CAT-354 ( DrugBank: - )


1 disease
IDDisease name (Link within this page)Number of trials
97Ulcerative colitis6

97. Ulcerative colitis


Clinical trials : 2,527 Drugs : 1,465 - (DrugBank : 259) / Drug target genes : 144 - Drug target pathways : 202
No.TrialIDDate_
enrollment
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registration
Public_titleScientific_titleConditionInterventionPrimary_
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Inclusion_
agemin
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agemax
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PhaseCountries
1EUCTR2011-004812-40-GB
(EUCTR)
12/04/201221/03/2012Evaluation of efficacy and safety of tralokinumab in patients with active, moderate-to-severe ulcerative colitis. A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitis Ulcerative Colitis
MedDRA version: 14.1;Level: LLT;Classification code 10045365;Term: Ulcerative colitis;System Organ Class: 10017947 - Gastrointestinal disorders;Therapeutic area: Diseases [C] - Digestive System Diseases [C06]
Product Name: tralokinumab
Product Code: CAT-354
INN or Proposed INN: tralokinumab
AstraZeneca ABNULLNot RecruitingFemale: yes
Male: yes
110Phase 2Czech Republic;Netherlands;Germany;Italy;United Kingdom
2NCT01482884
(ClinicalTrials.gov)
March 201229/11/2011Evaluation of Efficacy and Safety of Tralokinumab in Patients With Active, Moderate-to-severe Ulcerative ColitisA Phase IIa, Randomised, Double-blind, Placebo-controlled, Parallel-arm, Multicenter Study to Evaluate the Efficacy and Safety of Tralokinumab (CAT-354), a Recombinant Human Monoclonal Antibody Directed Against Interleukin-13 (IL-13), as add-on Therapy, on Clinical Response in Patients With Active, Moderate-to-severe, Ulcerative ColitisUlcerative ColitisDrug: tralokinumab;Drug: placeboAstraZenecaMedImmune LtdCompleted18 Years65 YearsAll147Phase 2Czech Republic;France;Germany;Italy;Poland;United Kingdom;Netherlands
3EUCTR2011-004812-40-DE
(EUCTR)
26/01/201225/11/2011Evaluation of efficacy and safety of tralokinumab in patients with active, moderate-to-severe ulcerative colitis. A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitis Ulcerative Colitis
MedDRA version: 14.1;Level: LLT;Classification code 10045365;Term: Ulcerative colitis;System Organ Class: 100000004856;Therapeutic area: Diseases [C] - Digestive System Diseases [C06]
Product Name: tralokinumab
Product Code: CAT-354
INN or Proposed INN: tralokinumab
AstraZeneca ABNULLNot RecruitingFemale: yes
Male: yes
110Phase 2Czech Republic;Netherlands;Germany;United Kingdom;Italy
4EUCTR2011-004812-40-NL
(EUCTR)
25/01/201222/12/2011Evaluation of efficacy and safety of tralokinumab in patients with active, moderate-to-severe ulcerative colitis. A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitis Ulcerative Colitis
MedDRA version: 15.0;Level: LLT;Classification code 10045365;Term: Ulcerative colitis;System Organ Class: 10017947 - Gastrointestinal disorders;Therapeutic area: Diseases [C] - Digestive System Diseases [C06]
Product Name: tralokinumab
Product Code: CAT-354
INN or Proposed INN: tralokinumab
AstraZeneca ABNULLNot RecruitingFemale: yes
Male: yes
110Phase 2Czech Republic;Netherlands;United Kingdom;Italy
5EUCTR2011-004812-40-CZ
(EUCTR)
24/01/201229/12/2011Evaluation of efficacy and safety of tralokinumab in patients with active, moderate-to-severe ulcerative colitis. A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitis Ulcerative Colitis
MedDRA version: 14.1;Level: LLT;Classification code 10045365;Term: Ulcerative colitis;System Organ Class: 100000004856;Therapeutic area: Diseases [C] - Digestive System Diseases [C06]
Product Name: tralokinumab
Product Code: CAT-354
INN or Proposed INN: tralokinumab
AstraZeneca ABNULLNot RecruitingFemale: yes
Male: yes
110Phase 2Czech Republic;Netherlands;United Kingdom;Italy
6EUCTR2011-004812-40-IT
(EUCTR)
12/12/201102/03/2012A phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitisA phase IIa, randomised, double-blind, placebo-controlled, parallel-arm, multicenter study to evaluate the efficacy and safety of tralokinumab (CAT-354), a recombinant human monoclonal antibody directed against interleukin-13 (IL-13), as add-on therapy, on clinical response in patients with active, moderate-to-severe, ulcerative colitis Ulcerative Colitis
MedDRA version: 14.1;Level: LLT;Classification code 10045282;Term: UC;System Organ Class: 10017947 - Gastrointestinal disorders;Therapeutic area: Diseases [C] - Digestive System Diseases [C06]
Product Name: tralokinumab
Product Code: CAT-354
INN or Proposed INN: tralokinumab
Other descriptive name: NA
ASTRAZENECANULLNot RecruitingFemale: yes
Male: yes
110Phase 2Czech Republic;Netherlands;Germany;United Kingdom;Italy