- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Fast food.
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EudraCT Number: 2012-005173-32 | Sponsor Protocol Number: K-489DK | Start Date*: 2013-07-09 |
Sponsor Name:FAST-consortium | ||
Full Title: FAST-Fish - Food Allergy Specific Treatment for fish allergy | ||
Medical condition: Fish Allergy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000276-10 | Sponsor Protocol Number: FAST2015 | Start Date*: 2015-07-02 |
Sponsor Name:FAST Consortium under EU 7. FWP | ||
Full Title: FAST – Food Allergy Specific ImmunoTherapy A multinational phase IIb study to investigate the efficacy and safety of subcutaneous immunotherapy with a modified fish- parvalbumin given in single ri... | ||
Medical condition: Food allergy to fish | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) DK (Completed) GR (Ongoing) NL (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004450-41 | Sponsor Protocol Number: TXRENAL-17 | Start Date*: 2018-05-31 |
Sponsor Name:Consorci Mar Parc de Salut | ||
Full Title: PHASE IV, OPEN, UNICENTRIC AND PILOT CLINICAL TRIAL TO EVALUATE THE INFLUENCE ON THE BIODISPONIBILITY AND PHARMACOKINETIC CHARACTERISTICS OF ENVARSUS® COMPARED WITH ADVAGRAF® OF FAST OR INGESTION I... | ||
Medical condition: Trasplante renal y inmunosupresión | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002273-29 | Sponsor Protocol Number: CX842A2106 | Start Date*: 2022-11-02 |
Sponsor Name:Cinclus Pharma Holding AB | ||
Full Title: A randomized, single dose, crossover study in healthy volunteers to investigate the relative bioavailability of linaprazan for a new oral tablet formulation of linaprazan glurate, and to assess the... | ||
Medical condition: Healthy voluneers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000685-11 | Sponsor Protocol Number: PR-30-5011-C | Start Date*: 2013-09-29 | |||||||||||
Sponsor Name:TESARO Inc. | |||||||||||||
Full Title: A Phase 3 Randomized Double-Blind Trial of Maintenance with Niraparib Versus Placebo in Patients with Platinum Sensitive Ovarian Cancer | |||||||||||||
Medical condition: Platinum Sensitive Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) AT (Completed) GB (GB - no longer in EU/EEA) DK (Completed) IT (Completed) HU (Completed) ES (Ongoing) BE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000284-27 | Sponsor Protocol Number: UOLDR0001N | Start Date*: 2011-05-16 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: A Randomised Controlled Trial for People with Established Type 2 Diabetes during Ramadan: Liraglutide versus a Sulphonylurea and/or Pioglitazone | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002408-42 | Sponsor Protocol Number: RB-UK-12-0004 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Reckitt Benckiser Pharmaceuticals Inc. | |||||||||||||
Full Title: An Open-label, Randomised, Three -Way, Cross-Over Study to Assess the Pharmacokinetics, Safety and Tolerability of Two Formulations of RBP-6300 10mg in Healthy Volunteers under a Naltrexone Block i... | |||||||||||||
Medical condition: Maintenance/substitution agent for the treatment of opioid dependence. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000723-14 | Sponsor Protocol Number: 20120119 | Start Date*: 2014-07-11 |
Sponsor Name:Amgen Inc. | ||
Full Title: A Double-blind, Randomized, Placebo-Controlled, Multicenter Study to Evaluate Safety and Efficacy of Evolocumab (AMG 145) in Combination With Statin Therapy in Diabetic Subjects With Hyperlipidemia... | ||
Medical condition: Hyperlipidemia or mixed dyslipidemia in Diabetic Subjects | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002026-20 | Sponsor Protocol Number: CT7001-001 | Start Date*: 2017-10-31 |
Sponsor Name:Carrick Therapeutics | ||
Full Title: A Modular, Multipart, Multiarm, Open-label, Phase I/IIa Study to Evaluate the Safety and Tolerability of CT7001 Alone and in Combination with Anti-cancer Treatments in Patients with Advanced Malign... | ||
Medical condition: Module 1A: All solid malignancies Module 1B: Solid malignancies, potentially including TNBC, SCLC, CRPC, ovarian cancer patients, and other appropriate cancer indications. Module 1B-1 (TNBC):... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2022-001485-35 | Sponsor Protocol Number: LPS17007 | Start Date*: 2022-10-03 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Open-Label, Parallel-Group Trial Comparing the Efficacy and Safety of Insulin Glargine 300 U/mL (Gla-300) and Insulin Degludec 100 U/mL (IDeg-100) in Insulin-Naï... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus and Renal Impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005110-30 | Sponsor Protocol Number: FASTRELIEF | Start Date*: 2017-02-23 | ||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | ||||||||||||||||||
Full Title: A multicenter randomized trial to evaluate the efficacy of fentanyl pectin nasal spray (FPNS) versus Physician Choice (PC) - Usual Care (UC), in reducing incidental predictable breakthrough pain (I... | ||||||||||||||||||
Medical condition: Patients with head and neck cancer . | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004250-26 | Sponsor Protocol Number: CO-338-010 | Start Date*: 2012-02-02 | |||||||||||||||||||||
Sponsor Name:Clovis Oncology Inc. | |||||||||||||||||||||||
Full Title: A Phase I/II, Open-Label, Safety, Pharmacokinetic, and Preliminary Efficacy Study of Oral Rucaparib in Patients with gBRCA Mutation Ovarian Cancer, or Other Solid Tumor | |||||||||||||||||||||||
Medical condition: Patients with locally advanced or metastatic solid tumors including lymphoma and germline BRCA (gBRCA) ovarian cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Completed) DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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