- Trials with a EudraCT protocol (3,192)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,192 result(s) found for: roche OR chugai OR genentech.
Displaying page 152 of 160.
| EudraCT Number: 2020-003956-34 | Sponsor Protocol Number: 73763989PAHPB2006 | Start Date*: 2021-01-16 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2, Open-label, Single-arm, Multicenter Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of Treatment With JNJ-73763989, JNJ-56136379, Nucleos(t)ide Analogs, and Pegylate... | |||||||||||||
| Medical condition: Chronic Hepatitis B Virus Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001780-23 | Sponsor Protocol Number: BTZ116577 | Start Date*: 2019-12-04 |
| Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
| Full Title: A Phase III, Randomized, Multicenter, Open-Label Study in Adolescent and Adult Participants Comparing the Efficacy and Safety of Gepotidacin to Ceftriaxone Plus Azithromycin in the Treatment of Unc... | ||
| Medical condition: Uncomplicated Urogenital Gonorrhea | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002981-15 | Sponsor Protocol Number: DanNORMS | Start Date*: 2020-12-15 | |||||||||||||||||||||
| Sponsor Name:Danish Multiple Sclerosis Center, Rigshospitalet | |||||||||||||||||||||||
| Full Title: Danish non-inferiority study of ocrelizumab and rituximab in MS (DanNORMS): A randomized study comparing the efficacy of ocrelizumab and rituximab in active multiple sclerosis. | |||||||||||||||||||||||
| Medical condition: Multiple sclerosis. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2022-000060-22 | Sponsor Protocol Number: 2020/0424/HP | Start Date*: 2023-04-03 | |||||||||||||||||||||
| Sponsor Name:CHU de Rouen | |||||||||||||||||||||||
| Full Title: Comparison of a personalized maintenance therapy based on the evolution of anti-desmoglein antibodies as biomarkers of pemphigus subclinical activity, with the standard treatment (rituximab + corti... | |||||||||||||||||||||||
| Medical condition: Pemphigus diseases (Pemphigus Vulgaris - PV and Pemphigus Foliaceus (PF). | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2022-000273-81 | Sponsor Protocol Number: UC-GIG-2203 | Start Date*: 2022-09-13 | |||||||||||||||||||||
| Sponsor Name:UNICANCER | |||||||||||||||||||||||
| Full Title: Randomised phase II study evaluating trifluridine/tipiracil plus oxaliplatin versus FOLFOX in patients with gastric, oesophagus or gastroesophageal junction adenocarcinoma locally advanced, recurre... | |||||||||||||||||||||||
| Medical condition: Patients with gastric, oesophagus or gastroesophageal junction adenocarcinoma locally advanced, recurrent or metastatic, ineligible for triplet chemotherapy. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2018-001347-31 | Sponsor Protocol Number: RF-2016-02361887 | Start Date*: 2018-07-30 | ||||||||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | ||||||||||||||||||
| Full Title: Anti-nerve reactivity as predictor of response to immune therapy in patients with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): A proof of concept study with rituximab in patie... | ||||||||||||||||||
| Medical condition: Chronic inflammatory demyelinating polyradiculoneuropathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-004666-26 | Sponsor Protocol Number: 2015/208/HP | Start Date*: 2017-07-19 | |||||||||||||||||||||
| Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||||||||||||
| Full Title: Randomised double blind double dummy control trial comparing the safety and efficacy of rituximab versus oral cyclophosphamide in severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
| Medical condition: severe forms of mucous membrane pemphigoid | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-000627-53 | Sponsor Protocol Number: P150922 | Start Date*: 2016-11-18 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: MAINtenance of remission with RITuximab versus azathioprine for patients with newly-diagnosed or relapsing Eosinophilic Granulomatosis with polyangiitis. A prospective, randomized, controlled, doub... | |||||||||||||
| Medical condition: Patients with newly diagnosed or relapsing EGPA, after achievement of remission. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004718-32 | Sponsor Protocol Number: NL72607.041.20 | Start Date*: 2020-10-09 |
| Sponsor Name:UMC Utrecht | ||
| Full Title: Upfront autologous hematopoietic stem cell transplantation versus immunosuppressive medication in early diffuse cutaneous systemic sclerosis: an international multicentre, open-label, randomized co... | ||
| Medical condition: Diffuse cutaneous systemic sclerosis according to the ACR/EULAR criteria | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001663-39 | Sponsor Protocol Number: D4190C00022 | Start Date*: 2015-11-27 | |||||||||||
| Sponsor Name:MedImmune | |||||||||||||
| Full Title: A Study of Safety, Tolerability, and Clinical Activity of MEDI4736 and Tremelimumab Administered as Monotherapy and in Combination to Subjects with Unresectable Hepatocellular Carcinoma | |||||||||||||
| Medical condition: Hepatocellular Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000111-84 | Sponsor Protocol Number: ACE-LY-003 | Start Date*: 2020-02-04 | |||||||||||||||||||||
| Sponsor Name:ACERTA PHARMA BV | |||||||||||||||||||||||
| Full Title: An Open-label, Phase 1b/2 Study of Acalabrutinib Alone or in Combination Therapy in Subjects with B-cell Non-Hodgkin Lymphoma | |||||||||||||||||||||||
| Medical condition: B-cell Non-Hodgkin Lymphoma | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2009-012813-22 | Sponsor Protocol Number: PRODIGE 14 - ACCORD 21/0905 | Start Date*: 2010-08-20 | |||||||||||
| Sponsor Name:Fédération Nationale des Centres de Lutte Contre le Cancer (FNCLCC) | |||||||||||||
| Full Title: Essai de phase II, randomisé multicentrique, évaluant le meilleur protocole de chimiothérapie associée à une thérapie ciblée choisie selon le statut KRAS dans les métastases hépatiques initialement... | |||||||||||||
| Medical condition: Cancer colorectal métastatique, première ligne de traitement, avec métastases hépatiques initialement non résécables. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003936-10 | Sponsor Protocol Number: D8220C00027 | Start Date*: 2022-06-28 | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: MAJIC: A Phase III Prospective, Multicenter, Randomized, Open-Label Trial of Acalabrutinib plus Venetoclax versus Venetoclax plus Obinutuzumab in Previously Untreated Chronic Lymphocytic Leukemia o... | ||||||||||||||||||
| Medical condition: Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) HU (Trial now transitioned) ES (Trial now transitioned) PL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-000862-49 | Sponsor Protocol Number: RG_15-011 | Start Date*: 2016-08-22 |
| Sponsor Name:The University of Birmingham | ||
| Full Title: Can we Save the rectum by watchful waiting or TransAnal surgery following (chemo)Radiotherapy versus Total mesorectal excision for early REctal Cancer? | ||
| Medical condition: Early rectal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Completed) SE (Trial now transitioned) BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000605-84 | Sponsor Protocol Number: XPORT-DLBCL-030 | Start Date*: 2020-09-16 | ||||||||||||||||
| Sponsor Name:Karyopharm Therapeutics Inc. | ||||||||||||||||||
| Full Title: A Phase 2/3, Multicenter Randomized Study of Rituximab-Gemcitabine-Dexamethasone-Platinum (R-GDP) With or Without Selinexor in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (RR DL... | ||||||||||||||||||
| Medical condition: Relapsed/Refractory Diffuse Large B-Cell Lymphoma (RR DLBCL) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Ongoing) FR (Ongoing) IT (Trial now transitioned) GR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-005061-31 | Sponsor Protocol Number: GATA | Start Date*: 2017-10-07 | |||||||||||||||||||||||||||||||
| Sponsor Name:LYSARC | |||||||||||||||||||||||||||||||||
| Full Title: A PHASE II TRIAL EVALUATING COMBINATION OF ATEZOLIZUMAB, WITH VENETOCLAX AND OBINUTUZUMAB FOR RELAPSED/REFRACTORY LYMPHOMAS | |||||||||||||||||||||||||||||||||
| Medical condition: - relapsed/refractory follicular lymphoma (FL) patients - relapsed/refractory aggressive (DLBCL) lymphoma patients - relapsed/refractory other indolent lymphoma patients | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-004699-21 | Sponsor Protocol Number: CP-MGAH22-06 | Start Date*: 2020-10-12 | |||||||||||||||||||||
| Sponsor Name:MacroGenics, Inc. | |||||||||||||||||||||||
| Full Title: A Phase 2/3 Trial to Evaluate Margetuximab in Combination with INCMGA00012 and Chemotherapy or MGD013 and Chemotherapy in Patients with Metastatic or Locally Advanced, Treatment-naïve, HER2-Positiv... | |||||||||||||||||||||||
| Medical condition: Metastatic or Locally Advanced, Treatment-naïve, HER2-Positive Gastric or Gastroesophageal Junction Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) PL (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-000758-39 | Sponsor Protocol Number: PREBEN | Start Date*: 2015-12-13 | ||||||||||||||||
| Sponsor Name:Department of Hematology, Aarhus University Hospital | ||||||||||||||||||
| Full Title: A phase 1/2 study of the combination of pixantrone, etoposide, bendamustine and, in CD-20 positive tumors, rituximab in patients with relapsed aggressive non-Hodgkin lymphomas of B- or T-cell pheno... | ||||||||||||||||||
| Medical condition: Relapse of aggressive non-Hodgkin lymphoma of B and T-cell phenotype | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Prematurely Ended) SE (Completed) FI (Prematurely Ended) NO (Completed) NL (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-020966-34 | Sponsor Protocol Number: ICORG10-05 | Start Date*: 2010-08-06 | |||||||||||
| Sponsor Name:ICORG | |||||||||||||
| Full Title: A phase II neoadjuvant study assessing TCH (Docetaxel, Carboplatin and Trastuzumab) and TCHL (Docetaxel, Carboplatin, Traztuzumab and Lapatinib) in Erb B2 positive breast cancer patients | |||||||||||||
| Medical condition: Her 2 positive locally advanced or primary breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003704-39 | Sponsor Protocol Number: NEAT22/SSAT060 | Start Date*: 2014-04-01 |
| Sponsor Name:St Stephen's AIDS Trust [...] | ||
| Full Title: An open label study examining the efficacy and cardiovascular risk of immediate versus deferred switch from a boosted PI to dolutegravir (DTG) in HIV infected patients with stable virological suppr... | ||
| Medical condition: HIV infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) BE (Completed) ES (Ongoing) IT (Completed) | ||
| Trial results: (No results available) | ||
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