- Trials with a EudraCT protocol (435)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
435 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: View results |
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 in patients with a complete, partial or stable response (NIVOPTIMIZE-trial) | ||
Medical condition: Patients with advanced or metastatic melanoma or renal cell carcinoma treated with nivolumab monotherapy in a 480mg or 6 mg/kg 4 weekly scheme (either from start or after combination therapy with i... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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 (Trial now transitioned) AT (Trial now transitioned) BE (Ongoing) FR (Trial now transitioned) CZ (Trial now transitioned) DK (Trial now transitioned) SE (Trial now transitioned) NO (Trial now transitioned) FI (Trial now transitioned) ES (Ongoing) IT (Ongoing) GR (Trial now transitioned) PT (Completed) Outside EU/EEA | ||||||||||||||||||
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 (Completed) PL (Completed) 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: 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 (Completed) DE (Completed) CZ (Completed) FR (Completed) PL (Completed) NL (Completed) BE (Completed) DK (Completed) FI (Completed) IE (Completed) ES (Ongoing) PT (Completed) 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: 2022-001150-35 | Sponsor Protocol Number: AxIn | Start Date*: 2022-11-10 | ||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||
Full Title: Phase II study of axitinib intensification plus nivolumab compared to nivolumab alone after induction with nivolumab plus ipilimumab in mRCC patients without previous complete response (AxIn study). | ||||||||||||||||||
Medical condition: Metastatic renal cell carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (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 (Trial now transitioned) PL (Trial now transitioned) CZ (Ongoing) PT (Trial now transitioned) FI (Trial now transitioned) IT (Ongoing) ES (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 (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) SE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) NO (Trial now transitioned) GR (Trial now transitioned) FI (Trial now transitioned) PL (Trial now transitioned) Outside EU/EEA IT (Ongoing) RO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004914-79 | Sponsor Protocol Number: CA017-003 | Start Date*: 2016-10-22 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2a Study of BMS-986205 Administered in Combination With Nivolumab (BMS-936558, Anti-PD-1 Monoclonal Antibody) in Advanced Malignant Tumors | |||||||||||||
Medical condition: Advanced Malignant Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) PL (Completed) NO (Completed) FI (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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 (Completed) HU (Completed) DE (Completed) PT (Completed) FR (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) IT (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: 2018-002676-40 | Sponsor Protocol Number: CA045-009 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Study of Neoadjuvant and Adjuvant Nivolumab Plus Bempegaldesleukin (NKTR-214), Versus Nivolumab Alone Versus Standard of Care in Participants with Muscle-Invasive Bladder Can... | |||||||||||||
Medical condition: Muscle-Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) AT (Completed) GR (Completed) ES (Ongoing) CZ (Completed) PL (Completed) FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) IT (Ongoing) | |||||||||||||
Trial results: View results |
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 (Completed) | |||||||||||||
Trial results: View results |
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