Tralokinumab

drug
On this page

Also known as AdtralzaAdbryCAT-354

Summary

Tralokinumab (CHEMBL1743081) is an approved antibody (ATC D11AH07); indicated across 7 conditions including atopic eczema and asthma.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: D11AH07
  • Indications: 7 conditions
  • Clinical trials: 34

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1743081
NameTralokinumab
TypeAntibody
Max phase4
ATCD11AH07

Also known as: Adtralza, Adbry, CAT-354, Tralokinumab, TRALOKINUMAB

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

7 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
atopic eczema4MONDO:0004980EFO:0000274
asthma3MONDO:0004979MONDO:0004979
alopecia areata2MONDO:0005340EFO:0004192
ulcerative colitis2MONDO:0005101EFO:0000729
idiopathic pulmonary fibrosis2MONDO:0800504EFO:0000768
exocrine pancreatic carcinoma1MONDO:0005192EFO:0002618

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 34.

Phase distribution

PhaseTrials
PHASE314
PHASE210
PHASE15
Not specified3
PHASE42

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07352566PHASE4NOT_YET_RECRUITINGUtilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT06773455PHASE4TERMINATEDTralokinumab for Dupilumab Failures
NCT06311682PHASE3RECRUITINGA Trial to Evaluate the Efficacy and Safety of Tralokinumab in Combination With Topical Corticosteroids in Children and Infants With Moderate-to-severe Atopic Dermatitis
NCT02161757PHASE3COMPLETEDA Phase 3 Study to Evaluate the Efficacy and Safety of Tralokinumab in Adults and Adolescents With Uncontrolled Asthma
NCT02194699PHASE3COMPLETEDA Phase 3 Study to Evaluate the Efficacy and Safety of Tralokinumab in Adults and Adolescents With Uncontrolled Asthma
NCT02281357PHASE3COMPLETEDPhase 3 Study to Evaluate the Efficacy & Safety of Tralokinumab in Adults & Adolescents With OCS Dependent Asthma
NCT02902809PHASE3TERMINATEDA Study to Evaluate the Safety of Tralokinumab in Adults and Adolescents With Uncontrolled Asthma
NCT03131648PHASE3COMPLETEDTralokinumab Monotherapy for Moderate to Severe Atopic Dermatitis - ECZTRA 1 (ECZema TRAlokinumab Trial no. 1)
NCT03160885PHASE3COMPLETEDTralokinumab Monotherapy for Moderate to Severe Atopic Dermatitis - ECZTRA 2 (ECZema TRAlokinumab Trial no. 2)
NCT03363854PHASE3COMPLETEDTralokinumab in Combination With Topical Corticosteroids for Moderate to Severe Atopic Dermatitis - ECZTRA 3
NCT03526861PHASE3COMPLETEDTralokinumab Monotherapy for Adolescent Subjects With Moderate to Severe Atopic Dermatitis - ECZTRA 6 (ECZema TRAlokinumab Trial no. 6).
NCT03587805PHASE3COMPLETEDLong-term Extension Trial in Subjects With Atopic Dermatitis Who Participated in Previous Tralokinumab Trials - ECZTEND
NCT03761537PHASE3COMPLETEDTralokinumab in Combination With Topical Corticosteroids in Subjects With Severe Atopic Dermatitis - ECZTRA 7
NCT04587453PHASE3COMPLETEDTralokinumab in Combination With Topical Corticosteroids in Japanese Subjects With Moderate-to-severe Atopic Dermatitis
NCT05194540PHASE3COMPLETEDEfficacy and Safety of Tralokinumab Administered by an Autoinjector in Adults and Adolescents With Moderate to Severe Atopic Dermatitis (INJECZTRA)
NCT05958407PHASE3COMPLETEDA 32-week Trial to Evaluate the Efficacy and Safety of Tralokinumab in Subjects With Moderate-to-severe Atopic Hand Eczema Who Are Candidates for Systemic Therapy
NCT00640016PHASE2TERMINATEDA Study to Assess the Efficacy, Safety, and Tolerability of CAT-354 in Subjects With Asthma
NCT00873860PHASE2COMPLETEDStudy to Evaluate the Safety and Efficacy of CAT-354
NCT01402986PHASE2COMPLETEDA Safety and Efficacy Study of Tralokinumab in Adults With Asthma
NCT01482884PHASE2COMPLETEDEvaluation of Efficacy and Safety of Tralokinumab in Patients With Active, Moderate-to-severe Ulcerative Colitis
NCT01629667PHASE2TERMINATEDA Phase 2, Randomized Dose-ranging Study to Evaluate the Efficacy of Tralokinumab in Adults With Idiopathic Pulmonary Fibrosis
NCT02449473PHASE2COMPLETEDStudy to Evaluate Efficacy & Safety of Tralokinumab in Subjects With Asthma Inadequately Controlled on Corticosteroids
NCT02684097PHASE2COMPLETEDA Pilot Study of Tralokinumab in Subjects With Moderate to Severe Alopecia Areata
NCT03562377PHASE2COMPLETEDVaccine Responses in Tralokinumab-Treated Atopic Dermatitis - ECZTRA 5 (ECZema TRAlokinumab Trial No. 5)
NCT04556461PHASE2COMPLETEDEffects of Tralokinumab Treatment of Atopic Dermatitis on Skin Barrier Function
NCT05388760PHASE2COMPLETEDTralokinumab Monotherapy for Children With Moderate-to-severe Atopic Dermatitis - TRAPEDS 1 (TRAlokinumab PEDiatric Trial no. 1)
NCT00974675PHASE1TERMINATEDA Study to Assess Pharmacokinetics, Safety and Tolerability of Multiple Doses of CAT-354 in Subjects With Moderate Asthma
NCT01093040PHASE1COMPLETEDA Study to Assess the Safety and Immunogenicity of the Drug CAT-354 in Healthy Japanese Subjects
NCT01592396PHASE1COMPLETEDA Phase 1, Open-label Study to Investigate the Pharmacokinetics of Tralokinumab (CAT-354) in Adolescents With Asthma
NCT02085473PHASE1COMPLETEDA Study of Tralokinumab When Delivered Subcutaneously at Different Flow Rates to Healthy Volunteers
NCT03556592PHASE1COMPLETEDDrug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4
NCT03358693Not specifiedRECRUITINGMolecular Signatures in Inflammatory Skin Disease
NCT05938478Not specifiedRECRUITINGMonitoring Pregnancy and Infant Outcomes Following Tralokinumab Exposure During Pregnancy in the US and Canada - PROTECT
NCT07444801Not specifiedRECRUITINGIntervention With Tralokinumab in Patients With Moderate-to-severe Atopic Dermatitis With Genital Impact

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).