- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Brain healing.
Displaying page 1 of 1.
EudraCT Number: 2012-001249-41 | Sponsor Protocol Number: KEK-ZH-2012-0249 | Start Date*: 2013-04-12 |
Sponsor Name:University Hospital of Zurich and City Hospital Waid | ||
Full Title: Vitamin D3 – Omega3 – Home Exercise – HeALTHy Ageing and Longevity Trial Randomized, double-blind, placebo-controlled, multi-centre clinical trial | ||
Medical condition: healthy ageing, functional decline | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) PT (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016501-41 | Sponsor Protocol Number: 400-09-001 | Start Date*: 2010-06-29 |
Sponsor Name:Omrix Biopharmaceuticals Ltd | ||
Full Title: A Randomized, Controlled Study to Evaluate the Safety and Effectiveness of Evicel as an Adjunct to Sutured Dural Repair | ||
Medical condition: tissue adhesion/sealing and suture support in neurosurgery and surgical procedures where contact with cerebrospinal fluid or dura mater can occur e.g. otologic, rhinologic, ophthalmic and vertebral... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) NL (Completed) FI (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004175-73 | Sponsor Protocol Number: HP-CD-CL-2002 | Start Date*: 2017-09-27 | |||||||||||
Sponsor Name:Herantis Pharma Plc | |||||||||||||
Full Title: A Phase I-II, Randomised, Double-Blind, Placebo Controlled, Safety and Tolerability Study of Intermittent Bilateral Intraputamenal Cerebral Dopamine Neurotrophic Factor (CDNF) Infusions Administere... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001554-33 | Sponsor Protocol Number: BGB-290-104 | Start Date*: 2018-01-24 |
Sponsor Name:BeiGene USA, Inc. | ||
Full Title: A Phase 1b/2 study to assess the safety, tolerability and efficacy of BGB-290 in combination with radiation therapy and/or temozolomide in subjects with first-line or recurrent/refractory glioblastoma | ||
Medical condition: glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004944-37 | Sponsor Protocol Number: MK-3475-054-07 | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC, a Subsidiary of Merck & Co. Inc | |||||||||||||
Full Title: Adjuvant immunotherapy with anti-PD-1 monoclonal antibody Pembrolizumab (MK-3475) versus placebo after complete resection of high-risk Stage III melanoma: A randomized, double-blind Phase 3 trial o... | |||||||||||||
Medical condition: Stage III melanoma (AJCC R0) with histologically confirmed cutaneous melanoma metastatic to lymph node, classified as (AJCC, 2010): Stage IIIA with metastasis > 1 mm; any Stage IIIB or IIIC (no in-... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) PT (Trial now transitioned) ES (Ongoing) DK (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) FI (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000975-32 | Sponsor Protocol Number: RPCE03L1801 | Start Date*: 2004-11-09 |
Sponsor Name:UCB S.A. - Pharma Sector | ||
Full Title: An exploratory, double blind, randomized, placebo-controlled, prallel group, multicenter study, for the assessment of the efficacy, safety and tolerability of ucb34714 50mg oral capsules in b.i.d. ... | ||
Medical condition: post-herpetic neuralgia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) CZ (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004053-91 | Sponsor Protocol Number: CO19/121741 | Start Date*: 2020-07-06 | |||||||||||
Sponsor Name:University of Leeds | |||||||||||||
Full Title: Brain Re-Irradiation Or Chemotherapy: a phase II randomised trial of re-irradiation and chemotherapy in patients with recurrent glioblastoma | |||||||||||||
Medical condition: Recurrent Glioblastoma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003896-35 | Sponsor Protocol Number: EORTC 26041_22041 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase I/II study on concomitant and adjuvant Temozolomide and Radiotherapy with or without PTK787/ZK222584 in newly diagnosed GBM | |||||||||||||
Medical condition: Glioblastoma multiforme | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) AT (Completed) GB (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001155-11 | Sponsor Protocol Number: OSI-904-202 | Start Date*: 2005-02-25 | |||||||||||
Sponsor Name:OSI Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Open Label, Phase II Study of OSI-7904L versus 5-FU/LV as First-Line Treatment in Patients with Unresectable, Locally Advanced or Metastatic Adenocarcinoma of the Biliary Tract | |||||||||||||
Medical condition: Unresectable, locally advanced or metastatic adenocarcinoma of the biliary tract | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006342-32 | Sponsor Protocol Number: 75111-10114 | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: Pertuzumab + trastuzumab (PH) versus PH plus metronomic chemotherapy (PHM) in the elderly HER2+ metastatic breast cancer population who may continue on T-DM1 alone following disease progression whi... | |||||||||||||
Medical condition: Newly diagnosed or recurrent (after surgery) stage IV (TNM/AJCC v.7) HER-2 positive (IHC 3+ or or HER-2 gene amplification by in situ hybridization) invasive breast cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) PT (Completed) NL (Completed) GB (GB - no longer in EU/EEA) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000874-67 | Sponsor Protocol Number: NO25390 | Start Date*: 2011-11-04 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: An open-label, multicenter, single-arm, Phase I dose-escalation with efficacy tail extension study of vemurafenib (RO5185426) in pediatric patients with surgically incurable and unresectable Stage ... | |||||||||||||
Medical condition: Metastatic Melanoma | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Completed) IT (Prematurely Ended) SK (Prematurely Ended) ES (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003024-33 | Sponsor Protocol Number: D5162C00048 | Start Date*: 2023-01-13 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: An Open-label, Single-arm, Phase II, Multinational, Multicentre Study to Assess the Efficacy and Safety of 5 Years of Osimertinib in Participants with Epidermal Growth Factor Receptor Mutation-Posi... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012857-39 | Sponsor Protocol Number: A4021032 | Start Date*: 2009-11-16 | |||||||||||
Sponsor Name:PFIZER, S.A. | |||||||||||||
Full Title: ESTUDIO DE FASE 2, ALEATORIZADO Y ABIERTO DE FIGITUMUMAB (CP-751,871) MÁS CISPLATINO (O CARBOPLATINO) Y ETOPOSIDO, FRENTE A CISPLATINO (O CARBOPLATINO) Y ETOPOSIDO SOLOS, COMO TRATAMIENTO DE PRIME... | |||||||||||||
Medical condition: Pacientes con cáncer de pulmón microcítico en estadio extendido que no hayan recibido quimioterapia previa para su enfermedad. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) BG (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003866-34 | Sponsor Protocol Number: 2553 | Start Date*: 2012-09-24 | |||||||||||
Sponsor Name:North Bristol NHS Trust (NBT) | |||||||||||||
Full Title: A Placebo-Controlled, Randomised, Double-Blind Trial to Assess the Safety and Efficacy of Intermittent Bilateral Intraputamenal Glial Cell Line-Derived Neurotrophic Factor (GDNF) Infusions Administ... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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. |
