- 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 5 of 8.
EudraCT Number: 2018-003298-90 | Sponsor Protocol Number: OPT-302-1003 | Start Date*: 2018-12-07 | ||||||||||||||||
Sponsor Name:Opthea Ltd | ||||||||||||||||||
Full Title: Phase 1b/2a study of OPT-302 in combination with aflibercept for persistent central-involved diabetic macular edema | ||||||||||||||||||
Medical condition: Persistent central-involved diabetic macular edema | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001764-29 | Sponsor Protocol Number: VGFTe-ROP-1920 | Start Date*: 2020-12-01 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals. Inc. | |||||||||||||
Full Title: Randomized, Controlled, Multi-Center Study to Assess the Efficacy, Safety, and Tolerability of Intravitreal Aflibercept Compared to Laser Photocoagulation in Patients with Retinopathy of Prematurity | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) CZ (Completed) BG (Completed) BE (Completed) PT (Completed) GR (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003695-23 | Sponsor Protocol Number: 69HCL14-0201 | Start Date*: 2015-07-21 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Phase II study evaluating the efficacy of aflibercept for the treatment of inflammatory choroidal neovascularization in young subjects: the ALINEA study | |||||||||||||
Medical condition: inflammatory choroidal neovascularization | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001063-82 | Sponsor Protocol Number: KS301P105 | Start Date*: 2021-01-14 | ||||||||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | ||||||||||||||||||||||||||||
Full Title: A Prospective, Randomized, Double-masked, Active Comparator-controlled, Multi-center, Two-arm, Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared with Intravitreal A... | ||||||||||||||||||||||||||||
Medical condition: Diabetic Macular Edema (DME) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Prematurely Ended) HU (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004648-12 | Sponsor Protocol Number: CLS1003-301 | Start Date*: 2018-01-15 |
Sponsor Name:Clearside Biomedical, Inc. | ||
Full Title: SAPPHIRE: A RANDOMIZED, MASKED, CONTROLLED TRIAL TO STUDY THE SAFETY AND EFFICACY OF SUPRACHOROIDAL CLS-TA IN CONJUNCTION WITH INTRAVITREAL AFLIBERCEPT IN SUBJECTS WITH RETINAL VEIN OCCLUSION | ||
Medical condition: Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) HU (Completed) DE (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) PT (Completed) DK (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-000362-42 | Sponsor Protocol Number: THR-687-002 | Start Date*: 2021-10-06 | ||||||||||||||||
Sponsor Name:Oxurion NV | ||||||||||||||||||
Full Title: A Phase 2, randomised, multicentre study to assess the dose level of multiple THR-687 injections and to evaluate the efficacy and safety of THR-687 versus aflibercept for the treatment of diabetic ... | ||||||||||||||||||
Medical condition: Diabetic macular oedema (DME) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Prematurely Ended) LT (Completed) LV (Prematurely Ended) HU (Prematurely Ended) PT (Prematurely Ended) DE (Ongoing) IT (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004530-11 | Sponsor Protocol Number: ALT-L9-03 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:Altos Biologics Inc. | |||||||||||||
Full Title: A Randomized, Phase 3, Double Masked, Parallel Group, Multicenter Study to Compare the Efficacy and Safety of ALT L9 Versus Eylea® in Patients With Neovascular Age Related Macular Degeneration (ALT... | |||||||||||||
Medical condition: Neovascular Age Related Macular Degeneration | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) LV (Completed) AT (Completed) ES (Ongoing) BG (Completed) EE (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002003-25 | Sponsor Protocol Number: | Start Date*: 2016-06-02 | |||||||||||
Sponsor Name:Barts Health NHS Trust | |||||||||||||
Full Title: A Phase II Trial of Aflibercept Monotherapy With Early Dynamic Contrast Enhanced Ultrasound Monitoring in Chemorefractory Metastatic Colorectal Cancer | |||||||||||||
Medical condition: Metastatic Colorectal Cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002567-26 | Sponsor Protocol Number: ΗΕ6Α/13 | Start Date*: 2014-03-04 | |||||||||||
Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||
Full Title: Single-arm phase II study of maintenance therapy with aflibercept after first-line treatment with FOLFIRI plus aflibercept in metastatic colorectal cancer patients | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003509-16 | Sponsor Protocol Number: FLIBER | Start Date*: 2018-03-02 | ||||||||||||||||
Sponsor Name:FONDAZIONE RICERCA TRASLAZIONALE (FORT) | ||||||||||||||||||
Full Title: Serum cytokine levels as predictors of the efficacy of aflibercept in combination with FOLFIRI in metastatic Colo-Rectal Cancer patients (mCRC) | ||||||||||||||||||
Medical condition: Metastatic Colo-Rectal Cancer | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000329-11 | Sponsor Protocol Number: Elderly | Start Date*: 2018-05-02 | ||||||||||||||||
Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | ||||||||||||||||||
Full Title: Aflibercept and 5-FU vs. FOLFOX as 1st line treatment for elderly or frail elderly patients with metastatic colorectal cancer | ||||||||||||||||||
Medical condition: metastatic colorectal cancer | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003428-35 | Sponsor Protocol Number: KSI-CL-102 | Start Date*: 2020-01-03 | |||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | |||||||||||||||||||||||
Full Title: A Phase 2b/3, Prospective, Randomised, Double-masked, Active Comparator-controlled, Multi-center Study to Investigate the Efficacy and Safety of Repeated Intravitreal Administration of KSI-301 in S... | |||||||||||||||||||||||
Medical condition: Neovascular (Wet) Age-related Macular Degeneration | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003515-10 | Sponsor Protocol Number: BP41783 | Start Date*: 2021-03-09 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A LONGITUDINAL, BIOMARKER STUDY OF ANTI-VEGF, TO EXPLORE THE RELATIONSHIP BETWEEN AQUEOUS HUMOR COMPOSITION AND MULTIMODAL RETINAL IMAGING IN NEOVASCULAR AGE-RELATED MACULAR DEGENERATION AND DIABET... | |||||||||||||
Medical condition: Treatment Naïve Neovascular Age-Related Macular Degeneration (nAMD) and Treatment Naïve diabetic macular edema (DME) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000975-21 | Sponsor Protocol Number: RET-AFLI-2014-01 | Start Date*: 2014-06-16 |
Sponsor Name:Fundación Retinaplus + | ||
Full Title: A phase IV study to evaluate the effectiveness of aflibercept in naive patients with macular edema secondary to Central Retinal Vein Occlusion (CRVO) on an individualized Treat and Extend regimen. ... | ||
Medical condition: Macular edema secondary to central retinal vein occlusion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002168-34 | Sponsor Protocol Number: FNB-OK-2013-01 | Start Date*: 2014-12-09 | |||||||||||||||||||||
Sponsor Name:Doc. MUDr. Petr Kolář, PhD, Oční klinika FN Brno | |||||||||||||||||||||||
Full Title: Study To Determine Efficacy of Aflibercept For Treatment Of Retinal Angiomatous Proliferation Secondary To Age Related Macular Degeneration | |||||||||||||||||||||||
Medical condition: Retinal angiomatous proliferation secondary to wet age related macular degeneration. | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000272-26 | Sponsor Protocol Number: HYKP1021 | Start Date*: 2014-09-04 |
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | ||
Full Title: A Multicentre Phase III Double-masked Randomised Controlled Non-Inferiority Trial comparing the clinical and cost effectiveness of intravitreal therapy with ranibizumab (Lucentis) vs aflibercept (E... | ||
Medical condition: Macular Oedema due to Central Retinal Vein Occlusion (CRVO). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001837-10 | Sponsor Protocol Number: PRODIGE25 | Start Date*: 2016-09-27 | |||||||||||
Sponsor Name:Fédération Francophone de Cancérologie Digestive | |||||||||||||
Full Title: PHASE II RANDOMIZED TRIAL EVALUATING AFLIBERCEPT ASSOCIATED WITH SCHEME LV5FU2 AS FIRST LINE TREATMENT OF NON-RESECTABLE METASTATIC COLORECTAL CANCERS | |||||||||||||
Medical condition: first line of treatment for metastatic colorectal cancer | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001062-11 | Sponsor Protocol Number: KS301P104 | Start Date*: 2021-01-20 | ||||||||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | ||||||||||||||||||||||||||||
Full Title: A Prospective, Randomized, Double-masked, Active Comparator-controlled, Multi-center, Two-arm, Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared with Intravitreal A... | ||||||||||||||||||||||||||||
Medical condition: Diabetic Macular Edema (DME) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) SK (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005263-33 | Sponsor Protocol Number: AUG-201202-EyNeP | Start Date*: 2015-04-29 | |||||||||||
Sponsor Name:Medizinische Fakultät der Universität Bonn | |||||||||||||
Full Title: Intravitreal Aflibercept (Eylea®) for therapy of choroidal neovascularization and fibrovascular proliferation in patients with Pseudoxanthoma elasticum | |||||||||||||
Medical condition: Choroidal neovascularizations and fibrovascular proliferations in patients with Pseudoxanthoma elasticum | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003133-42 | Sponsor Protocol Number: 1672_2019 | Start Date*: 2020-02-14 |
Sponsor Name:Medical University of Vienna, Department of Ophthalmology and Optometry | ||
Full Title: Personalized treatment aided by automated analysis of fluid in active neovascular age-related macular degeneration (nAMD) in a prospective, multicenter, randomized study | ||
Medical condition: Nevoascular age related macular degneration (nAMD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
