- Trials with a EudraCT protocol (5,192)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5,192 result(s) found for: antibody.
Displaying page 191 of 260.
| EudraCT Number: 2022-002594-28 | Sponsor Protocol Number: APHP200036 | Start Date*: 2022-10-05 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Graft Acute kidney injury: vitamin B3 to facilitate renal Recovery In the Early Life of a transplant | |||||||||||||
| Medical condition: Patients with end-stage renal failure treated with extrarenal purification (hemodialysis using a catheter or a fistula, or peritoneal dialysis), registered on the national kidney donation waiting l... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000101-28 | Sponsor Protocol Number: AMB-051-07 | Start Date*: 2022-12-08 | |||||||||||
| Sponsor Name:AmMax Bio, Inc. | |||||||||||||
| Full Title: A Phase 2, Open-Label, Adaptive, Dose-Ranging Study with Long-Term Extension to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Intra-articular AMB-05X Injections in Subjects w... | |||||||||||||
| Medical condition: Tenosynovial Giant Cell Tumor | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) IT (Prematurely Ended) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012324-83 | Sponsor Protocol Number: UZB-BN-09-001 | Start Date*: 2009-07-04 | |||||||||||
| Sponsor Name:Prof Bart Neyns | |||||||||||||
| Full Title: CeCil: A randomized, non-comparative phase II clinical trial of the effect of radiation therapy plus Temozolomide combined with Cilengitide or Cetuximab on the 1-year overall survival of patients w... | |||||||||||||
| Medical condition: Subjects with newly diagnosed glioblastoma, who have met all eligibility criteria for the CENTRIC study (EMD 121974-011 study, EudraCT 2007-004344-78) with the exception of NOT having a tumor with ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006075-42 | Sponsor Protocol Number: ALXN1210-NMO-317 | Start Date*: 2022-05-17 | |||||||||||
| Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2/3, Open-label, Historical-controlled, Single-arm, Multicenter Study to Evaluate the Efficacy, Pharmacokinetics, Pharmacodynamics, and Safety of Ravulizumab in Children and Adolescents Wit... | |||||||||||||
| Medical condition: Neuromyelitis Optica Spectrum Disorder (NMOSD) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) DE (Ongoing) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002841-31 | Sponsor Protocol Number: PEOPLE | Start Date*: 2018-01-26 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
| Full Title: Phase II study to test Pembrolizumab (MK-3475) in first line treatment of advanced NSCLC patients with PD-L1 low tumors (<50%)_ PEOPLE TRIAL (Pembrolizumab in Pd-L1 low Expressors) | |||||||||||||
| Medical condition: Advanced NSCLC patients with PD-L1 low tumors (<50%) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002340-90 | Sponsor Protocol Number: HPV-Xneutra-001 | Start Date*: 2013-06-26 | |||||||||||
| Sponsor Name:Ghent University Hospital | |||||||||||||
| Full Title: Study of the molecular mechanisms underlying the cross-neutralizing capacity of AS04-adjuvanted HPV vaccine (Cervarix®) in comparison with the aluminiumhydroxyphosphate sulphate adjuvanted HPV vacc... | |||||||||||||
| Medical condition: vaccin against the human papillomavirus | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000765-20 | Sponsor Protocol Number: ANTIVEGFVEP | Start Date*: 2015-11-27 | |||||||||||||||||||||
| Sponsor Name:Kuopion yliopistollinen sairaala/silmätautien poliklinikka | |||||||||||||||||||||||
| Full Title: The Effect of Intravitreal Bevacizumab Injections in Patients with Macular Oedema Caused by AMD, CRVO or DME on the Plasticity of Nerves Studied by Visual Evoked Potentials | |||||||||||||||||||||||
| Medical condition: Wet age-related macular degeneration, diabetic macular edema, central retinal vein occlusion | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-004628-31 | Sponsor Protocol Number: FIL_V-RBAC | Start Date*: 2018-05-15 | |||||||||||
| Sponsor Name:Fondazione Italiana Linfomi ONLUS | |||||||||||||
| Full Title: Rituximab, bendamustine and cytarabine followed by venetoclax (V-RBAC) in high-risk elderly patients with mantle cell lymphoma (MCL) | |||||||||||||
| Medical condition: Mantle Cell Lymphoma in elderly patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001819-12 | Sponsor Protocol Number: CIS-COV | Start Date*: 2022-10-13 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
| Full Title: Cysteamine in association with standard therapy for the treatment of hospitalized patients with COVID-19 pneumonia: phase 2 study on safety of a new antiviral and direct therapy on the host | |||||||||||||
| Medical condition: Covid-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000729-13 | Sponsor Protocol Number: 2020_0068 | Start Date*: 2021-01-21 |
| Sponsor Name:Hôpital Foch | ||
| Full Title: Evaluation of Glucocorticoids plus Rituximab compared to Glucocorticoids plus Placebo for the treatment of patients with newly-diagnosed or relapsing IgA vasculitis : A prospective, randomized, con... | ||
| Medical condition: Patients with a diagnosis of IgAV according to Chapel Hill Consensus Conference definitions. Patients will require having a biopsy-proven diagnosis of IgAV. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004330-15 | Sponsor Protocol Number: D20180138 | Start Date*: 2019-01-10 | |||||||||||
| Sponsor Name:Assistance Publique - Hôpitaux de Paris (AP-HP) | |||||||||||||
| Full Title: A multi-center phase III randomized study comparing continuous versus fixed duration therapy with Daratumumab, Lenalidomide, and Dexamethasone for relapsed multiple myeloma | |||||||||||||
| Medical condition: multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000569-18 | Sponsor Protocol Number: RECHMPL20_0094 | Start Date*: 2020-10-02 |
| Sponsor Name:University Hospital of Montpellier | ||
| Full Title: NEOADUVANT ATEZOLIZUMAB AND ADJUVANT ATEZOLIZUMAB + BEVACIZUMAB IN COMBINATION WITH PERCUTANEOUS RADIOFREQUENCY ABLATION OF SMALL HCC: A MULTICENTER RANDOMIZED PHASE II TRIAL | ||
| Medical condition: Digestive oncology | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000547-24 | Sponsor Protocol Number: CCRG11-001 | Start Date*: 2012-02-27 | ||||||||||||||||
| Sponsor Name:Antwerp University Hospital | ||||||||||||||||||
| Full Title: Therapeutic efficacy of Wilms' tumor gene (WT1) mRNA-electroporated autologous dendritic cell vaccination in patients with solid tumors: a phase I/feasibility study | ||||||||||||||||||
| Medical condition: Therapeutic vaccination with dendritic cells loaded with Wilms' tumor 1 protein in patients with solid tumors | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-000297-17 | Sponsor Protocol Number: 69HCL19_0153 | Start Date*: 2021-01-21 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: IMMUNOGAST: An umbrella phase 2 trial to assess personalized targeted IMMUNOtherapy-based regimens in recurrent advanced/metastatic GASTric adenocarcinoma patients | |||||||||||||
| Medical condition: For patients with advanced/metastatic gastric adenocarcinomas in progression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000637-12 | Sponsor Protocol Number: P170909J | Start Date*: 2019-03-29 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Efficacy and safety of rituximab in the treatment of good prognosis microscopic polyangiitis | |||||||||||||
| Medical condition: Patients with newly diagnosed or relapsing MPA, without any poor prognosis marker (FFS=0). Stratification will be made according to peripheral nerve involvement. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001936-45 | Sponsor Protocol Number: matab4 | Start Date*: 2011-05-25 |
| Sponsor Name: | ||
| Full Title: Pertussis vaccination in pregnancy | ||
| Medical condition: The number of reported pertussis cases is rising, also in very young infants. Different strategies are possible to close the gap of susceptibility between the loss of maternal antibodies and prote... | ||
| Disease: | ||
| Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003466-39 | Sponsor Protocol Number: Protocol_MAMA_studie_22/05/2018 | Start Date*: Information not available in EudraCT |
| Sponsor Name:University of Antwerp | ||
| Full Title: Pertussis immunization during pregnancy: assessment of the role of maternal antibodies on immune responses in term and preterm infants (the MAMA study) | ||
| Medical condition: The effect of pertussis vaccination during pregnancy on the immune response after infant and childhood vaccinations in term and preterm infants. | ||
| Disease: | ||
| Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000505-80 | Sponsor Protocol Number: BT-001.01 | Start Date*: 2021-01-21 | |||||||||||
| Sponsor Name:TRANSGENE | |||||||||||||
| Full Title: A phase I/IIa study of intra-tumoral BT-001 (TG6030) administered alone and in combination with pembrolizumab in patients with cutaneous or, subcutaneous lesions or easily injectable lymph nodes of... | |||||||||||||
| Medical condition: Phase I: Advanced or metastatic solid tumors including Non-Hodgkin Lymphoma (NHL) and preferably Soft Tissue Sarcoma, Merkel Cell Carcinoma, Melanoma, Triple Negative Breast Cancer, Non Smal Cell L... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003555-38 | Sponsor Protocol Number: CP-MGC018-01 | Start Date*: 2019-08-05 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:MacroGenics, Inc. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1/2, First-in-Human, Open-Label, Dose-Escalation Study of MGC018 (Anti–B7-H3 Antibody Drug Conjugate) Alone and in Combination with MGA012 (Anti–PD-1 Antibody) in Patients with Advanced Sol... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Advanced Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: PL (Completed) ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-001360-39 | Sponsor Protocol Number: SU2C-SARC032 | Start Date*: 2019-06-24 | ||||||||||||||||
| Sponsor Name:SARC | ||||||||||||||||||
| Full Title: A Phase II Randomized Controlled Trial of Neoadjuvant Pembrolizumab with Radiotherapy and Adjuvant Pembrolizumab in Patients with High-Risk, Localized Soft Tissue Sarcoma of the Extremity | ||||||||||||||||||
| Medical condition: This trial investigates whether neoadjuvant radiotherapy combined with pembrolizumab followed by surgical resection and adjuvant pembrolizumab improves disease-free survival for patients with high-... | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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