- Trials with a EudraCT protocol (53)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
53 result(s) found for: Aspergillosis.
Displaying page 1 of 3.
EudraCT Number: 2021-004554-32 | Sponsor Protocol Number: PC_ASP_006 | Start Date*: 2022-07-09 | |||||||||||
Sponsor Name:Pulmocide Ltd | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled study to assess the safety and efficacy of nebulized PC945 when added to systemic antifungal therapy for the treatment of refractory invasive pulmonar... | |||||||||||||
Medical condition: Refractory invasive pulmonary aspergillosis (IPA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) AT (Trial now transitioned) GR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004988-27 | Sponsor Protocol Number: FG-463-21-20 | Start Date*: 2006-07-27 | |||||||||||
Sponsor Name:Astellas Pharma BV | |||||||||||||
Full Title: A PHASE II, MULTICENTRE, RANDOMISED, OPEN-LABEL, ACTIVE CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF MICAFUNGIN SALVAGE MONO THERAPY VERSUS ACTIVE CONTROL INTRAVENOUS SALVAGE MONO THE... | |||||||||||||
Medical condition: Patients with haematopoietic stem cell transplantation (HSCT), acute leukaemia, myelodysplastic syndrome (MDS) and with proven (probable only in case of pulmonary aspergillosis) invasive aspergillo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) ES (Completed) HU (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001936-30 | Sponsor Protocol Number: Uni-Koeln-687 | Start Date*: 2006-09-21 | |||||||||||
Sponsor Name:Universität zu Köln | |||||||||||||
Full Title: A phase II dose escalation study of caspofungin in patients with invasive aspergillosis | |||||||||||||
Medical condition: proven or probable aspergillosis in immunocompromised patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003921-40 | Sponsor Protocol Number: 2016IF002 | Start Date*: 2017-07-21 | |||||||||||||||||||||||||||||||
Sponsor Name:University Hospital of South Manchester NHS Foundation Trust | |||||||||||||||||||||||||||||||||
Full Title: Open label study of the efficacy and safety of isavuconazole for the treatment of Chronic Pulmonary Aspergillosis | |||||||||||||||||||||||||||||||||
Medical condition: Chronic Pulmonary Aspergillosis | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002445-20 | Sponsor Protocol Number: A8851009 | Start Date*: 2007-11-01 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED TRIAL COMPARING THE EFFICACY OF ANIDULAFUNGIN AND VORICONAZOLE IN COMBINATION TO THAT OF VORICONAZOLE ALONE WHEN USED FOR PRIMARY THERAPY OF PROVEN OR PROBABLE INVASIVE AS... | |||||||||||||
Medical condition: INVASIVE ASPERGILLOSIS | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) NL (Ongoing) FR (Completed) GB (Completed) ES (Completed) IT (Completed) DE (Completed) CZ (Completed) BE (Completed) PT (Completed) GR (Completed) IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006648-23 | Sponsor Protocol Number: CIGE025A2437 | Start Date*: 2008-11-12 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: An exploratory, randomized, double-blind, placebo controlled study to assess the efficacy of multiple doses of omalizumab in cystic fibrosis complicated with allergic bronchopulmonary aspergillosis | ||||||||||||||||||
Medical condition: Patients with cystic fibrosis complicated by allergic bronchopulmonary aspergillosis. | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) NL (Prematurely Ended) GB (Prematurely Ended) IE (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002944-90 | Sponsor Protocol Number: EORTC 65041 | Start Date*: 2005-07-26 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: A Multicenter, Open, Phase II Study to Estimate the activity and safety of Caspofungin (CASP) in the First-line Treatment of probable and proven Invasive Aspergillosis 'IA) in Patients with Hematol... | |||||||||||||
Medical condition: Invasive aspergillosis in patients with haematological malignancies (HM)/autologous Hematopoietic Stem Cell Transplantation (HSCT) – group A- and patients with allogeneic HSCT transplantation – gro... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) ES (Completed) IT (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001841-16 | Sponsor Protocol Number: VOCARE-07-01 | Start Date*: 2008-09-17 | |||||||||||
Sponsor Name:Melchor Riera Jaume | |||||||||||||
Full Title: ENSAYO CLÍNICO ALEATORIZADO Y CONTROLADO DE VORICONAZOL FRENTE A PLACEBO EN LA PROFILAXIS DE ASPERGILOSIS PULMONAR EN PACIENTES COLONIZADOS CON PATOLOGÍA RESPIRATORIA CRÓNICA (ESTUDIO VOCARE) | |||||||||||||
Medical condition: Aspergilosis pulmonar invasiva | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005275-10 | Sponsor Protocol Number: A1501080 | Start Date*: 2009-03-24 | |||||||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||||||||||||
Full Title: A PROSPECTIVE, OPEN-LABEL, NON-RANDOMIZED, MULTI-CENTER STUDY TO INVESTIGATE THE SAFETY AND TOLERABILITY OF VORICONAZOLE AS PRIMARY THERAPY FOR TREATMENT OF INVASIVE ASPERGILLOSIS AND MOLDS SUCH AS... | |||||||||||||||||||||||
Medical condition: Treatment of proven or probable invasive aspergillosis (IA) and rare molds such as Scedosporium or Fusarium species. | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) HU (Completed) CZ (Prematurely Ended) ES (Prematurely Ended) DE (Completed) BG (Prematurely Ended) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003270-14 | Sponsor Protocol Number: POSA-FLU | Start Date*: 2017-11-06 |
Sponsor Name:UZ Leuven | ||
Full Title: A phase IV, interventional, non-blinded, randomized, controlled, multicenter study of Posaconazole prophylaxis for the prevention of influenza-associated aspergillosis (IAA) in critically ill patients | ||
Medical condition: invasive aspergillosis in critically ill patients with influenza pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) NL (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021231-14 | Sponsor Protocol Number: A1501095 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PROSPECTIVE, RANDOMIZED TRIAL COMPARING THE SAFETY, TOLERABILITY, AND EFFICACY OF VORICONAZOLE AND ANIDULAFUNGIN IN COMBINATION TO THAT OF VORICONAZOLE ALONE WHEN USED FOR PRIMARY THERAPY OF INVA... | |||||||||||||
Medical condition: Primary therapy of invasive aspergillosis (IA) in pediatric subjects aged 2 to 17 years. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) FR (Ongoing) NL (Ongoing) DK (Prematurely Ended) PL (Completed) DE (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000499-32 | Sponsor Protocol Number: FSJD-ABELNEB-2010 | Start Date*: 2011-09-29 | |||||||||||
Sponsor Name:FUNDACIÓ SANT JOAN DE DEU | |||||||||||||
Full Title: A PHASE II CLINICAL TRIAL TO EVALUATE THE SAFETY AND TOLERABILITY OF AMPHOTERICIN B LIPID COMPLEX (ABELCET®) FOR THE PROPHYLAXIS OF INVASIVE PULMONARY ASPERGILLOSIS DURING PROLONGED NEUTROPENIA IN ... | |||||||||||||
Medical condition: Invasive pulmonary aspergillosis in patients with acute myeloblastic or lymphoblastic leukaemia. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000972-14 | Sponsor Protocol Number: CPAAARI | Start Date*: 2018-07-04 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Therapeutic efficacy comparison of a six-month treatment by itraconazole and nebulised Ambisome® versus treatment by itraconazole alone in non- or mildly- immunocompromised patients with Chronic Pu... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002289-33 | Sponsor Protocol Number: 601-0018 | Start Date*: 2023-02-01 | ||||||||||||||||
Sponsor Name:Pulmatrix, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Evaluate the Effect of Dose and Duration of Treatment of Itraconazole Administered as a Dry Powder for Inhalation (PUR1900) on S... | ||||||||||||||||||
Medical condition: Allergic bronchopulmonary aspergillosis (ABPA) in patients with asthma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000627-40 | Sponsor Protocol Number: IA-DUET | Start Date*: 2020-12-28 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Azole-echinocandin combination therapy for invasive aspergillosis. A randomized pragmatic superiority trial (IA-DUET) | |||||||||||||
Medical condition: Invasive aspergillosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002949-11 | Sponsor Protocol Number: 601-0014 | Start Date*: 2019-08-05 | |||||||||||
Sponsor Name:Pulmatrix, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center, Placebo-Controlled Phase 2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Itraconazole Administered as a Dry Powder for Inhalation (PU... | |||||||||||||
Medical condition: Asthma with Allergic Bronchopulmonary Aspergillosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003868-59 | Sponsor Protocol Number: WSA-CS-004 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:Astellas Global Pharma Development, Inc. | |||||||||||||
Full Title: A phase III, double blind, randomized study to evaluate safety and efficacy of BAL8557 versus voriconazole for primary treatment of invasive fungal disease caused by Apsergillus species or other fi... | |||||||||||||
Medical condition: Invasive fungal disease caused by Aspergillus species or other filamentous fungi. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) HU (Completed) ES (Completed) NL (Completed) IT (Completed) GB (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006633-19 | Sponsor Protocol Number: TFF-V2-001 | Start Date*: 2022-08-02 | |||||||||||
Sponsor Name:TFF Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label, Randomized, Safety, Pharmacokinetic, and Efficacy Study of Voriconazole Inhalation Powder Compared to Oral Voriconazole Tablets in Subjects with Acute Invasive Pulmonary Aspe... | |||||||||||||
Medical condition: Invasive pulmonary aspergillosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) ES (Ongoing) BE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002619-24 | Sponsor Protocol Number: R668-ABPA-1923 | Start Date*: 2020-09-08 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Dupilumab in Patients with Allergic Bronchopulmonary Aspergillosis | |||||||||||||
Medical condition: Allergic bronchopulmonary aspergillosis (ABPA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (GB - no longer in EU/EEA) NL (Completed) BG (Completed) FR (Prematurely Ended) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003435-11 | Sponsor Protocol Number: VL2397-201 | Start Date*: 2018-08-14 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Vical Incorporated | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 2 Study of VL-2397 Compared to Standard First-Line Treatment for Invasive Aspergillosis in Immunocompromised Adults | ||||||||||||||||||||||||||||||||||||||
Medical condition: Invasive Aspergillosis | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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