- Trials with a EudraCT protocol (257)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
257 result(s) found for: Entry inhibitors.
Displaying page 10 of 13.
| EudraCT Number: 2007-006031-30 | Sponsor Protocol Number: GIM8 OVER | Start Date*: 2007-12-20 | |||||||||||
| Sponsor Name:CONSORZIO ONCOTECH | |||||||||||||
| Full Title: A Randomized Trial with factorial Design comparing Fulvestrant ± Lapatinib ± Aromatase Inhibitor in metastatic breast cancer progressing after Aromatase Inhibitor therapy | |||||||||||||
| Medical condition: breast cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002448-42 | Sponsor Protocol Number: GMI-1271-201 | Start Date*: 2015-03-12 | |||||||||||
| Sponsor Name:GlycoMimetics, Inc. | |||||||||||||
| Full Title: A Phase I/II, open-label multicenter study to determine safety, pharmacokinetics and efficacy of GMI-1271 in combination with chemotherapy in patients with acute myeloid leukemia | |||||||||||||
| Medical condition: Acute myeloid leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-003736-77 | Sponsor Protocol Number: E7080-A001-216 | Start Date*: 2023-03-28 |
| Sponsor Name:Eisai Inc. | ||
| Full Title: A Phase 1/2 Study of Lenvatinib in Combination with Everolimus in Recurrent and Refractory Pediatric Solid Tumors, Including CNS Tumors | ||
| Medical condition: Recurrent and Refractory Solid Tumors | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003847-39 | Sponsor Protocol Number: AK580 | Start Date*: 2018-03-12 | |||||||||||
| Sponsor Name:Akari Therapeutics Plc. | |||||||||||||
| Full Title: CAPSTONE: Phase III Confirmatory Assessment Protocol: rVA576 Safety and Efficacy in Three-Part, Two-Arm, Randomised Open Label Evaluation in patients with Paroxysmal Nocturnal Haemoglobinuria (PNH) | |||||||||||||
| Medical condition: Paroxysmal Nocturnal Haemoglobinuria (PNH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004040-28 | Sponsor Protocol Number: MS200647_0024 | Start Date*: 2019-04-11 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: A Phase Ib/II, Open-Label Study of M7824 in Combination with Chemotherapy in Participants with Stage IV Non-small Cell Lung Cancer | |||||||||||||
| Medical condition: Stage IV Non-small Cell Lung Cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001923-11 | Sponsor Protocol Number: 18-BI-1206-03 | Start Date*: 2019-12-09 | |||||||||||
| Sponsor Name:BioInvent International AB | |||||||||||||
| Full Title: Phase 1/2a Clinical Trial of BI-1206, a Monoclonal Antibody to CD32b (FcγRIIB), in Combination with Pembrolizumab in Subjects with Advanced Solid Tumors Previously Treated with Anti-PD1 or Anti-PDL... | |||||||||||||
| Medical condition: Advanced solid tumors who have relapsed or are refractory to anti-PD1 or anti-PDL1 therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001940-25 | Sponsor Protocol Number: IFG-05-2019 | Start Date*: 2021-08-25 | |||||||||||||||||||||||||||||||
| Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||||||||||||||||||||||
| Full Title: A PHASE II OPEN-LABEL STUDY FOR THE COMPREHENSIVE ANALYSIS OF PREDICTORS OF THE TREATMENT WITH PEMBROLIZUMAB AND OLAPARIB IN PATIENTS WITH UNRESECTABLE OR METASTATIC HER2 NEGATIVE BREAST CANCER AND... | |||||||||||||||||||||||||||||||||
| Medical condition: patients with unresectable or metastatic HER2 negative breast cancer and a deleterious germline mutation in BRCA 1/2, ATM, BARD1, CHEK2, FANCC, PALB2, RAD51C, RAD51D, SLX4, XRCC2 or a homologous re... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-000027-12 | Sponsor Protocol Number: IJB-IRAES-2020 | Start Date*: 2022-06-26 | |||||||||||
| Sponsor Name:Institut Jules Bordet | |||||||||||||
| Full Title: Immunological variables associated to ICI toxicity in cancer patients IRAES | |||||||||||||
| Medical condition: solid tumour | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003780-35 | Sponsor Protocol Number: AIO-TRK-0221 | Start Date*: 2019-04-01 | |||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
| Full Title: Randomized phase II, open-label efficacy and safety study of second-line durvalumab plus tremelimumab versus platinum-based chemotherapy alone in patients with NSCLC and first-line checkpoint-inhib... | |||||||||||||
| Medical condition: Non-small cell lung cancer stage IV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001223-31 | Sponsor Protocol Number: KAISII | Start Date*: 2016-10-11 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Incidence of Invasive Fungal Disease in Patients receiving Immunosuppressive Therapy, Intensive Chemotherapy or Reduced Intensity Haematopoietic Stem Cell Transplantation on Posaconazole Prophylaxis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Aplastic Anaemia, Myelodysplastic syndromes, Acute Myeloid Leukaemia undergoing immunosuppression therapy, high dose chemotherapy or reduced intensity stem cell transplantation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-004111-22 | Sponsor Protocol Number: CSOM230B2305 | Start Date*: 2007-01-05 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized, double-blind study to assess the safety and efficacy of different dose levels of Pasireotide (SOM230) s.c. over a 6 month treatment period in patients with de novo, persistent or recu... | |||||||||||||
| Medical condition: Cushing’s disease is rare disease that is caused by an adrenocorticotropic hormone (ACTH) secreting pituitary adenoma. The elevated ACTH secreted by these tumors stimulates the adrenal glands to pr... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) BE (Completed) IT (Completed) FI (Completed) FR (Completed) DE (Completed) PT (Completed) GR (Completed) GB (Completed) HU (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007788-17 | Sponsor Protocol Number: A3921045 | Start Date*: 2009-05-20 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: PHASE 3, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED STUDY OF THE EFFICACY AND SAFETY OF 2 DOSES OF CP 690,550 MONOTHERAPY IN PATIENTS WITH ACTIVE RHEUMATOID ARTHRITIS | |||||||||||||
| Medical condition: CP 690,550 is being studied as a DMARD for the treatment of moderate to severe active RA in adults. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005854-21 | Sponsor Protocol Number: RDEA806-201 | Start Date*: 2008-01-15 | |||||||||||
| Sponsor Name:Ardea Biosciences Inc. | |||||||||||||
| Full Title: A multicenter Phase 2a, randomized, double-blind, placebo-controlled, proof-of-concept trial to determine the antiviral activity, pharmacokinetics, tolerability and safety of RDEA806 in HIV-1 posit... | |||||||||||||
| Medical condition: HIV-1 | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003997-28 | Sponsor Protocol Number: GENA-15 | Start Date*: 2014-01-15 | |||||||||||
| Sponsor Name:Octapharma Pharmazeutika Produktions GmbH, | |||||||||||||
| Full Title: Extension Study for Patients who completed GENA-05 (NuProtect) – to Investigate Immunogenicity, Efficacy and Safety of Treatment with Human-cl rhFVIII | |||||||||||||
| Medical condition: Severe Haemophilia A | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) DE (Prematurely Ended) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002177-25 | Sponsor Protocol Number: 19-255-03 | Start Date*: 2021-11-08 | ||||||||||||||||||||||||||
| Sponsor Name:Nektar Therapeutics | ||||||||||||||||||||||||||||
| Full Title: A Phase 1b/2, Open-label, Multicenter, Dose Escalation and Dose Expansion Study of NKTR-255 in Combination with Cetuximab as a Salvage Regimen for Solid Tumors | ||||||||||||||||||||||||||||
| Medical condition: Relapsed or refractory (R/R) head and neck squamous cell carcinoma (HNSCC) or colorectal carcinoma (CRC) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-003512-20 | Sponsor Protocol Number: IN11004 | Start Date*: 2016-05-09 | |||||||||||
| Sponsor Name:Intec Pharma, Ltd. | |||||||||||||
| Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled Study Comparing the Efficacy and Safety of Gastric Retentive, Controlled Release Accordion Pill™ Carbidopa/Levodo... | |||||||||||||
| Medical condition: Parkinson's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) GB (Completed) SK (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-004193-91 | Sponsor Protocol Number: DPB100925 | Start Date*: 2005-03-07 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A 12-Week, Parallel-Group, Double-Blind, Randomized, Placebo-Controlled, Multicenter, Dose Ranging Study to Evaluate the Efficacy, Safety and Tolerability of GW823093 (2.5mg, 7.5mg, 15mg, 30mg and ... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DE (Completed) SE (Completed) CZ (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002128-10 | Sponsor Protocol Number: BP39144 | Start Date*: 2016-09-14 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: An adaptive Phase I/II study to assess safety, efficacy, pharmacokinetics and pharmacodynamics of RO7112689 in healthy volunteers and patients with paroxysmal nocturnal hemoglobinuria (PNH) | |||||||||||||
| Medical condition: Paroxysmal nocturnal hemoglobinuria (PNH) | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) DE (Trial now transitioned) HU (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003974-29 | Sponsor Protocol Number: D6186C00001 | Start Date*: 2019-08-15 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Biomarker-Directed Phase 2 Platform Study in Patients with Advanced Non-Small Cell Lung Cancer whose Disease has Progressed on First-Line Osimertinib Therapy | |||||||||||||
| Medical condition: Advanced Non-Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) NO (Trial now transitioned) DK (Completed) ES (Ongoing) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005042-21 | Sponsor Protocol Number: I4X-MC-JFCU | Start Date*: 2015-04-21 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Single-Arm, Multicenter, Phase 1b Study with an Expansion Cohort to Evaluate Safety and Efficacy of Necitumumab in Combination with Abemaciclib in Treatment of Patients with Stage IV Non-Small Ce... | |||||||||||||
| Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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