- 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 9 of 22.
EudraCT Number: 2012-003030-17 | Sponsor Protocol Number: 3475-002 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Randomized, Phase II Study of MK-3475 versus Chemotherapy in Patients with Advanced Melanoma | |||||||||||||
Medical condition: Advanced melanoma (unresectable or metastatic) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) NO (Completed) SE (Completed) IT (Completed) NL (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002957-67 | Sponsor Protocol Number: CA209-010 | Start Date*: 2011-11-23 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Randomized, Blinded, Phase 2 Dose-Ranging Study of BMS-936558 (MDX-1106) in Subjects With Progressive Advanced/Metastatic Clear-Cell Renal Cell Carcinoma Who Have Received Prior Anti-Angiogenic T... | ||||||||||||||||||
Medical condition: Advanced/Metastatic renal cell carcinoma with a clear cell component | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003500-33 | Sponsor Protocol Number: TCD16843 | Start Date*: 2023-03-21 | |||||||||||
Sponsor Name:Synthorx, A Sanofi Company | |||||||||||||
Full Title: An Open-Label, Multicenter Phase 1/2 Dose Escalation and Expansion Study of THOR-707 as a Single Agent and as a Combination Therapy in Adult Subjects with Advanced or Metastatic Solid Tumors | |||||||||||||
Medical condition: Cancer, metastasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001992-22 | Sponsor Protocol Number: ADVANCE | Start Date*: 2018-06-12 | ||||||||||||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||||||||||||
Full Title: Phase II open label randomised safety and efficacy study of the viral vectored ChAd-MVA 5T4 vaccine in combination with PD-1 checkpoint blockade in low- or intermediate-risk localized or locally ad... | ||||||||||||||||||||||||||||
Medical condition: Low- and intermediate-risk prostate cancer and advanced metastatic prostate cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002447-18 | Sponsor Protocol Number: MK3475-055 | Start Date*: 2015-09-23 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | ||
Full Title: A Phase II Clinical Trial of Single Agent Pembrolizumab (MK-3475) in Subjects with Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) Who Have Failed Platinum and Cetuximab | ||
Medical condition: Recurrent/metastatic head and neck squamous cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002934-32 | Sponsor Protocol Number: D4884C00001 | Start Date*: 2015-12-15 | |||||||||||||||||||||
Sponsor Name:AstraZenenca AB | |||||||||||||||||||||||
Full Title: A Phase II, Multi-Center, Open-Label Study of Tremelimumab Monotherapy in Patients with Advanced Solid Tumors | |||||||||||||||||||||||
Medical condition: Adult patients (age ≥18 years) with advanced and metastatic solid tumors including but not limited to histologically or cytologically documented UBC, PDAC, or TNBC. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002328-35 | Sponsor Protocol Number: CANTABRICO | Start Date*: 2020-11-11 | |||||||||||
Sponsor Name:AstraZeneca Farmacéutica Spain, S.A | |||||||||||||
Full Title: A Phase IIIB, Single Arm Study, of Durvalumab in Combination with Platinum-Etoposide for Untreated Patients with Extensive-Stage Small Cell Lung Cancer reflecting Real World Clinical Practice in Sp... | |||||||||||||
Medical condition: Extensive-Stage Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000914-39 | Sponsor Protocol Number: 2018-21 | Start Date*: 2018-11-15 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | |||||||||||||
Full Title: Precision Immuno-Oncology for advanced Non-small cell lung cancer patients with PD-1 ICI Resistance (PIONeeR clinical study) | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002327-11 | Sponsor Protocol Number: 213403 | Start Date*: 2021-02-05 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||||||||||||||||||
Full Title: A RANDOMIZED, PHASE 2, DOUBLE-BLIND STUDY TO EVALUATE THE EFFICACY OF DOSTARLIMAB PLUS CHEMOTHERAPY VERSUS PEMBROLIZUMAB PLUS CHEMOTHERAPY IN METASTATIC NON-SQUAMOUS NON-SMALL CELL LUNG CANCER | ||||||||||||||||||
Medical condition: Metastatic non-squamous non-small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002986-36 | Sponsor Protocol Number: NIBIT-ML-1 | Start Date*: 2020-06-19 | |||||||||||
Sponsor Name:FONDAZIONE NIBIT NETWORK ITALIANO PER LA BIOTERAPIA DEI TUMORI | |||||||||||||
Full Title: A randomized, run-in, phase II study of nivolumab combined with ipilimumab and guadecitabine or nivolumab combined with ipilimumab in melanoma and NSCLC patients resistant to anti-PD-1/PD-L1 | |||||||||||||
Medical condition: MM and NSCLC patients resistant to anti-PD-1/PD-L1 therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002611-34 | Sponsor Protocol Number: 54767414MMY2036 | Start Date*: 2017-10-16 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Open-label, Multicenter, Multiphase Study of JNJ-63723283, an Anti-PD-1 Monoclonal Antibody, Administered in Combination with Daratumumab, Compared with Daratumumab Alone in Subjects ... | |||||||||||||
Medical condition: Relapsed or Refractory Multiple Myeloma (MM). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Prematurely Ended) FR (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004792-36 | Sponsor Protocol Number: CA209-017 | Start Date*: 2012-09-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: An Open-Label Randomized Phase III Trial of BMS-936558 (Nivolumab) versus Docetaxel in Previously Treated Advanced or Metastatic Squamous Cell Non-small Cell Lung Cancer (NSCLC) Revised Protocol N... | |||||||||||||
Medical condition: Squamous cell Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) ES (Ongoing) AT (Completed) HU (Completed) CZ (Completed) NO (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004482-24 | Sponsor Protocol Number: MK3475-087 | Start Date*: 2015-06-02 |
Sponsor Name:Merck Sharp & Dohme LLC | ||
Full Title: A Phase II clinical trial of MK-3475 (pembrolizumab) in subjects with relapsed or refractory (R/R) classical Hodgkin Lymphoma (cHL) | ||
Medical condition: Hodgkin lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) NO (Completed) ES (Completed) NL (Prematurely Ended) DE (Completed) AT (Completed) HU (Completed) IE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004850-31 | Sponsor Protocol Number: C4221016 | Start Date*: 2021-07-29 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND STUDY OF ENCORAFENIB AND BINIMETINIB PLUS PEMBROLIZUMAB VERSUS PLACEBO PLUS PEMBROLIZUMAB IN PARTICIPANTS WITH BRAF V600E/K MUTATION-POSITIVE METASTATIC OR UNRES... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Metastatic or unresectable locally advanced BRAF V600E/K mutation positive melanoma | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) AT (Prematurely Ended) SK (Trial now transitioned) CZ (Trial now transitioned) NO (Prematurely Ended) PL (Trial now transitioned) GR (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002997-29 | Sponsor Protocol Number: D9106C00001 | Start Date*: 2019-01-07 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III, Double-blind, Placebo-controlled, Multi-center International Study of Neoadjuvant/adjuvant Durvalumab for the Treatment of Patients with Resectable Stages II and III Non-small Cell Lun... | |||||||||||||
Medical condition: Patients with resectable Non-small Cell Lung Cancer (Stage IIA to IIIB; either squamous or non-squamous) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) AT (Trial now transitioned) BG (Completed) ES (Ongoing) NL (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004429-15 | Sponsor Protocol Number: GEM-1402 | Start Date*: 2016-02-16 | |||||||||||
Sponsor Name:GRUPO ESPAÑOL MULTICISPLINAR DE MELANOMA | |||||||||||||
Full Title: Phase II multicente, non randomized, open label trial of nivolumab in combination with ipilimumab in subjects with previously untreated metastatic uveal melanoma. | |||||||||||||
Medical condition: Metastatic uveal melanoma non suitable for radical resection. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004682-11 | Sponsor Protocol Number: AUTO3-DB1 | Start Date*: 2017-07-19 | |||||||||||||||||||||||||||||||
Sponsor Name:Autolus Limited | |||||||||||||||||||||||||||||||||
Full Title: A Single Arm, Open-Label, Multi-Centre, Phase I/II Study Evaluating the Safety and Clinical Activity of AUTO3, a CAR T Cell Treatment Targeting CD19 and CD22 with Anti PD-1 Antibody in Patients wi... | |||||||||||||||||||||||||||||||||
Medical condition: Relapsed or refractory Diffuse Large B Cell Lymphoma (DLBCL) and large B cell lymphoma subsets | |||||||||||||||||||||||||||||||||
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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: 2016-003279-23 | Sponsor Protocol Number: MOMEL27 | Start Date*: 2020-01-13 |
Sponsor Name:Radboudumc | ||
Full Title: Phase 2 Study testing the COmbination of Vemurafenib With Cobimetinib in BRAF V600 mutated Melanoma Patients to Normalize LDH and Optimize immunotherapY with Nivolumab and Ipilimumab (COWBOY) | ||
Medical condition: Stage IV or unresectable stage III, BRAFV600E/K mutation positive melanoma, naïve for BRAF/MEK, PD-1/PD-L1 or CTLA-4 targeting therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001327-39 | Sponsor Protocol Number: C/37/2017 | Start Date*: 2018-11-05 |
Sponsor Name:Imperial College London | ||
Full Title: A Phase II, Two-Stage, Trial of Pembrolizumab in Cancer of unknown primary - CUPem | ||
Medical condition: CUP, Cancer of Unknown Primary | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004501-24 | Sponsor Protocol Number: CT-2011-01 | Start Date*: 2012-03-06 | |||||||||||
Sponsor Name:CureTech Ltd. | |||||||||||||
Full Title: Phase II study to evaluate the safety, tolerability and efficacy of CT-011 administered intravenously to patients with metastatic melanoma | |||||||||||||
Medical condition: Metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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