- Trials with a EudraCT protocol (3,005)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (31)
3,005 result(s) found for: C value.
Displaying page 113 of 151.
| EudraCT Number: 2007-003148-31 | Sponsor Protocol Number: P05115 | Start Date*: 2007-10-12 | ||||||||||||||||||||||||||
| Sponsor Name:Schering-Plough Research Institute, A Division of Schering Corporation | ||||||||||||||||||||||||||||
| Full Title: A Phase 4 Study of the Pharmacokinetics of Oral Posaconazole Among Patients with Compromised Gastrointestinal Function and at High Risk for Invasive Fungal Infection. | ||||||||||||||||||||||||||||
| Medical condition: Acute Myeloid Leukemia, Neutropenia, Antifungal Prophylaxis, Gastrointestinal Disorders | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2009-011148-21 | Sponsor Protocol Number: D0520C00012 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A 12-week, randomised, double-blind, placebo-controlled, parallel group, multinational, phase IIb dose range finding study to evaluate the efficacy and safety of AZD9668 administered orally at 3 do... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022437-28 | Sponsor Protocol Number: 40929837ASH2001 | Start Date*: 2010-11-03 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo- and Active-Controlled Crossover Study to Evaluate the Efficacy of JNJ 40929837 for the Treatment of Asthma Using a Bronchial Allergen Challenge Model | |||||||||||||
| Medical condition: JNJ-40929837 is being developed for the treatment of asthma. | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012598-37 | Sponsor Protocol Number: DUT-MD-304 | Start Date*: 2010-01-29 | |||||||||||
| Sponsor Name:Forest Research Institute, Inc. | |||||||||||||
| Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE SAFETY AND EFFICACY OF DUTOGLIPTIN IN PATIENTS WITH TYPE 2 DIABETES MELLITUS ON BACKGROUND TREATMENT WIT... | |||||||||||||
| Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000050-10 | Sponsor Protocol Number: FORMaT001 | Start Date*: 2023-01-02 | |||||||||||
| Sponsor Name:University of Queensland | |||||||||||||
| Full Title: Finding the Optimal Regimen for Mycobacterium abscessus Treatment | |||||||||||||
| Medical condition: Mycobacterium abscessus pulmonary disease | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001828-22 | Sponsor Protocol Number: 101 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Y-mAbs Therapeutics A/S | |||||||||||||
| Full Title: A Multicenter Phase 2/3 Trial of the Efficacy and Safety of Intracerebroventricular Radioimmunotherapy using 131I-omburtamab for Neuroblastoma Central Nervous System/Leptomeningeal Metastases | |||||||||||||
| Medical condition: Treatment of pediatric neuroblastoma patients with CNS relapse as evidenced by CNS/LM metastases | |||||||||||||
|
|||||||||||||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003456-36 | Sponsor Protocol Number: CL1-95012-001 | Start Date*: 2021-08-09 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: A first in human Phase 1/2 open-label, multicenter, dose escalation and expansion study of PRS-344/S095012 in patients with solid tumors | |||||||||||||
| Medical condition: Advanced and/or metastatic solid tumors | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003005-30 | Sponsor Protocol Number: AR-DEX-22-03 | Start Date*: 2023-06-28 | |||||||||||
| Sponsor Name:Areteia Therapeutics, Inc. | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, parallel-group study to assess the efficacy, safety, and tolerability of dexpramipexole administered orally for 24 weeks in participants with eosinop... | |||||||||||||
| Medical condition: Eosinophilic Asthma | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003226-33 | Sponsor Protocol Number: 0480 | Start Date*: 2018-09-13 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Dean of the Medical Faculty of the Friedrich-Alexander University Erlangen-Nürnberg Prof. Dr. Markus Neurath | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: First-line treatment of locally advanced HNSCC with double checkpoint blockade and radiotherapy dependent on intratumoral CD8+ T cell infiltration (CheckRad-CD8) | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced head and neck squamous cell carcinoma (HNSCC) | |||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-005091-36 | Sponsor Protocol Number: 2020-005091-36 | Start Date*: 2021-08-30 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Stichting Catharina Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Signal TrAnsduction Pathway activity analysis for OVarian cancER treatment. STAPOVER study | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Ovarian cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2017-000242-22 | Sponsor Protocol Number: STR001-202 | Start Date*: 2017-06-28 | |||||||||||
| Sponsor Name:STREKIN AG | |||||||||||||
| Full Title: A Phase III multicenter, double-blind, placebo-controlled, study evaluating the safety, and efficacy of STR001 treatment in adults with Sudden Sensorineural Hearing Loss | |||||||||||||
| Medical condition: Sudden Sensorineural Hearing Loss (SSHL) including - idiopathic unilateral Sensorineural Hearing Loss - acute uni- or bilateral acoustic trauma-induced Sensorineural Hearing Loss | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001955-37 | Sponsor Protocol Number: CQAB149B2335S | Start Date*: 2007-04-29 | |||||||||||
| Sponsor Name:Novartis Farmacéutica S.A | |||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, doble ciego, doble enmascarado, controlado con placebo, con grupos paralelos y diseño adaptativo, de 26 semanas de tratamiento, para evaluar la eficacia, seguri... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) SE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004143-30 | Sponsor Protocol Number: CQAB149B2311 | Start Date*: 2008-01-22 | |||||||||||
| Sponsor Name:Novartis Farmaceutica S.A. | |||||||||||||
| Full Title: Estudio fase III, multicéntrico, aleatorizado, doble ciego, controlado con placebo, de 2 periodos cruzados, para evaluar el efecto de indacaterol (300 µg o.d.) en pacientes con enfermedad pulmonar ... | |||||||||||||
| Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) de moderada a crónica | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) BE (Completed) DK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002603-17 | Sponsor Protocol Number: 1218.89 | Start Date*: 2013-01-14 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A phase IIIb, multicenter, multinational, randomized, double-blind, placebo controlled, parallel group study to evaluate the glycemic and renal efficacy of once daily administration of linagliptin ... | |||||||||||||
| Medical condition: Type 2 diabetes patients receiving treatment with ACEi or ARB with micro- or macroalbuminuria (UACR between 30 and 3000 mg/g creatinine). [ACEi=Angiotensin Converting Enzyme inhibitor; ARB=Angioten... | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) FI (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010198-19 | Sponsor Protocol Number: CLCQ908A2204 | Start Date*: 2009-05-27 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A Phase 2 12-week multi-center, randomized, double-blind, placebo-controlled, parallel-group adaptive design study to evaluate the safety and efficacy of LCQ for weight reduction and reduced LDL ch... | ||||||||||||||||||
| Medical condition: Obesity and mixed dyslipidemia | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Prematurely Ended) GB (Completed) ES (Completed) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-001122-18 | Sponsor Protocol Number: CNTO1275ARA2001 | Start Date*: 2012-06-13 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Study Evaluating the Efficacy and Safety of Ustekinumab (STELARA®) and CNTO 1959 Administered Subcutaneously in... | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006976-31 | Sponsor Protocol Number: CQAB149B2341 | Start Date*: 2009-03-04 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized, double-blind, controlled, parallel group, 12-week treatment study to compare the efficacy and safety of the combination of indacaterol 150 μg once daily with open label tiotropium 18 ... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) ES (Completed) DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004794-31 | Sponsor Protocol Number: KIN-1902-2001 | Start Date*: 2022-08-19 | |||||||||||
| Sponsor Name:Kinevant Sciences GmbH | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study with Open-label Extension to Assess the Efficacy and Safety of Namilumab in Subjects with Chronic Pulmonary Sarcoidosis | |||||||||||||
| Medical condition: chronic pulmonary sarcoidosis | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003337-41 | Sponsor Protocol Number: CS1003-305 | Start Date*: 2021-04-15 | |||||||||||
| Sponsor Name:CStone Pharmaceuticals (Suzhou) Co., Ltd. | |||||||||||||
| Full Title: A Multi-Center, Double-Blind, Randomized, Phase III Study to Investigate the Efficacy and Safety of CS1003 in Combination with Lenvatinib Compared to Placebo in Combination with Lenvatinib as First... | |||||||||||||
| Medical condition: unresectable advanced hepatocellular carcinoma | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) PL (Trial now transitioned) ES (Restarted) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002326-27 | Sponsor Protocol Number: COG0201 | Start Date*: 2022-09-14 | |||||||||||
| Sponsor Name:Cognition Therapeutics, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, PHASE 2 STUDY TO EVALUATE THE SAFETY AND EFFICACY OF CT1812 IN SUBJECTS WITH MILD TO MODERATE ALZHEIMER’S DISEASE | |||||||||||||
| Medical condition: Mild to Moderate Alzheimer's Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) ES (Completed) CZ (Completed) | |||||||||||||
| 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
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| 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. | |
Query did not match any studies.