- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Tildrakizumab.
Displaying page 1 of 1.
EudraCT Number: 2019-003485-40 | Sponsor Protocol Number: CCR5163 | Start Date*: 2020-10-01 |
Sponsor Name:The Institute of Cancer Research | ||
Full Title: ACTION: Phase I/II Trial of Abiraterone Acetate in Combination with Tildrakizumab (anti-IL23 targeting monoclonal antibody) in Men with Metastatic Castration-Resistant Prostate Cancer (mCRPC) | ||
Medical condition: Metastatic castration resistant prostate cancer | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002255-42 | Sponsor Protocol Number: MK-3222-010 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:Sun Pharma Global FZE | |||||||||||||
Full Title: A 64-Week, Phase 3, Randomized, Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222), Followed by an Optiona... | |||||||||||||
Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000706-10 | Sponsor Protocol Number: 22-00274 | Start Date*: 2022-09-12 | |||||||||||
Sponsor Name:University Medical Center of the Johannes Gutenberg- University Mainz | |||||||||||||
Full Title: Pilot study on Administration of Tildrakizumab in patients with Hidradenitis Suppurativa. | |||||||||||||
Medical condition: Hidradenitis suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001377-88 | Sponsor Protocol Number: MK-3222-011 | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:Sun Pharma Global FZE | |||||||||||||
Full Title: A 52-Week, Phase 3, Randomized, Active Comparator and Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222 / MK-3222)... | |||||||||||||
Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) AT (Completed) BE (Completed) CZ (Completed) IT (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003936-19 | Sponsor Protocol Number: CLR_16_22 | Start Date*: 2017-03-20 |
Sponsor Name:SUN Pharmaceuticals Global FZE | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 2a Study to Evaluate the Efficacy and Safety of Tildrakizumab in Subjects with Active Ankylosing Spondylitis or Non-Radiographic Axial Spondyloa... | ||
Medical condition: Ankylosing spondylitis (AS) and Non-Radiographic Axial Spondyloarthritis (nr-axSpA) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-003218-15 | Sponsor Protocol Number: M-14745-44 | Start Date*: 2019-11-03 | |||||||||||
Sponsor Name:Almirall S.A. | |||||||||||||
Full Title: A phase IV interventional study to assess the disease-modifying effect of long-term treatment with tildrakizumab in adult patients with moderate-to-severe plaque psoriasis | |||||||||||||
Medical condition: Moderate to severe plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003937-62 | Sponsor Protocol Number: CLR_16_23 | Start Date*: 2017-03-20 | |||||||||||
Sponsor Name:SUN Pharma Global FZE | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multiple Dose, Phase 2b Study to Demonstrate the Safety and Efficacy of Tildrakizumab in Subjects with Active Psoriatic Arthritis | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001060-35 | Sponsor Protocol Number: CLR_18_07 | Start Date*: 2018-08-29 | |||||||||||||||||||||
Sponsor Name:Sun Pharmaceutical Industries Limited (SPIL) | |||||||||||||||||||||||
Full Title: A Long-Term Extension Study to Demonstrate Safety of Tildrakizumab in Subjects with Psoriatic Arthritis who Have Previously Completed Study with Tildrakizumab | |||||||||||||||||||||||
Medical condition: Psoriatic Arthritis (PsA) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) ES (Ongoing) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002804-42 | Sponsor Protocol Number: M-14745-42 | Start Date*: 2019-11-27 | |||||||||||
Sponsor Name:Almirall S.A. | |||||||||||||
Full Title: An international, multicentre, open label, interventional phase IV clinical study to investigate the efficacy and safety of tildrakizumab 100 mg in patients with moderate-to-severe chronic plaque p... | |||||||||||||
Medical condition: Moderate to severe chronic plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000955-11 | Sponsor Protocol Number: TILD-19-07 | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:Sun Pharmaceutical industries Ltd | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study to Demonstrate the Efficacy and Safety of Tildrakizumab in Anti-TNF Experienced Subjects with Active Psoriatic Arthritis I (INSPIRE 1) | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) EE (Trial now transitioned) SK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003551-11 | Sponsor Protocol Number: TILD-19-12 | Start Date*: 2020-08-17 |
Sponsor Name:Sun Pharma Advanced Research Company Ltd. | ||
Full Title: A Multicenter, Randomized, Placebo and Active Comparator-Controlled Clinical trial to Study the Efficacy, Safety and Pharmacokinetics (PK) of Tildrakizumab in Pediatric Subjects from 6 to <18 Years... | ||
Medical condition: moderate to severe chronic plaque psoriasis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) SK (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000817-35 | Sponsor Protocol Number: M-14745-41 | Start Date*: 2019-07-26 | |||||||||||
Sponsor Name:Almirall | |||||||||||||
Full Title: An open-label, randomized, Phase IV study, to assess the efficacy and safety of tildrakizumab in patients with moderate to severe chronic plaque psoriasis who are non-responders to dimethyl fumarat... | |||||||||||||
Medical condition: Moderate to severe chronic plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) NL (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000956-37 | Sponsor Protocol Number: TILD-19-19 | Start Date*: 2021-06-18 | |||||||||||
Sponsor Name:Sun Pharmaceutical industries Ltd | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study to Demonstrate the Efficacy and Safety of Tildrakizumab in Anti-TNF Naive Subjects with Active Psoriatic Arthritis II (INSPIRE 2) | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004230-42 | Sponsor Protocol Number: 18562 | Start Date*: 2020-07-31 | |||||||||||||||||||||
Sponsor Name:Radboudumc | |||||||||||||||||||||||
Full Title: Dose reduction of the new generation biologics (IL17 and IL23 inhibitors) in psoriasis: A pragmatic, multicentre, randomized, controlled, non-inferiority study - BeNeBio study | |||||||||||||||||||||||
Medical condition: psoriasis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001740-54 | Sponsor Protocol Number: MK-3222-012 | Start Date*: 2013-12-16 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp, a subsidiary of Merck & Co, Inc. | |||||||||||||
Full Title: A 28-Week, Phase 3, Randomized, Active Comparator and Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous SCH 900222 / MK-3222, Followed by... | |||||||||||||
Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
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