IP Library Granted Patent US 9,260,521
Granted Patent B2
US 9,260,521 · App. 14/045,019 · Granted Feb 16, 2016

Treatment of tumors using specific anti-L1 antibody

Inventors: Daniela Kelm (Steinheim an der Murr, DE); Peter Altevogt (Neckargemuend, DE); Gerhard Moldenhauer (Bad Arolsen, DE); Frank Breitling (Heidelberg, DE); Achim Krueger (Munich, DE); Silke Baerreiter (Weinheim, DE); Sandra Luettgau (Schongau, DE); Ulrich Moebius (Gauting, DE); Yi Li (Wantage, GB); Susanne Sebens (Kiel, DE); Heiner Schaefer (Kiel, DE)
Assignees: MEDIGENE AG; DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFUNG DES OFFENTLICHEN RECHTS
C07K16/2803A61K39/39558A61K45/06A61N5/02A61N5/0613A61N5/10G01N33/57492A61K2039/505A61N2005/0661A61N2005/1087A61N2005/1089C07K2317/24C07K2317/41C07K2317/622C07K2317/73C07K2317/76C07K2317/92C07K2319/30
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Quick Facts
Patent No.
US 9,260,521
App. No.
14/045,019
Granted
Feb 16, 2016
Kind
B2
Abstract

The present invention relates to the anti-L1 monoclonal antibody 9.3 as well as to related antibodies or binding molecules and well as to the uses thereof, especially in tumor treatment.

Claims (25)

1. A purified binding molecule capable of binding L1CAM

(i) comprising the following six CDR sequences RASQDISNYLN (SEQ ID No: 1), YTSRLHS (SEQ ID No: 2), QQGNTLPWT (SEQ ID No: 3), RYWML (SEQ ID No: 4), EINPRNDRTNYNEKFKT (SEQ ID No: 5), and GGGYAMDY (SEQ ID No: 6),

or

(ii) which is capable of binding to the same L1CAM epitope recognized by the monoclonal antibody 9.3, produced by the hybridoma cell deposited under DSMZ ACC2841, or

(iii) comprising the following six CDR sequences QDISNY (SEQ ID No: 7), YTS, QQGNTLPWT (SEQ ID No: 8), GYTFTRYW (SEQ ID No: 9), INPRNDRT (SEQ ID No: 10), and ALGGGYAMDY (SEQ ID No: 11),

wherein the purified binding molecule capable of binding L1CAM is selected from the group consisting of single chain antibody (scFv), a multimer of scFv, a diabody, a triabody, a tetrabody, an antigen-binding fragment of a monoclonal antibody, a Fab, a tandab, a flexibody, a bispecific antibody, and a chimeric antibody.

2. The purified binding molecule capable of binding L1CAM of claim 1 , wherein the binding molecule binds L1CAM with an affinity (KD) of at least 10 −8 M, 10 −9 M, 10 −10 M, or 10 −11 M.

3. The purified binding molecule capable of binding L1CAM of claim 1 , linked to an active substance.

4. The purified binding molecule capable of binding L1CAM of claim 3 , wherein the active substance is a toxin, a cytokine, a nanoparticle or a radionuclide.

5. The purified binding molecule capable of binding L1CAM of claim 1 , wherein the epitope is within the first immunoglobulin-like domain of L1CAM.

6. A method for treating a tumor disease, wherein a binding molecule capable of binding L1CAM of claim 1 is administered to a subject in an effective amount to treat said disease.

7. The method of claim 6 for sensitizing tumor cells in a patient for the treatment with a chemotherapeutic drug or with radiotherapy.

8. The method of claim 6 for sensitizing tumor cells in a patient for the treatment with a chemotherapeutic drug or with radiotherapy, wherein the cells are at least partially resistant to the treatment with said chemotherapeutic drug or to radiotherapy.

9. The method of claim 6 for sensitizing tumor cells in a patient for the treatment with a chemotherapeutic drug or with radiotherapy, wherein after the sensitization with the binding molecule the patient is further treated with said chemotherapeutic drug or with radiotherapy.

10. The method of claim 6 for the treatment of a tumor disease in a patient previously treated with a chemotherapeutic drug or with radiotherapy.

11. The method of claim 10 for the treatment of a tumorigenic disease in a patient at least partially resistant to the treatment with said chemotherapeutic drug or with radiotherapy.

12. The method of claim 6 , wherein the binding molecule is administered in combination with a chemotherapeutic drug or with radiotherapy.

13. The method of claim 6 , wherein the binding molecule is administered in combination with a chemotherapeutic drug or with radiotherapy, wherein the chemotherapeutic drug or the radiotherapy is administered prior to the binding molecule.

14. The method of claim 6 , wherein the tumor disease is selected from the group consisting of astrocytoma, oligodendroglioma, meningioma, neurofibroma, glioblastoma, ependymoma, Schwannoma, neurofibrosarcoma, medulloblastoma, melanoma, pancreatic cancer, prostate carcinoma, head and neck cancer, breast cancer, lung cancer, ovarian cancer, endometrial cancer, renal cancer, neuroblastomas, squamous carcinomas, hepatoma, colon cancer and mesothelioma and epidermoid carcinoma.

15. The method of claim 6 , wherein the tumor disease bears the tumor cells from an epithelial tumor or the tumor disease is an epithelial tumor.

16. The method of claim 15 , wherein the epithelial tumor is pancreatic cancer, colon cancer, ovarian cancer or endometrial cancer.

17. The method of claim 6 for sensitizing tumor cells in a patient for the treatment with a chemotherapeutic drug or with radiotherapy, wherein the chemotherapeutic drug is a DNA damaging agent.

18. The method of claim 17 , wherein the DNA damaging agent is selected from the group consisting of actinomycin-D, mitomycin C, cisplatin, doxorubicin, etoposide, verapamil, podophyllotoxin, 5-FU and taxans, paclitaxel and carboplatin.

19. The method of claim 6 for sensitizing tumor cells in a patient for the treatment with a chemotherapeutic drug or with radiotherapy, wherein the radiotherapy is selected from the group consisting of X-ray radiation, UV-radiation, γ-irradiation, α- or β-irradiation, and microwaves.

20. A pharmaceutical composition, comprising a purified binding molecule capable of binding L1CAM of claim 1 .

Assignments (1)
CHANGE OF NAME Recorded Aug 13, 2014
From: MEDIGENE AG
To: MEDIGENE AG
Reel/Frame 033531/0777 →
Continuity (4)
Continuation 13367178 · Feb 6, 2012
Division 12139006 · Jun 13, 2008
Provisional Application 60944359 · Jun 15, 2007
Related Publication 20140120117A1 · May 1, 2014