- Trials with a EudraCT protocol (497)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (68)
497 result(s) found for: Combinations.
Displaying page 14 of 25.
| EudraCT Number: 2011-006162-40 | Sponsor Protocol Number: NODAT-BELATAC | Start Date*: 2013-05-28 | ||||||||||||||||
| Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | ||||||||||||||||||
| Full Title: NEW-ONSET DIABETES MELLITUS AFTER RENAL TRANSPLANTATION. A MULTICENTRE, PROSPECTIVE, RANDOMIZED, OPEN STUDY TO EVALUATE BELATACEPT-BASED VERSUS TACROLIMUS-BASED IMMUNOSUPPRESSION | ||||||||||||||||||
| Medical condition: Adult kidney transplant recipients older than 45 years old with risk of developing prediabetes states after renal transplantation (PREDAT) and diabetes mellitus after renal transplantation (NODAT) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-004981-52 | Sponsor Protocol Number: GEMNABCCC-001 | Start Date*: 2016-09-28 | |||||||||||
| Sponsor Name:University Hospital Essen | |||||||||||||
| Full Title: Nab-Paclitaxel (Abraxane®) and Gemcitabine as first line therapy in patients with cholangiocarcinoma ineligible for cisplatin-based chemotherapy – a pilot study The NACHO trial (GEMNABCCC-001) | |||||||||||||
| Medical condition: unresecable, metastatic or recurrent cholangiocarcinoma (intrahepatic cholangiocellular carcinoma, bile duct cancer, gall bladder carcinoma) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000486-37 | Sponsor Protocol Number: CHF201701 | Start Date*: 2019-03-27 |
| Sponsor Name:Heart Initiative | ||
| Full Title: STRONG-HF: Safety, Tolerability and efficacy of Rapid Optimization, helped by NT-proBNP testing, of Heart Failure therapies | ||
| Medical condition: Acute Heart Failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) HR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-002238-35 | Sponsor Protocol Number: CLI-05993CB1-01 | Start Date*: 2020-01-27 | |||||||||||
| Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
| Full Title: A SINGLE-DOSE, UNCONTROLLED, OPEN LABEL, NON-RANDOMIZED, CLINICAL PHARMACOLOGY STUDY OF CHF 5993 100/6/12.5 μg PMDI (FIXED COMBINATION OF BECLOMETASONE DIPROPIONATE PLUS FORMOTEROL FUMARATE PLUS GL... | |||||||||||||
| Medical condition: asthma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005392-39 | Sponsor Protocol Number: 213357 | Start Date*: 2022-02-25 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline, S.A. | ||||||||||||||||||
| Full Title: OPAL Master Protocol: A Phase 1B/2 Multicohort Umbrella Study to Evaluate the Safety and Efficacy of Novel Treatments and/or Combinations of Treatments in Participants with Ovarian Cancer (OPAL). C... | ||||||||||||||||||
| Medical condition: Ovarian cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-005217-41 | Sponsor Protocol Number: 51-03FPAEU | Start Date*: 2021-09-06 |
| Sponsor Name:Lead Chemical Company Ltd | ||
| Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of a Flurbiprofen 40 mg cutaneous hydrogel medicated plaster vs. placebo and vs. a marketed active comparator in the l... | ||
| Medical condition: pain in acute strains, sprains or bruises of the soft tissues following blunt trauma, e.g. sports injuries | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003398-79 | Sponsor Protocol Number: MH21HEM | Start Date*: 2023-05-11 |
| Sponsor Name:Princess Máxima Center for pediatric oncology | ||
| Full Title: International proof of concept therapeutic Stratification trial of Molecular Anomalies in Relapsed or Refractory HEMatological malignancies in children Subprotocol D: Trametinib + Dexamethasone + C... | ||
| Medical condition: Molecularly profiled r/r ALL/LBL whose tumor harbors an actionable event that can be targeted by the investigational agents. In this subprotocol, patients must present alterations in the RAS signal... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006958-31 | Sponsor Protocol Number: 2021/3401 | Start Date*: 2022-05-24 |
| Sponsor Name:Gustave Roussy | ||
| Full Title: An Interventional and Translational Study investigating Sotorasib in Previously Treated Locally Advanced or Metastatic NSCLC Subjects With Mutated KRAS p.G12C | ||
| Medical condition: Locally-advanced and unresectable or metastatic non-small-cell lung cancer with KRAS G12C mutation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001202-42 | Sponsor Protocol Number: D419QC00002 | Start Date*: 2016-11-09 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase II, Open-Label, Multi-Arm Study to Determine the Preliminary Efficacy of Novel Combinations of Treatment in Patients with Platinum Refractory Extensive-Stage Small-Cell Lung Cancer | |||||||||||||
| Medical condition: Patients with extensive-stage small-cell lung cancer (ED-SCLC) who have refractory or resistant disease from prior platinum-based chemotherapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001165-24 | Sponsor Protocol Number: UC-0150/1704 | Start Date*: 2018-06-12 |
| Sponsor Name:UNICANCER | ||
| Full Title: A Multicentre, Randomised, Open-label, Phase 2 trial of mifamurtide combined with post-operative chemotherapy for newly diagnosed high risk osteosarcoma patients (metastatic osteosarcoma at diagnos... | ||
| Medical condition: Patients ≤50 years old with high-risk osteosarcoma (defined as metastatic osteosarcoma at diagnosis or localised osteosarcoma with poor histological response) after pre-operative chemotherapy and s... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004961-42 | Sponsor Protocol Number: BC-6226 | Start Date*: 2020-08-06 | |||||||||||
| Sponsor Name:Ghent University Hospital | |||||||||||||
| Full Title: SPondyloArthritis: inducing drug-free Remission by early TNF-Alpha bloCkade Under guidance of Single cell RNA sequencing and epigenetic profiling | |||||||||||||
| Medical condition: peripheral spondyloarthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003543-29 | Sponsor Protocol Number: 48-04LXPU | Start Date*: 2021-05-07 |
| Sponsor Name:Lead Chemical Company Ltd. | ||
| Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of a Loxoprofen sodium 60 mg medicated plaster vs. placebo and vs. a marketed comparator in the local symptomatic and ... | ||
| Medical condition: Acute blunt, soft tissue injuries of the muscles or limbs | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-004670-25 | Sponsor Protocol Number: CQ-001-19 | Start Date*: 2022-11-16 | |||||||||||
| Sponsor Name:Corequest sagl | |||||||||||||
| Full Title: Peritoneal Ultrafiltration in cardio Renal syndrome to prevent heart failure Exacerbation: The PURE Study | |||||||||||||
| Medical condition: Congestive Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003465-18 | Sponsor Protocol Number: BCT1902 | Start Date*: 2021-10-06 |
| Sponsor Name:Breast Cancer Trials | ||
| Full Title: A randomised phase II trial evaluating the efficacy of a nivolumab monotherapy lead in “window” or commencement of nivolumab concurrently with paclitaxel and carboplatin as neoadjuvant therapy in e... | ||
| Medical condition: Early stage triple negative breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003939-30 | Sponsor Protocol Number: CA209-142 | Start Date*: 2014-03-21 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 2 Clinical Trial of Nivolumab and Nivolumab Plus Ipilimumab in Recurrent and Metastatic Microsatellite High (MSI-H) Colon Cancer | |||||||||||||
| Medical condition: MSI Positive Colorectal Cancer MSI Negative Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) BE (Trial now transitioned) IE (Completed) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004074-25 | Sponsor Protocol Number: ABc2 | Start Date*: 2020-08-12 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
| Full Title: A Phase II Open-Label Randomized COntrolled Pre-Surgical Feasibility Study of Antibiotic COmbinations in Early Breast Cancer | |||||||||||||
| Medical condition: We investigated, in a population of patients with breast cancer, the combined effect of azithrocyn, docyciclin and vitamin C on biomarkers associated with cell proliferation | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000636-40 | Sponsor Protocol Number: PNOC022 | Start Date*: 2022-10-20 | |||||||||||||||||||||
| Sponsor Name:Pacific Pediatric Neuro-Oncology Consortium (PNOC) | |||||||||||||||||||||||
| Full Title: PNOC022: A Combination Therapy Trial using an Adaptive Platform Design for Children and Young Adults with Diffuse Midline Gliomas (DMGs) including Diffuse Intrinsic Pontine Gliomas (DIPGs) at Initi... | |||||||||||||||||||||||
| Medical condition: Diffuse Midline Gliomas, H3K27M mutant | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2013-004916-23 | Sponsor Protocol Number: MORE | Start Date*: 2014-04-28 | |||||||||||
| Sponsor Name:Ospedale San Raffaele | |||||||||||||
| Full Title: Monotherapy with Ofatumumab for RElapsed/refractory Splenic B-cell marginal zone lymphoma (MORE) | |||||||||||||
| Medical condition: Splenic B-cell marginal zone lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000782-53 | Sponsor Protocol Number: UNITO-MM-01/FORTE | Start Date*: 2015-01-12 |
| Sponsor Name:Università degli Studi di Torino-Dipartimento di Biotecnologie Molecolari e Scienze della Salute | ||
| Full Title: A MULTICENTER, RANDOMIZED, OPEN LABEL PHASE II STUDY OF CARFILZOMIB, CYCLOPHOSPHAMIDE AND DEXAMETHASONE (CCyd) as pre transplant INDUCTION and post transplant consolidation or CARFILZOMIB, LENALIDO... | ||
| Medical condition: NEWLY DIAGNOSED MULTIPLE MYELOMA (MM) PATIENTS ELEGIBLE FOR AUTOLOGOUS TRANSPLANT | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000042-17 | Sponsor Protocol Number: M21SAD | Start Date*: 2021-12-29 | |||||||||||||||||||||||||||||||
| Sponsor Name:Netherlands Cancer Institute | |||||||||||||||||||||||||||||||||
| Full Title: Sarcomas and DDR-Inhibition; a neoadjuvant phase I combined modality study – SADDRIN-1 | |||||||||||||||||||||||||||||||||
| Medical condition: soft tissue sarcomas | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
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