- Trials with a EudraCT protocol (424)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
424 result(s) found for: PD-1.
Displaying page 6 of 22.
EudraCT Number: 2016-002722-36 | Sponsor Protocol Number: RAGTIME | Start Date*: 2017-03-29 | |||||||||||
Sponsor Name:FUNDACIÓ LLUITA CONTRA LA SIDA | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled clinical trial to evaluate the effect of Raltegravir intensification (1.200 mg QD) on the gut microbiota of chronically HIV-1 infected subject over time... | |||||||||||||
Medical condition: HIV-1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004509-42 | Sponsor Protocol Number: CTL-101-023 | Start Date*: 2018-04-23 | |||||||||||||||||||||
Sponsor Name:Celleron Therapeutics Ltd | |||||||||||||||||||||||
Full Title: A Phase Ib/ II Trial to Assess the Safety and Efficacy of CXD101 in Combination with the PD-1 Inhibitor Nivolumab in Patients with Metastatic, Previously-Treated, Microsatellite-Stable Colorectal C... | |||||||||||||||||||||||
Medical condition: Metastatic, Previously-Treated, Microsatellite-Stable Colorectal Carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
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: 2015-004475-75 | Sponsor Protocol Number: IFCT-1501 | Start Date*: 2016-02-08 | |||||||||||
Sponsor Name:IFCT | |||||||||||||
Full Title: A randomized phase II study evaluating efficacy and safety of 2nd or 3rd line treatment by Nivolumab monotherapy or Nivolumab plus Ipilimumab, for unresectable Malignant Pleural Mesothelioma (MPM) ... | |||||||||||||
Medical condition: Malignant Pleural Mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003553-42 | Sponsor Protocol Number: AIO-HEP-0217 | Start Date*: 2018-05-03 | ||||||||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||||||||||||
Full Title: A Phase II single-arm, open-label study of transarterial chemoembolization (TACE) in combination with nivolumab performed for intermediate stage hepatocellular carcinoma (HCC) | ||||||||||||||||||||||||||||
Medical condition: intermediate stage hepatocellular carcinoma (HCC) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002846-61 | Sponsor Protocol Number: ACT15319 | Start Date*: 2018-04-10 | ||||||||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | ||||||||||||||||||
Full Title: A Phase 1/2 Open-label, Multi-center, Safety, Preliminary Efficacy and Pharmacokinetic (PK) Study of Isatuximab (SAR650984) in Combination with REGN2810, or Isatuximab alone, in Patients with Advan... | ||||||||||||||||||
Medical condition: - Prostate cancer - Non-small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022388-37 | Sponsor Protocol Number: TUD-RELA02-048 | Start Date*: 2011-09-23 | ||||||||||||||||
Sponsor Name:Technische Universität Dresden | ||||||||||||||||||
Full Title: Treatment of patients with MDS or AML with an impending hematological relapse with Azacitidin (Vidaza) | ||||||||||||||||||
Medical condition: Patients with AML or MDS >= 18 years of age after conventional chemotherapy or stem cell transplantation with significant residual disease or an increase of MRD (e.g. t(6,9), NPM1 or CD34+ or CD117... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004353-32 | Sponsor Protocol Number: GECP16/06 | Start Date*: 2017-09-01 |
Sponsor Name:Spanish Lung Cancer Group (SLCG/GECP) | ||
Full Title: Survival, quality of life and self-reported outcomes of elderly patients with advanced non-small cell lung cancer (NSCLC), treated with pembrolizumab (MK-3475) in the first line setting | ||
Medical condition: First line treatment in PD-L1 positive advanced non-small cell lung cancer patients | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2014-004419-35 | Sponsor Protocol Number: GN13RH410 | Start Date*: 2015-03-18 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Inhibition of Co-Stimulation in Rheumatoid Arthritis | |||||||||||||
Medical condition: Rheumatoid Arthritis: patients who are dual ACPA and HLA-DR4 positive | |||||||||||||
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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: 2020-005984-29 | Sponsor Protocol Number: NL76248.091.20 | Start Date*: 2021-06-28 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: [89Zr]Df-IAB22M2C anti-CD8 minibody PET/CT imaging to assess the in vivo distribution of CD8+ T-cells in COVID-19 patients | ||
Medical condition: Proven COVID-19. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000875-34 | Sponsor Protocol Number: MM1807 | Start Date*: 2018-05-30 | |||||||||||
Sponsor Name:National Center for Cancer Immune Therapy | |||||||||||||
Full Title: Efficacy of immunotherapy in melanoma patients with brain metastases treated with steroids | |||||||||||||
Medical condition: Metastatic melanoma with brain metastasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003698-41 | Sponsor Protocol Number: MK-3475-048 | Start Date*: 2015-02-19 | |||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a Subsidiary of Merck & Co. Inc. | |||||||||||||||||||||||
Full Title: A Phase 3 Clinical Trial of Pembrolizumab (MK-3475) in First Line Treatment of Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma. | |||||||||||||||||||||||
Medical condition: Recurrent/metastatic head and neck squamous cell carcinoma. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) EE (Completed) LV (Completed) DK (Completed) FI (Completed) AT (Completed) CZ (Completed) NL (Completed) HU (Completed) ES (Completed) RO (Ongoing) GR (Completed) DE (Completed) IT (Completed) GB (GB - no longer in EU/EEA) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000040-30 | Sponsor Protocol Number: 202100912 | Start Date*: 2023-03-06 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: An open label pilot study of [18AlF]-Resca-IL2 (Interleukin-2 PET tracer) for positron emission tomography imaging in patients treated with immune checkpoint inhibitors. | ||
Medical condition: patients with stage IV non-small-cell lung carcinoma (NSCLC), renal cell carcinoma (RCC), CSCC, urothelial cell cancer (UCC), and head and neck squamous cell carcinoma (HNSCC), eligible for ICI the... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001461-16 | Sponsor Protocol Number: 4280-003 | Start Date*: 2019-02-13 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 1/Phase 2 Clinical Study to Evaluate the Safety and Efficacy of a Combination of MK-4280 and Pembrolizumab (MK-3475) in Participants with Hematologic Malignancies | |||||||||||||
Medical condition: Hematologic malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003556-23 | Sponsor Protocol Number: PROMIT | Start Date*: 2019-10-15 | |||||||||||
Sponsor Name:University Hospital of the Friedrich-Alexander University Erlangen-Nürnberg | |||||||||||||
Full Title: A Phase 2, single arm study on dacarbazine (DTIC) followed by immunotherapy re-challenge in unresectable or metastatic melanoma with primary resistance to PD-1/PD-L1 or PD-1 + CTLA4 Blockade Pre... | |||||||||||||
Medical condition: Melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005793-10 | Sponsor Protocol Number: 01012121 | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:Jakob Benedict Seidelin | |||||||||||||
Full Title: Open label Randomized Controlled clinical Trial of vedolizumab versus conventional treatment for Checkpoint Inhibitor induced Colitis | |||||||||||||
Medical condition: Immune check point inhibitor induced colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001252-22 | Sponsor Protocol Number: MP-LALC | Start Date*: 2017-08-02 | |||||||||||
Sponsor Name:DIPARTIMENTO DI ONCOLOGIA-UNIVERSITA' DEGLI STUDI DI TORINO | |||||||||||||
Full Title: Pembrolizumab (MK-3475) as maintainance unresectable stage III NSCLC after chemo-radiotherapy (MP-LALC- Maintainance Pembrolizumab in Locally Advanced Lung Cancer). | |||||||||||||
Medical condition: unresectable stage IIIA/B Non Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003203-14 | Sponsor Protocol Number: TUXEDO-2 | Start Date*: 2023-05-02 |
Sponsor Name:Med. Univ. Wien, Klinik f. Innere Medizin I, Onkologie | ||
Full Title: Phase II Study of daTopotamab-derUXtecan (Dato-DXd; DS-1026a) in triple-negative brEast cancer patients with newly Diagnosed or prOgressing brain metastases | ||
Medical condition: triple negative breast cancer with newly diagnosed or progressing brain metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005427-36 | Sponsor Protocol Number: NL75654.078.20 | Start Date*: 2021-05-26 |
Sponsor Name:Erasmus MC Cancer Center [...] | ||
Full Title: A multicenter, open label non-randomized phase I/II dose escalation study with extension cohort to determine the safety, tolerability and immune modulating effects of the therapeutic LRPAP1 synthet... | ||
Medical condition: non small cell lung cancer (NSCLC) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
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 |
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