Combination therapy with an anti-axl antibody-drug conjugate
The present disclosure relates to combination therapies for the treatment of pathological conditions, such as cancer. In particular, the present disclosure relates to combination therapies comprising treatment with an Antibody Drug Conjugate (ADC) and a secondary agent.
1. A method for treating cancer in an individual, the method comprising administering to the individual an effective amount of ADC×AXL and a secondary agent;
wherein ADC×AXL has the chemical structure:
Ab-(DL) p
wherein:
DL is:
p is from 1 to 8;
and Ab is an antibody that binds to AXL, the antibody comprising:
(a) a heavy chain having the sequence according to SEQ ID NO. 3; and
(b) a light chain having the sequence according to SEQ ID NO. 4.
2. A method according to claim 1 , wherein the secondary agent is Fludarabine or Cytarabine.
3. A method according to claim 1 , wherein the secondary agent is a PD1 antagonist.
4. A method according to claim 3 , wherein the PD 1 antagonist is selected from the group consisting of pembrolizumab, nivolumab, MEDI0680, PDR001 (spartalizumab), Camrelizumab, AUNP12, Pidilizumab Cemiplimab (REGN-2810), AMP-224, BGB-A317 (Tisleizumab), and BGB-108.
5. A method according to claim 1 , wherein the secondary agent is a PD-L1 antagonist.
6. A method according to claim 5 , wherein the PD-L1 antagonist is selected from the group consisting of atezolizumab (Tecentriq), BMS-936559/MDX-1105, durvalumab/MEDI4736, and MSB0010718C (Avelumab).
7. A method according to claim 1 , wherein the secondary agent is a GITR (Glucocorticoid-Induced TNFR-Related protein) agonist.
8. A method according to claim 7 , wherein the GITR (Glucocorticoid-Induced TNFR-Related protein) agonist is selected from the group consisting of MEDI1873, TRX518, GWN323, MK-1248, MK 4166, BMS-986156 and INCAGN1876.
9. A method according to claim 1 , wherein the secondary agent is an OX40 agonist.
10. A method according to claim 9 , wherein the OX40 agonist is selected from the group consisting of MEDI0562, MEDI6383, MOXR0916, RG7888, OX40mAb24, INCAGN1949, GSK3174998, and PF-04518600.
11. A method according to claim 1 , wherein the secondary agent is a CTLA-4 antagonist.
12. A method according to claim 11 , wherein the CTLA-4 antagonist is ipilimumab or Tremelimumab.
13. A method according to claim 1 , wherein the secondary agent is a hypomethylating agent.
14. A method according to claim 13 , wherein the hypomethylating agent is azacitidine or decitabine.
15. A method according to claim 1 , wherein the secondary agent is a PARP inhibitor (PARPi).
16. A method according to claim 15 , wherein the PARPi is selected from the group consisting of Olaparib, CEP-9722, BMN-673/talazoparib, Rucaparib, Iniparib/SAR24-550/BSI-201, Veliparib (ABT-888), Niraparib/MK-4827, BGB-290, 3-aminobenzamide, and E7016.
17. A method according to claim 1 , wherein the secondary agent is an agent that upregulates HER2 expression.
18. A method according to claim 17 , wherein the agent that upregulates HER2 expression is gemcitabine or tamoxifen.
19. A method according to claim 1 , wherein the secondary agent is an AXL-kinase inhibitor (AXLi), a BRAF inhibitor (BRAFi), or a MEK inhibitor (MEKi).
20. A method according to claim 19 , wherein:
the AXLi is selected from the group consisting of BGB324 (bemcentinib), TP0903, Gilteritinib (ASP2215), Cabozantinib (XL184), SGI7079, Merestinib, amuvatinib (MP-470), bosutinib (SKI-606), MGCD265, and foretinib (GSK1363089/XL880);
the BRAFi is selected from the group consisting of vemurafenib, PLX4720, dabrafenib, Sorafenib, Encorafenib, and GDC0879; and
the MEKi is selected from the group consisting of Trametinib, Cobimetinib, Binimetinib, Selumetinib, PD-325901, CI-1040, PD035901, U0126, and TAK-733.
21. A method according to claim 1 , wherein the cancer comprises AXL+ve neoplastic cells, both AXL+ve and AXL−ve neoplastic cells, or AXL−ve neoplastic cells infiltrated with AXL+ve cells.