- Trials with a EudraCT protocol (422)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
422 result(s) found for: nivolumab.
Displaying page 1 of 22.
EudraCT Number: 2019-003310-14 | Sponsor Protocol Number: SHO20190708 | Start Date*: 2019-12-05 |
Sponsor Name:Department of Dermatology, Bispebjerg Hospital | ||
Full Title: Laser immunotherapy with and without topical anti-PD1 in basal cell carcinomas | ||
Medical condition: Basal cell carcinoma in 24-30 patients | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001707-32 | Sponsor Protocol Number: NIVOPTIMIZE-trial | Start Date*: 2021-07-08 |
Sponsor Name:Erasmus Medical Center Rotterdam | ||
Full Title: Nivolumab dose optimization during nivolumab therapy in melanoma patients after achieving a complete or partial response (NIVOPTIMIZE-trial) | ||
Medical condition: Patients with advanced or metastatic melanoma treated with nivolumab monotherapy in a 480 mg 4 weekly scheme (either from start or after combination therapy with ipilimumab), have a confirmed CR or... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003208-42 | Sponsor Protocol Number: CA209-6GE | Start Date*: 2022-06-15 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Open Label, Randomized, Non-Inferiority Pharmacokinetic Study of Nivolumab Administered Subcutaneously (Nivo SC) Versus Intravenous Administration of Nivolumab in Participants with Stage... | ||||||||||||||||||
Medical condition: Resected Stage IIIA/B/C/D or Stage IV melanoma in an adjuvant setting | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Temporarily Halted) BE (Ongoing) PL (Prematurely Ended) DE (Prematurely Ended) IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004760-11 | Sponsor Protocol Number: CA209-408 | Start Date*: 2016-08-25 |
Sponsor Name:VU Medical Centre | ||
Full Title: 89Zirconium-labeled nivolumab and 18F-labeled anti-PD-L1 as predictive imaging biomarkers of response and toxicity in nivolumab treated patients with non-small-cell lung cancer – a feasibility study | ||
Medical condition: Non-small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002499-14 | Sponsor Protocol Number: CA017-055 | Start Date*: 2018-03-01 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind Study of BMS-986205 Combined with Nivolumab versus Nivolumab in Participants with Metastatic or Unresectable Melanoma that is Previously Untreated | |||||||||||||
Medical condition: Metastatic or Unresectable Melanoma that is Previously Untreated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Completed) GB (Completed) IE (Completed) CZ (Completed) GR (Completed) PL (Completed) FR (Completed) Outside EU/EEA IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001641-13 | Sponsor Protocol Number: CA224-098 | Start Date*: 2022-01-11 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-blind Study of Adjuvant Immunotherapy with Nivolumab +Relatlimab Fixed-dose Combination versus Nivolumab Monotherapy after Complete Resection of Stage III-IV Melanoma | ||||||||||||||||||
Medical condition: participants with completely resected Stage III or Stage IV melanoma | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) AT (Ongoing) BE (Ongoing) FR (Ongoing) DK (Ongoing) SE (Ongoing) NO (Ongoing) FI (Ongoing) ES (Ongoing) IT (Ongoing) GR (Ongoing) Outside EU/EEA | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004816-39 | Sponsor Protocol Number: CA012-004 | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2a Study of BMS-986178 Administered Alone and in Combination with Nivolumab or Ipilimumab in Advanced Solid Tumors | |||||||||||||
Medical condition: Advanced Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002469-37 | Sponsor Protocol Number: CA209-7FL | Start Date*: 2020-01-29 | |||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-blind, Placebo-controlled Phase 3 Study of Nivolumab Versus Placebo in Combination With Neoadjuvant Chemotherapy and Adjuvant Endocrine Therapy in Patients With Hi... | |||||||||||||||||||||||
Medical condition: Patients With High-risk, Estrogen Receptor-Positive (ER+), Human Epidermal Growth Factor Receptor 2-Negative (HER2-) Primary Breast Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Ongoing) DE (Ongoing) CZ (Ongoing) FR (Ongoing) PL (Ongoing) NL (Ongoing) BE (Ongoing) DK (Ongoing) FI (Ongoing) IE (Ongoing) ES (Ongoing) PT (Ongoing) GB (GB - no longer in EU/EEA) IT (Ongoing) RO (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002441-61 | Sponsor Protocol Number: CA209-451 | Start Date*: 2016-01-27 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Phase 3 Study of Nivolumab, Nivolumab in Combination with Ipilimumab, or Placebo as Maintenance Therapy in Subjects with Extensive-Stage Disease Small Cell ... | |||||||||||||
Medical condition: Extensive stage disease small cell lung cancer who have completed first line chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) GR (Completed) SE (Completed) DE (Completed) ES (Completed) GB (GB - no longer in EU/EEA) IE (Completed) FI (Completed) PL (Completed) NL (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003108-10 | Sponsor Protocol Number: GOING | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | |||||||||||||
Full Title: The GOING Study: Regorafenib followed by Nivolumab in patients with Hepatocellular Carcinoma progressing under sorafenib | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002939-21 | Sponsor Protocol Number: AARON | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: An Open-Label Phase II Study of Relatlimab (BMS-986016) with Nivolumab (BMS- 936558) in Combination with 5-Azacytidine for the Treatment of Patients with Refractory/Relapsed Acute Myeloid Leukemia ... | |||||||||||||
Medical condition: Subjects with Acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003655-15 | Sponsor Protocol Number: CA209-67T | Start Date*: 2021-06-02 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Open-label, Randomized, Noninferiority Trial of Subcutaneous Formulation of Nivolumab Versus Intravenous Nivolumab in Participants With Advanced or Metastatic Clear Cell Renal Cell Carci... | |||||||||||||
Medical condition: Metastatic Clear Cell Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) PL (Ongoing) CZ (Ongoing) PT (Ongoing) FI (Ongoing) IT (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003738-34 | Sponsor Protocol Number: CA209-143 | Start Date*: 2014-06-05 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Randomized Phase 3 Open Label Study of Nivolumab versus Bevacizumab and a Safety Study of Nivolumab or Nivolumab in Combination with Ipilimumab in Adult Subjects with Recurrent Glioblastoma (GBM)... | |||||||||||||
Medical condition: Recurrent glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) ES (Completed) BE (Ongoing) DK (Completed) PL (Completed) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002673-28 | Sponsor Protocol Number: NL82177.078.22 | Start Date*: 2023-01-31 |
Sponsor Name:Erasmus MC | ||
Full Title: Safe Stop IPI-NIVO Trial: Early discontinuation of nivolumab upon achieving a (confirmed) complete or partial response in patients with irresectable stage III or metastatic melanoma treated with fi... | ||
Medical condition: Stage III irresectable or metastatic melanoma treated with first-line ipilimumab-nivolumab | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003583-12 | Sponsor Protocol Number: CA224-047 | Start Date*: 2018-05-30 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined with Nivolumab versus Nivolumab in Participants with Previously Untreated Metastatic or Unresectable Melanoma | ||||||||||||||||||
Medical condition: Previously Untreated Metastatic or Unresectable Melanoma | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Ongoing) DE (Ongoing) AT (Ongoing) GB (GB - no longer in EU/EEA) SE (Ongoing) DK (Ongoing) FR (Ongoing) ES (Ongoing) GR (Ongoing) FI (Ongoing) PL (Ongoing) Outside EU/EEA IT (Ongoing) RO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001018-76 | Sponsor Protocol Number: CA209-649 | Start Date*: 2016-10-10 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 3 Study of Nivolumab Plus Ipilimumab versus Oxaliplatin plus Fluoropyrimidine in Subjects with Previously Untreated Advanced or Metastatic Gastric or Ga... | ||||||||||||||||||
Medical condition: Gastric or Gastroesophageal Junction Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) GR (Ongoing) PL (Ongoing) HU (Ongoing) DE (Restarted) PT (Ongoing) CZ (Ongoing) GB (GB - no longer in EU/EEA) IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002544-32 | Sponsor Protocol Number: UCL/15/0515 | Start Date*: 2018-03-01 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: A phase II study of nivolumab monotherapy in patients with relapsed/refractory Hodgkin lymphoma, fit for autologous stem cell transplant, who fail to reach complete metabolic remission after first ... | ||||||||||||||||||
Medical condition: Relapsed/refractory Hodgkin lymphoma | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000603-91 | Sponsor Protocol Number: CA013-004 | Start Date*: 2016-08-30 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2a Study of BMS-986179 Administered in Combination with Nivolumab (BMS- 936558) in Subjects with Advanced Solid Tumors | |||||||||||||
Medical condition: Solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003334-25 | Sponsor Protocol Number: Uni-Koeln-2785 | Start Date*: 2017-01-26 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Cologne | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase II trial of nivolumab in combination with ipilimumab to evaluate efficacy and safety in relapsed lung cancer and to evaluate biomarkers predictive for response to immune checkpoint inhibition | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) and patients with Small cell lung cancer (SCLC) after failure of platinum-based first-line therapy. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000416-21 | Sponsor Protocol Number: CA030-001 | Start Date*: 2019-01-31 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2 First-in-Human Study of BMS-986249 Alone and in Combination with Nivolumab in Advanced Solid Tumors | |||||||||||||
Medical condition: Advanced Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) DE (Ongoing) PL (Ongoing) FI (Ongoing) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
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