- Trials with a EudraCT protocol (1,116)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (53)
1,116 result(s) found for: Immunotherapy.
Displaying page 1 of 56.
EudraCT Number: 2012-004194-12 | Sponsor Protocol Number: CS-BM32-nasal-001 | Start Date*: 2012-10-23 |
Sponsor Name:Medizinische Universität Wien, HNO Klinik | ||
Full Title: The effect of BM32, a recombinant hypoallergenic vaccine for immunotherapy of grass pollen allergy, on immunoglobulin levels in nasal secretions of patients suffering from seasonal allergic rhinitis | ||
Medical condition: Grass pollen allergy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002769-44 | Sponsor Protocol Number: ESAP | Start Date*: 2015-09-28 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: Efficacy and safety of an accelerated outpatient protocol for hymenoptera venom immunotherapy | |||||||||||||
Medical condition: Immunotherapy against systemic anaphylactic sting reactions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016815-39 | Sponsor Protocol Number: il-ASIT1 | Start Date*: 2010-01-15 |
Sponsor Name:Allergy Unit Department of Oto-rhino-Laryngology Lund/Malmö University Hospital | ||
Full Title: Is Intralymphatic Allergen Immunotherapy effective and safe: A human randomized clinical trial | ||
Medical condition: Seasonal Allergic rhinitis due to pollen from grass and betula verrucosa | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002944-18 | Sponsor Protocol Number: BIA-HDMP-201 | Start Date*: 2016-11-14 |
Sponsor Name:Bial Industrial Farmacéutica S.A. | ||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE BLIND CLINICAL TRIAL PHASE II, WITH SUBCUTANEOUS POLYMERIZED DEPOT IMMUNOTHERAPY AT DIFFERENT DOSES IN PARALLEL PLACEBO-CONTROLLED GROUPS IN PATIENTS WITH ALLERGIC R... | ||
Medical condition: The disease under study is allergic rhinoconjunctivitis secondary to sensitization to DPT and DF. Included in the study are patients diagnosed with that disease who also have associated mild asthma... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023536-16 | Sponsor Protocol Number: ITN043AD | Start Date*: 2011-02-25 |
Sponsor Name:University of California, San Francisco, Immune Tolerance Network | ||
Full Title: A Randomised, Double-blind, Single-centre, Placebo controlled Study of Sublingual Immunotherapy and Subcutaneous Immunotherapy in Adults with Seasonal Allergic Rhinitis (ITN043AD) | ||
Medical condition: Grass-pollen induced rhinoconjunctivitis (hay fever). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003746-42 | Sponsor Protocol Number: om 145 | Start Date*: 2003-02-11 | |||||||||||
Sponsor Name:OSPEDALE ONCOLOGICO DI BARI | |||||||||||||
Full Title: Immunotherapy vs immuno-chemotherapy in patients with metastatic kidney carcinoma | |||||||||||||
Medical condition: metastatic kidney carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001459-22 | Sponsor Protocol Number: BIA-PAR-DEPOT | Start Date*: 2015-02-20 |
Sponsor Name:Bial Industrial Farmacéutica S.A. | ||
Full Title: OPEN CLINICAL TRIAL, MULTICENTER, WITH SUBCUTANEOUS IMMUNOTHERAPY IN DEPOT PRESENTATION, IN PATIENTS WITH ALLERGY RHINOCONJUNCTIVITIS SENSITIZED TO PARIETARIA JUDAICA | ||
Medical condition: PATIENTS WITH RHINOCONJUNCTIVITIS SENSITISED TO PARIETARIA JUDAICA | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000513-29 | Sponsor Protocol Number: CLU-2008-001 | Start Date*: 2008-09-30 |
Sponsor Name:ROXALL Medizin GmbH | ||
Full Title: Efficacy and safety of subcutaneous cluster immunotherapy with cluster-allergoid CLUSTOID® (glutaraldehyde-polymerized allergen extract of mixtures of grass and rye allergens – Holcus lanatus, Dact... | ||
Medical condition: This clinical trial will evaluate the benefit of subcutaneous cluster immunotherapy with cluster-allergoid CLUSTOID® over placebo in patients with allergic rhinoconjunctivits. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005768-74 | Sponsor Protocol Number: ImmunoSep | Start Date*: 2021-02-18 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: PERSONALIZED IMMUNOTHERAPY IN SEPSIS: A MULTICENTRE AND MULTINATIONAL, DOUBLE-BLIND, DOUBLE-DUMMY RANDOMIZED CLINICAL TRIAL (THE IMMUNOSEP TRIAL) | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) NL (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003616-13 | Sponsor Protocol Number: TPX-0005-01 | Start Date*: 2020-05-12 | |||||||||||
Sponsor Name:Turning Point Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 1/2, Open-Label, Multi-Center, First-in-Human Study of the Safety, Tolerability, Pharmacokinetics, and Anti-Tumor Activity of TPX-0005 in Patients with Advanced Solid Tumors Harboring ALK, ... | |||||||||||||
Medical condition: advanced solid tumors | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) NL (Ongoing) DE (Ongoing) PL (Ongoing) ES (Ongoing) BE (Ongoing) HU (Ongoing) DK (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005115-32 | Sponsor Protocol Number: 213824 | Start Date*: 2022-09-16 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Phase 2, Randomized, Open-label Platform Study Utilizing a Master Protocol to Evaluate Novel Immunotherapy Combinations in Participants with Previously Untreated Locally Advanced/Metastatic Prog... | |||||||||||||
Medical condition: Non-small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) ES (Ongoing) NL (Ongoing) BE (Ongoing) DE (Ongoing) IT (Ongoing) PL (Ongoing) PT (Ongoing) HU (Ongoing) GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004583-30 | Sponsor Protocol Number: BIA-DPT-P2-001 | Start Date*: 2012-01-16 |
Sponsor Name:BIAL Industrial Farmaceutica | ||
Full Title: A MULTICENTER, PHASE II, RANDOMISED, DOUBLE?BLIND, PLACEBO CONTROLED CLINICAL TRIAL OF THE SUBCUTANEOUS IMMUNOTHERAPY IN DIFFERENT DOSES WITH PARALLEL GROUPS IN SUBJECTS WITH ALLERGIC RHINOCONJUNCT... | ||
Medical condition: Allergic rhinoconjunctivitis with or without associated asthma. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000254-21 | Sponsor Protocol Number: MO39839 | Start Date*: 2021-04-20 | ||||||||||||||||
Sponsor Name:University Hospital Essen | ||||||||||||||||||
Full Title: Window of opportunity study of preoperative immunotherapy with atezolizumab (Tecentriq®) with or without tocilizumab (Actemra®) in local head and neck squamous cell carcinoma | ||||||||||||||||||
Medical condition: local squamous cell carcinoma of the head and neck | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006251-11 | Sponsor Protocol Number: HLS05/2011 | Start Date*: 2012-03-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Pilot clinical trial, controlled and randomized, Phase III, to evaluate security and efficacy of oral specific immunotherapy in HIV infected patients who suffer from grass pollen allergy. | |||||||||||||
Medical condition: HIV+ subjects with grass pollen allergy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003809-26 | Sponsor Protocol Number: SP010 | Start Date*: 2013-12-04 | |||||||||||
Sponsor Name:SOTIO a.s. | |||||||||||||
Full Title: Open-label, one-arm, multi-centre phase II clinical trial with second cycle of active cellular immunotherapy DCVAC/PCa in patients with localized prostate cancer after primary radical prostatectomy... | |||||||||||||
Medical condition: Localized prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003408-33 | Sponsor Protocol Number: ESR-21-21536 | Start Date*: 2023-04-25 | |||||||||||
Sponsor Name:TheraOp gGmbH | |||||||||||||
Full Title: PACCELIO - FDG-PET based small volume accelerated immuno chemoradio-therapy in locally advanced NSCLC | |||||||||||||
Medical condition: Locally advanced, unresectable non-small-cell lung cancer (NSCLC) (Stage III) with a PD-L1-expression of ≥ 1% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000594-24 | Sponsor Protocol Number: 12/014/TAR | Start Date*: 2012-04-19 | |||||||||||
Sponsor Name:Royal Sussex County Hospital | |||||||||||||
Full Title: An open study to investigate the effects of injection immunotherapy on allergen-specific T and B cell responses in adult patients with seasonal allergic rhinitis. | |||||||||||||
Medical condition: Allergic Rhinitis due to birch or grass pollen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003832-96 | Sponsor Protocol Number: ChIm-NB-PL | Start Date*: 2021-10-13 | |||||||||||||||||||||
Sponsor Name:Jagiellonian University Medical College | |||||||||||||||||||||||
Full Title: Immunotherapy with dinutuximab beta in combination with chemotherapy for the treatment of patients with primary neuroblastoma refractory to standard therapy and with relapsed or progressive disease | |||||||||||||||||||||||
Medical condition: Recurrent or progression of neuroblastoma or neuroblastoma refractory to first-line treatment | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004566-99 | Sponsor Protocol Number: CO39612 | Start Date*: 2020-03-27 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER, RANDOMIZED UMBRELLA STUDY EVALUATING THE EFFICACY AND SAFETY OF MULTIPLE IMMUNOTHERAPY-BASED TREATMENT COMBINATIONS IN PATIENTS WITH METASTATIC COLORECTAL CA... | |||||||||||||
Medical condition: Colorectal cancer (CRC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005576-28 | Sponsor Protocol Number: VB-C-01 | Start Date*: 2015-07-13 |
Sponsor Name:VACCIBODY A.S. | ||
Full Title: An Exploratory Safety and Immunogenicity Study of Human Papillomavirus (HPV16+) Immunotherapy VB10.16 in Women with High Grade Cervical Intraepithelial Neoplasia (HSIL; CIN 2/3) | ||
Medical condition: High grade cervical intraepithelial neoplasia (HSIL, CIN 2/3) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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