- Trials with a EudraCT protocol (66)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
66 result(s) found for: Nintedanib.
Displaying page 1 of 4.
EudraCT Number: 2018-000525-32 | Sponsor Protocol Number: 1199-0248 | Start Date*: 2019-01-31 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | |||||||||||||
Full Title: An open-label extension trial of the long term safety of nintedanib in patients with Progressive Fibrosing Interstitial Lung Disease (PF-ILD) | |||||||||||||
Medical condition: Progressive Fibrosing Interstitial Lung Disease (PF-ILD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Completed) GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005554-23 | Sponsor Protocol Number: 1199-0378 | Start Date*: 2021-11-24 | |||||||||||
Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | |||||||||||||
Full Title: An open-label trial of the long-term safety and tolerability of nintedanib per os, on top of standard of care, over at least 2 years, in children and adolescents with clinically significant fibrosi... | |||||||||||||
Medical condition: Interstitial Lung Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) HU (Prematurely Ended) BE (Trial now transitioned) NL (Ongoing) GR (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) FI (Completed) DK (Ongoing) IT (Trial now transitioned) NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004530-14 | Sponsor Protocol Number: 1199-0337 | Start Date*: 2019-10-15 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | |||||||||||||
Full Title: A double blind, randomised, placebo-controlled trial to evaluate the dose-exposure and safety of nintedanib per os on top of standard of care for 24 weeks, followed by open label treatment with nin... | |||||||||||||
Medical condition: Interstitial Lung Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Completed) FI (Completed) NO (Completed) DK (Completed) FR (Completed) CZ (Completed) PL (Completed) GR (Completed) HU (Completed) GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002114-40 | Sponsor Protocol Number: APHP200527 | Start Date*: 2020-07-30 |
Sponsor Name:Assistance Publique - Hôpitaux de Paris | ||
Full Title: Nintedanib for the treatment of SARS-Cov-2 induced pulmonary fibrosis | ||
Medical condition: Patients 2 to 6 months after Covid-19 acute pneumonia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003891-22 | Sponsor Protocol Number: BIO_LUME_1 | Start Date*: 2015-10-06 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: Nintedanib (BIBF 1120) plus docetaxel in NSCLC patients progressing after first-line CTX: angiogenic biomarker identification, phase II trial | ||
Medical condition: The project aims for screening for potential biomarkers and biomarker combinations relevant for second line setting in NSCLC during combinational therapy with docetaxel and nintedanib. The predicit... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
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: 2012-005201-48 | Sponsor Protocol Number: 1199.93 | Start Date*: 2013-07-16 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: LUME-Meso: Double blind, randomised, multicentre, phase II/III study of nintedanib in combination with pemetrexed / cisplatin followed by continuing nintedanib monotherapy versus placebo in combina... | |||||||||||||
Medical condition: Unresectable Malignant Pleural Mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Prematurely Ended) GB (Completed) FR (Completed) DK (Completed) ES (Prematurely Ended) BE (Completed) NL (Prematurely Ended) SE (Completed) PT (Completed) CZ (Completed) AT (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003360-37 | Sponsor Protocol Number: 1199.247 | Start Date*: 2017-02-28 |
Sponsor Name:Boehringer Ingelheim | ||
Full Title: A double blind, randomized, placebo-controlled trial evaluating the efficacy and safety of nintedanib over 52 weeks in patients with Progressive Fibrosing Interstitial Lung Disease (PF-ILD) | ||
Medical condition: The aim of the current study is to investigate the efficacy and safety of 150 mg bid nintedanib over 52 weeks in patients with Progressive Fibrosing Interstitial Lung Disease (PF-ILD) defined as pa... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) ES (Completed) BE (Completed) DE (Completed) GB (Completed) PL (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000521-38 | Sponsor Protocol Number: EORTC-08112 | Start Date*: 2017-06-30 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Nintedanib as maintenance treatment of malignant pleural mesothelioma (NEMO): a double-blind randomized phase II study of the EORTC Lung Cancer Group | |||||||||||||
Medical condition: Malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000095-42 | Sponsor Protocol Number: 1199.52 | Start Date*: 2014-10-08 | |||||||||||
Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled Phase III study of nintedanib plus best supportive care (BSC) versus placebo plus BSC in patients with colorectal cancer refractory to standard therap... | |||||||||||||
Medical condition: Patients with metastatic colorectal cancer refractory to standards therapies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LU (Completed) IT (Completed) SE (Completed) AT (Completed) DK (Completed) BE (Completed) DE (Completed) PT (Completed) NL (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002109-73 | Sponsor Protocol Number: NiCCC2013 | Start Date*: 2013-11-14 | ||||||||||||||||
Sponsor Name:Greater Glasgow Health Board | ||||||||||||||||||
Full Title: A Randomised Phase II Study of Nintedanib (BIBF1120) Compared to Chemotherapy in Patients with Recurrent Clear Cell Carcinoma of the Ovary or Endometrium | ||||||||||||||||||
Medical condition: Recurrent clear cell carcinoma of the ovary or endometrium | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Completed) FR (Completed) NL (Completed) DK (Prematurely Ended) FI (Prematurely Ended) NO (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2015-000640-42 | Sponsor Protocol Number: 1199.222 | Start Date*: 2015-08-26 | |||||||||||
Sponsor Name:Boehringer Ingelheim France | |||||||||||||
Full Title: A twelve week, open-label, randomised, parallel-group study evaluating safety, tolerability and pharmacokinetics (PK) of oral nintedanib in combination with oral pirfenidone, compared to treatment ... | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001747-31 | Sponsor Protocol Number: P160907 | Start Date*: 2019-04-09 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: A Multi-center, Randomised, Double-blind Trial of Nintedanib in Lung Tranplant (LTx) recipients with bronchiolitis obliterans sydrome (BOS) grade 1-2 | |||||||||||||
Medical condition: Bronchiolitis Obliterating Syndrome (SBO) grade 1 or 2 in patients with pulmonary transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004895-21 | Sponsor Protocol Number: NEO-BLADE | Start Date*: 2014-01-17 | |||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
Full Title: Phase II randomised placebo controlled NEOadjuvant chemotherapy study of Nintedanib with Gemcitabine and Cisplatin in locally advanced muscle invasive BLADder cancEr | |||||||||||||
Medical condition: Muscle invasive bladder cancer - localised muscle invasive carcinoma (T2-T4a N0 M0) | |||||||||||||
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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: 2015-003280-11 | Sponsor Protocol Number: MA29895 | Start Date*: 2016-02-25 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: AN EXPLORATORY MULTICENTER, OPEN-LABEL, SINGLE ARM STUDY OF THE SAFETY AND TOLERABILITY OF PIRFENIDONE (ESBRIET®) IN COMBINATION WITH NINTEDANIB (OFEV®) IN PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS | |||||||||||||
Medical condition: Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) DK (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002619-14 | Sponsor Protocol Number: 1199.36 | Start Date*: 2016-07-21 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: INSTAGE(TM): A 24-week, double-blind, randomized, parallel-group study evaluating the efficacy and safety of oral nintedanib coadministrated with oral sildenafil, compared to treatment with ninteda... | |||||||||||||
Medical condition: patients with idiopathic pulmonary fibrosis (IPF) and advanced lung function impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) BE (Completed) GB (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005814-12 | Sponsor Protocol Number: UCL10/0470 | Start Date*: 2013-08-19 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Phase II, randomised, placebo controlled, multicentre, feasibility study of low dose (metronomic) cyclophosphamide with or without nintedanib (BIBF 1120) in advanced ovarian cancer (METRO-BIBF) | |||||||||||||
Medical condition: Advanced ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004458-34 | Sponsor Protocol Number: Nipawilma_2013 | Start Date*: 2014-11-12 | |||||||||||
Sponsor Name:University of Essen | |||||||||||||
Full Title: A Phase I/II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Efficacy and Safety of Nintedanib/Vargatef in Combination With Paclitaxel Chemotherapy for Treatment of ... | |||||||||||||
Medical condition: Advanced (unresectable stage III or IV) BRAF V600 wildtype cutaneous malignant melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002093-12 | Sponsor Protocol Number: 1506-STBSG | Start Date*: 2017-07-04 | ||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of | ||||||||||||||||||
Full Title: A Phase II multicenter study comparing the efficacy of the oral angionenesis inhibitor nintedanib with the intravenous cytotoxis compound ifosfamide for treatment of patients with advanced metastat... | ||||||||||||||||||
Medical condition: Metastatic soft tissue sarcoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) NL (Completed) ES (Completed) LT (Completed) | ||||||||||||||||||
Trial results: View results |
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