- Trials with a EudraCT protocol (79)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
79 result(s) found for: Drug-drug interactions.
Displaying page 4 of 4.
EudraCT Number: 2007-002918-19 | Sponsor Protocol Number: VEG110190 | Start Date*: 2007-09-06 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithkline Research & Development Limited | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase II, Open-Label, Multicenter Feasibility Study of Pazopanib, Carboplatin, and Paclitaxel in Women with Previously Untreated, Advanced Gynaecological Tumors | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: previously untreated, advanced gynaecological tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003785-14 | Sponsor Protocol Number: 200249 | Start Date*: 2014-03-03 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A Phase I/II Study to Assess the Safety and Efficacy of Pazopanib and MK-3475 in Subjects with Advanced Renal Cell Carcinoma | ||||||||||||||||||
Medical condition: Renal Cell Carcinoma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001617-14 | Sponsor Protocol Number: CRLX030A2205 | Start Date*: 2012-08-17 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An adaptive multicentre, randomized, partially doubleblind, placebo controlled study to assess the safety, PK and PD/efficacy of RLX030 in women with pre-eclampsia | |||||||||||||
Medical condition: Pre-eclampsia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004442-15 | Sponsor Protocol Number: HISTORY | Start Date*: 2013-09-11 | ||||||||||||||||
Sponsor Name:University Leipzig | ||||||||||||||||||
Full Title: High-dose intravenous silibinin infusions during 10 days as add-on treatment to triple therapy (telaprevir, peginterferon alpha and ribavirin) in cirrhotic GT 1 hepatitis C virus infected patients ... | ||||||||||||||||||
Medical condition: High-dose intravenous silibinin infusions during 10 days as add-on treatment to triple therapy (telaprevir, peginterferon alpha and ribavirin) in cirrhotic GT 1 hepatitis C virus infected patients ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000415-23 | Sponsor Protocol Number: PM14-A-002-20 | Start Date*: 2021-05-25 | |||||||||||
Sponsor Name:Pharma Mar, S.A. | |||||||||||||
Full Title: Phase I/II, Multicenter, Open-label, Clinical and Pharmacokinetic Study of PM14 in Combination with Irinotecan in Pretreated Patients with Selected Advanced Solid Tumors | |||||||||||||
Medical condition: Advanced Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005437-53 | Sponsor Protocol Number: ITCC053 | Start Date*: 2016-11-03 |
Sponsor Name:Erasmus Medical Center | ||
Full Title: A phase 1B of crizotinib either in combination or as single agent in pediatric patients with ALK, ROS1 or MET positive malignancies Study ITCC 053 | ||
Medical condition: Malignancies carrying a genetic alteration of ALK, MET or ROS1 | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) DE (Trial now transitioned) IE (Completed) ES (Ongoing) DK (Trial now transitioned) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005533-39 | Sponsor Protocol Number: Debio0932-201 | Start Date*: 2012-02-27 | ||||||||||||||||
Sponsor Name:Debiopharm International SA | ||||||||||||||||||
Full Title: A Phase I-II evaluation of the safety and efficacy of the oral HSP90 inhibitor Debio 0932 in combination with standard of care in first- and second-line therapy of patients with Stage IIIb or IV No... | ||||||||||||||||||
Medical condition: Non-small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001848-21 | Sponsor Protocol Number: ALRN-6924-1-03 | Start Date*: 2019-09-12 | ||||||||||||||||
Sponsor Name:Aileron Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 1b/2 Study of the Dual MDMX/MDM2 Inhibitor, ALRN-6924, for the Prevention of Chemotherapy-induced Myelosuppression | ||||||||||||||||||
Medical condition: Small Cell Lung Cancer and Non small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Prematurely Ended) ES (Prematurely Ended) NL (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005758-36 | Sponsor Protocol Number: UTX-TGR-304 | Start Date*: 2016-10-28 | |||||||||||
Sponsor Name:TG Therapeutics | |||||||||||||
Full Title: A Phase 3, Randomized Study to Assess the Efficacy and Safety of Ublituximab in Combination with TGR-1202 (Umbralisib) Compared to Obinutuzumab in Combination with Chlorambucil in Patients with Chr... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) BG (Prematurely Ended) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001476-37 | Sponsor Protocol Number: PENTA17 | Start Date*: 2015-12-16 | |||||||||||
Sponsor Name:Fondazione PENTA ONLUS | |||||||||||||
Full Title: SMILE: Strategy for Maintenance of HIV suppression with elvitegravir+darunavir/ritonavir in children (PENTA 17) - A two-arm, Phase 2/3 multicentre, open-label, randomised study evaluating safety ... | |||||||||||||
Medical condition: Paediatric HIV-1 Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) GB (GB - no longer in EU/EEA) BE (Completed) DE (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001035-58 | Sponsor Protocol Number: A4001056 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:Pfizer, S. A. | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO ASSESS THE SAFETY AND EFFICACY OF MARAVIROC (UK-427,857) IN THE TREATMENT OF RHEUMATOID ARTHRITIS IN SUBJECTS RECEI... | |||||||||||||
Medical condition: ARTRITIS REUMATOIDE RHEUMATOID ARTHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004718-90 | Sponsor Protocol Number: UTX-TGR-205 | Start Date*: 2017-10-10 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:TG Therapeutics | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2b Randomized Study to Assess the Efficacy and Safety of the Combination of Ublituximab + TGR-1202 with or without Bendamustine and TGR-1202 alone in Patients with Previously Treated Non-Ho... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Non-Hodgkin lymphoma | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001551-31 | Sponsor Protocol Number: BGB-3111-304 | Start Date*: 2017-12-04 | ||||||||||||||||
Sponsor Name:BeiGene, Ltd. | ||||||||||||||||||
Full Title: An International, Phase 3, Open-label, Randomized Study of BGB-3111 Compared with Bendamustine plus Rituximab in Patients with Previously Untreated Chronic Lymphocytic Leukemia or Small Lymphocytic... | ||||||||||||||||||
Medical condition: Untreated Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Prematurely Ended) CZ (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022293-14 | Sponsor Protocol Number: ANRS146OPTIMAL | Start Date*: 2012-08-22 |
Sponsor Name:Inserm-ANRS | ||
Full Title: Optimized Phase III Trial of Immuno-stimulation with Maraviroc, a CCR5 antagonist, combined with Anti Retroviral Therapy (cART) in advanced, Late diagnosed HIV-1 infected patients with an AIDS-defi... | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003953-16 | Sponsor Protocol Number: CICL670A2409 | Start Date*: 2007-05-20 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A one-year, open-label, single arm, multi-centre trial evaluating the efficacy and safety of oral ICL670 (20 mg/kg/day) in patients diagnosed with transfusion-dependent iron overload | ||
Medical condition: Transfusional iron overload | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) IT (Completed) DK (Completed) BE (Completed) DE (Completed) NO (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003056-31 | Sponsor Protocol Number: CC-122-CLL-001 | Start Date*: 2015-08-24 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Celgene Corporation | ||||||||||||||||||||||||||||||||||||||
Full Title: Phase 1/2 Study to Determine the Safety, Pharmacokinetics, and Efficacy of Single Agent CC-122 and the Combinations of CC-122 and Ibrutinib and CC-122 and Obinutuzumab in Subjects with Chronic Lymp... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) based on modified International Workshop on Chronic Lymphocytic Leukemia (IWCLL) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002102-19 | Sponsor Protocol Number: VEG108844 | Start Date*: 2008-11-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study VEG108844, a Study of Pazopanib versus Sunitinib in the Treatment of Subjects with Locally Advanced and/or Metastatic Renal Cell Carcinoma | |||||||||||||
Medical condition: Locally Advanced and/or Metastatic Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) ES (Completed) SE (Completed) NL (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005575-41 | Sponsor Protocol Number: CAIN457F2320 | Start Date*: 2015-03-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, phase III multicenter study of subcutaneous secukinumab (150 mg) with and without a subcutaneous loading regimen to assess efficacy, safety, and tole... | |||||||||||||
Medical condition: Ankylosing Spondylitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) AT (Completed) NL (Completed) FI (Completed) NO (Completed) DK (Completed) GB (Completed) ES (Completed) SK (Completed) BG (Completed) PL (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002381-18 | Sponsor Protocol Number: VEG107769 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An Open-Label Extension Study to Assess the Safety and Efficacy of Pazopanib in Subjects with Renal Cell Carcinoma previously enrolled on Protocol VEG105192 | |||||||||||||
Medical condition: Renal Cell Carcinoma | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) AT (Prematurely Ended) SK (Completed) LT (Completed) EE (Completed) GR (Prematurely Ended) CZ (Completed) IT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
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