- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Benzamide.
Displaying page 1 of 2.
EudraCT Number: 2004-002952-33 | Sponsor Protocol Number: CAAE581A2203E1 | Start Date*: 2005-03-17 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 2-year extension to study 2203, partially randomized, double-blind, placebo-controlled in the first year and open label in the second year, to assess the safety of the dose of AAE581 selected for... | ||
Medical condition: Osteoporosis is a metabolic bone disease characterized by low bone mass and micro architectural deterioration of bone tissue, leading to enhanced fragility and a consequent increase in fracture risk. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SK (Prematurely Ended) AT (Completed) IT (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002243-25 | Sponsor Protocol Number: CAAE581A2203E2 | Start Date*: 2007-08-28 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An observational, safety follow-up extension to studies 2203 and 2203E1 to assess the safety of AAE581 in postmenopausal women with osteopenia/osteoporosis | ||
Medical condition: Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: PL (Completed) FR (Completed) AT (Completed) ES (Completed) CZ (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001754-92 | Sponsor Protocol Number: AAE581C2201 | Start Date*: 2005-02-14 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase II, 12-month, double-blind, placebo-controlled, dose-finding, multicenter study to evaluate the safety, tolerability, and disease modifying efficacy of daily oral AAE581 (10, 25 and 50 mg t... | ||
Medical condition: Osteoarthritis (OA) is a disease with a complex pathophysiology leading to the degeneration of articular cartilage and bone. It is characterized by pain, biochemical and enzymatic changes, cartilag... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000686-37 | Sponsor Protocol Number: PR-20-5006-C | Start Date*: 2013-09-11 | ||||||||||||||||
Sponsor Name:Tesaro, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2a, Open-Label, Dose Escalation and Cohort Expansion Trial of Oral TSR-011 in Patients with Advanced Solid Tumors and Lymphomas | ||||||||||||||||||
Medical condition: Solid tumors or lymphomas that have failed standard therapies or for which no standard treatment option(s) exist. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002384-16 | Sponsor Protocol Number: TTD-11-01/AXI-IIG-01 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Grupo de Tratamiento de los Tumores Digestivos (TTD) | |||||||||||||
Full Title: A Phase II study of Axitinib as maintenance for patients with advanced colorectal carcinoma. | |||||||||||||
Medical condition: Advanced colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018585-23 | Sponsor Protocol Number: A4061051 | Start Date*: 2010-12-21 | |||||||||||
Sponsor Name:Pfizer Inc 235 East 42nd Street, New York, NY10017 | |||||||||||||
Full Title: AG-013736 (axitinib) for the treatment of metastatic renal cell cancer (mRCC) | |||||||||||||
Medical condition: metastatic renal cell cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000051-15 | Sponsor Protocol Number: A4061008 | Start Date*: Information not available in EudraCT |
Sponsor Name:Pfizer Pharma GmbH | ||
Full Title: Continuing Access to the Tyrosine Kinase Inhibitor of VEGFR-2, AG-013736 (A406) for Patients Previously Receiving AG-013736 in Clinical Trials | ||
Medical condition: Patients who have been treated in previous AG-013736 oncology studies | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) CZ (Completed) IT (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005010-43 | Sponsor Protocol Number: COL MIG-202 | Start Date*: 2009-06-22 | |||||||||||
Sponsor Name:CoLucid Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Double Blind Randomized Placebo-Controlled Parallel Group Dose-Ranging Study of Oral COL-144 in the Acute Treatment of Migraine | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) BE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021590-37 | Sponsor Protocol Number: A4061058 | Start Date*: 2011-01-03 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY10017,USA | |||||||||||||
Full Title: A MULTICENTER, GLOBAL, RANDOMIZED, DOUBLE-BLIND STUDY OF AXITINIB PLUS BEST SUPPORTIVE CARE VERSUS PLACEBO PLUS BEST SUPPORTIVE CARE IN PATIENTS WITH ADVANCED HEPATOCELLULAR CARCINOMA FOLLOWING FAI... | |||||||||||||
Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SK (Completed) GB (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002183-13 | Sponsor Protocol Number: O304-2016-02 | Start Date*: 2016-08-27 |
Sponsor Name:Betagenon AB | ||
Full Title: Effect on fasting plasma glucose (FPG) of once daily oral administration during 28 days of O304 suspension in subjects with Type 2 Diabetes (T2D). A single-centre, randomised, parallel-group, doubl... | ||
Medical condition: Type 2 Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003501-90 | Sponsor Protocol Number: A4061011 | Start Date*: 2006-01-18 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: Phase 2 Study of the Anti-Angiogenesis Agent AG-013736 as Second- or Later-Line Treatment in Patients with Advanced Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: Second-or Later Line treatment in patients with advanced Non-Small Cell lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000053-30 | Sponsor Protocol Number: A4061016 | Start Date*: 2005-07-21 | |||||||||||
Sponsor Name:Pfizer Inc. - La Jolla laboratories | |||||||||||||
Full Title: A randomized phase 2 study of the anti-angiogenesis agent AG-013736 in combination with gemcitabine in patients with chemotherapy-naïve advanced pancreatic cancer preceded by a phase 1 portion | |||||||||||||
Medical condition: Treatment of patients with chemotherapy-naïve, locally advanced or metastatic epithelial cancer of the exocrine pancreas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007786-23 | Sponsor Protocol Number: A4061046 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: ESTUDIO EN FASE 2 ALEATORIZADO Y DOBLE CIEGO DE AXITINIB (AG-013736) CON O SIN AJUSTE DE LA DOSIS EN PACIENTES CON CANCER DE CELULAS RENALES METASTASICO RANDOMIZED, DOUBLE-BLIND PHASE 2 STUDY OF A... | |||||||||||||
Medical condition: CCR metastásico Metastatic RCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002361-17 | Sponsor Protocol Number: AML2521 | Start Date*: 2021-11-17 | ||||||||||||||||||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | ||||||||||||||||||||||||||||
Full Title: A multicentric phase 2 study of venetoclax and azacitidine for the management of the molecular relapse/progression in adult NPM1- mutaded acute myeloid leukemia. | ||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukemia with NPM1 mutation. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002579-12 | Sponsor Protocol Number: CLL2222 | Start Date*: 2023-04-04 | |||||||||||
Sponsor Name:FONDAZIONE GIMEMA (GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL' ADULTO) FRANCO MANDELLI ONLUS | |||||||||||||
Full Title: Front-Line Venetoclax and Obinutuzumab combination followed by Venetoclax or Venetoclax and Zanubrutinib combination in patients with residual disease: a minimal residual disease (MRD) tailored tre... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005584-10 | Sponsor Protocol Number: 103 PH GL 2007 CL003 | Start Date*: 2008-02-27 | ||||||||||||||||
Sponsor Name:Pharmion Corporation [...] | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Open-Label Study of Single Agent Azacitidine (Vidaza®) vs. Single Agent MGCD0103 vs. Azacitidine in Combination With MGCD0103 for the Treatment of Elderly Subjects With Newly... | ||||||||||||||||||
Medical condition: Newly diagnosed Acute Myeloid Leukemia and Intermediate-2, or high-risk Myelodysplastic Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Ongoing) SE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004412-11 | Sponsor Protocol Number: CBX-001 | Start Date*: 2015-01-16 | |||||||||||
Sponsor Name:Canbex Therapeutics Ltd | |||||||||||||
Full Title: A Phase II Proof of Concept (PoC), Double-Blind, Randomised, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of VSN16R for the Treatment of Spasticity in Subjects wi... | |||||||||||||
Medical condition: Multiple Sclerosis | |||||||||||||
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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: 2006-003903-38 | Sponsor Protocol Number: COL MIG-201 | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:CoLucid Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Placebo-Controlled Group Sequential Adaptive Treatment Assignment Study of Intravenous COL-144 (LY573144) in the Acute Treatment of Migraine | |||||||||||||
Medical condition: Migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000405-23 | Sponsor Protocol Number: Versio_1 | Start Date*: 2018-03-27 | |||||||||||
Sponsor Name:Juha Rinne / PET Centre | |||||||||||||
Full Title: In vivo PET imaging of neuroinflammation in Parkinson’s disease using the purinergic P2X7 receptor ligand [11C]SMW139 (PRI-PD) | |||||||||||||
Medical condition: Parkinson´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001550-29 | Sponsor Protocol Number: AXI-IIG-02 | Start Date*: 2011-08-11 | |||||||||||
Sponsor Name:Grupo Español de Tumores Neuroendocrinos | |||||||||||||
Full Title: A Phase II randomized double-blind study of Santostatin LAR in combination with Axitinib versus Placebo in patients with progressive advanced well-differentiated neuroendocrine carcinomas of non-pa... | |||||||||||||
Medical condition: Patients with progressive advanced well-differentiated neuroendocrine carcinomas of non-pancreatic origin (carcinoids) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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