- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Bone meal.
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| EudraCT Number: 2015-005585-32 | Sponsor Protocol Number: 111111733104 | Start Date*: 2016-06-24 | |||||||||||
| Sponsor Name:Department of Biomedical Sciences, Faculty of Health Sciences, University of Copenhagen | |||||||||||||
| Full Title: Synergy effect of the appetite hormone GLP-1 (LiragluTide) and Exercise on maintenance of weight loss and health after a low calorie diet - the S-LiTE randomized trial | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002407-10 | Sponsor Protocol Number: 17/0238 | Start Date*: 2018-03-23 | ||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||
| Full Title: A double-blinded, randomised, placebo-controlled trial of liraglutide 3.0 mg in patients with poor weight-loss and a suboptimal glucagon-like peptide-1 response following bariatric surgery. | ||||||||||||||||||
| Medical condition: Obesity. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-003226-25 | Sponsor Protocol Number: Abifood01 | Start Date*: 2013-07-12 | |||||||||||
| Sponsor Name:Fundacion Publica Andaluza para la Gestion de la Investigacion en Salud de Sevilla | |||||||||||||
| Full Title: Phase I, randomized, open design trial to evaluate the effect of food (fasting, fat meal and standard meal) on the pharmacokinetics of abiraterone acetate at reduced doses, compared with convention... | |||||||||||||
| Medical condition: metastatic prostatic cancer after castration-resistant progression to docetaxel | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000154-19 | Sponsor Protocol Number: UC-0105/1701 | Start Date*: 2017-07-19 |
| Sponsor Name:UNICANCER | ||
| Full Title: A phase II randomized trial comparing alpelisib and fulvestrant versus chemotherapy as maintenance therapy in patients with PIK3CA mutated advanced breast cancer | ||
| Medical condition: PIK3CA mutated, HR+/Her2- metastatic breast cancer who do not present progressive disease after 6-8 cycles of 1st or second line chemotherapy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004083-21 | Sponsor Protocol Number: E7438-G000-101 | Start Date*: 2015-02-02 |
| Sponsor Name:Epizyme, Inc. | ||
| Full Title: An Open-Label, Multicenter, Phase 1/2 Study of Tazemetostat (EZH2 Histone Methyl Transferase [HMT] Inhibitor) as a Single Agent in Subjects With Advanced Solid Tumors or With B Cell Lymphomas | ||
| Medical condition: Relapsed or refractory Diffuse Large B Cell Lymphoma, Follicular Lymphoma, Advanced solid tumor | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005153-39 | Sponsor Protocol Number: LX4211.1-310-T1DM | Start Date*: 2015-04-28 | |||||||||||
| Sponsor Name:Lexicon Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of LX4211 as Adjunct Therapy in Adult Patients with Typ... | |||||||||||||
| Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) AT (Completed) ES (Completed) LT (Completed) DE (Completed) GB (Completed) HU (Completed) BE (Completed) SE (Completed) NL (Completed) PL (Completed) BG (Completed) RO (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003942-18 | Sponsor Protocol Number: ASTX727-06 | Start Date*: 2021-09-03 | ||||||||||||||||||||||||||
| Sponsor Name:Taiho Oncology, Inc. | ||||||||||||||||||||||||||||
| Full Title: An Open-Label, Multicenter, Extension Study for Subjects Who Participated in Prior Clinical Studies of ASTX727 (Standard Dose) | ||||||||||||||||||||||||||||
| Medical condition: Acute myeloid lymphoma (AML), myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML) or solid tumors | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SK (Trial now transitioned) BG (Trial now transitioned) ES (Completed) LT (Completed) HU (Trial now transitioned) AT (Ongoing) FR (Completed) DE (Trial now transitioned) IT (Completed) RO (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-001959-37 | Sponsor Protocol Number: E7449-E044-101 | Start Date*: 2011-10-17 | |||||||||||||||||||||||||||||||
| Sponsor Name:Eisai Limited | |||||||||||||||||||||||||||||||||
| Full Title: An open label, multicenter, Phase 1/2 Study of Poly(ADP-Ribose) Polymerase (PARP) Inhibitor E7449 as Single Agent in Subjects with Advanced Solid Tumours or with B-cell Malignancies and in Combinat... | |||||||||||||||||||||||||||||||||
| Medical condition: Advanced solid tumors (including ovarian cancer, triple negative breast cancer, and advanced melanoma) and B-cell lymphomas | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2009-016622-13 | Sponsor Protocol Number: CA187-016 | Start Date*: 2010-06-23 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: An Open-Label Randomized, Parallel, Two-Arm Phase II Study Comparing BMS-690514 + Letrozole with Lapatinib + Letrozole in Recurrent or Metastatic Breast Cancer Patients Who Are Hormone Receptor Pos... | |||||||||||||
| Medical condition: Locally recurrent or metastatic hormone receptor positive (HR+) breast cancer and either: • HER2+ disease with progression while on adjuvant antiendocrine therapy or at any time after adjuvant anti... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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