- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Sarcopenia.
Displaying page 1 of 2.
EudraCT Number: 2014-003482-25 | Sponsor Protocol Number: CBYM338E2202 | Start Date*: 2015-01-30 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A 28 week, randomized, double-blind, placebo-controlled, multi-center, parallel group dose range finding study to assess the effect of monthly doses of bimagrumab 70, 210, and 700 mg on skeletal mu... | |||||||||||||
Medical condition: sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Completed) BE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003134-33 | Sponsor Protocol Number: R1033-SRC-1239 | Start Date*: 2014-01-31 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY OF THE SAFETY AND EFFICACY OF 3-MONTH SUBCUTANEOUS REGN1033 TREATMENT IN PATIENTS WITH SARCOPENIA | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000471-27 | Sponsor Protocol Number: CBYM338E2202E1 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A 28 week randomized withdrawal extension of a doubleblind, placebo-controlled, parallel group study to assess durability of effect on skeletal muscle strength and function upon withdrawal of bimag... | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006354-98 | Sponsor Protocol Number: L00074 TD 304 | Start Date*: 2007-06-07 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: “Transdermal testosterone supplementation in elderly hypogonadal men with sarcopenia: effects on muscle function, physical performance, body composition and quality of life.” A randomized, double-b... | |||||||||||||
Medical condition: ELDERLY HYPOGONADAL MEN WITH SARCOPENIA | |||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003455-61 | Sponsor Protocol Number: 2013GR06 | Start Date*: 2015-02-11 | |||||||||||
Sponsor Name:Tayside Academic Sciences Centre | |||||||||||||
Full Title: Perindopril and Leucine to improve muscle function in older people | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002383-95 | Sponsor Protocol Number: 0773-005-00 | Start Date*: 2007-08-08 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase IIa Randomized, Placebo-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0773 in Patients with Sarcopenia | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) ES (Completed) FR (Completed) GB (Completed) FI (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002373-12 | Sponsor Protocol Number: R&D:2008GR01 | Start Date*: 2008-10-02 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Effect of Spironolactone on Exercise Capacity in functionally impaired older people without heart failure: a double blind placebo controlled trial | |||||||||||||
Medical condition: Older people with impairment in activities of daily living (sarcopenia) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003932-35 | Sponsor Protocol Number: BIO101-CL03 | Start Date*: 2018-02-20 | |||||||||||
Sponsor Name:Biophytis S.A. | |||||||||||||
Full Title: Safety and Efficacy of BIO-101 175 mg b.i.d. and 350 mg b.i.d. 26-week oral administration to patients suffering from age-related SARcopenia, including sarcopenic obesity, Aged ≥65 years and at ris... | |||||||||||||
Medical condition: Sarcopenia including sarcopenic obesity | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002509-22 | Sponsor Protocol Number: 0677-032 | Start Date*: 2005-09-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A 24-Week, Double-Blind, Randomized, Placebo-Controlled, Multicenter Study to Assess the Safety and Efficacy of MK-0677 for the Treatment of Sarcopenia in Patients Recovering From Hip Fracture | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012621-12 | Sponsor Protocol Number: R&D2008GR03 | Start Date*: 2009-08-06 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Maximising physical function in later life: a 2 centre randomised trial of progressive resistance exercise training in combination with ACE inhibition | |||||||||||||
Medical condition: Age related decline in muscle function (sarcopenia) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005401-28 | Sponsor Protocol Number: AOI2021ME_PICKERING | Start Date*: 2022-01-26 |
Sponsor Name:University Hospital of Clermont-Ferrand | ||
Full Title: Effects of the combination of magnesium bisphosphonates versus bisphosphonates alone on bone remodeling: Randomized pilot clinical trial | ||
Medical condition: postmenopausal osteoporosis | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005874-11 | Sponsor Protocol Number: 0822-035 | Start Date*: 2009-02-24 | ||||||||||||||||
Sponsor Name:Laboratoires Merck Sharp & Dhome-Chibret | ||||||||||||||||||
Full Title: A Substudy to Explore Biomarkers of Physical Function in the Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) to Reduce the Risk of ... | ||||||||||||||||||
Medical condition: This is an exploratory sub-study of Protocol 018 (Eudract N°2007-002693-66) to identify biomarkers of physical function. This biomarker sub-study will use an ongoing clinical study (Protocol 018) ... | ||||||||||||||||||
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Population Age: Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005920-39 | Sponsor Protocol Number: UC-IMM-2106 | Start Date*: 2022-07-12 |
Sponsor Name:Unicancer | ||
Full Title: A phase II study of durvalumab (MEDI 4736) maintenance in frail limited disease small cell lung cancer patients after thoracic chemoradiotherapy (CRT) | ||
Medical condition: Histologically confirmed frail Limited Disease Small Cell Lung Cancer (ECOG PS 2, ECOG PS 0-1 and older than 70 or did not receive a concomitant thoracic CRT because of comorbidities) previously un... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003899-13 | Sponsor Protocol Number: NL65803.078.18 | Start Date*: 2018-12-20 |
Sponsor Name: | ||
Full Title: The effect of IntraDialytic Parenteral Nutrition on nutritional status and quality of life in hemodialysis patients | ||
Medical condition: Malnutrition / Sarcopenia (loss of muscle mass) in hemodialyse patients. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000359-42 | Sponsor Protocol Number: GOOD-WP2 | Start Date*: 2019-02-18 | ||||||||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
Full Title: Geriatric outcomes among older Type 2 diabetic patients treated with DPP4 inhibitors or glinides: focus on sarcopenia markers of muscle and physical performance status (GOOD-WP2) | ||||||||||||||||||
Medical condition: Elderly patients suffering from type 2 diabetes mellitus in treatment with metformina | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003915-11 | Sponsor Protocol Number: CarniValI (Uni-Koeln-1107) | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:University of Utah | |||||||||||||
Full Title: Phase I/II Trial of Valproic Acid and Carnitine in Infants with Spinal Muscular Atrophy Type I (CARNI-VAL Type I) | |||||||||||||
Medical condition: Spinal Muscular Atrophy Type I in infants | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003703-19 | Sponsor Protocol Number: 18-002 | Start Date*: 2020-04-20 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: The Effect of Higher Protein Dosing in Critically Ill Patients: A Multicenter Randomized Trial | ||
Medical condition: Nutritionally high-risk critically ill mechanically ventilated patients. In this sub-study, eligible and enrolled patients randomized to the high protein dose group will achieve its protein goals b... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004406-18 | Sponsor Protocol Number: INRCA-2017-01 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:IRCC INRCA | |||||||||||||
Full Title: Geriatric outcomes among older Type 2 diabetic patients treated with DPP4 inhibitors or glinides: focus on pro-inflammatory and oxidative stress markers (GOOD-WP1) | |||||||||||||
Medical condition: TYPE 2 DIABETES | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000252-18 | Sponsor Protocol Number: 35RC20_9803_RePERSO | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:Rennes University Hospital | |||||||||||||
Full Title: Evaluation of treatment PERSOnalization based on its therapeutic monitoring in patients with metastatic colorectal cancer treated with regorafenib | |||||||||||||
Medical condition: metastatic colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003663-26 | Sponsor Protocol Number: UC-GTG-2006 | Start Date*: 2021-11-19 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A double-blind randomised phase III trial evaluating the efficacy of ADT +/- darolutamide in de novo metastatic prostate cancer patients with vulnerable functional ability and not elected for docet... | |||||||||||||
Medical condition: Adenocarcinoma of the prostate | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) IE (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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