- Trials with a EudraCT protocol (45)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
45 result(s) found for: Cryotherapy.
Displaying page 2 of 3.
EudraCT Number: 2015-005820-24 | Sponsor Protocol Number: IIS-PICATO1264 | Start Date*: 2016-09-09 | |||||||||||
Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | |||||||||||||
Full Title: A randomized study to evaluate the efficacy of ingenol mebutate on actinic keratoses and field cancerization compared to cryotherapy | |||||||||||||
Medical condition: actinic keratoses and field cancerization | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000478-42 | Sponsor Protocol Number: 008285QM | Start Date*: 2013-02-18 |
Sponsor Name:Queen Mary, University of London | ||
Full Title: NEPTUNE: A Randomised Phase II Study of Neoadjuvant TAK-700 and Leuprorelin Acetate versus Surgery Alone in Intermediate and High Risk Clinically Localized Prostate Cancer | ||
Medical condition: High or Intermediate Risk, Untreated, Clinically Localised Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-022054-16 | Sponsor Protocol Number: X-03016-3284 | Start Date*: 2011-09-05 | |||||||||||
Sponsor Name:MEDA Pharma GmbH & Co. KG | |||||||||||||
Full Title: Long-term effects of Aldara® 5% cream and Solaraze® 3% gel in the treatment of actinic keratoses on the face or scalp with respect to the risk of progression to in-situ and invasive squamous cel... | |||||||||||||
Medical condition: This study will compare the long term effects of Aldara® and Solaraze® of the actinic keratoses on the face or scalp. Actinic keratoses (AKs) are defined as keratotic macules, papules or plaques w... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004901-12 | Sponsor Protocol Number: SFOLFOX/SFOLFIRI vs FOLFOX/FOLFIRI | Start Date*: 2005-05-13 | |||||||||||
Sponsor Name:TEVA Pharma Belgium | |||||||||||||
Full Title: Phase II randomized study of Combined Infusional Leucovorin Sodium and 5-FU Versus the Classical Sequential administration of Leucovorin Calcium followed by 5-FU both in combination with standard ... | |||||||||||||
Medical condition: Histologically confirmed adenocarcinoma of the colon or the rectum and unresectable metastases or advanced locoregional disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000824-32 | Sponsor Protocol Number: IMDZ-04-1702 | Start Date*: 2018-10-19 |
Sponsor Name:Immune Design Corp. | ||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy and Safety of CMB305 in Unresectable Locally-advanced or Metastatic NY-ESO-1+ Synovial Sarcoma Subjects Follo... | ||
Medical condition: Unresectable locally-advanced or metastatic synovial sarcoma | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-001302-15 | Sponsor Protocol Number: BIO-CT-001 | Start Date*: 2019-09-13 | |||||||||||
Sponsor Name:BIOKOSMOS S.A. | |||||||||||||
Full Title: Phase III study of Positron/Computerized Tomography (PETCT) with F-18-PSMA-1007 versus F-18-Fluorocholine to compare the detection rate of prostate cancer lesions in patients with biochemical recur... | |||||||||||||
Medical condition: Prostate cancer recurrent | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005276-27 | Sponsor Protocol Number: FE 200486 CS35 | Start Date*: 2009-07-17 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: An Open-Label, Multi-Centre, Randomised, Parallel-Arm One-Year Trial, Comparing the Efficacy and Safety of Degarelix Three-Month Dosing Regimen with Goserelin Acetate in Patients with Prostate Canc... | |||||||||||||
Medical condition: prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: HU (Completed) NL (Completed) DE (Completed) FI (Completed) CZ (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006854-24 | Sponsor Protocol Number: ALA-AK-CT002 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, observer blind, multinational phase III study to evaluate the safety and efficacy of a nanoemulsion gel formulation BF-200 ALA, in comparison with Metvix® and placebo, for the treatme... | |||||||||||||
Medical condition: Actinic keratosis (AK) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004235-24 | Sponsor Protocol Number: ABX-CT-303 | Start Date*: 2021-06-09 | |||||||||||||||||||||
Sponsor Name:ABX GmbH | |||||||||||||||||||||||
Full Title: Phase III study of [18F]PSMA-1007 positron emission tomography for the detection of prostate cancer lesions in patients with biochemical recurrence after previous definitive treatment for localized... | |||||||||||||||||||||||
Medical condition: Suspicion of prostate cancer recurrence or persistence after previous definitive treatment, based on American Society for Radiation Oncology (ASTRO) criteria of 3 consecutive PSA rises and/or ASTRO... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013052-76 | Sponsor Protocol Number: VHLSUT09 | Start Date*: 2010-02-12 | |||||||||||
Sponsor Name:ARTIC (Association pour la Recherche de Thérapeutiques Innovantes en Cancérologie) | |||||||||||||
Full Title: A single-arm, phase II study of SU11248 (sunitinib) in patients with von Hippel-Lindau (VHL) disease. | |||||||||||||
Medical condition: von Hippel-Lindau (VHL) disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000287-34 | Sponsor Protocol Number: ARO-012 | Start Date*: 2017-05-30 | |||||||||||
Sponsor Name:Arog Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Trial of Crenolanib in Subjects with Advanced or Metastatic Gastrointestinal Stromal Tumors with a D842V Mutation in the PDGFRA Gene. | |||||||||||||
Medical condition: Advanced or metastatic gastrointestinal stromal tumor (GIST) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000545-39 | Sponsor Protocol Number: DERMAQ-001 | Start Date*: 2018-04-30 | |||||||||||
Sponsor Name:ASL 1 AVEZZANO-SULMONA-L'AQUILA | |||||||||||||
Full Title: A randomized half-side comparative study of Methyl aminolevulinate (MAL, Metvix®) Daylight photodynamic therapy (DL-PDT) with or without pre-treatment with calcitriol (Silkis®) for Actinic Keratosi... | |||||||||||||
Medical condition: Actinic Keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006474-21 | Sponsor Protocol Number: TCD6511 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: A dose-escalating, multicenter, single arm, open-label study of XRP9881 in combination with capecitabine (Xeloda®), in metastatic breast cancer patients with disease progressing after anthracycline... | |||||||||||||
Medical condition: Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004382-83 | Sponsor Protocol Number: ALA-AK-CT009 | Start Date*: 2016-06-09 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, observer-blind, intra-individual phase III study to evaluate the safety and efficacy of BF 200 ALA (Ameluz®) in combination with daylight-PDT (photodynamic therapy) in comparison with... | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003241-42 | Sponsor Protocol Number: ALA-BCC-CT008 | Start Date*: 2013-12-23 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, observer blind, multinational phase III study to evaluate the safety and efficacy of BF-200 ALA (Ameluz®) in comparison to Metvix® in the treatment of non-aggressive basal cell carcin... | |||||||||||||
Medical condition: Basal cell carcinoma (BCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000486-72 | Sponsor Protocol Number: ALA-AK-CT010 | Start Date*: 2017-07-28 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, double-blind, intra-individual, multi-center phase III study to evaluate the safety and efficacy of BF 200 ALA (Ameluz®) versus placebo in the treatment of mild to severe actinic kera... | |||||||||||||
Medical condition: Actinic keratosis (AK) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002510-12 | Sponsor Protocol Number: ALA-AK-CT007 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, double-blind, phase III multi-center study to evaluate the safety and efficacy of BF-200 ALA (Ameluz®) versus placebo in the field-directed treatment of mild to moderate actinic kerat... | |||||||||||||
Medical condition: Actinic keratosis (AK) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005193-11 | Sponsor Protocol Number: METAL | Start Date*: 2015-03-31 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: METformin And Longevity (METAL): A window of opportunity study investigating biological effects of metformin in localised prostate cancer | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002975-16 | Sponsor Protocol Number: ABX-CT-301 | Start Date*: 2018-10-31 | |||||||||||||||||||||
Sponsor Name:ABX GmbH | |||||||||||||||||||||||
Full Title: Phase III study of F-18-PSMA-1007 vs F-18-Fluorocholine PET to compare the detection rate of prostate cancer lesions in patients with biochemical recurrence after previous definitive treatment for ... | |||||||||||||||||||||||
Medical condition: Suspicion of prostate cancer recurrence after previous definitive treatment, based on American Society for Radiation Oncology (ASTRO) criteria of 3 consecutive PSA rises and/or ASTRO/Phoenix criter... | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001410-33 | Sponsor Protocol Number: UZB-VUB-11-01 | Start Date*: 2016-03-10 | ||||||||||||||||
Sponsor Name:UZ BRUSSEL | ||||||||||||||||||
Full Title: Randomized phase II clinical trial on mRNA electroporated autologous dendritic cells for stage III/IV melanoma in patients who are free from measurable tumor lesions following the local treatment o... | ||||||||||||||||||
Medical condition: stage III/IV melanoma in patients who are free from measurable tumor lesions following the local treatment of macro metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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