- Trials with a EudraCT protocol (1,581)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (529)
1,581 result(s) found for: Connective tissue disease.
Displaying page 1 of 80.
EudraCT Number: 2014-001101-40 | Sponsor Protocol Number: 13/0417 | Start Date*: 2015-02-24 | ||||||||||||||||
Sponsor Name:University College London (UCL) | ||||||||||||||||||
Full Title: Sclero XIII: A phase II ,double-blind, randomized, placebo-controlled study to investigate pharmacokinetics (PK), safety and efficacy of intravenous factor XIII treatment in patients with systemic... | ||||||||||||||||||
Medical condition: Systemic Sclerosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003633-42 | Sponsor Protocol Number: RBHIPF004 | Start Date*: 2013-10-18 | |||||||||||||||||||||||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||||||||||||||||||||||
Full Title: A randomized, double blind controlled trial comparing rituximab against intravenous cyclophosphamide in connective tissue disease associated interstitial lung disease | |||||||||||||||||||||||||||||||||
Medical condition: A diagnosis of connective tissue disease associated interstitial lung disease, based on internationally accepted criteria, in one of the following categories: o Systemic sclerosis o Idiopathic inte... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005323-27 | Sponsor Protocol Number: IM101-344 | Start Date*: 2015-09-16 | ||||||||||||||||
Sponsor Name:University of Michigan | ||||||||||||||||||
Full Title: A phase II study to evaluate subcutaneous abatacept vs. placebo in diffuse cutaneous systemic sclerosis—a double-blind, placebo-controlled, randomized controlled trial | ||||||||||||||||||
Medical condition: Diffuse Cutaneous Systemic Sclerosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004937-19 | Sponsor Protocol Number: CMHV370A12201 | Start Date*: 2021-09-08 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A multi-center, randomized, participant- and investigator- blinded, placebo-controlled, parallel group basket study to evaluate the safety, tolerability and efficacy of MHV370 in participants with ... | ||||||||||||||||||
Medical condition: Sjögren’s syndrome Mixed connective tissue disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018904-94 | Sponsor Protocol Number: 2010-018904-94 | Start Date*: 2010-05-31 | |||||||||||
Sponsor Name:FONDAZIONE SALVATORE MAUGERI - CLINICA DEL LAVORO E DELLA RIABILITAZIONE | |||||||||||||
Full Title: EFFICACY AND SAFETY OF INTRAMUSCULAR NERIDRONATE IN OSTEOPOROTIC PATIENTS AFFECTED BY PARKINSON'S DISEASE | |||||||||||||
Medical condition: Osteoporosis in patients affected by Parkinson's disaease at the stages 1-2-3-4 following Hoehn and Yahr criteria | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005357-23 | Sponsor Protocol Number: 01 | Start Date*: 2013-01-27 | |||||||||||
Sponsor Name:AUSL VITERBO | |||||||||||||
Full Title: Preventing injection pain by Clostridium Histolyticum Collagenase Administration for teatment of Dupuytrens contracture | |||||||||||||
Medical condition: Dupuytren s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003372-18 | Sponsor Protocol Number: NERI-AS001-07 | Start Date*: 2007-12-03 | |||||||||||
Sponsor Name:ABIOGEN PHARMA | |||||||||||||
Full Title: A randomised, double-blind, placebo controlled study to assess the safety and the efficacy of neridronate 100 mg - 4 i.v. infusions in a course of 10 days treatment - in patients with algodystrophi... | |||||||||||||
Medical condition: Algodystrophic Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003200-39 | Sponsor Protocol Number: 13/0077 | Start Date*: 2014-04-01 | ||||||||||||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||||||||||||
Full Title: A phase II, single centre, randomised, placebo-controlled, 3-part trial to assess the safety, tolerability and efficacy of Zibotentan in patients with renal disease secondary to scleroderma | ||||||||||||||||||||||||||||
Medical condition: Renal complications of systemic sclerosis (scleroderma renal crisis and chronic kidney disease). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005626-29 | Sponsor Protocol Number: IRFMN-SARCO-7953 | Start Date*: 2021-05-05 | ||||||||||||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||||||||||||
Full Title: A phase II study on trabectedin in combination with PPARg agonist pioglitazone in patients with round cell myxoid liposarcomas or dedifferentiated G1 and G2 liposarcomas with stable disease after a... | ||||||||||||||||||||||||||||
Medical condition: Patients with myxoid/round cell liposarcoma treated with at least 4 cycle of T alone with a stable disease at the last tumor evaluation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000494-67 | Sponsor Protocol Number: 1.2 | Start Date*: 2013-10-22 | |||||||||||
Sponsor Name:Klinik for håndkirurgi, Gentofte hospital | |||||||||||||
Full Title: Needle fasciotomi vs collagenase for treatment of Dupuytrens contracture in 2nd, 3rd, 4th and 5th metacarpophalangeal joint. | |||||||||||||
Medical condition: Dupuytrens contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005661-20 | Sponsor Protocol Number: SKP-021-01-11 | Start Date*: 2012-07-13 | |||||||||||
Sponsor Name:PROMO INTERNATIONAL SRL | |||||||||||||
Full Title: A double-blind, randomised, parallel group, active controlled, multicentre study to assess the therapeutic non-inferiority of SKP-021, a 0.3% ketoprofen patch, versus diclofenac sodium patch in pat... | |||||||||||||
Medical condition: patients with painful and inflammatory conditions (e.g.: back pain, bruise, contusion, sprain, strains) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006205-95 | Sponsor Protocol Number: 2011-006205-95 | Start Date*: 2012-10-05 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: Toremifene in desmoid tumor: prospective clinical trial and identification of potential molecular targets | |||||||||||||
Medical condition: Primary or recurrent sporadic desmoid tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017160-17 | Sponsor Protocol Number: ALGO-01 | Start Date*: 2010-02-24 | ||||||||||||||||
Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | ||||||||||||||||||
Full Title: NSAID USED IN MESOTHERAPY VS NSAID INTRAMUSCOLAR INJECTION IN algodistrophy TREATMENT: A RANDOMIZED, CONTROLLED STUDY | ||||||||||||||||||
Medical condition: SUFFERED FROM ALGODISTROPHY PATIENTS | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001075-20 | Sponsor Protocol Number: IOV-2018-STS-METROPHOLYS | Start Date*: 2018-05-25 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO - IRCCS | |||||||||||||
Full Title: The METROPHOLYS Study - Metronomic cyclophosphamide vs doxorubicin in elderly patients with advanced soft tissue sarcomas. Randomized, controlled open label clinical trial | |||||||||||||
Medical condition: soft tissue sarcomas | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000745-37 | Sponsor Protocol Number: AC-052-413 | Start Date*: 2004-10-11 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: Uncontrolled extension trial to protocol AC-052-406 to evaluate the long-term effects of bosentan therapy in patients with pulmonary arterial hypertension related to connective tissue disease (TRUS... | ||
Medical condition: Pulmonary arterial hypertension (PAH) is characterized by increased pulmonary arterial pressure and pulmonary vascular resistance leading to right ventricular failure. PAH is a serious complication... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001252-52 | Sponsor Protocol Number: CZOL446H2337 | Start Date*: 2009-03-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo controlled efficacy and safety trial of intravenous zoledronic acid twice yearly compared to placebo in osteoporotic children treated with glucocort... | |||||||||||||
Medical condition: Treatment of osteoporosis in a paediatric population (aged 5 to 17 years old) treated with systemic glucocorticoids (i.v. or oral) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FI (Prematurely Ended) BE (Completed) DE (Prematurely Ended) PL (Prematurely Ended) Outside EU/EEA HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004852-62 | Sponsor Protocol Number: FARM7KWBZ4 | Start Date*: 2009-02-09 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA` DEGLI STUDI DI NAPOLI | ||||||||||||||||||
Full Title: Safety and clinical efficacy of abetimus sodium (LJP-394) in prevention of renal flares in patients with systemic lupus erythematosus and a history of renal disease. | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000343-14 | Sponsor Protocol Number: AS0007 | Start Date*: 2017-01-04 | |||||||||||
Sponsor Name:UCB Biopharma SPRL. | |||||||||||||
Full Title: Multicenter, Open-Label Study To Assess The Effects Of Certolizumab Pegol On The Reduction Of Anterior Uveitis Flares In Axial Spondyloarthritis Subjects With A History Of Anterior Uveitis (C-VIEW) | |||||||||||||
Medical condition: Anterior Uveitis in subjects with Axial Spondyloarthritis (axSpA) and a history of AU. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001108-11 | Sponsor Protocol Number: EORTC protocol 62033 | Start Date*: 2004-11-08 | |||||||||||
Sponsor Name:European Organisation for the Research and Treatment of Cancer | |||||||||||||
Full Title: A phase II study of intravenous TZT-1027, administered weekly times two, every three weeks, to patients with advanced or metastatic soft tissue sarcomas (STS) with prior exposure to doxorubicin-bas... | |||||||||||||
Medical condition: Soft Tissue Sarcoma (STS) is a rare group of heterogeneous mesenchymal cancers originating from connective tissue. There are multiple histological subtypes of STS. At present all these subtypes are... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005157-29 | Sponsor Protocol Number: PHRR-04/PG/SPAXIM | Start Date*: 2007-04-27 | ||||||||||||||||
Sponsor Name:CHRU-TOURS | ||||||||||||||||||
Full Title: EFFET DU METHOTREXATE SUR LA RELATION DOSE - EFFET DE L'INFLIXIMAB DANS LA SPONDYLARTHRITE ANKYLOSANTE | ||||||||||||||||||
Medical condition: Les patients seront traités par infliximab, avec ou sans méthotrexate associé, selon la pratique habituelle en accord avec le libellé de l’A.M.M. Seuls le nombre de prélèvements sanguins et de visi... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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