Claims for Patent: 8,697,080

Summary for Patent: 8,697,080

Title:	Methods and compositions for treatment of human immunodeficiency virus infection with conjugated antibodies or antibody fragments
Abstract:	The present invention concerns methods and compositions for treatment of HIV infection in a subject. The compositions may comprise a targeting molecule against an HIV antigen, such as an anti-HIV antibody or antibody fragment. The anti-HIV antibody or fragment may be conjugated to a variety of cytotoxic agents, such as doxorubicin. In a preferred embodiment, the antibody or fragment is P4/D10. Other embodiments may concern methods of imaging, detection or diagnosis of HIV infection in a subject using an anti-HIV antibody or fragment conjugated to a diagnostic agent. In alternative embodiments, a bispecific antibody with at least one binding site for an HIV antigen and at least one binding site for a carrier molecule may be administered, optionally followed by a clearing agent, followed by administration of a carrier molecule conjugated to a therapeutic agent.
Inventor(s):	Goldenberg; David M. (Mendham, NJ), Chang; Chien-Hsing (Downingtown, PA), Rossi; Edmund A. (Morris Plains, NJ), McBride; William J. (Boonton, NJ)
Assignee:	Immunomedics Inc. (Morris Plains, NJ)
Application Number:	13/675,422
Patent Claims:	1. A pharmaceutical composition comprising a P4/D10 antibody or fragment thereof against an HIV surface envelope antigen, the antibody or fragment conjugated to a cytotoxic drug, wherein exposure to the conjugated antibody or fragment is effective to reduce HIV infection or to limit the intercellular transmission of HIV to uninfected cells when administered to a subject. 2. The composition of claim 1, wherein the subject is a human subject. 3. The composition of claim 1, wherein the conjugated antibody or fragment is a chimeric, humanized or human antibody or fragment. 4. The composition of claim 1, wherein the cytotoxic drug is doxorubicin. 5. The composition of claim 1, wherein the cytotoxic drug is aplidin, azaribine, anastrozole, azacytidine, bleomycin, bortezomib, bryostatin-1, busulfan, calicheamycin, camptothecin, 10-hydroxycamptothecin, carmustine, celebrex, chlorambucil, cisplatin, irinotecan (CPT-11), SN-38, carboplatin, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dactinomycin, daunomycin glucuronide, daunorubicin, doxorubicin, 2-pyrrolinodoxorubicine (2P-DOX), cyano-morpholino doxorubicin, doxorubicin glucuronide, epirubicin glucuronide, estramustine, etoposide, etoposide glucuronide, etoposide phosphate, floxuridine (FUdR), 3',5'-O-dioleoyl-FudR (FUdR-dO), fludarabine, flutamide, fluorouracil, gemcitabine, hydroxyurea, idarubicin, Ifosfamide, L-asparaginase, leucovorin, lomustine, mechlorethamine, melphalan, mercaptopurine, 6-mercaptopurine, methotrexate, mitoxantrone, mithramycin, mitomycin, mitotane, phenyl butyrate, procarbazine, paclitaxel, pentostatin, PSI-341, semustine, streptozocin, tamoxifen, taxanes, taxol, thalidomide, thioguanine, thiotepa, teniposide, topotecan, uracil mustard, velcade, vinblastine, vinorelbine, vincristine or a combination thereof. 6. The composition of claim 1, wherein the antibody or fragment is a bispecific antibody, a bispecific antibody fragment, an scFv, a Fab, a Fab', a F(ab).sub.2, a F(ab').sub.2, an Fv, an sFv, an scFv, an scFv-Fc fusion, a single chain antibody, a diabody, a triabody or a tetrabody. 7. The composition of claim 1, wherein the antibody or fragment is a neutralizing antibody. 8. The composition of claim 1, further comprising a second antibody or fragment thereof, wherein the second antibody or fragment binds to an HIV surface envelope antigen. 9. The composition of claim 8, wherein the second antibody or fragment binds to the same HIV surface envelope antigen as the P4/D10 antibody. 10. The composition of claim 8, wherein the second antibody or fragment binds to a different HIV surface envelope antigen than the P4/D10 antibody. 11. The composition of claim 8, wherein the second antibody or fragment thereof is selected from the group consisting of 4E10, 2F5, 3D6, C37, 1ACY, 1F58, 1GGGC, 2G12 and X5. 12. The composition of claim 1, further comprising an anti-retroviral agent selected from the group consisting of efavirenz, zidovudine, tenofovir, lamivudine, emtricitabine, didanosine, abacavir, stavudine, nevirapine, lopinavir, ritonavir, atazanavir, fosamprenavir, indinavir, nelfinavir and saquinavir. 13. The composition of claim 1, wherein exposure to the conjugated antibody or fragment is effective to reduce HIV infection or to limit the intercellular transmission of HIV to uninfected cells in vivo. 14. The composition of claim 1, wherein the conjugated antibody or fragment thereof is a bispecific antibody or fragment thereof. 15. The composition of claim 14, wherein the bispecific antibody further comprises a second antibody or fragment thereof and the second antibody or fragment thereof binds to a hapten on a targetable construct. 16. The composition of claim 14, wherein the bispecific antibody or fragment comprises at least one scFv, Fab, Fab', F(ab).sub.2, F(ab').sub.2, Fv, sFv, scFv-Fc fusion, single chain antibody, diabody, triabody or tetrabody. 17. The composition of claim 15, wherein the hapten is HSG (histamine-succinyl-glycine) or In-DTPA. 18. The composition of claim 15, wherein the bispecific antibody or fragment comprises one or more 679 antibodies or antibody fragments that bind to HSG. 19. A pharmaceutical composition comprising an antibody or fragment thereof against an HIV surface envelope antigen, the antibody or fragment conjugated to a cytotoxic drug, wherein the antibody or fragment competes for binding to gp120 with the P4/D10 antibody, wherein exposure to the conjugated antibody or fragment is effective to reduce HIV infection or to limit the intercellular transmission of HIV to uninfected cells when administered to a subject. 20. The composition of claim 19, wherein the subject is a human subject. 21. The composition of claim 19, wherein the conjugated antibody or fragment is a chimeric, humanized or human antibody or fragment. 22. The composition of claim 19, wherein the cytotoxic drug is doxorubicin. 23. The composition of claim 19, wherein the cytotoxic drug is aplidin, azaribine, anastrozole, azacytidine, bleomycin, bortezomib, bryostatin-1, busulfan, calicheamycin, camptothecin, 10-hydroxycamptothecin, carmustine, celebrex, chlorambucil, cisplatin, irinotecan (CPT-11), SN-38, carboplatin, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dactinomycin, daunomycin glucuronide, daunorubicin, doxorubicin, 2-pyrrolinodoxorubicine (2P-DOX), cyano-morpholino doxorubicin, doxorubicin glucuronide, epirubicin glucuronide, estramustine, etoposide, etoposide glucuronide, etoposide phosphate, floxuridine (FUdR), 3',5'-O-dioleoyl-FudR (FUdR-dO), fludarabine, flutamide, fluorouracil, gemcitabine, hydroxyurea, idarubicin, ifosfamide, L-asparaginase, leucovorin, lomustine, mechlorethamine, melphalan, mercaptopurine, 6-mercaptopurine, methotrexate, mitoxantrone, mithramycin, mitomycin, mitotane, phenyl butyrate, procarbazine, paclitaxel, pentostatin, PSI-341, semustine, streptozocin, tamoxifen, taxanes, taxol, thalidomide, thioguanine, thiotepa, teniposide, topotecan, uracil mustard, velcade, vinblastine, vinorelbine, vincristine or a combination thereof. 24. The composition of claim 19, wherein the antibody or fragment is a bispecific antibody, a bispecific antibody fragment, an scFv, a Fab, a Fab', a F(ab).sub.2, a F(ab').sub.2, an Fv, an sFv, an scFv, an scFv-Fc fusion, a single chain antibody, a diabody, a triabody or a tetrabody. 25. The composition of claim 19, wherein the antibody or fragment is a neutralizing antibody.

Details for Patent 8,697,080

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Recordati Rare Diseases, Inc.	ELSPAR	asparaginase	For Injection	101063	01/10/1978		2026-05-15
Jubilant Hollisterstier Llc	N/A	positive skin test control-histamine	Injection	103891	03/13/1924		2026-05-15