- Trials with a EudraCT protocol (147)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
147 result(s) found for: Aflibercept.
Displaying page 7 of 8.
EudraCT Number: 2015-003723-65 | Sponsor Protocol Number: MICM1014 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:Moorfields Eye Hospital | |||||||||||||
Full Title: Aflibercept (Eylea®) for macular oedema associated with underlying Retinitis Pigmentosa (AMOUR) | |||||||||||||
Medical condition: Retinitis Pigmentosa associated Cystoid Macular Oedema | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002152-32 | Sponsor Protocol Number: GR40306 | Start Date*: 2019-04-30 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FARICIMAB IN PATIENTS WITH NEOVASCULAR AGE-RELATED MACULAR DEGENERATIO... | |||||||||||||
Medical condition: Neovascular age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (GB - no longer in EU/EEA) PL (Completed) ES (Ongoing) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001441-14 | Sponsor Protocol Number: IFOM-CPT002/2018/PO001 | Start Date*: 2018-10-29 | |||||||||||
Sponsor Name:IFOM - Istituto FIRC di Oncologia Molecolare - Milano | |||||||||||||
Full Title: PEMBROLIZUMAB IN MMR-PROFICIENT METASTATIC COLORECTAL CANCER PHARMACOLOGICALLY PRIMED TO TRIGGER DYNAMIC HYPERMUTATION STATUS | |||||||||||||
Medical condition: RAS mutated metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004042-42 | Sponsor Protocol Number: GR40844 | Start Date*: 2019-05-22 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FARICIMAB IN PATIENTS WITH NEOVASCULAR AGE-RELATED MACULAR DEGENERATIO... | |||||||||||||
Medical condition: Neovascular age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) PT (Completed) DE (Completed) HU (Completed) DK (Completed) ES (Completed) PL (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000440-63 | Sponsor Protocol Number: GR41984 | Start Date*: 2020-09-30 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FARICIMAB IN PATIENTS WITH MACULAR EDEMA SECONDARY TO BRANCH RETINAL ... | |||||||||||||
Medical condition: Macular edema secondary to Branch Retinal Vein Occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) PT (Completed) AT (Completed) CZ (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005104-10 | Sponsor Protocol Number: GR40349 | Start Date*: 2018-11-08 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF RO6867461 IN PATIENTS WITH DIABETIC MACULAR EDEMA (YOSEMITE) | |||||||||||||
Medical condition: Diabetic Macular Edema (DME) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BG (Completed) DE (Completed) HU (Completed) AT (Completed) PL (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005105-12 | Sponsor Protocol Number: GR40398 | Start Date*: 2018-09-18 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FARICIMAB (RO6867461) IN PATIENTS WITH DIABETIC MACULAR EDEMA (RHINE) | |||||||||||||
Medical condition: Diabetic Macular Edema (DME) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) DE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000621-39 | Sponsor Protocol Number: Sym004-11 | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Symphogen A/S | |||||||||||||
Full Title: An Open-label, Multicenter, Phase 2 Trial Investigating Sym004 in Patients with Metastatic Colorectal Cancer and Acquired Resistance to Anti-EGFR Monoclonal Antibodies and Documented Mutation of Ex... | |||||||||||||
Medical condition: Metastatic Colorectal Cancer and Acquired Resistance to Anti-EGFR Monoclonal Antibodies and Documented Mutation of Extra Cellular Doman of EGFR | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000642-35 | Sponsor Protocol Number: HL217-201 | Start Date*: 2019-09-19 | |||||||||||
Sponsor Name:HANLIM PHARM CO., LTD | |||||||||||||
Full Title: A phase IIa randomized, double-blind, multicentre study to evaluate safety and efficacy of HL217 topical ophthalmologic solution in the treatment of exudative Age-Related Macular Degeneration (AMD) | |||||||||||||
Medical condition: AMD (age-related macular degeneration) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005875-10 | Sponsor Protocol Number: VGFTe-ROP-2036 | Start Date*: 2022-03-10 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals. Inc. | |||||||||||||
Full Title: An Extension Study to Evaluate the Long-Term Outcomes of Patients Who Received Treatment for Retinopathy of Prematurity in the VGFTe-ROP-1920 Study | |||||||||||||
Medical condition: Retinopathy of prematurity (ROP) | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Trial now transitioned) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003147-27 | Sponsor Protocol Number: B1261009 | Start Date*: 2014-01-10 | ||||||||||||||||
Sponsor Name:Pfizer Inc 235 East 42nd Street, New York, NY 10017 US | ||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-MASKED, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTI-CENTER STUDY TO COMPARE THE EFFICACY AND SAFETY OF A CHEMOKINE CCR2/5 RECEPTOR ANTAGONIST (PF-04634817) WITH THAT OF ... | ||||||||||||||||||
Medical condition: PF-04634817 is a small molecule chemokine CCR2/5 receptor antagonist that is being developed for the treatment of diabetic nephropathy and diabetic macular edema. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001221-40 | Sponsor Protocol Number: 1336-0007 | Start Date*: 2019-05-06 | |||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||||||||||||
Full Title: Safety, tolerability and pharmacodynamics of single rising intravitreal and multiple rising intravitreal doses of BI 836880 in patients with wAMD (open label, non-randomized, uncontrolled). | |||||||||||||||||||||||
Medical condition: wet age-related macular degeneration (wAMD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004162-99 | Sponsor Protocol Number: RAMTAS | Start Date*: 2018-08-09 | |||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH am Krankenhaus Nordwest | |||||||||||||
Full Title: RAMTAS A Phase III study of RAMucirumab in combination with TAS102 vs. TAS102 monotherapy in chemotherapy refractory metastatic colorectal cancer patients | |||||||||||||
Medical condition: Advanced metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002834-35 | Sponsor Protocol Number: PARERE | Start Date*: 2020-09-24 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: Randomized phase II study of PAnitumumab REchallenge followed by REgorafenib versus the reverse sequence in RAS and BRAF WILD-TYPE chemorefractory metastatic colorectal cancer patients. | |||||||||||||
Medical condition: RAS and BRAF wild-type chemorefractory metastatic colorectal cancer 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: 2018-001096-20 | Sponsor Protocol Number: UCL-mCRC-2018-MS100070-0095 | Start Date*: 2018-08-03 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Avelumab combined with cetuximab and irinotecan for treatment refractory metastatic colorectal microsatellite stable cancer – A proof of concept, open label non-randomized Phase IIa study. | ||
Medical condition: TREATMENT FOR REFRACTORY METASTATIC MICROSATELLITE STABLE COLORECTAL CANCER | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000441-13 | Sponsor Protocol Number: GR41986 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-MASKED, ACTIVE COMPARATOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FARICIMAB IN PATIENTS WITH MACULAR EDEMA SECONDARY TO CENTRAL RETINAL ... | |||||||||||||
Medical condition: Macular edema secondary to Central Retinal or Hemiretinal Vein Occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Completed) AT (Completed) CZ (Completed) HU (Completed) FR (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000257-39 | Sponsor Protocol Number: PM60184-B-002-17 | Start Date*: 2017-12-01 | |||||||||||
Sponsor Name:Pharma Mar, S.A. | |||||||||||||
Full Title: A Phase II, Open-label, Multicenter Study of PM060184 in Patients with Advanced Colorectal Cancer after Standard Treatment | |||||||||||||
Medical condition: Advanced Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005655-16 | Sponsor Protocol Number: Regard-CrC_2012 | Start Date*: 2013-07-03 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Regorafenib Assessment in Refractory advanced Colorectal cancer | |||||||||||||
Medical condition: Advanced refractory colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002533-14 | Sponsor Protocol Number: REVERT | Start Date*: 2021-02-15 | ||||||||||||||||
Sponsor Name:DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA | ||||||||||||||||||
Full Title: REVERT – taRgeted thErapy for adVanced colorEctal canceR paTients. | ||||||||||||||||||
Medical condition: unresectable metastatic colorectal cancer (mCRC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006280-21 | Sponsor Protocol Number: CORIOLAN | Start Date*: 2012-04-27 | ||||||||||||||||
Sponsor Name:Jules Bordet Institute | ||||||||||||||||||
Full Title: Correlating the tumoral metabolic progression index measured by serial FDG PET-CT and apparent diffusion coefficient measured by MRI to patient's outcome in advance colorectal cancer | ||||||||||||||||||
Medical condition: Advanced colorectal cancer, refractory to all available medications | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
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