- Trials with a EudraCT protocol (3,190)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,190 result(s) found for: roche OR chugai OR genentech.
Displaying page 149 of 160.
EudraCT Number: 2012-000571-16 | Sponsor Protocol Number: GS-US-334-0109 | Start Date*: 2012-09-21 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
Full Title: An Open-Label Study of GS-7977+ Ribavirin for 12 Weeks in Subjects with Chronic HCV Infection who Participated in Prior Studies Evaluating GS-7977. | ||||||||||||||||||
Medical condition: Chronic Genotype 2 or 3 HCV Infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) GB (Completed) SE (Completed) EE (Completed) DE (Completed) NL (Completed) ES (Completed) PL (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018389-22 | Sponsor Protocol Number: LAP113957 / SOLTI-1001 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A randomized, multicentre, open-label, Phase II study of the efficacy and safety of lapatinib plus epirubicin and cyclophosphamide (EC90-L) followed by weekly paclitaxel and lapatinib (PX-L) compar... | |||||||||||||
Medical condition: patients with previously untreated ErbB2-overexpressing Stage I - IIIA invasive breast cancer with primary tumour size > 1cm. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) AT (Prematurely Ended) FR (Completed) NO (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002565-38 | Sponsor Protocol Number: CD-ON-MEDI-551-1088 | Start Date*: 2012-07-17 | ||||||||||||||||
Sponsor Name:MedImmune, LLC | ||||||||||||||||||
Full Title: A Phase 2 Randomized Open-label Study of MEDI-551 in Adults With Relapsed or Refractory DLBCL | ||||||||||||||||||
Medical condition: Relapsed or refractory diffuse large B-cell lymphoma(DLBCL) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) ES (Completed) HU (Completed) IT (Temporarily Halted) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004061-87 | Sponsor Protocol Number: Debio1562-201 | Start Date*: 2016-01-25 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Debiopharm International S.A. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Study to Evaluate the Efficacy and Tolerability of Debio 1562 in Combination with Rituximab in Patients with Relapsed and/or Refractory Diffuse Large B-Cell Lymphoma and Other Forms of No... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with Relapsed and/or Refractory Diffuse Large B-Cell Lymphoma and Other Forms of Non-Hodgkin’s Lymphoma | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) HU (Completed) BG (Completed) CZ (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002491-39 | Sponsor Protocol Number: SGNTUC-028 | Start Date*: 2022-02-11 | |||||||||||||||||||||
Sponsor Name:Seagen Inc. | |||||||||||||||||||||||
Full Title: A randomized, double-blind, phase 3 study of tucatinib or placebo in combination with trastuzumab and pertuzumab as maintenance therapy for metastatic HER2+ breast cancer (HER2CLIMB-05) | |||||||||||||||||||||||
Medical condition: Unresectable locally-advanced or metastatic HER2+ breast cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) PT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) IT (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) CZ (Trial now transitioned) FI (Trial now transitioned) NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002966-29 | Sponsor Protocol Number: CCTL019H2301 | Start Date*: 2018-11-22 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Tisagenlecleucel versus standard of care in adult patients with relapsed or refractory aggressive B-cell non-Hodgkin lymphoma: A randomized, open label, phase III trial (BELINDA) | |||||||||||||
Medical condition: adult patients with aggressive B-cell NHL after failure of rituximab and anthracycline containing first line immunochemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) NL (Trial now transitioned) BE (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005476-33 | Sponsor Protocol Number: I4C-MC-JTBB | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Controlled Phase 2 Study Evaluating LY2875358 plus Erlotinib versus Erlotinib as First-Line Treatment in Metastatic Non–Small Cell Lung Cancer Patients with Activating EGFR Mutations ... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Ongoing) IT (Completed) FR (Completed) ES (Ongoing) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005725-24 | Sponsor Protocol Number: M22-132 | Start Date*: 2022-04-25 | |||||||||||||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||||||||||||
Full Title: Phase 1b/2, Open-Label Study to Evaluate Safety and Tolerability of Epcoritamab in Combination with Anti-Neoplastic Agents in Subjects with Non-Hodgkin Lymphoma | |||||||||||||||||||||||
Medical condition: B-cell Non-Hodgkin's lymphoma, diffuse large B-cell lymphoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) NL (Trial now transitioned) DK (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006158-16 | Sponsor Protocol Number: UMCN-AKF08.02 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||
Full Title: Study on Pharmacokinetics of newly developed ANtiretroviral agents in HIV-infected pregNAnt women (PANNA) | |||||||||||||
Medical condition: HIV-infection in pregnant women | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) IE (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001755-39 | Sponsor Protocol Number: ACE-LY-312(D8227C00001) | Start Date*: 2020-11-30 | |||||||||||
Sponsor Name:Acerta Pharma B.V. (A Member of the AstraZeneca Group) | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Acalabrutinib in Combination with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Subjects ≤75 Yea... | |||||||||||||
Medical condition: Diffuse large B-cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) AT (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002342-36 | Sponsor Protocol Number: JHL-CLIN-1101-03 | Start Date*: 2019-02-01 | |||||||||||
Sponsor Name:JHL Biotech (Hong Kong) Limited | |||||||||||||
Full Title: A Multinational, Randomized, Double-blind, Positive-controlled, Parallel Group Clinical Study to Compare the Efficacy and Safety of the JHL1101 in Combination with CHOP (J-CHOP) versus Rituximab in... | |||||||||||||
Medical condition: Diffuse Large B-Cell Lymphoma (DLBCL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001534-17 | Sponsor Protocol Number: MS201943-0029 | Start Date*: 2019-01-03 | |||||||||||||||||||||
Sponsor Name:Merck KGaA | |||||||||||||||||||||||
Full Title: A Phase II, Randomized, Open-label Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of M6620 in Combination with Avelumab and Carboplatin in Comparison to Standard of Care... | |||||||||||||||||||||||
Medical condition: PARPi-resistant Recurrent Ovarian, Primary Peritoneal, or Fallopian Tube Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) BE (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001220-30 | Sponsor Protocol Number: EGF117165 | Start Date*: 2014-07-25 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: An Open-Label, Phase II, Study to Evaluate Biomarkers Associated with Response to Subsequent Therapies in Subjects with HER2-Positive Metastatic Breast Cancer Receiving Treatment with Trastuzumab i... | |||||||||||||
Medical condition: HER2 positive Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002716-28 | Sponsor Protocol Number: 673-301 | Start Date*: 2014-05-03 | |||||||||||
Sponsor Name:Medivation, Inc. | |||||||||||||
Full Title: A Phase 3, Open-Label, Randomized, Parallel, 2-Arm, Multi-Center Study of Talazoparib (BMN 673) versus Physician’s Choice in Germline BRCA Mutation Subjects with Locally Advanced and/or Metastatic ... | |||||||||||||
Medical condition: Germline BRCA Mutation Subjects with Locally Advanced and/or Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) IT (Completed) IE (Completed) FR (Completed) ES (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001362-25 | Sponsor Protocol Number: RAM-MS | Start Date*: 2018-05-02 | |||||||||||
Sponsor Name:Helse Bergen HF, Haukeland University Hospital | |||||||||||||
Full Title: Randomized autologous hematopoietic stem cell transplantation versus alemtuzumab, cladribine or ocrelizumab for patients with relapsing remitting Multiple Sclerosis | |||||||||||||
Medical condition: Relapsing remitting multiple sclerosis. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002979-35 | Sponsor Protocol Number: 209348 | Start Date*: 2020-12-22 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Phase IIb Multi-Center, Randomised, Open Label Study to Assess the Efficacy and Safety of Sequential Treatment with GSK3228836 followed by Pegylated Interferon Alpha 2a in Participants with Chron... | |||||||||||||
Medical condition: Chronic Hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001483-38 | Sponsor Protocol Number: BAY1163877/19131 | Start Date*: 2019-09-02 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: An international, multicenter, Phase 1b/2 study of rogaratinib (BAY 1163877) in combination with atezolizumab as first-line treatment in cisplatin-ineligible patients with FGFR-positive locally adv... | |||||||||||||
Medical condition: FGFR-positive locally advanced or metastatic urothelial carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004978-26 | Sponsor Protocol Number: 73763989PAHPB2005 | Start Date*: 2020-10-12 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, randomized, open-label, multicenter study to evaluate efficacy, pharmacokinetics, safety, and tolerability of response-guided treatment with JNJ-73763989 + JNJ-56136379 + nucleos(t)ide a... | |||||||||||||
Medical condition: Chronic Hepatitis B Virus Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021587-15 | Sponsor Protocol Number: ICORG10-04NSABP-B46I | Start Date*: 2010-09-08 | |||||||||||
Sponsor Name:ICORG | |||||||||||||
Full Title: A Phase III Clinical Trial Comparing TC to TAC for Women with Node-Positive or High-Risk Node-Negative, HER2-Negative Breast Cancer | |||||||||||||
Medical condition: Adjuvant Breast Cancer: Node positive or high risk node negative and HER 2 negative | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002641-11 | Sponsor Protocol Number: GS-US-334-0153 | Start Date*: 2013-10-07 | ||||||||||||||||
Sponsor Name:Gilead Sciences Inc. | ||||||||||||||||||
Full Title: A Phase 3B Randomized, Open-Label, Multi-Center Trial Assessing Sofosbuvir + Ribavirin for 16 or 24 Weeks and Sofosbuvir + Pegylated Interferon + Ribavirin for 12 Weeks in Subjects with Genotype 2 ... | ||||||||||||||||||
Medical condition: Hepatitis C Virus Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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