- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
24 result(s) found for: Teratogenicity.
Displaying page 1 of 2.
| EudraCT Number: 2009-012151-23 | Sponsor Protocol Number: SPON 671-09 | Start Date*: 2009-11-11 |
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised phase II study of Irinotecan, 5-Fluorouracil and Folinic Acid (FOLFIRI) with or without the addition of an endothelin receptor antagonist in patients with metastatic colorectal cancer ... | ||
| Medical condition: Metastatic Colorectal Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003792-34 | Sponsor Protocol Number: DIA-2-REDESIGN | Start Date*: 2015-03-25 |
| Sponsor Name:GWT-TUD GmbH | ||
| Full Title: RANDOMIZED DOUBLE BLIND PARALLEL DESIGN STUDY COMPARING RISK OF NOCTURNAL HYPOGLYCEMIA AND CRITICAL ARRHYTHMIAS WITH SITAGLIPTIN VERSUS GLIMEPIRIDE IN PATIENTS WITH TYPE 2 DIABETES INSUFFICIENTLY C... | ||
| Medical condition: Patients with diabetes mellitus type 2 inadequately controlled on metformin monotherapy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-004287-56 | Sponsor Protocol Number: CHUBX2016/44 | Start Date*: 2019-11-21 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Randomized placebo-controlled trial comparing Methotrexate vs. Methotrexate/Metformin association in rheumatoid arthritis patients: METorMET² study | |||||||||||||
| Medical condition: rheumatoid arthritis (RA) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003119-13 | Sponsor Protocol Number: 14/0172 | Start Date*: 2015-02-11 | ||||||||||||||||
| Sponsor Name:Joint Research Office- UCL | ||||||||||||||||||
| Full Title: Can simvastatin significantly reduce the amount of immunosuppressive medication required by patients with sight threatening uveitis? A phase IIb, single site, randomized, placebo controlled, double... | ||||||||||||||||||
| Medical condition: Uveitis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-006187-47 | Sponsor Protocol Number: AI424-494 | Start Date*: 2012-11-20 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A 48-Week, Randomized, Open-Label Phase 3b Study Comparing the Antiviral Efficacy and Safety of ATV/RTV Plus 3TC with ATV/RTV plus TDF/FTC in HIV-1-Infected, Treatment-Naive Subjects, Followed by a... | |||||||||||||
| Medical condition: HIV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000786-24 | Sponsor Protocol Number: NET-2013-02355002 | Start Date*: 2017-03-07 | |||||||||||
| Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
| Full Title: Thalidomide, a novel immunological treatment to modify the natural history of paediatric Crohn's disease: a new proposal from a well-established paediatric research network | |||||||||||||
| Medical condition: Crohn's Disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001642-17 | Sponsor Protocol Number: AMB116457 | Start Date*: 2013-04-26 | |||||||||||
| Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
| Full Title: An open-label extension study of the long-term safety, tolerability and efficacy of ambrisentan in subjects with inoperable chronic thromboembolic pulmonary hypertension (CTEPH) | |||||||||||||
| Medical condition: Subjects with inoperable chronic thromboembolic pulmonary hypertension (CTEPH). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) AT (Completed) DE (Completed) GB (Prematurely Ended) CZ (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021572-29 | Sponsor Protocol Number: AMB114588 | Start Date*: 2010-11-23 | |||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development, Ltd | |||||||||||||||||||||||||||||||||
| Full Title: An open-label, long term extension study for treatment of pulmonary arterial hypertension in paediatric patients aged 8 years up to 18 years who have participated in AMB112529 and in whom continued... | |||||||||||||||||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GR (Prematurely Ended) DE (Completed) NL (Ongoing) ES (Completed) HU (Completed) IT (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-006719-21 | Sponsor Protocol Number: IMCL CP13-0707 | Start Date*: 2008-08-07 | ||||||||||||||||
| Sponsor Name:ImClone LLC | ||||||||||||||||||
| Full Title: A Five-Tier, Phase 2 Open-Label Study of IMC-A12 Administered as a Single Agent Every 2 Weeks in Patients With Previously- Treated, Advanced or Metastatic Soft Tissue and Ewing's Sarcoma/PNET | ||||||||||||||||||
| Medical condition: Previously-treated, advanced or metastatic soft tissue and Ewing’s sarcoma/peripheral primitive neuroectodermal tumor (PNET) | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) ES (Completed) DE (Completed) NL (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-000850-48 | Sponsor Protocol Number: CA184-156 | Start Date*: 2012-06-15 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: Randomized, Multicenter, Double-Blind, Phase 3 Trial Comparing the Efficacy of Ipilimumab plus Etoposide/Platinum versus Etoposide/Platinum in Subjects with Newly Diagnosed Extensive-Stage Disease ... | |||||||||||||
| Medical condition: Extensive Stage Disease Small Cell Lung Cancer (ED-SCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FI (Completed) IT (Completed) SE (Completed) DE (Completed) CZ (Completed) AT (Completed) GB (Completed) PT (Completed) HU (Completed) ES (Completed) NL (Completed) IE (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002018-29 | Sponsor Protocol Number: A3921165 | Start Date*: 2020-12-09 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF TOFACITINIB FOR TREATMENT OF SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS (sJIA) WITH ACTIVE SYSTEMIC FEATURES IN CHILDREN AND ADOLESCENT SUBJECTS | |||||||||||||
| Medical condition: Systemic Juvenile Idiopathic Arthritis (sJIA) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) PL (Completed) DE (Completed) BE (Completed) IT (Completed) NL (Prematurely Ended) SE (Prematurely Ended) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-009035-30 | Sponsor Protocol Number: CP15-0802 | Start Date*: 2009-10-27 | |||||||||||
| Sponsor Name:ImClone LLC | |||||||||||||
| Full Title: Randomized Phase 2 Trial Investigating Liposomal Doxorubicin With or Without Anti Platelet Derived Growth Factor Receptor-Alpha (PDGFRα) Monoclonal Antibody IMC-3G3 in Patients With Platinum-Refrac... | |||||||||||||
| Medical condition: Platinium-refractory or Platinium-resistant Advanced Ovarian Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001356-10 | Sponsor Protocol Number: Revail | Start Date*: 2012-01-12 | |||||||||||
| Sponsor Name:LYSARC | |||||||||||||
| Full Title: STUDY OF THE EFFICACY AND SAFETY OF FIRST LINE TREATMENT WITH CHOP AND LENALIDOMIDE (Rev-CHOP) IN PATIENTS AGED FROM 60 TO 80 YEARS WITH PREVIOUSLY UNTREATED ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ... | |||||||||||||
| Medical condition: Angioimmunoblastic T-cell Lymphoma (AITL) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001883-12 | Sponsor Protocol Number: GI1616 | Start Date*: 2016-09-14 | ||||||||||||||||
| Sponsor Name:Herlev & Gentofte Hospital, Oncology Dept. | ||||||||||||||||||
| Full Title: A PROSPECTIVE RANDOMIZED, OPEN-LABEL PHASE 2 STUDY OF IMMUNE CHECKPOINT INHIBITION, NIVOLUMAB WITH OR WITHOUT IPILIMUMAB IN COMBINATION WITH RADIATION THERAPY IN PRETREATED PATIENTS WITH METASTATIC... | ||||||||||||||||||
| Medical condition: Patients with metastatic pancreatic cancer or metastatic biliary tract cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-004792-30 | Sponsor Protocol Number: HE316 | Start Date*: 2018-10-03 | |||||||||||
| Sponsor Name:Hellenic Cooperative Oncology Group (HeCOG) | |||||||||||||
| Full Title: Phase Ib-II study of Ramucirumab combined with standard Nab-paclitaxel and Gemcitabine as first-line treatment in patients with advanced pancreatic adenocarcinoma | |||||||||||||
| Medical condition: Advanced pancreatic adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003759-13 | Sponsor Protocol Number: GI1931 | Start Date*: 2019-12-20 | ||||||||||||||||
| Sponsor Name:Department of Oncology, Herlev & Gentofte | ||||||||||||||||||
| Full Title: Phase 1/2 study in borderline resectable, locally advanced or metastatic pancreatic cancer to assess safety and potential efficacy of dual checkpoint inhibition in combination with gemcitabine and ... | ||||||||||||||||||
| Medical condition: Locally advanced pancreatic cancer, non-resectable or borderline resectable, or metastatic pancreatic cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-004531-23 | Sponsor Protocol Number: CV181-206 | Start Date*: 2013-07-26 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A 24-Week International, Multi-center, Randomized, Parallel-group, Double-blind Trial to Evaluate Metformin Extended Release Monotherapy Compared to Metformin Immediate Release Monotherapy in Adult... | |||||||||||||
| Medical condition: Type 2 Diabetes. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) HU (Completed) GB (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019547-19 | Sponsor Protocol Number: AMB112529 | Start Date*: 2010-07-16 | |||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development, Ltd | |||||||||||||||||||||||||||||||||
| Full Title: A randomized, open label study comparing safety and efficacy parameters for a high and a low dose of ambrisentan (adjusted for body weight) for the treatment of pulmonary arterial hypertension in ... | |||||||||||||||||||||||||||||||||
| Medical condition: Pulmonary Arterial Hypertension | |||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GR (Prematurely Ended) NL (Completed) HU (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) Outside EU/EEA | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-000508-24 | Sponsor Protocol Number: 7406 | Start Date*: 2015-06-12 | |||||||||||
| Sponsor Name:Newcastle Upon Tyne Hospitals NHS Trust | |||||||||||||
| Full Title: A Feasibility Study of Bezafibrate in Mitochondrial Myopathy | |||||||||||||
| Medical condition: Mitochondrial myopathy due to mt.3243A>G mutation | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004438-40 | Sponsor Protocol Number: GI1950 | Start Date*: 2020-04-06 | |||||||||||||||||||||
| Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | |||||||||||||||||||||||
| Full Title: Phase 2 study in pretreated patients with advanced pancreatic cancer to assess efficacy of ipilimumab, nivolumab and tocilizumab in combination with radiation. | |||||||||||||||||||||||
| Medical condition: Pretreated patients with advanced pancreatic cancer. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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