- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Clavicle.
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EudraCT Number: 2006-003381-33 | Sponsor Protocol Number: EMR-62202-717 | Start Date*: 2007-08-30 |
Sponsor Name:Institute of Oncology Ljubljana | ||
Full Title: Induction chemotherapy followed by chemoradiation with cetuximab and cisplatin for inoperable squamous cell carcinoma of the head and neck. | ||
Medical condition: Inoperable squamous cell carcinoma of the head and neck. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002403-13 | Sponsor Protocol Number: Ularitide-1502 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:PDL BioPharma Inc | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blinded, Placebo-controlled Study of Ularitide in the Treatment of Subjects with Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) LT (Prematurely Ended) AT (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002692-98 | Sponsor Protocol Number: GH001 | Start Date*: 2017-10-04 | |||||||||||
Sponsor Name:GAMA Healthcare | |||||||||||||
Full Title: An evaluation of the efficacy of HEXI-PREP by Clinell Wipes versus placebo and ChloraPrep, for use in pre-operative skin preparation | |||||||||||||
Medical condition: For disinfection of the skin, immediately prior to invasive medical procedures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001153-17 | Sponsor Protocol Number: 262 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:MSD | |||||||||||||
Full Title: Phase III (Phase V Program), Open-Label, Randomized, Referred- Care-Controlled, Clinical Trial to Evaluate the Efficacy and Safety of MK-0217A/Alendronate Sodium 70 mg/Vitamin D3 5600 I.U. Combinat... | |||||||||||||
Medical condition: Postmenopausal women with osteoporosis at increased risk of falls. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) LT (Completed) GB (Completed) BE (Completed) LV (Completed) FR (Completed) IE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017039-16 | Sponsor Protocol Number: CL3-12911-036 | Start Date*: 2010-05-05 | ||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | ||||||||||||||||||
Full Title: Effect of strontium ranelate (2g per day) in the management of long bone fractures with delayed-union or non union: an international open label study | ||||||||||||||||||
Medical condition: Delayed and non-united fractures | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) FR (Completed) IT (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002693-66 | Sponsor Protocol Number: 0822-018 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:MERCK SHARP & DOHME CORP. | |||||||||||||
Full Title: A Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of MK-0822 to Reduce the Risk of Fracture in Osteoporotic Postmenopausal Women Treated With Vitamin D an... | |||||||||||||
Medical condition: Postmenopausal Osteoporosis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: LT (Completed) DK (Completed) CZ (Prematurely Ended) PL (Prematurely Ended) GB (Prematurely Ended) DE (Completed) FR (Prematurely Ended) BE (Prematurely Ended) LV (Completed) EE (Completed) IT (Completed) ES (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019952-35 | Sponsor Protocol Number: CS001P3 | Start Date*: 2010-09-14 |
Sponsor Name:CEL-SCI Corporation | ||
Full Title: A Phase III, Open-label, Randomized, Multi-center Study of the Effects of Leukocyte Interleukin, Injection [Multikine] Plus Standard of Care (Surgery + Radiotherapy or Surgery + Concurrent Chemorad... | ||
Medical condition: Subjects with Advanced Primary Sqamous Cell Carcinoma of the oral Cavity/Soft Palate | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) PL (Completed) GB (GB - no longer in EU/EEA) AT (Prematurely Ended) RO (Ongoing) HR (Ongoing) ES (Prematurely Ended) IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001170-32 | Sponsor Protocol Number: H3E-MC-JMIG | Start Date*: 2008-09-05 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company limited | ||||||||||||||||||
Full Title: Protocol H3E-MC-JMIG Phase 3 Study of Pemetrexed, Cisplatin, and Radiotherapy Followed by Consolidation Pemetrexed versus Etoposide, Cisplatin, and Radiotherapy Followed by Consolidation Cytoto... | ||||||||||||||||||
Medical condition: patients with locally advanced, unresectable/inoperable, Stage III, nonsquamous NSCLC without malignant pleural/pericardial effusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) HU (Completed) ES (Completed) NL (Completed) BE (Completed) FR (Completed) DE (Completed) GB (Completed) IE (Completed) | ||||||||||||||||||
Trial results: View results |
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