Anti-betacellulin antibodies, fragments thereof, and multi-specific binding molecules
Anti-betacellulin (BTC) antibodies, methods of producing the antibodies, pharmaceutical compositions comprising the antibodies, and methods of using the antibodies. Multi-specific binding molecules, including bispecific antibodies, comprising a BTC binding moiety and an anti-vascular endothelial growth factor (VEGF) binding moiety.
1 . A method of treating an ophthalmic disorder in a subject in need thereof, comprising administering to the subject an effective amount of a pharmaceutical composition, wherein the pharmaceutical composition comprises a multi-specific binding molecule comprising 1) an anti-betacellulin (BTC) binding moiety and 2) an anti-vascular endothelial growth factor (VEGF) binding moiety, wherein the ophthalmic disorder is selected from the group consisting of macular edema, diabetic macular edema (DME), neovascular age-related macular degeneration (nAMD), and retinal vein occlusion (RVO), and wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 as set forth in:
a. SEQ ID NOs: 1, 2, 3, 14, 15, and 16, respectively; SEQ ID NOs: 4, 2, 3, 14, 15, and 16, respectively; SEQ ID NOs: 5, 6, 3, 17, 18, and 19, respectively; or SEQ ID NOs: 7, 8, 9, 20, 18, and 16, respectively;
b. SEQ ID NOs: 25, 26, 27, 38, 39, and 40, respectively; SEQ ID NOs: 28, 26, 27, 38, 39, and 40, respectively; SEQ ID NOs: 29, 30, 27, 41, 42, and 43, respectively; or SEQ ID NOs: 31, 32, 33, 44, 42, and 40, respectively;
c. SEQ ID NOs: 25, 49, 50, 58, 59, and 60, respectively; SEQ ID NOs: 28, 49, 50, 58, 59, and 60, respectively; SEQ ID NOs: 29, 51, 50, 61, 62, and 63, respectively; or SEQ ID NOs: 31, 52, 53, 64, 62, and 60, respectively; or
d. SEQ ID NOs: 69, 70, 71, 82, 83, and 84, respectively; SEQ ID NOs: 72, 70, 71, 82, 83, and 84, respectively; SEQ ID NOs: 73, 74, 71, 85, 18, and 86, respectively; or SEQ ID NOs: 75, 76, 77, 87, 18, and 84, respectively.
2 . The method of claim 1 , wherein the anti-VEGF binding moiety is an anti-VEGF antibody or antigen binding fragment thereof in a format selected from the group consisting of an isolated antibody, a Fab, a Fab′, a F(ab′) 2 , a Fv, and a scFv.
3 . The method of claim 2 , wherein the anti-BTC binding moiety is an anti-BTC Fab and the anti-VEGF binding moiety is an anti-VEGF Fab, wherein the anti-BTC Fab comprises a heavy chain (HA) and a light chain (LA), and wherein the anti-VEGF Fab comprises a heavy chain (HB) and a light chain (LB).
4 . The method of claim 3 , wherein the HA and the HB are linked in the format from the N-terminus to the C-terminus: N-HA-linker 1-HB-C, and wherein the LA and the LB are linked in the format from the N-terminus to the C-terminus: N-LA-linker 2-LB-C.
5 . The method of claim 1 , wherein the anti-BTC binding moiety comprises a VH and a VL comprising an amino acid sequence with at least 90% sequence identity to:
a. SEQ ID NOs: 10 and 21, respectively;
b. SEQ ID NOs: 34 and 45, respectively;
c. SEQ ID NOs: 54 and 65, respectively; or
d. SEQ ID NOs: 78 and 88, respectively.
6 . The method of claim 5 , wherein the anti-BTC binding moiety comprises a heavy chain and a light chain with an amino acid sequence as set forth in:
a. SEQ ID NOs: 12 and 23, respectively;
b. SEQ ID NOs: 36 and 47, respectively;
c. SEQ ID NOs: 56 and 67, respectively; or
d. SEQ ID NOs: 80 and 90, respectively.
7 . The method of claim 1 , wherein the anti-VEGF binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 as set forth in:
a. SEQ ID NOs: 92, 93, 94, 105, 106, and 107 respectively;
b. SEQ ID NOs: 95, 93, 94, 105, 106, and 107, respectively;
c. SEQ ID NOs: 96, 97, 94, 108, 109, and 110, respectively; or
d. SEQ ID NOs: 98, 99, 100, 111, 109, and 107, respectively.
8 . The method of claim 7 , wherein the anti-VEGF binding moiety comprises a VH and VL comprising an amino acid sequence with at least 90% sequence identity to SEQ ID NOs: 101 and 112, respectively.
9 . The method of claim 7 , wherein the anti-VEGF binding moiety comprises a VH and VL encoded by the nucleic acid sequence as set forth in:
a. SEQ ID NOs: 102 and 113, respectively;
b. SEQ ID NOs: 117 and 123, respectively;
c. SEQ ID NOs: 128 and 133, respectively;
d. SEQ ID NOs: 138 and 143, respectively; or
e. SEQ ID NOs: 148 and 152, respectively.
10 . The method of claim 7 , wherein the anti-VEGF binding moiety comprises a heavy chain and a light chain with the amino acid sequence as set forth in SEQ ID NOs: 103 and 114, respectively, or wherein the heavy chain and light chain are encoded by a nucleic acid sequence with at least 90%-sequence identity to SEQ ID NOs: 104 and 115, respectively.
11 . The method of claim 1 , wherein the anti-BTC binding moiety comprises a variable heavy chain domain (VHA) and a variable light chain domain (VLA) that bind to BTC, and wherein the anti-VEGF binding moiety comprises a variable heavy chain domain (VHB) and a variable light chain domain (VLB) that bind to VEGF, wherein the multi-specific binding molecule is in the format from the N-terminus to C-terminus as: N-VHA-heavy chain constant domain (CHIA)-linker 1-VHB-heavy chain constant domain (CH1B)-C and N-VLA-light chain constant domain (CKA)-linker 2-VLB-light chain constant domain (CKB)-C, which comprises a heavy chain comprising the VHA, CHIA, linker 1, VHB, and CH1B, and which comprises a light chain comprising the VLA, CKA, linker 2, VLB, and CKB, wherein the heavy chain and the light chain is as set forth in:
a. SEQ ID NOs: 120 and 125, respectively;
b. SEQ ID NOs: 130 and 135, respectively;
c. SEQ ID NOs: 140 and 145, respectively; or
d. SEQ ID NOs: 149 and 154, respectively.
12 . The method of claim 1 , wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 and the anti-VEGF binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3, which are as set forth in:
a. SEQ ID NOs: 1, 2, 3, 14, 15, 16, 92, 93, 94, 105, 106, and 107, respectively;
b. SEQ ID NOs: 4, 2, 3, 14, 15, 16, 95, 93, 94, 105, 106, and 107, respectively;
c. SEQ ID NOs: 5, 6, 3, 17, 18, 19, 96, 97, 94, 108, 109, and 110, respectively; or
d. SEQ ID NOs: 7, 8, 9, 20, 18, 16, 98, 99, 100, 111, 109, and 107, respectively.
13 . The method of claim 1 , wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 and the anti-VEGF binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3, which are as set forth in:
a. SEQ ID NOs: 25, 26, 27, 38, 39, 40, 92, 93, 94, 105, 106, and 107, respectively;
b. SEQ ID NOs: 28, 26, 27, 38, 39, 40, 95, 93, 94, 105, 106, and 107, respectively;
c. SEQ ID NOs: 29, 30, 27, 41, 42, 43, 96, 97, 94, 108, 109, and 110, respectively; or
d. SEQ ID NOs: 31, 32, 33, 44, 42, 40, 98, 99, 100, 111, 109, and 107, respectively.
14 . The method of claim 1 , wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 and the anti-VEGF binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3, which are as set forth in:
a. SEQ ID NOs: 25, 49, 50, 58, 59, 60, 92, 93, 94, 105, 106, and 107, respectively;
b. SEQ ID NOs: 28, 49, 50, 58, 59, 60, 95, 93, 94, 105, 106, and 107, respectively;
c. SEQ ID NOs: 29, 51, 50, 61, 62, 63, 96, 97, 94, 108, 109, and 110, respectively; or
d. SEQ ID NOs: 31, 52, 53, 64, 62, 60, 98, 99, 100, 111, 109, and 107, respectively.
15 . The method of claim 1 , wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 and the anti-VEGF binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3, which are as set forth in:
a. SEQ ID NOs: 69, 70, 71, 82, 83, 84, 92, 93, 94, 105, 106, and 107 respectively;
b. SEQ ID NOs: 72, 70, 71, 82, 83, 84, 95, 93, 94, 105, 106, and 107, respectively;
c. SEQ ID NOs: 73, 74, 71, 85, 18, 86, 96, 97, 94, 108, 109, and 110, respectively; or
d. SEQ ID NOs: 75, 76, 77, 87, 18, 84, 98, 99, 100, 111, 109, and 107, respectively.
16 . The method of claim 1 , further comprising administering intravitreally to the subject the multi-specific binding molecule at a dose of about 0.25 mg/eye.
17 . The method of claim 1 , further comprising administering intravitreally to the subject the multi-specific binding molecule at a dose of about 0.75 mg/eye.
18 . The method of claim 1 , further comprising administering intravitreally to the subject the multi-specific binding molecule at a dose of about 2.5 mg/eye.
19 . The method of claim 1 , further comprising administering intravitreally to the subject the multi-specific binding molecule at a dose of about 7.5 mg/eye.
20 . A method of improving vision or visual acuity in a subject in need thereof, comprising administering to the subject an effective amount of a pharmaceutical composition, wherein the pharmaceutical composition comprises a multi-specific binding molecule comprising 1) an anti-betacellulin (BTC) binding moiety and 2) an anti-vascular endothelial growth factor (VEGF) binding moiety, wherein the subject has an ophthalmic disorder selected from the group consisting of macular edema, diabetic macular edema (DME), neovascular age-related macular degeneration (nAMD), and retinal vein occlusion (RVO), and wherein the anti-BTC binding moiety comprises HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 as set forth in:
a. SEQ ID NOs: 1, 2, 3, 14, 15, and 16, respectively; SEQ ID NOs: 4, 2, 3, 14, 15, and 16, respectively; SEQ ID NOs: 5, 6, 3, 17, 18, and 19, respectively; or SEQ ID NOs: 7, 8, 9, 20, 18, and 16, respectively;
b. SEQ ID NOs: 25, 26, 27, 38, 39, and 40, respectively; SEQ ID NOs: 28, 26, 27, 38, 39, and 40, respectively; SEQ ID NOs: 29, 30, 27, 41, 42, and 43, respectively; or SEQ ID NOs: 31, 32, 33, 44, 42, and 40, respectively;
c. SEQ ID NOs: 25, 49, 50, 58, 59, and 60, respectively; SEQ ID NOs: 28, 49, 50, 58, 59, and 60, respectively; SEQ ID NOs: 29, 51, 50, 61, 62, and 63, respectively; or SEQ ID NOs: 31, 52, 53, 64, 62, and 60, respectively; or
d. SEQ ID NOs: 69, 70, 71, 82, 83, and 84, respectively; SEQ ID NOs: 72, 70, 71, 82, 83, and 84, respectively; SEQ ID NOs: 73, 74, 71, 85, 18, and 86, respectively; or SEQ ID NOs: 75, 76, 77, 87, 18, and 84, respectively.