Maridebart cafraglutide

Highest phase reached
Drug type
Antibody drug conjugate

Listing at source
Listed
Highest phase reached

Drug type
Antibody drug conjugate
Drug name
Maridebart cafraglutide

  • amg 133
  • AMG 133
  • AMG-133
  • gamma1 heavy chain Homo sapiens (1-450) [VH (Homo sapiens IGHV3-33*01 (92.9%) -(IGHD) -IGHJ4*01 (100%), CDR-IMGT [8.8.13] (26-33.51-58.97-109)) (1-120) -Homo sapiens IGHG1*03v, G1m3>G1m17, nG1m1 CH1 K120, CH3 E12, M14, G1v64 CH2 C36, G1v54-30 CH2 C83, G84.4, C85 (CH1 R120>K (217) (121-218), hinge 1-15 (219-233), CH2 E36>C (275), R83>C (295), N84.4>G (300), V85>C (305) (234-343), CH3 E12 (359), M14 (361) (344-448), CHS (449-450)) (121-450)], (223-214')-disulfide with kappa light chain Homo sapiens (1'-214') [V-KAPPA (Homo sapiens IGKV3-15*01 (97.9%)-IGKJ4*01 (100%), CDR-IMGT [6.3.9] (27-32.51-53.89-97)) (1'-107') -Homo sapiens IGKC*01 (100%), Km3 A45.1 (153), V101 (191) (108'-214')]; dimer (229-229'':232-232'')-bisdisulfide, produced in Chinese hamster ovary (CHO) cells, glycoform alfa; 275,275''-bis(thioether) conjugated to a glucagon-like peptide 1(GLP-1) analogue (GCG (glucagon) 98-126, GLP-1 7-35 A8>methylalanine (2), V16>Y (10), G22>E (16)), via a fused 18-mer linker (diglycyl- tris(tetraglycyl-seryl)-lysinamide
  • gamma1 heavy chain homo sapiens 1 450 vh homo sapiens ighv3 33 01 92 9 ighd ighj4 01 100 cdr imgt 8 8 13 26 33 51 58 97 109 1 120 homo sapiens ighg1 03v g1m3 g1m17 ng1m1 ch1 k120 ch3 e12 m14 g1v64 ch2 c36 g1v54 30 ch2 c83 g84 4 c85 ch1 r120 k 217 121 218 hinge 1 15 219 233 ch2 e36 c 275 r83 c 295 n84 4 g 300 v85 c 305 234 343 ch3 e12 359 m14 361 344 448 chs 449 450 121 450 223 214 disulfide with kappa light chain homo sapiens 1 214 v kappa homo sapiens igkv3 15 01 97 9 igkj4 01 100 cdr imgt 6 3 9 27 32 51 53 89 97 1 107 homo sapiens igkc 01 100 km3 a45 1 153 v101 191 108 214 dimer 229 229 232 232 bisdisulfide produced in chinese hamster ovary cho cells glycoform alfa 275 275 bis thioether conjugated to a glucagon like peptide 1 glp 1 analogue gcg glucagon 98 126 glp 1 7 35 a8 methylalanine 2 v16 y 10 g22 e 16 via a fused 18 mer linker diglycyl tris tetraglycyl seryl lysinamide
  • immunoglobulin g1 anti glucose dependent insulinotropic polypeptide receptor 275 cysteine 295 cysteine 300 glycine 305 cysteine human γ1 chain disulfide with human κ chain dimer
  • immunoglobulin g1 anti glucose dependent insulinotropic polypeptide receptor 275 cysteine 295 cysteine 300 glycine 305 cysteine human γ1 chain disulfide with human κ chain dimer 275 275 bis thioether with 7 37 glucagon like peptide i 8 2 methylalanine 16 tyrosine 22 glutamic acid 36 glycine human fusion protein with peptide linker ggggs 3 n6 2 mercaptoacetyl lysinamide
  • immunoglobulin g1 kappa anti homo sapiens gipr gastric inhibitory polypeptide receptor homo sapiens monoclonal antibody gamma1 heavy chain homo sapiens 1 450 vh homo sapiens ighv3 33 01 92 9 ighd ighj4 01 100 cdrimgt 8 8 13 26 33 51 58 97 109 1 120 homo sapiens ighg1 03v g1m3 g1m17 ng1m1 ch1 k120 ch3 e12 m14 g1v64 ch2 c36 g1v54 30 ch2 c83 g84 4 c85 ch1 r120 k 217 121 218 hinge 1 15 219 233 ch2 e36 c 275 r83 c 295 n84 4 g 300 v85 c 305 234 343 ch3 e12 359 m14 361 344 448 chs 449 450 121 450 223 214 disulfide with kappa light chain homo sapiens 1 214 vkappa homo sapiens igkv3 15 01 97 9 igkj4 01 100 cdr imgt 6 3 9 27 32 51 53 89 97 1 107 homo sapiens igkc 01 100 km3 a45 1 153 v101 191 108 214 dimer 229 229 232 232 bisdisulfide produced in chinese hamster ovary cho cells glycoform alfa
  • Immunoglobulin G1-kappa, anti-[Homo sapiens GIPR (gastric inhibitory polypeptide receptor)], Homo sapiens monoclonal antibody; gamma1 heavy chain Homo sapiens (1-450) [VH (Homo sapiens IGHV3-33*01 (92.9%)-(IGHD) -IGHJ4*01 (100%), CDRIMGT [8.8.13] (26-33.51-58.97-109)) (1-120) -Homo sapiens IGHG1*03v, G1m3>G1m17, nG1m1 CH1 K120, CH3 E12, M14, G1v64 CH2 C36, G1v54-30 CH2 C83, G84.4, C85 (CH1 R120>K (217) (121-218), hinge 1-15 (219-233), CH2 E36>C (275), R83>C (295), N84.4>G (300), V85>C (305) (234-343), CH3 E12 (359), M14 (361) (344-448), CHS (449-450)) (121-450)], (223-214')-disulfide with kappa light chain Homo sapiens (1'-214') [VKAPPA (Homo sapiens IGKV3-15*01 (97.9%) -IGKJ4*01 (100%), CDR-IMGT [6.3.9] (27-32.51-53.89-97)) (1'-107') -Homo sapiens IGKC*01 (100%), Km3 A45.1 (153), V101 (191) (108'-214')]; dimer (229-229'':232-232'')-bisdisulfide, produced in Chinese hamster ovary (CHO) cells, glycoform alfa
  • Immunoglobulin G1, anti-(glucose-dependent insulinotropic polypeptide receptor) [275-cysteine,295-cysteine,300-glycine,305-cysteine] (human γ1-chain), disulfide with human κ-chain, dimer
  • Immunoglobulin G1, anti-(glucose-dependent insulinotropic polypeptide receptor) [275-cysteine,295-cysteine,300-glycine,305-cysteine] (human γ1-chain), disulfide with human κ-chain, dimer, 275,275′-bis(thioether) with 7-37-glucagon-like peptide I [8-(2-methylalanine),16-tyrosine,22-glutamic acid,36-glycine] (human) fusion protein with peptide linker ((GGGGS)3-N6-(2-mercaptoacetyl)lysinamide)
  • maridebart cafraglutida
  • Maridebart cafraglutida
  • maridebart cafraglutide
  • Maridebart cafraglutide
  • Maridebart Cafraglutide
  • maridebart cafraglutide [INN]
  • MARIDEBART CAFRAGLUTIDE [USAN]
  • maridebart cafraglutide inn
  • maridebart cafraglutide usan

CAS registry numbers
  • 2760218-55-9
ChEMBL ID
CHEMBL5314751
FDA ingredient codes (UNII)
  • Z24U3U73HN

First in class
No
Orphan designation
No

Pharmacology name
maridebart cafraglutide
Type
Antibody
Drug name stem
-bart; -tide

  • Action
    Agonist
    Action type
    Agonist
    Target
    GLP-1 receptor
    Gene symbol
    GLP1R
    Protein identifier
    P43220
    Median affinity
    7.61
    Affinity units
    pEC50
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    GIP receptor
    Gene symbol
    GIPR
    Protein identifier
    P48546
    Median affinity
    7.37
    Affinity units
    pIC50

  • Condition identifier
    EFO_0001073
    Highest recorded phase
    3
  • Condition identifier
    EFO_0003918
    Highest recorded phase
    3
  • Condition identifier
    HP_0001513
    Highest recorded phase
    3
  • Condition identifier
    HP_0025502
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0005148
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0005148
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0007147
    Highest recorded phase
    3

Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Natural product
No

  • Component
    Heavy chain
    Type
    Protein
    Sequence
    QVQLVESGGGVVQPGRSLRLSCAASGFTFSNYGMHWVRQAPGEGLEWVAAIWFDASDKYYADAVKGRETISRDNSKNTLYLQMNSLRAEDTAVYYCARDQAIFGVVPDYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPCVKENWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVESCSVMHEALHNHYTQKSLSLSPGK
  • Component
    Disulfide bridges
    Sequence
    22-96 $ 22''-96'' $ 23'-88' $ 23'''-88''' $ 134'-194' $ 134'''-194''' $ 147-203 $ 147''-203'' $ 223-214' $ 223''-214''' $ 229-229'' $ 232-232'' $ 264-324 $ 264''-324'' $ 295-305 $ 295''-305'' $ 370-428 $ 370''-428''
  • Component
    Light chain
    Type
    Protein
    Sequence
    EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYGAATRATGIPARVSGSGSGTEFTLTISSLQSEDFAVYYCQQYNNWPLTEGGGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
  • Component
    Glycosylation sites (N)
    Sequence
    300 $ 300''

Related records

Trials (20)

In development for (3)