- Trials with a EudraCT protocol (38)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38 result(s) found for: Inducers.
Displaying page 1 of 2.
EudraCT Number: 2018-004520-10 | Sponsor Protocol Number: ACNS1021 | Start Date*: 2019-06-25 |
Sponsor Name:National Cancer Institute (NCI) | ||
Full Title: 2018-004520-10 | ||
Medical condition: Recurrent, Refractory or Progressive High Grade Glioma and Ependymoma Tumors | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2021-005024-37 | Sponsor Protocol Number: 202100647 | Start Date*: 2022-01-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Evaluation of [18F]MC225 to measure P-glycoprotein function in neurodegenerative disease | ||
Medical condition: - Alzheimer's disease - Mild Cognitive Impairment - Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004104-34 | Sponsor Protocol Number: SNDX-5613-0700 | Start Date*: 2022-04-20 | |||||||||||
Sponsor Name:Syndax Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 1/2, Open-label, Dose-Escalation and Dose-Expansion Cohort Study of SNDX-5613 in Patients with Relapsed/Refractory Leukemias, Including Those Harboring an MLL/KMT2A Gene Rearrangement or Nu... | |||||||||||||
Medical condition: Relapsed or Refractory Acute Leukemias | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) LT (Trial now transitioned) DE (Temporarily Halted) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002910-37 | Sponsor Protocol Number: TEA | Start Date*: 2019-10-07 |
Sponsor Name:Erasmus MC | ||
Full Title: Study on the pharmacokinetic interaction between green tea and tamoxifen in patients with breast cancer. “the TEA study” | ||
Medical condition: Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001284-20 | Sponsor Protocol Number: BIOGIO | Start Date*: 2017-07-05 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The effects of the proton pump inhibitor esomeprazole on the bioavailability of afatinib (Giotrif®) in patients with non-small cell lung cancer (NSCLC) 'the BIO-GIO study' | ||
Medical condition: Non small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003265-38 | Sponsor Protocol Number: PTC743-NEU-005-FA | Start Date*: 2022-10-22 |
Sponsor Name:PTC Therapeutics, Inc. | ||
Full Title: An Open-Label Study to Evaluate Pharmacokinetics, Safety, and Efficacy of Vatiquinone in Children With Friedreich Ataxia Younger Than 7 Years of Age | ||
Medical condition: Friedreich Ataxia | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2009-012802-38 | Sponsor Protocol Number: UMCNONCO200903 | Start Date*: 2009-07-01 |
Sponsor Name:University Medical Centre Nijmegen St Radboud | ||
Full Title: Evaluation of the activity of temsirolimus with FLT-PET in patients with renal cell cancer | ||
Medical condition: advanced (stage IV or recurrent disease) RCC | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004378-92 | Sponsor Protocol Number: EdomTHC | Start Date*: 2019-05-27 | |||||||||||
Sponsor Name:Fundació Clínic per la Recerca Biomèdica | |||||||||||||
Full Title: Effect of cannabinoids (THC / CBD) on hyperalgesia in patients with deep endometriosis | |||||||||||||
Medical condition: Deep endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006656-19 | Sponsor Protocol Number: HE 17/08 | Start Date*: 2008-06-03 |
Sponsor Name:Hellenic Cooperative Oncology Group | ||
Full Title: INVESTIGATION OF THE EFFICACY OF LAPATINIB MONOTHERAPY AND TEMOZOLOMIDE PLUS LAPATINIB COMBINATION, IN RECURRENT HIGH GRADE GLIOMAS. A PHASE I/II STUDY. | ||
Medical condition: Refractory glioblastoma multiforme. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006371-67 | Sponsor Protocol Number: RLBUHT 3729 | Start Date*: 2009-09-10 |
Sponsor Name:Royal Liverpool and Broadgreen University Hospital [...] | ||
Full Title: EFFECT OF THIENOPYRIDINE DERIVATIVE (CLOPIDOGREL) ON THE DISPOSITION OF EFAVIRENZ AND NEVIRAPINE IN HIV POSITIVE PATIENTS | ||
Medical condition: To determine whether anti-platelet agent clopidigrel influences the disposition of NNRTIs (efavirenz and nevirapine) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-005722-23 | Sponsor Protocol Number: N01274 | Start Date*: 2007-05-15 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Open-label, single-arm, multi-center, pharmacokinetic, safety and tolerability study of levetiracetam intravenous infusion in children (4 - 16 years old) with epilepsy. | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004854-27 | Sponsor Protocol Number: PROTAM | Start Date*: 2020-02-27 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The influence of UGT inhibition on endoxifen exposure in cancer patients treated with tamoxifen: A proof of concept study. “The PROTAM study” | ||
Medical condition: Hormone positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002426-28 | Sponsor Protocol Number: 81896-PREDICTAM | Start Date*: 2022-11-14 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: Predicting an accurate tamoxifen dose: a feasibility study in patients with hormone positive breast cancer | ||
Medical condition: Hormone positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005732-18 | Sponsor Protocol Number: DU176b-A-U157 | Start Date*: 2016-06-29 | ||||||||||||||||
Sponsor Name:Daiichi Sankyo , Inc. | ||||||||||||||||||
Full Title: A Phase 1, Open-Label, Single-dose, Non-randomized Study to Evaluate Pharmacokinetics and Pharmacodynamics of Edoxaban in Pediatric Patients | ||||||||||||||||||
Medical condition: Edoxaban is being investigated for use in pediatric patients who may require anticoagulation therapy. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) FR (Ongoing) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002500-91 | Sponsor Protocol Number: RPC01-3001 | Start Date*: 2015-10-12 | |||||||||||
Sponsor Name:Celgene International II Sàrl (CIS II) | |||||||||||||
Full Title: A Multi-Site, Open-Label Extension Trial of Oral RPC1063 in Relapsing Multiple Sclerosis | |||||||||||||
Medical condition: Relapsing Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) ES (Completed) BG (Completed) SK (Completed) GR (Completed) PL (Completed) LV (Completed) EE (Completed) LT (Completed) PT (Completed) SE (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003517-13 | Sponsor Protocol Number: N01275 | Start Date*: 2007-12-11 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Open-label, single-arm, multi-center, pharmacokinetic, safety and tolerability study of levetiracetam intravenous infusion in children (1 month to 4 years old) with epilepsy. | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001017-16 | Sponsor Protocol Number: FARM9A8J83 | Start Date*: 2012-04-16 | ||||||||||||||||
Sponsor Name:IRCCS FONDAZIONE ISTITUTO NEUROLOGICO C. MONDINO | ||||||||||||||||||
Full Title: A randomized controlled trial of generic substitution of antiepileptic drugs | ||||||||||||||||||
Medical condition: Epilepsy or other diseases in which using: carbamazepine, lamotrigine, levetiracetam, oxcarbazepine, topiramate and valproate in mono or politerapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002667-33 | Sponsor Protocol Number: 24051 | Start Date*: 2007-06-18 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase I/II study on induction chemotherapy followed by chemoradiation with or without lapatinib, a dual EGFR/ErbB2 kinase inhibitor, in patients with locally advanced resectable larynx and hypophar... | |||||||||||||
Medical condition: locally advanced resectable larynx and hypopharynx squamous cell carcinoma | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000082-41 | Sponsor Protocol Number: 2021-0486 | Start Date*: 2022-03-31 |
Sponsor Name:Fundación para la Investigación en Urología | ||
Full Title: Impact of pitavastatin use in prostate cancer patients treated with new generation androgen therapy: multicenter clinical trial | ||
Medical condition: We propose a multicenter, prospective, randomized, single-blind clinical trial, without conflict of interest, to determine the clinical benefit of statins (Pitavastatin 2 mg) in prostate cancer pa... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015981-73 | Sponsor Protocol Number: GERICO 09/0907 | Start Date*: 2009-12-08 | ||||||||||||||||
Sponsor Name:FNCLCC (Fédération Nationale des Centres de Lutte Contre le Cancer) | ||||||||||||||||||
Full Title: Phase II study evaluating the toxicity and activity of the combination lapatinib + capecitabine in elderly patients aged 70 and over with metastatic breast cancer over expressing HER2 | ||||||||||||||||||
Medical condition: Locally advanced or metastatic breast cancer over expressing HER2 and ≥ 70 years old | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: View results |
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