- Trials with a EudraCT protocol (170)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
170 result(s) found for: LEO Pharma.
Displaying page 5 of 9.
EudraCT Number: 2016-004201-13 | Sponsor Protocol Number: LP0162-1326 | Start Date*: 2017-06-30 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, phase 3 trial to evaluate the efficacy and safety of tralokinumab monotherapy in subjects with moderate to severe atopic dermatitis who are candidate... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005573-12 | Sponsor Protocol Number: LP0162-1335 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A single (assessor) blinded, randomised, parallel-group, monotherapy trial to evaluate the pharmacokinetic and safety of tralokinumab in children (age 2 to <12 years) with moderate-to-severe atopic... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
|
|||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000746-19 | Sponsor Protocol Number: LP0162-1337 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: An open-label, single-arm, multi-centre, long-term extension trial to evaluate the safety and efficacy of tralokinumab in subjects with atopic dermatitis who participated in previous tralokinumab c... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) DE (Completed) PL (Completed) BE (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002019-97 | Sponsor Protocol Number: EX0401ES | Start Date*: 2005-01-25 | |||||||||||
Sponsor Name:FARMACUSI, S.A. | |||||||||||||
Full Title: Long term subcutaneous tinzaparin compared with tinzaparin and oral anticoagulants in the treatment of acute pulmonary embolism. A multicentre, prospective, randomised, open, parallel group clinica... | |||||||||||||
Medical condition: Patients with clinical suspicion of Pulmonar Thromboembolism confirmed according to the PIOPED criteria. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001230-18 | Sponsor Protocol Number: PRO-001 | Start Date*: 2019-01-30 | |||||||||||
Sponsor Name:Hellenic Genito-Urinary Cancer Group (HGUCG) | |||||||||||||
Full Title: Long-term thromboprophylaxis with tinzaparin in high-risk prostate or breast cancer patients. A prospective, randomised, international multicentre, open-label, blinded-endpoint Phase III study. PRO... | |||||||||||||
Medical condition: Long-term thromboprophylaxis with tinzaparin in high-risk prostate or breast cancer patients. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001793-87 | Sponsor Protocol Number: M/37779/23 | Start Date*: 2007-07-31 | |||||||||||
Sponsor Name:Laboratorios Almirall, S.A. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-Group, Vehicle and Active Controlled Trial, to Assess the Efficacy and Safety of LAS37779 Cream for the Treatment of Chronic Plaque Psoriasis | |||||||||||||
Medical condition: Male and female patients, 18 to 70 years of age, with a diagnosis of chronic plaque psoriasis. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003215-78 | Sponsor Protocol Number: MBL 0202 INT | Start Date*: 2005-11-16 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to Betamethasone Dipropionate in the Gel Vehicle, Calcipotriol in the Gel Vehicle and the Gel Vehicle alone in Psoriasis Vulgaris. | |||||||||||||
Medical condition: Psoriasis vulgaris on the trunk and/or limbs | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) IE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003704-31 | Sponsor Protocol Number: ARG-16 | Start Date*: 2019-05-17 |
Sponsor Name:Uppsala University | ||
Full Title: Impact on the intestinal microbiota during antibiotic treatment | ||
Medical condition: Impact on the intestinal microbiota during antibiotic treatment | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000704-14 | Sponsor Protocol Number: S241-GB-07 | Start Date*: Information not available in EudraCT |
Sponsor Name:Stiefel Laboratories International Division | ||
Full Title: Human 96 Hour Repeat Open Application Test for Assessment of Skin Irritation | ||
Medical condition: Not applicable (Healthy Volunteer Study) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005897-54 | Sponsor Protocol Number: S241-GB-08 | Start Date*: 2006-02-01 |
Sponsor Name:Stiefel Laboratories Maidenhead Ltd | ||
Full Title: A Phase 1, Single-Centre, Single-blind, CPO Solution Human Patch Test in Healthy Subjects | ||
Medical condition: Not Applicable (Healthy Volunteer Study) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001776-21 | Sponsor Protocol Number: NCT00687882 | Start Date*: 2016-03-10 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für | ||
Full Title: Prospective Multi-Center Evaluation of the Duration of Therapy for Thrombosis in Children | ||
Medical condition: Thrombosis in pediatric patients | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2005-002864-27 | Sponsor Protocol Number: MBL 0503 INT | Start Date*: 2005-10-07 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Calcipotriol plus Betamethasone Dipropionate Gel Compared to DAIVONEX/DOVONEX Scalp Solution in Patients with Scalp Psoriasis. A phase III study comparing a gel containing calcipotriol 50 mcg/g plu... | |||||||||||||
Medical condition: Psoriasis of the scalp Clinical signs of psoriasis vulgaris on trunk and/or limbs, or earlier diagnosed with psoriasis vulgaris on trunk and/or limbs Extent of scalp psoriasis involving 10% or more... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004460-66 | Sponsor Protocol Number: KARAASS-1 | Start Date*: 2014-04-01 | ||||||||||||||||
Sponsor Name:Jørgen Jeppesen | ||||||||||||||||||
Full Title: Oral potassium supplementation in healthy men - interactions with the renin-angiotensin-aldosterone system and the sympathetic nervous system | ||||||||||||||||||
Medical condition: Blood pressure regulation and hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001440-38 | Sponsor Protocol Number: 42647 | Start Date*: 2014-05-22 | |||||||||||
Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
Full Title: Methods to increase PpIX formation in the skin of healthy volunteers | |||||||||||||
Medical condition: Healthy volunteers - no medical condition is investigated but pharmaco kinetics | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001059-63 | Sponsor Protocol Number: 2015.009 | Start Date*: 2015-09-23 | |||||||||||
Sponsor Name:Aalborg University | |||||||||||||
Full Title: BONATHIAD - Bone Association with Thiazide Diuretics. | |||||||||||||
Medical condition: The effect of bendroflumethiazide with potassium supplement when used as an adjuvant to oral bisphosphonates in the treatment of newly diagnosed osteoporosis among post-menopausal women above 50 ye... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001204-23 | Sponsor Protocol Number: MUFU001-SA-01 | Start Date*: 2008-09-01 |
Sponsor Name:Dra. Beatriz Sanchez Sobrino | ||
Full Title: Estudio comparativo de mupirocina versus acido fusidico tópico en la erradicación de portadores nasales de Staphylococcus aureus en pacientes con insuficiencia renal crónica en hemodiálisis por cat... | ||
Medical condition: Pacientes con insuficiencia renal crónica estadio 5 en Hemodialisis que se encuentren realizando la técnica mediante un acceso vascular tipo catéter central permanente tunelizado portadores nasales... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017589-22 | Sponsor Protocol Number: AGO/2009/013 | Start Date*: 2010-01-14 | |||||||||||
Sponsor Name:University Hospital Ghent | |||||||||||||
Full Title: Interacties tussen hart en nieren tijdens de behandeling van gedecompenseerd hartfalen: diuretica versus ultrafiltratie (CRUF Trial) | |||||||||||||
Medical condition: Patiënten met ernstig gedecompenseerd hartfalen | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002496-33 | Sponsor Protocol Number: 1111 | Start Date*: 2020-09-16 |
Sponsor Name:Helsingin ja Uudenmaan sairaanhoitopiiri [...] | ||
Full Title: TROMBOOSIPROFYLAKSIA JA HYYTYMISAKTIVAATIO HAIMASYÖVÄN NEOADJUVANTTIHOIDON AIKANA – YHTEYS ENNUSTEESEEN JA TAUDIN UUSIUTUMISEEN | ||
Medical condition: Tutkimme tehostetun tromboosiprofylaksian hyödyllisyyttä ja turvallisuutta haimasyövän neoadjuvanttihoitojen yhteydessä | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002223-25 | Sponsor Protocol Number: AGO/2015/007 | Start Date*: 2015-08-18 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Eradication of methicillin-susceptible Staphylococcus aureus nasal carriage in patients undergoing dialysis: can fusidic acid be used as an alternative to mupirocin? | ||
Medical condition: persistent nasal Staphylococcus aureus carriage | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002583-80 | Sponsor Protocol Number: 38814 | Start Date*: 2013-09-06 | |||||||||||
Sponsor Name:Department of Dermatology, Bispebjerg University Hospital | |||||||||||||
Full Title: Treatment of Actinic Keratoses with Ingenol Mebutate and topical glucocorticosteroid - a safety study | |||||||||||||
Medical condition: Actinic Keratoses | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (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. |
