- Trials with a EudraCT protocol (243)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
243 result(s) found for: Degenerative diseases.
Displaying page 1 of 13.
EudraCT Number: 2019-002473-65 | Sponsor Protocol Number: PET-PiB | Start Date*: 2021-06-16 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: PET-CT study of cerebral regional amyloid burden in Patients with suspected Alzheimer’s disease | |||||||||||||
Medical condition: Patients with amnestic or non-amnestic MCI or early dementia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002963-92 | Sponsor Protocol Number: CLRX712A12201 | Start Date*: 2020-02-05 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, subject and investigator blinded study investigating the safety, tolerability and preliminary efficacy of 8-week treatment with intra-articular LRX712 to regenerat... | |||||||||||||
Medical condition: Cartilage injuries | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001955-29 | Sponsor Protocol Number: 024PKAN15004 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Retrophin, Inc. | |||||||||||||
Full Title: Efficacy, Safety, and Tolerability of Fosmetpantotenate (RE-024), a Phosphopantothenate replacement therapy, in patients with Pantothenate Kinase-associated Neurodegeneration (PKAN): A Randomized, ... | |||||||||||||
Medical condition: Pantothenate kinase associated neurodegeneration (PKAN), an autosomal recessive genetic disorder, the most common form of Neurodegeneration with Brain Iron Accumulation (NBIA). It is a progressive,... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) NO (Completed) FR (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002494-75 | Sponsor Protocol Number: CL3-12911-018 | Start Date*: 2006-04-26 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: The efficacy and safety of two doses of strontium ranelate (1g and 2g per day) versus placebo administered orally for 3 years in the treatment of knee osteoarthritis. A prospective multicentre, int... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) BE (Completed) GB (Completed) ES (Completed) IT (Completed) DK (Completed) PT (Completed) LT (Completed) EE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004049-26 | Sponsor Protocol Number: MTX-071-P02 | Start Date*: 2017-11-23 | |||||||||||
Sponsor Name:Mestex | |||||||||||||
Full Title: Lopain (MTX-071 / resiniferatoxin) An open label, single dose phase Ib/IIa study to determine the safety and clinical effects of intra-articular injections of low doses of Lopain (MTX-071) in pa... | |||||||||||||
Medical condition: chronic osteoarthritic knee-joint pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003232-31 | Sponsor Protocol Number: TDU11685-ACT12505 | Start Date*: 2011-11-03 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: A two part protocol to assess, using double blind placebo control, the safety, tolerability, and pharmacokinetics of ascending single doses of a new intra-articular administration formulation of SA... | |||||||||||||
Medical condition: KNEE OSTEOARTHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000178-13 | Sponsor Protocol Number: RDORTH01 | Start Date*: 2017-04-13 | |||||||||||
Sponsor Name:Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust | |||||||||||||
Full Title: How Effective are Topical NSAIDs in the Treatment of Hip Osteoarthritis: An In Vivo Study in Patients Undergoing Total Hip Arthroplasty | |||||||||||||
Medical condition: Osteoarthritis of the hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004046-18 | Sponsor Protocol Number: CL3-12911-040 | Start Date*: 2012-02-23 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Knee joint replacement over 5 years in patients with knee osteoarthritis. A long term follow up study in patients of the CL3-12911-018 study. | |||||||||||||
Medical condition: Osteoarthritis The medical condition investigated in the CL3-12911-018 study was osteoarthritis. The applied CL3-12911-040 trial, CL3-12911-018 follow-up study, is thus performed in osteoarthrit... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Prematurely Ended) AT (Completed) BE (Completed) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) DK (Prematurely Ended) LT (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003315-63 | Sponsor Protocol Number: ARPA-AMANTADINA-2012 | Start Date*: 2012-10-24 |
Sponsor Name:FIBHULP | ||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, STUDY OF EFFECTIVENESS, TOLERABILITY AND SAFETY OF THERAPY WITH AMANTADINE IN DEGENERATIVE ATAXIAS | ||
Medical condition: Degenerative ataxias | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003467-60 | Sponsor Protocol Number: M13-741 | Start Date*: 2014-06-11 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2a Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981 in Patients with Knee Osteoarthritis | |||||||||||||
Medical condition: Adult male and female patients with mild to moderate, symptomatic, radiographic and inflammatory osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003797-51 | Sponsor Protocol Number: D5680C00003 | Start Date*: 2021-07-20 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomised, Double-blind, Placebo-controlled, Dose-response Study of the Efficacy and Safety of MEDI7352 in Subjects with Painful Osteoarthritis of the Knee | |||||||||||||
Medical condition: Painful osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003956-20 | Sponsor Protocol Number: 2003-35-RTA-3 | Start Date*: 2005-03-09 | |||||||||||
Sponsor Name:HEXAL AG | |||||||||||||
Full Title: Multi-center, double-blind, double-dummy, controlled, randomized phase III study on the tolerability and efficacy of Diclofenac Sodium 150 mg o.d. in comparison to Voltaren® 50 t.i.d. and Voltaren®... | |||||||||||||
Medical condition: Symptomatic treatment for pain and inflammation associated with irritations of degenerative joint diseases, e.g. ostheoarthitis of the hip, knee or fingers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004052-30 | Sponsor Protocol Number: CLNA043X2202 | Start Date*: 2017-04-28 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, patient and investigator blinded, Proof of Concept study investigating the safety, tolerability and preliminary efficacy of multiple intra-articular LNA043 injecti... | |||||||||||||
Medical condition: Acute cartilage injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003154-80 | Sponsor Protocol Number: 2020CLI | Start Date*: 2020-12-08 | |||||||||||
Sponsor Name:Mucos Pharma GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Crossover Study to Investigate the Mechanism of Action of an Oral Enzyme Treatment with Bromelain, Trypsin and Rutoside versus Placebo in Subjects wi... | |||||||||||||
Medical condition: Subjects suffering from knee Osteoarthitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001427-79 | Sponsor Protocol Number: TIRCON2012V1-EXT | Start Date*: 2015-03-27 |
Sponsor Name:ApoPharma Inc. | ||
Full Title: Long-term Safety and Efficacy Study of Deferiprone in Patients with Pantothenate Kinase-Associated Neurodegeneration (PKAN) | ||
Medical condition: Pantothenate kinase-associated neurodegeneration (PKAN) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004444-30 | Sponsor Protocol Number: Disc_allo_MSV | Start Date*: 2013-04-23 |
Sponsor Name:Citospin | ||
Full Title: Treatment of degenerative disc disease with allogenic mesenchymal cells—MSV-- | ||
Medical condition: Treatment of degenerative disc disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004313-41 | Sponsor Protocol Number: 47659 | Start Date*: 2014-05-19 | |||||||||||||||||||||
Sponsor Name:UMCG | |||||||||||||||||||||||
Full Title: Effect of pre-operative pain treatment by means of duloxetine on postoperative outcome after total hip or knee arthroplasty | |||||||||||||||||||||||
Medical condition: Osteoarthritis (knee or hip) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004581-10 | Sponsor Protocol Number: CL2-201086-002 | Start Date*: 2018-09-04 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Efficacy and safety of 3 doses of S201086/GLPG1972 administered orally once daily in patients with knee osteoarthritis. A 52-week international, multi-regional, multi-center, randomized, double-bli... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) DK (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004805-34 | Sponsor Protocol Number: TDU13828-ACT13830 | Start Date*: 2015-04-02 | |||||||||||
Sponsor Name:Sanofi-aventis Research & Development | |||||||||||||
Full Title: A Two Part Protocol Using Double Blind Placebo Control to Assess the Safety, Tolerability, and Pharmacokinetics of Single Escalating Intra-articular Doses Followed by Assessment of Efficacy, Safety... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005040-28 | Sponsor Protocol Number: 1289.7 | Start Date*: 2015-05-11 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim Italia S.p.A. | ||||||||||||||||||
Full Title: A multi-centre, double-blind, parallel-group, randomised controlled study to investigate efficacy, safety and tolerability of orally administered BI 409306 during a 12-week treatment period compa... | ||||||||||||||||||
Medical condition: Cognitive impairment due to Alzheimer's Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) PT (Completed) AT (Completed) GB (Completed) BE (Completed) NL (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
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