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Drug ReportsLebrikizumab
Ebglyss(lebrikizumab)
Ebglyss (lebrikizumab) is an antibody pharmaceutical. Lebrikizumab was first approved as Ebglyss on 2023-11-16. It has been approved in Europe to treat atopic dermatitis.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
Ebglyss
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Lebrikizumab
Tradename
Proper name
Company
Number
Date
Products
Ebglysslebrikizumab-lbkzEli LillyN-761306 RX2024-09-13
2 products
Labels
FDA
EMA
Brand Name
Status
Last Update
ebglyssBiologic Licensing Application2024-09-19
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
41 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Atopic dermatitisD003876EFO_0000274L2031720
EczemaD004485HP_0000964L30.931720
DermatitisD003872HP_0011123L30.931720
AsthmaD001249EFO_0000270J457512
Inborn genetic diseasesD030342EFO_000050811
Skin diseasesD012871L00-L9911
Genetic skin diseasesD01287311
SinusitisD012852EFO_0007486J3211
Nasal polypsD009298HP_0100582J3311
PolypsD011127EFO_000066211
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
FibrosisD00535511
Idiopathic pulmonary fibrosisD054990J84.11211
Pulmonary fibrosisD01165811
Chronic obstructive pulmonary diseaseD029424EFO_0000341J44.911
Lung diseasesD008171HP_0002088J98.411
Obstructive lung diseasesD008173HP_000653611
InflammationD007249MP_000184511
Airway obstructionD00040211
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients44
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PruritusD011537HP_0000989L2911
HypersensitivityD006967HP_0012393T78.4011
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLebrikizumab
INNlebrikizumab
Description
Lebrikizumab (humanized mab)
Classification
Antibody
Drug classmonoclonal antibodies
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
>4I77:H|Lebrikizumab heavy chain QVTLRESGPALVKPTQTLTLTCTVSGFSLSAYSVNWIRQPPGKALEWLAMIWGDGKIVYNSALKSRLTISKDTSKNQVVL TMTNMDPVDTATYYCAGDGYYPYAMDNWGQGSLVTVSSASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWN SGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESK >4I77:L|Lebrikizumab light chain DIVMTQSPDSLSVSLGERATINCRASKSVDSYGNSFMHWYQQKPGQPPKLLIYLASNLESGVPDRFSGSGSGTDFTLTIS SLQAEDVAVYYCQQNNEDPRTFGGGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQS GNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Identifiers
PDB4I77
CAS-ID
RxCUI
ChEMBL IDCHEMBL1743035
ChEBI ID
PubChem CID
DrugBankDB11914
UNII IDU9JLP7V031 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 1,213 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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14 adverse events reported
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