to a standard protocol. After this synthesis, a PCR reaction was carried out with the primers R1b and PCR-ON. The PCR was run for 30 cycles at the following temperatures and times: 94 C. (30 seconds) and 68 C. (3 minutes). The PCR product was analysed on an agarose gel, which was then used for Southern Blotting. The blotting onto nylon membrane was done by using a standard protocol. Fragment 1 from the canine EGF-receptor was labeled and the membrane was hybridized over night. Again, a PCR reaction was performed with these primers and analysed on gel. According to the bands, that appeared after scanning the blot, the bands were cut out of the gel. The DNA was isolated, ligated into the TA-vector and transformed into one shot competent cells using the protocol provided with the TA-vector-system. After plasmid isolation with alkaline lyses the inserts in the plasmids were sequenced.

[0092] Tables 1 and 2 show the sequence comparison of the subcloned fragments and the human EGFR-sequence, tables 3 and 4 show the comparison of the complete EGFR-sequences, or the kinase domains respectively, between different species.

TABLE 1
Homology Between The Canine And Human EGFR Sequence
	similarity index	similarity index
fragment	in DNA-sequence	in amino acid sequence
1	85.9%	90.4%
2	91.5%	99.3%
3	86.7%	87.9%

[0093]

TABLE 2
Comparison Of The DNA And Amino Acid Level Of Various
Fragments From Domains Of The Human And Canine EGFR
		similarity index
fragment	domain	DNA level	amino acid level
1	kinase domain	91.5%	100.0%
2	kinase domain	92.3%	100.0%
2	Mg-ATP binding site (1)	100.0%	100.0%
2	Mg-ATP binding site (2)	100.0%	100.0%
2	PI3K	100.0%	100.0%

[0094]

TABLE 3
Comparison Of The EGFR Sequences Between
Different Species
	DNA level	amino acid level
	rat/mice:	87.6%	95.6%
	canine/rat:	79.1%	90.4%
	canine/mice:	81.9%	90.1%

[0095]

TABLE 4
Comparison Of The EGFR Kinase Domains Between Different
Species, Based On The Articles By Ullrich et al., 1984;
Peth et al., 1990; Luetteke et al., 1994.
	DNA-sequence
	sequence	amino acid
	human/mice:	86.8%	100%
	human/rat:	88.1%	100%
	human/canine:	90.7%	100%

[0096] As can be seen, homology on the DNA level between human and dog is the highest; there are no differences on the amino acid level.

[0097] To analyse if the EGF receptor is expressed in different tumor cell lines (see below) and whether there is a correlation between its expression and an inhibition of cell proliferation by BIBX1382, an expression analysis on Northern Blot and by PCR and a ³H-Thymidin proliferation assay were performed:

[0098] a) EGFR Expression Analysis by Northern Blot

[0099] The cell lines SLU-1 (Hellmn, 1992 and 1993; van Leeuwen et al., 1996), SLU-2 (Hellmn, 2000), SLU-3 (Hellmn, 1992 and 1993), SLU-4 (Hellmn, 1992 and 1993; van Leeuwen et al., 1996) and T5 were cultured in T25 or T75 tissue culture bottles at 37 C. and 5% CO₂. The medium was RPMI (Gibco cat 21980-32) supplemented with 10% FCS (PAA) and standard antibiotics. Cultures were split at ratios of between 1:3 and 1:10.

[0100] The tumor cells T5 were isolated from a fresh canine mixed mamma-tumor. The tumor was cut down into small pieces, picked up in medium and was run through a cell strainer. The flow through was centrifuged for ten minutes at 200-250 g, resuspended and again centrifuged. Cells were suspended in medium and were cultured in a T25 tissue culture bottle. Afterwards the cells were cultured in T25 or T75 tissue culture bottles (Greiner) at 37 C. and 5% CO₂. The medium was RPMI supplemented with 10% fetal calf serum (FCS, PAA), non-essential amino acids (GIBCO BRL) and a standard complement of antibiotics (penicillin/streptomycin, GIBCO BRL). Cultures were split with Trypsin-EDTA (GIBCO BRL) when they were subconfluent. The split ration was 1:2. The tumor cell lines p114 (van Leeuwen et al., 1996) and SH1b (van der Burg et al., 1989; van Leeuwen et al., 1996) were also cultured in T25, T75 or T175 tissue culture bottles (Greiner) at 37 C. and 5% CO₂. The medium was again Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 10% fetal calf serum (FCS, PAA), non-essentiell amino acids (GIBCO BRL) and a standard complement of antibiotics (penicillin/streptomycin, GIBCO BRL). Cultures were split with Trypsin-EDTA (GIBCO BRL) when they were subconfluent. The split ration was 1:5 to 1:10.

[0101] The cell lines CCL-34, CRL-6230 and CR1-6234 were purchased from ATCC, they were grown as described for cell line CCl-34 in Example 1.

[0102] To determine the level of EGFR expression, mRNA from all samples was prepared and polyA mRNA was isolated. These RNAs were separated by gel electrophoresis and Northern Blot analysis was performed. By using the expression level of the house-keeping gene GAPDH the EGFR expression levels of all cell lines except SH1b were determined.

[0103] EGF receptor expression of all used cell lines was examined on Northern Blots. For these Northern Blots fragment 3 (see FIG. 1) was used as a probe for the EGF receptor and GAPDH as the control.

[0104] Specifically, 1 g polyA RNA was separated on agarose gel, blotted onto nylon membranes and hybridized using a standard protocol. Hybridisation was always performed using the probe of interesta probe selective for the EGFRin combination with the house-keeping gene GAPDH. To detect the canine EGF-receptor the fragment 3 of the receptor was used. The same amount of both DNA probes was labeled with the same batch of ³²P-ATP and the same amount of incorporated cpm per ml was used for the hybridisation (410⁶ cpm/ml). The evaluation of the blots was done using a phosphoimager (Molecular Dynamics).

[0105] The cell line SLU-1 showed the highest expression of EGF receptor, SLU-2, SLU-4 and CCL-34 had lower, but detectable, expression. The last four cell lines, SLU-3, p114 (van Leeuwen et al., 1996), CRL-6230 and CRL-6234, did not express detectable levels of EGF receptor.

[0106] b) Expression Analysis Using RT-PCR

[0107] From the mRNA of the cell lines SH1b, p114, CCL-34, SLU-1 and A431 (as a positive control) cDNA was made using a standard protocol. With these cDNAs PCR was performed using the primer pair F3 (SEQ ID NO:7) and R3 (SEQ ID NO:8).

[0108] The PCR for was run with different numbers of cycles (12, 16, 20, 24, 28 cycles) at the following temperatures and times: 95 C. (30 seconds), 59 C. (30 seconds) and 72 C. (1 minute). The PCR fragments were analysed at an agarose gel (the Northern Blot is shown in FIG. 2).

[0109] c) ³H-Thymidin Proliferation Assay

[0110] The ability of BIBX1382 to inhibit the proliferation of cells in culture was tested with a ³H-Thymidin proliferation assays. This assay was performed with three tumor cell lines (SLU-1, SLU-4, SH1b) and a normal cell line (CRL-6234).

[0111] A pilot experiment with 500 to 12.000 cells per well in a 96-well plate in the presence of different concentrations of FCS (0% to 10%) was performed. After different proliferation times (24 h, 48 h, 72 h and 96 h), 10 l ³H-Thymidin (1:100 in PBS) were added, after incubation the plate was frozen, then thawed and the cells were harvested. The ³H-Thymidin incorporation rate was determined. For subsequent experiments the conditions (number of cells, FCS concentration) were chosen that showed the highest uptake of ³H-Thymidin. To determine a possible growth inhibitory effect of the inhibitor BIBX1382 on the cell lines, different concentrations (5 nM-10000 nM) of the inhibitor were used. Again ³H-Thymidin was added, after incubation the plate was frozen, then thawed and the cells were harvested. The ³H-Thymidin incorporation rate was determined in dependance of the concentration of inhibitor.

[0112] Cells of the cell line SLU-1 were inhibited in their proliferation rate by BIBX1382. The proliferation rate of SLU-4 cells was not affected by BIBX1382. For the cell line CRL-6234, BIBX1382 had toxic effects at high concentrations, at lower concentration CRL-6234 cells were not inhibited.

[0113] The ³H-Thymidin proliferation assay was also done with the tumor cell line SH1b. This cell line was inhibited in its proliferation time by BTBX1382 (FIG. 3).

[0114] Effect of the EGFR Inhibitor BIBX1382 on Tumor Growth in Nude Mice

[0115] The cell line SLU-1 was cultured as described in Example 2. For use in tumor experiments, cells were trypsinised, washed and suspended in PBS5% FCS at 10⁷ cells/ml. 210⁶ SLU-1 cells were injected into 40 nude mice (5-10 week-old female Hsd:NMRI-nu/nu purchased from Harlan, The Netherlands for the in vivo experiment with BIBX1382.

[0116] When tumors were established and had reached diameters of approximately 5 mm as measured with a calliper, mice were randomly distributed into groups of 10 animals so that each tumor size was equally represented in each treatment group. The time span between cell injection and randomisation/start of treatment was sixteen days. Starting ten days after randomisation, mice were treated once daily (at 24 hour intervals) with various doses of the test compound. Administration was intragastral using a gavage needle (Infusionskanule Olive A, Acufirm, No. 14 64 11-1). Therefore, the compound was suspended in 2.5% aqueous HP-beta-CD (hydroxy-propyl-beta-cyclodextrine)/1% aqueous Natrosol (hydroxyethylcellulose). Control mice received the vehicle only. The administration volume was 2.5 to 10 ml per kg mouse body weight. The solutions were proportioned and kept at 20 C.

[0117] The low dose group received 25 mg/kg/day (day 10-22) and 50 mg/kg/day (day 23-46) of BIBX1382; whereas the high dose group received 50 mg/kg/day (day 10-22), 70 mg/kg/day (day 23-30) and 100 mg/kg/day (day 31-46) of BIBX1382. The control group was treated with vehicle only.

[0118] Tumors were measured three times a week (Monday, Wednesday and Friday) with a calliper. Volumes in mm³ were then calculated according to the formula (tumor volumelength*diameter²*/6). To monitor side effects of treatment, mice were inspected daily for abnormalities and weighed three times (Monday, Wednesday and Friday) a week.

[0119] Tumor volumes were expressed as mean absolute tumor volumes in mm³ and plotted over days of treatment.

[0120] The specific relative tumor volumes (T/C %, i.e. the mean relative tumor volumes of groups of compound-treated tumors in % of the mean relative tumor volume of the vehicle-treated control tumors: T/C %100*mean V_rel compound-treated/mean V_rel vehicle-treated) were determined on the day following the final day of treatment.

[0121] Experiments were usually terminated when vehicle control mice had to be killed because of large tumor sizes (1200 to 1700 mm³).

[0122] As shown in FIGS. 4 and 5, BIBX1382 influenced SLU-1 tumor growth at all tested doses in the tumor inhibiting experiment. The volumes of all 10 tumors in the vehicle control mice increased (on average >60-fold over 7 weeks, albeit at different individual rates and with frequent intervals of growth interruption). The low dose group was treated with 25 mg/kg/day BIBX1382 from day 10 to day 22. During this time period 9 of 10 tumors showed a 8-fold increase in size, whereas the volume of one tumor did not change at all. From day 23 to day 46 this low dose group was treated with 50 mg/kg/day BIBX1382. All 10 tumors grew during this period showing a 3-6-fold increase in size. Looking at the whole period of treatment (day 10-46), the tumor size increased on average 35-fold.

[0123] The treatment of the high dose group started with a dose of 50 mg/kg/day from day 10 to day 22. During this period all ten tumors increased in size and showed at maximum a 5-6-fold increase. After increasing the dose to 70 mg/kg/day (day 23-30) the tumors grew by about 2-fold. From day 31 to day 46 the dose was raised to 100 mg/kg/day and the size of the tumors increased about 1.5-1.9-fold. Looking at the whole period of treatment again, the tumors increased in size on average 20-fold.

[0124] These responses of SLU-1 tumors to BTBX1382 are also reflected by T/C %-values (Table 5). After treatment of the low dose group with 25 mg/kg/day (day 10-22) the T/C-value was 78%. Raising the dose to 50 mg/kg/day (day 23-46) led to a decrease of the T/C-value to 62%. BIBX1382 treatment in the high dose group started with a dose of 50 mg/kg/day (day 10-22) leading to a T/C-value of 52%. Increasing the doses to 70 mg/kg/day (day 23-30) resulted in a T/C-value of 53%. After raising the dose to 100 mg/kg/day (day 31-46) the T/C-value decreased to 38%. Statistical analysis revealed that the T/C values of both dose groups (low and high) were significantly lower (standard T-test) compared to the vehicle control group.

[0125] The plasma levels of BIBX1382 determined after the last compound administration are shown in Table 6. These data demonstrated that plasma levels of approximately 4000 mmol/l at 2 hours after oral compound administration are able to reduce the tumor growth rate of SLU-1 as subcutaneous xenograft to a T/C value of 38%. With plasma levels of 3000 mmol/l at 2 hours after oral compound administration a reduction of the growth rate to a T/C value of 62% was achieved.

[0126] The results of the tumor inhibiting experiment are presented as plots of the mean absolute tumor volumes by group. T/C % along with the evaluations of tumor responses are shown in Table 5.

TABLE 5
Response Of SLU-1 Tumors To BIBX1382
		Daily	Duration
Ex-		oral	of
periment		dose	treatment	T/C	Tumor
1	Group	mg/kg4	days2	%3	response
DMT05/00	1	25 50	13, 24	62	partial
					growth
					suppression
	2	50 70 100	13, 8, 16	38	growth
					suppression
	control	vehicle	37	100
1Start of treatment was 16 days after injection of 2 106 SLU-1 cells in experiment DMT05/00.
2The first number indicates the length of the treatment period for the first dose followed by the figures indicating the length of treatment at the following doses.
3Determined on the day following the final day of treatment of the vehicle control group (day 47).
4Doses were raised to obtain a maximum difference between the BIBX1382-treated and vehicle-treated mice.

[0127]

TABLE 6
Plasma Levels Of Bibx1382 Of The Treated Mice
	50 mg/kg BIBX1382		100 mg/kg BIBX1382
	mean		mean
time h *	nmol/l	/	nmol/l	/
2	3172	1085	4159	1063
6	2852	930	4094	2174
24	394	161	591	252
* Hours after last compound administration on day 46 of experiment.

[0128] a) Histological Examination of Paraffin Sections of Canine Mamma-Adenocarcinomas with Anti-EGFR Antibodies

[0129] Immunohistochemical stainings were performed with paraffin sections of canine mamma-adenocarcinomas in order to determine whether the canine EGF receptor can be detected with a human EGFR-antibody.

[0130] Specific staining on the paraffin sections of canine mamma-adenocarcinomas was done with a human EGFR antibody (Santa Cruz cat sc-03). The sections were stained using a standard protocol for the streptavidin-biotin-complex method.

[0131] The paraffin sections of 22 different tumors were stained with this antibody. In two cases the sections could not be analysed. All other cases showed a specific staining of the EGF receptor. The levels of EGF receptor expression of the tumor cells are comparable to those of, for example, normal skin cells. This means that the EGF receptor is not overexpressed in these tumor samples, but it is expressed in 91% of the tested samples (FIG. 6).

[0132] b) Detection of EGFR on the Cellular Level

[0133] The cytospin analysis was performed with the cell lines SLU-1, SLU-2, SLU-3, SLU-4, T5, p114, SH1b and CCL-34. 10.000 cells were centrifuged (10 minutes, 800 rpm) onto a slide and fixed with paraformaldehyd. The staining was done using the streptavidin-biotin-complex method used for the staining of the paraffin-sections.

[0134] The cell lines SLU-1, CCL-34 and SLU-4 showed a high expression of the EGF-receptor, SH1b, SLU-2 and SLU-3 had lower expression. On the cytospin of the cell lines p114 only a few cells were stained, on the slide of T5 no cell was stained (FIG. 7). These data show that this antibody can be used for the analysis of canine tumor biopsies.

[0135] For these experiments, the same methods are applied as for cloning of the canine EGFR described in Example 1.

[0136] For cloning the canine HER2 receptor, following a strategy similar to that described for the canine EGFR in Example 1, the major part of the intracellular domain, the whole transmembrane and a small part of the extracellular domain are used as templates (Coussens et al; 1985). Three PCR primer pairs (SEQ ID NO:9 and SEQ ID NO:10; SEQ ID NO:11 and SEQ ID NO:12; SEQ ID NO:13 and SEQ ID NO:14) are used to encompass these defined area of the human sequence.

[0137] The positions of the primers in the human HER2-receptor sequence are the following:

[0138] SEQ ID NO: 9: 1800-1819, SEQ ID NO: 10: 3140-3124;

[0139] SEQ ID NO: 11 2807-2828, SEQ ID NO: 12 3783-3764;

[0140] SEQ ID NO: 13 3458-3481, SEQ ID NO: 14 4481-4458.

[0141] Messenger RNA from normal canine cell lines (e.g. CRL-6230, CRL-6234 and CCL-34) is isolated and transcribed into cDNA. These cDNA samples are used in different PCR reactions with the three primer pairs defined above. The resulting three PCR-fragments from the different primer pairs are subcloned into the TA vector system and sequenced. Cloning of the HER2 receptor can be completed using the SMART-PCR technology, as described in Example 1.

[0142] a) Coated Tablets Containing 75 mg of BIBX1382

[0143] 1 tablet core contains:

	BIBX1382	75.0	mg
	calcium phosphate	93.0	mg
	corn starch	35.5	mg
	polyvinylpyrrolidone	10.0	mg
	hydroxypropylmethylcellulose	15.0	mg
	magnesium stearate	1.5	mg
		230.0	mg

[0144] Preparation:

[0145] BIBX1382 is mixed with calcium phosphate, corn starch, polyvinylpyrrolidone, hydroxypropylmethylcellulose and half the specified amount of magnesium stearate. Blanks 13 mm in diameter are produced in a tablet-making machine and these are then rubbed through a screen with a mesh size of 1.5 mm using a suitable machine and mixed with the rest of the magnesium stearate. This granulate is compressed in a tablet-making machine to form tablets of the desired shape.

	Weight of core:	230	mg
	Diameter:	9	mm, convex

[0146] The tablet cores thus produced are coated with a film consisting essentially of hydroxypropylmethylcellulose. The finished film-coated tablets are polished with beeswax.

[0147] Weight of coated tablet: 245 mg.

[0148] b) Tablets Containing 100 mg of BIBX1382

[0149] Composition:

[0150] 1 tablet contains:

	BIBX1382	100.0	mg
	lactose	80.0	mg
	corn starch	34.0	mg
	polyvinylpyrrolidone	4.0	mg
	magnesium stearate	2.0	mg
		220.0	mg

[0151] Preparation:

[0152] BIBX1382, lactose and starch are mixed together and uniformly moistened with an aqueous solution of the polyvinylpyrrolidone. After the moist composition has been screened (2.0 mm mesh size) and dried in a rack-type drier at 50 C. it is screened again (1.5 mm mesh size) and the lubricant is added. The finished mixture is compressed to form tablets.

	Weight of tablet:	220 mg
	Diameter:	10 mm, biplanar,
		facetted on both sides and notched
		on side.

[0153] c) Tablets Containing 150 mg of BIBX1382

[0154] Composition:

[0155] 1 tablet contains:

	BIBX1382	150.0	mg
	powdered lactose	89.0	mg
	corn starch	40.0	mg
	colloidal silica	10.0	mg
	polyvinylpyrrolidone	10.0	mg
	magnesium stearate	1.0	mg
		300.0	mg

[0156] Preparation:

[0157] BIBX1382 mixed with lactose, corn starch and silica is moistened with a 20% aqueous polyvinylpyrrolidone solution and passed through a screen with a mesh size of 1.5 mm. The granules, dried at 45 C., are passed through the same screen again and mixed with the specified amount of magnesium stearate. Tablets are pressed from the mixture.

	Weight of tablet:	300	mg
	Diameter:	10	mm, flat

[0158] d) Hard Gelatine Capsules Containing 150 mg of BIBX1382

[0159] 1 capsule contains:

	BIBX1382		150.0	mg
	corn starch (dried)	approx.	180.0	mg
	lactose (powdered)	approx.	87.0	mg
	magnesium stearate		3.0	mg
		approx.	420.0	mg

[0160] Preparation:

[0161] BIBX1382 is mixed with the excipients, passed through a screen with a mesh size of 0.75 mm and homogeneously mixed using a suitable apparatus. The finished mixture is packed into size 1 hard gelatine capsules.

	Capsule filling:	approx. 320 mg
	Capsule shell:	size 1 hard qelatine capsule.

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[0190] All publications and patents mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.

[0191] While the invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications and this application is intended to cover any variations, uses, or adaptations of the invention following, in general, the principles of the invention and including such departures from the present disclosure as come within known or customary practice within the art to which the invention pertains and as may be applied to the essential features hereinbefore set forth.