Claims for Patent: 8,679,767

Summary for Patent: 8,679,767

Title:	Multiple reaction monitoring LC-MS/MS method to detect therapeutic antibodies in animal samples using framework signature peptides
Abstract:	Methods are disclosed to detect, characterize, measure, and quantitate human and humanized antibodies, and their conjugates, present in pre-clinical animal biological samples, including plasma/serum and tissue samples.
Inventor(s):	Kaur; Surinder (Lafayette, CA), Saad; Ola (Walnut Creek, CA), Xu; Keyang (Belmont, CA)
Assignee:	Genentech, Inc. (South San Francisco, CA)
Application Number:	13/469,332
Patent Claims:	1. A method of detecting human or humanized antibodies comprising the steps of: (a) treating a biological sample comprising a human or humanized antibody with a digestive enzyme to form a digested antibody sample, wherein the biological sample is serum, plasma, tissue, or cells from an animal selected from a cynomolgus monkey, a rat and a mouse that has been treated with said human or humanized antibody; and (b) analyzing the digested antibody sample by mass spectrometry to detect one or more human framework peptides, wherein the human framework peptides comprise one or more sequences selected from SEQ ID NOS. 1-8: TABLE-US-00015 GPSVFPLAPSSK SEQ ID NO: 1 STSGGTAALGCLVK SEQ ID NO: 2 TPEVTCVVVDVSHEDPEVK SEQ ID NO: 3 FNWYVDGVEVHNAK SEQ ID NO: 4 VVSVLTVLHQDWLNGK SEQ ID NO: 5 ALPAPIEK SEQ ID NO: 6 GFYPSDIAVEWESNGQPENNYK SEQ ID NO: 7 TTPPVLDSDGSFFLYSK. SEQ ID NO: 8 2. The method of claim 1 wherein the digestive enzyme is trypsin. 3. The method of claim 1 further comprising contacting the digested antibody sample with an affinity capture media or chromatography adsorbent and eluting said enriched digested antibody sample. 4. The method of claim 1 further comprising contacting the biological sample with an affinity capture media or chromatography adsorbent and eluting said enriched biological sample then treating the enriched biological sample with the digestive enzyme. 5. The method of claim 3 or 4 wherein the affinity capture media is bead-supported Protein A/G. 6. The method of claim 3 or 4 wherein the chromatography adsorbent is a solid-phase extraction (SPE) adsorbent. 7. The method of claim 1 wherein the biological sample is serum or plasma. 8. The method of claim 1 wherein the concentration of digested antibody sample is measured. 9. The method of claim 1 wherein the human or humanized antibody binds to one or more tumor-associated antigens or cell-surface receptors selected from (1)-(36): (1) BMPR1B (bone morphogenetic protein receptor-type IB); (2) E16 (LAT1, SLC7A5); (3) STEAP1 (six transmembrane epithelial antigen of prostate); (4) 0772P (CA125, MUC16); (5) MPF (MPF, MSLN, SMR, megakaryocyte potentiating factor, mesothelin); (6) Napi3b (NAPI-3B, NPTIIb, SLC34A2, solute carrier family 34 (sodium phosphate), member 2, type II sodium-dependent phosphate transporter 3b); (7) Sema 5b (F1110372, KIAA1445, Mm.42015, SEMASB, SEMAG, Semaphorin 5b Hlog, sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B); (8) PSCA hlg; (9) ETBR (Endothelin type B receptor); (10) MSG783 (RNF124, hypothetical protein F1120315); (11) STEAP2 (HGNC 8639, IPCA-1, PCANAP1, STAMP1, STEAP2, STMP, prostate cancer associated gene 1, prostate cancer associated protein 1, six transmembrane epithelial antigen of prostate 2, six transmembrane prostate protein); (12) TrpM4 (BR22450, F1120041, TRPM4, TRPM4B, transient receptor potential cation channel, subfamily M, member 4); (13) CRIPTO (CR, CR1, CRGF, CRIPTO, TDGF1, teratocarcinoma-derived growth factor); (14) CD21 (CR2 (Complement receptor 2) or C3DR (C3d/Epstein Barr virus receptor) or Hs 73792); (15) CD79b (CD79B, CD79.beta., IGb (immunoglobulin-associated beta), B29); (16) FcRH2 (IFGP4, IRTA4, SPAP1A (SH2 domain containing phosphatase anchor protein 1a), SPAP1B, SPAP1C); (17) HER2 (ErbB2); (18) NCA; (19) MDP; (20) IL20R.alpha.; (21) Brevican; (22) EphB2R; (23) ASLG659; (24) PSCA; (25) GEDA; (26) BAFF-R (B cell-activating factor receptor, BLyS receptor 3, BR3); (27) CD22 (B-cell receptor CD22-B isoform); (28) CD79a (CD79A, CD79.alpha., immunoglobulin-associated alpha); (29) CXCR5 (Burkitt's lymphoma receptor 1); (30) HLA-DOB (Beta subunit of MHC class II molecule (Ia antigen)); (31) P2X5 (Purinergic receptor P2X ligand-gated ion channel 5); (32) CD72 (B-cell differentiation antigen CD72, Lyb-2); (33) LY64 (Lymphocyte antigen 64 (RP105), type I membrane protein of the leucine rich repeat (LRR) family); (34) FcRH1 (Fc receptor-like protein 1); (35) IRTA2 (FcRH5, Immunoglobulin superfamily receptor translocation associated 2); and (36) TENB2 (putative transmembrane proteoglycan). 10. The method of claim 1 wherein the human or humanized antibody is selected from trastuzumab, ocrelizumab, pertuzumab, anti-PDLL, anti-neuropilin-1, anti-MUC16, rituximab, anti-mesothelin, and anti-LY6E. 11. The method of claim 1 wherein the human or humanized antibody is conjugated to a drug moiety. 12. The method of claim 11 wherein the drug moiety is selected from a maytansinoid, dolastatin, auristatin, calicheamicin, pyrrolobenzodiazepine (PBD), PNU-159682, anthracycline, duocarmycin, vinca alkaloid, taxane, trichothecene, CC1065, duocarmycin, camptothecin, elinafide, and stereoisomers, isosteres, analogs or derivatives thereof.

Details for Patent 8,679,767

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2039-02-26
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2039-02-26
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2039-02-26
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2039-02-26
Genentech, Inc.	PERJETA	pertuzumab	Injection	125409	06/08/2012		2039-02-26