- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
58 result(s) found for: Systemic Sclerosis (SSc).
Displaying page 1 of 3.
EudraCT Number: 2018-004655-20 | Sponsor Protocol Number: LIGHT | Start Date*: 2019-05-30 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: CLINICAL EFFICACY OF INHIBITION OF ORGAN DYSFUNCTION THROUGH BERMEKIMAB IN SYSTEMIC SCLEROSIS: A PROOF-OF-CONCEPT DOUBLE-BLIND RANDOMIZED CLINICAL TRIAL (THE LIGHT TRIAL) | |||||||||||||
Medical condition: CLINICAL EFFICACY OF INHIBITION OF ORGAN DYSFUNCTION THROUGH BERMEKIMAB IN SYSTEMIC SCLEROSIS: A PROOF-OF-CONCEPT DOUBLE-BLIND RANDOMIZED CLINICAL TRIAL (THE LIGHT TRIAL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000392-28 | Sponsor Protocol Number: 1199.214 | Start Date*: 2015-11-02 | |||||||||||||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim bv | |||||||||||||||||||||||||||||||||
Full Title: A double blind, randomised, placebo-controlled trial evaluating efficacy and safety of oral nintedanib treatment for at least 52 weeks in patients with Systemic Sclerosis associated Interstitial Lu... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with Systemic Sclerosis and associated Interstitial Lung Disease | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) GB (Completed) PT (Completed) DK (Completed) BE (Completed) ES (Completed) GR (Completed) FR (Completed) PL (Completed) IE (Completed) FI (Completed) NO (Completed) SE (Completed) AT (Completed) HU (Prematurely Ended) CZ (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000230-33 | Sponsor Protocol Number: HYDROXYSSc | Start Date*: 2022-01-26 | |||||||||||||||||||||||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||||||||||||||||||||||
Full Title: A DOUBLE BLIND, RANDOMIZED, PLACEBO-CONTROLLED, ADD-ON TRIAL EVALUATING EFFICACY AND SAFETY OF HYDROXYCHLOROQUINE IN EARLY SYSTEMIC SCLEROSIS (SSc)- HYDROXYSSc | |||||||||||||||||||||||||||||||||
Medical condition: Systemic Sclerosis (SSc) is a rare and orphan disease (DPCM 12 gennaio 2017-GU SG n°65-S.O. n°15 - 18/03/2017), characterized by immunological, vascular and fibrotic abnormalities. The estimated in... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001667-44 | Sponsor Protocol Number: 11575705 | Start Date*: 2011-06-28 | ||||||||||||||||
Sponsor Name:Active Biotech AB | ||||||||||||||||||
Full Title: An open-label study to evaluate biomarkers and safety in systemic sclerosis patients treated with ABR-215757 (paquinimod) | ||||||||||||||||||
Medical condition: Systemic Sclerosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001719-65 | Sponsor Protocol Number: CALC-SSc | Start Date*: 2018-12-10 |
Sponsor Name:University Medial Center Groningen | ||
Full Title: CALCification as an early marker of vasculopathy and organ involvement in Systemic Sclerosis CALC-SSc study | ||
Medical condition: Systemic sclerosis (SSc) is a rare progressive autoimmune disease hallmarked by severe vasculopathy. Patients are prone to enhanced calcification of skin and the vasculature. Active calcifications ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000224-27 | Sponsor Protocol Number: SSc/CYC/MP | Start Date*: 2008-10-15 | |||||||||||
Sponsor Name:Newcastle upon Tyne NHS Foundation Trust | |||||||||||||
Full Title: Systemic sclerosis associated interstitial lung disease: A longitudinal observational study assessing optimum treatment regimens. | |||||||||||||
Medical condition: Systemic Sclerosis associated interstitial lung disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003203-35 | Sponsor Protocol Number: VP-C21-004 | Start Date*: 2019-12-13 | ||||||||||||||||
Sponsor Name:Vicore Pharma AB | ||||||||||||||||||
Full Title: A Phase 2, single-center, randomised, double-blind, placebo-controlled, cross-over, cold challenge study investigating the effect of C21 on cold-induced vasoconstriction in subjects with Raynaud’s ... | ||||||||||||||||||
Medical condition: Systemic sclerosis (SSc) Raynaud’s phenomenon (RP) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003430-16 | Sponsor Protocol Number: APHP180613 | Start Date*: 2020-07-28 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Safety and efficacy of itacitinib in adults with systemic sclerosis: a phase II, randomized, controlled trial - SCLERITA | |||||||||||||
Medical condition: Patients with newly or active diffuse Systemic sclerosis (SSc) at the time of screening | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004669-17 | Sponsor Protocol Number: CSTI571E2205 | Start Date*: 2008-02-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, open-label, Proof of Concept (PoC) study to evaluate the efficacy and tolerability of STI571 for the treatment of fibrosis in patients with systemic sclerosis | |||||||||||||
Medical condition: Skin fibrosis in systemic sclerosis patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005023-11 | Sponsor Protocol Number: EMR200017-014 | Start Date*: 2016-07-08 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A Phase II, randomized, double-blind, placebo controlled, parallel-group, multicenter trial to evaluate the efficacy and safety of abituzumab in subjects with systemic sclerosis-associated intersti... | |||||||||||||
Medical condition: Systemic sclerosis-associated interstitial lung disease (SSc-ILD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005230-20 | Sponsor Protocol Number: NOT AVAILABLE | Start Date*: 2006-07-14 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: EX VIVO EFFECT OF AMINAFTONE (CAPILLAREMA) ON THE ENDOTELIAL FUNCTION IN SYSTEMIC SCLEROSIS. Effetto ex vivo dell’aminaftone (Capillarema) sulla funzione endoteliale nella Sclerosi Sistemica | |||||||||||||
Medical condition: Variazione della gravita' del fenomeno di Raynaud misurata mediante diario dei sintomi e scala analogica visiva VAS ヨ Visual Analogic Scale (6). Variazione dello stato globale di malattia valutat... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003403-66 | Sponsor Protocol Number: 1199.225 | Start Date*: 2017-11-06 | |||||||||||||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim bv | |||||||||||||||||||||||||||||||||
Full Title: An open-label extension trial to assess the long term safety of nintedanib in patients with ‘Systemic Sclerosis associated Interstitial Lung Disease’ (SSc-ILD) | |||||||||||||||||||||||||||||||||
Medical condition: Systemic Sclerosis associated Interstitial Lung Disease | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) ES (Completed) PT (Completed) GB (GB - no longer in EU/EEA) FR (Completed) DK (Completed) BE (Completed) AT (Completed) CZ (Completed) GR (Completed) SE (Completed) NO (Completed) FI (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022710-77 | Sponsor Protocol Number: AC-055C301 | Start Date*: 2011-06-16 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: Prospective, randomized, placebo-controlled, double-blind, multicenter, parallel group study to assess the efficacy, safety and tolerability of macitentan in patients with ischemic digital ulcers a... | |||||||||||||
Medical condition: Ischemic digital ulcers associated with systemic sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) DK (Prematurely Ended) BG (Completed) FI (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001353-28 | Sponsor Protocol Number: PSSc-001 | Start Date*: 2013-10-04 |
Sponsor Name:InterMune Inc. | ||
Full Title: An Open-Label, Randomized, Phase 2 Study of the Safety and Tolerability of Pirfenidone when Administered to Patients with Systemic Sclerosis-Related Interstitial Lung Disease | ||
Medical condition: Systemic Sclerosis-Related Interstitial Lung Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001882-28 | Sponsor Protocol Number: 2014-05ED | Start Date*: 2014-10-13 |
Sponsor Name:Thoraxklinik-Heidelberg gGmbH | ||
Full Title: Early Treatment of Borderline Pulmonary Arterial Hypertension Associated with Systemic Sclerosis (SSc-APAH) | ||
Medical condition: Systemic sclerosis-patients (SSc) with borderline pulmonary arterial hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003836-31 | Sponsor Protocol Number: AGO/2006/007 | Start Date*: 2006-09-06 | |||||||||||
Sponsor Name:University Hospital Gent | |||||||||||||
Full Title: A protocol based treatment for early and severe systemic sclerosis with (anti-CD-20) rituximab | |||||||||||||
Medical condition: systemic sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002796-28 | Sponsor Protocol Number: CEASESTIFFNESS | Start Date*: 2016-04-12 |
Sponsor Name:University Medical Center Groningen (UMCG) | ||
Full Title: The Clinical Efficacy And Subclinical Effects on arterial STIFFNESS of bosentan therapy added to usual care in patients with systemic sclerosis with digital ulcers. | ||
Medical condition: Systemic sclerosis (SSc) is characterized by skin fibrosis and visceral disease, mainly of the lungs, kidneys and the heart, accompanied by microvascular damage ultimately leading to digital ischem... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005764-62 | Sponsor Protocol Number: HZNP-HZN-825-301 | Start Date*: 2021-06-29 | |||||||||||
Sponsor Name:Horizon Therapeutics Ireland DAC | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Repeat-dose, Multicenter Trial to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of HZN-825 in Patients with Diffuse Cutaneous Syst... | |||||||||||||
Medical condition: Diffuse Cutaneous Systemic Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) IT (Trial now transitioned) NL (Ongoing) PL (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001004-15 | Sponsor Protocol Number: A1334-02 | Start Date*: 2022-04-22 | |||||||||||||||||||||||||||||||
Sponsor Name:ACCELERON PHARMA INC. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 1b/2 Open-Label, Multiple-Ascending Dose Study Followed by a Randomized, Double-Blind, Placebo Controlled Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamic Effects, and Effica... | |||||||||||||||||||||||||||||||||
Medical condition: Systemic sclerosis (SSc), a rare connective tissue disorder characterized by fibrosis, inflammation, and microvascular injury with heterogeneous presentations; Interstitial lung disease (ILD), a co... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002081-13 | Sponsor Protocol Number: GS-2001 | Start Date*: 2020-09-08 | ||||||||||||||||
Sponsor Name:Gesynta Pharma AB | ||||||||||||||||||
Full Title: A Phase II, randomised, multi-centre placebo-controlled, double-blind study to investigate the safety of GS-248, and efficacy on Raynaud’s phenomenon (RP) and peripheral vascular blood flow in pati... | ||||||||||||||||||
Medical condition: Raynaud's phenomenon (RP) in patients with Systemic sclerosis (SSc) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
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