Lutikizumab
Highest phase reached
Phase 3
Drug type
Antibody
- Listing at source
- Listed
- Highest phase reached
- Phase 3
- Drug type
- Antibody
- Drug name
- Lutikizumab
- a 1234138
- A-1234138
- abt 981
- Abt-981
- ABT-981
- immunoglobulin anti interleukin 1β interleukin 1α synthetic human a 1234138 heavy chain disulfide with synthetic human a 1234138 light chain dimer
- immunoglobulin g1 kappa anti homo sapiens il1a interleukin 1 alpha and homo sapiens il1b interleukin 1 beta il 1b 1l1f2 humanized monoclonal antibody tetravalent bispecific gamma1 heavy chain 1 577 humanized vh anti il1b homo sapiens ighv3 23 04 80 60 ighd ighj4 01 8 8 12 1 119 6 mer linker 120 125 homo sapiens vh anti il1a ighv3 30 03 88 80 ighd ighj1 01 8 8 15 126 247 homo sapiens ighg1 01 ch1 248 345 hinge 346 360 ch2 l1 3 a 364 l1 2 a 365 361 470 ch3 471 575 chs 576 577 248 577 350 327 disulfide with kappa light chain 1 327 humanized v kappa anti il1b homo sapiens igkv1 27 01 82 10 igkj2 01 6 3 9 1 106 7 mer linker homo sapiens v kappa anti il1a igkv1 12 01 92 60 igkj4 01 6 3 9 114 220 homo sapiens igkc 01 km3 221 327 dimer 356 356 359 359 bisdisulfide
- Immunoglobulin G1-kappa, anti-[Homo sapiens IL1A (interleukin 1 alpha) and Homo sapiens IL1B (interleukin 1 beta, IL-1B, 1L1F2)], humanized monoclonal antibody, tetravalent bispecific; gamma1 heavy chain (1-577) [humanized VH anti-IL1B (Homo sapiens IGHV3-23*04 (80.60%) -(IGHD)-IGHJ4*01) [8.8.12] (1-119) -6-mer linker (120-125)-Homo sapiens VH anti-IL1A (IGHV3-30*03 (88.80%) -(IGHD)-IGHJ1*01) [8.8.15] (126-247) -Homo sapiens IGHG1*01 (CH1 (248- 345), hinge (346-360), CH2 L1.3>A (364), L1.2>A (365), (361-470), CH3 (471-575), CHS (576-577)) (248-577)], (350-327')-disulfide with kappa light chain (1’-327’) [humanized V-KAPPA anti-IL1B (Homo sapiens IGKV1- 27*01 (82.10%) -IGKJ2*01) [6.3.9] (1'-106') -7-mer linker-Homo sapiens V-KAPPA anti-IL1A (IGKV1-12*01 (92.60%) -IGKJ4*01) [6.3.9] (114'-220')-Homo sapiens IGKC*01, Km3 (221'-327')]; dimer (356-356":359-359")-bisdisulfide
- Immunoglobulin, anti-(interleukin 1β/interleukin 1α) (synthetic human A-1234138 heavy chain), disulfide with synthetic human A-1234138 light chain, dimer
- lutikizumab
- Lutikizumab
- lutikizumab [INN]
- LUTIKIZUMAB [USAN]
- Lutikizumab [WHO-DD]
- lutikizumab inn
- lutikizumab usan
- lutikizumab who dd
- CAS registry numbers
- 1791411-57-8
- ChEMBL ID
- CHEMBL4594518
- FDA ingredient codes (UNII)
- 15FAZ725S0
- First in class
- No
- Orphan designation
- No
- Pharmacology name
- lutikizumab
- Type
- Antibody
- Drug name stem
- -mab; -mab
- Action
- Binding
- Action type
- Binding
- Target
- IL-1α
- Gene symbol
- IL-1α
- Median affinity
- 11.12
- Affinity units
- pKd
- Primary target
- Yes
- Action
- Binding
- Action type
- Binding
- Target
- IL-1β
- Gene symbol
- IL-1β
- Median affinity
- 10.68
- Affinity units
- pKd
- Primary target
- Yes
- Mechanism
- Interleukin-1 alpha inhibitor
- Action type
- Inhibitor
- Target
- Interleukin-1 alpha
- Protein identifier
- P01583
- Mechanism
- Interleukin-1 beta inhibitor
- Action type
- Inhibitor
- Target
- Interleukin-1 beta
- Protein identifier
- P01584
- Mechanism
- Interleukin-1 alpha inhibitor
- Action type
- Inhibitor
- Target
- Interleukin-1 alpha
- Mechanism
- Interleukin-1 beta inhibitor
- Action type
- Inhibitor
- Target
- Interleukin-1 beta
- Condition
- Colitis, Ulcerative
- Highest recorded phase
- 2
- Condition identifier
- EFO:0000729
- Subject identifier
- D003093
- Condition
- Osteoarthritis, Knee
- Highest recorded phase
- 2
- Condition identifier
- EFO:0004616
- Subject identifier
- D020370
- Condition
- Hidradenitis Suppurativa
- Highest recorded phase
- 3
- Condition identifier
- EFO:1000710
- Subject identifier
- D017497
- Condition
- Osteoarthritis
- Highest recorded phase
- 1
- Condition identifier
- MONDO:0005178
- Subject identifier
- D010003
- Condition identifier
- EFO_0000274
- Highest recorded phase
- 2
- Condition identifier
- EFO_0000729
- Highest recorded phase
- 2
- Condition identifier
- EFO_0004616
- Highest recorded phase
- 2
- Condition identifier
- EFO_1000710
- Highest recorded phase
- 3
- Condition identifier
- MONDO_0002400
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0004980
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0005011
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0005101
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0005178
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0005416
- Highest recorded phase
- 1
- Condition identifier
- MONDO_0006559
- Highest recorded phase
- 3
- Condition identifier
- MONDO_0008383
- Highest recorded phase
- 2
- Condition identifier
- MONDO_0011849
- Highest recorded phase
- 2
- NCT01668511
- NCT02087904
- NCT05139602
- NCT06468228
- NCT06257875
- Prodrug
- No
- Chirality
- Single enantiomer
- Inorganic
- No
- Natural product
- No
- Component
- Glycosylation sites (N)
- Sequence
- 427 $ 427''''
- Component
- Heavy chain
- Type
- Protein
- Sequence
- EVQLQESGPGLVKPSETLSLTCAVTGYSITSGYSWHWIRQFPGNGLEWMGYIHSSGSTNYNPSLKSRISISRDTSKNQFFLKLSSVTAADTAVYYCAGYDDYFEYWGQGTTVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPEAAGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
- Component
- Glycosylation sites (N)
- Sequence
- 427 $ 427''
- Component
- Light chain
- Type
- Protein
- Sequence
- DIQMTQSPSSLSASVGDRVTITCKASQNVGFNVAWYQQKPGKSPKALIYSASYRYSGVPSRFSGSGSGTDFTLTISSLQPEDFAEYFCQQYNWYPFTFGQGTKLEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
- Component
- Heavy chain
- Type
- Protein
- Sequence
- EVQLVESGGGVVQPGRSLRLSCSASGFIFSRYDMSWVRQAPGKGLEWVAYISHGGAGTYYPDSVKGRFTISRDNSKNTLFLQMDSLRPEDTGVYFCARGGVTKGYFDVWGQGTPVTVSSASTKGPQVQLVESGGGVVQPGRSLRLSCTASGFTFSMFGVHWVRQAPGKGLEWVAAVSYDGSNKYYAESVKGRFTISRDNSKNILFLQMDSLRLEDTAVYYCARGRPKVVIPAPLAHWGQGTLVTFSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPEAAGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
- Component
- Disulfide bridges
- Sequence
- 22-96 $ 22''-96'' $ 23'-88' $ 23'''-88''' $ 136'-201' $ 136'''-201''' $ 147-221 $ 147''-221'' $ 247-307' $ 247''-307''' $ 274-330'' $ 274-330'' $ 350-327' $ 350''-327'' $ 356-356'' $ 359''-359'' $ 391-451 $ 391''-451'' $ 359''-359'' $ 497-555 $ 497''-555''
- Component
- Disulfide bridges
- Sequence
- 22-96 $ 22''-96'' $ 23'-88' $ 23'''-88''' $ 134'-194' $ 134'''-194''' $ 143-199 $ 143''-199'' $ 219-214' $ 219''-214''' $ 225-225'' $ 228-228'' $ 260-320 $ 260''-320'' $ 366-424 $ 366''-424''
Related records
Trials (12)
- A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With Erosive Hand Osteoarthritis
- A Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981 in Patients With Knee Osteoarthritis
- A Study to Assess Adverse Events and Change in Disease Activity From Intravenous (IV) and Subcutaneous (SC) Lutikizumab in Adult Participants With Active Ulcerative Colitis
- A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa
- A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are Naïve to Biologic Therapy
- A Study to Assess Molecular Changes in Adult Participants With Moderate to Severe Hidradenitis Suppurativa or With Moderate to Severe Atopic Dermatitis Receiving Subcutaneous Injections of Lutikizumab
- A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid Arthritis
- A Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or in Combination, for the Treatment of Moderate to Severe Atopic Dermatitis
- A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple Subcutaneous Injections of ABT-981 in Patients With Osteoarthritis of the Knee
- Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, Safety, and Tolerability of Lutikizumab in Chinese Participants
- Study of Targeted Therapies for the Treatment of Adult Participants With Active Psoriatic Arthritis
- Study of Targeted Therapies for the Treatment of Adult Participants With Moderate to Severe Crohn's Disease
In development for (5)
- Atopic eczema Phase 2
- Hidradenitis suppurativa Phase 3
- Osteoarthritis Phase 1
- Osteoarthritis, knee Phase 2
- Ulcerative colitis Phase 2