- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Topical drug delivery.
Displaying page 1 of 1.
EudraCT Number: 2006-001784-35 | Sponsor Protocol Number: DicloMD | Start Date*: 2006-05-12 |
Sponsor Name:Nuvo research Inc | ||
Full Title: Validation of the microdialysis technique as a tool to assess local delivery of topical drugs used in the treatment of osteoarthritis of superficial joints | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001816-20 | Sponsor Protocol Number: 1.1000 | Start Date*: 2014-08-28 |
Sponsor Name:Academic Medical Center, Amsterdam | ||
Full Title: Fractional CO2 laser assisted delivery of topical anesthetics: a randomized controlled pilot study | ||
Medical condition: local anesthesia of the skin prior to minor cutaneous surgical procedures | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004890-21 | Sponsor Protocol Number: NL72427.068.19 | Start Date*: 2021-01-18 |
Sponsor Name:Academic Hospital Maastricht (azM) | ||
Full Title: Effectiveness of Periocular drug Injection in CATaract surgery | ||
Medical condition: cystoid macular edema (CME) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-005003-14 | Sponsor Protocol Number: Pro_MC2-01_13_Biotek | Start Date*: 2014-04-02 |
Sponsor Name:Drug Delivery Solutions ApS | ||
Full Title: A randomized, multi-centre, observer-blind, controlled exploratory study to assess efficacy and safety of new topical formulations (MC2-01) in patients with plaque psoriasis | ||
Medical condition: Patients with stable plaque type psoriasis (sufficient number and size of psoriatic plaques(s) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000685-12 | Sponsor Protocol Number: MC2-01-C6 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:MC2 Therapeutics Ltd | |||||||||||||
Full Title: A Multicentre, Open-label, Single-group Maximal Use Trial, Evaluating the Safety and Pharmacokinetic Profile of the Active Ingredients and their Metabolites after application of MC2-01 Cream in Ado... | |||||||||||||
Medical condition: Extensive Psoriasis Vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000737-36 | Sponsor Protocol Number: 206207-015 | Start Date*: 2006-05-17 |
Sponsor Name:Allergan Limited | ||
Full Title: A 6-Week, Multicenter, Masked, Randomized Trial (with a 20-Week Masked Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segment Drug Delivery System (DEX PS... | ||
Medical condition: Non-infectious ocular inflammation of the anterior segment in anterior uveitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000736-26 | Sponsor Protocol Number: 206207-014 | Start Date*: 2006-05-17 |
Sponsor Name:Allergan Limited | ||
Full Title: An 8-Week, Multicenter, Masked, Randomized Trial (with an 18-Week Masked Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segment Drug Delivery System (DEX ... | ||
Medical condition: Non-infectious ocular inflammation of the posterior segment in intermediate or posterior uveitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) AT (Completed) IT (Completed) PT (Completed) BE (Completed) CZ (Completed) DE (Completed) GR (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005091-42 | Sponsor Protocol Number: 192024-041D | Start Date*: 2012-05-08 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: An Open Label (Stage 1) and Randomized (Stage 2), 24-Month Study of Safety and Efficacy of Bimatoprost Drug Delivery System in Patients With Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: open-angle glaucoma (OAG) and ocular hypertension (OHT) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001727-39 | Sponsor Protocol Number: POP03 | Start Date*: 2018-10-16 | ||||||||||||||||
Sponsor Name:Polpharma S.A. | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSSOVER, COMPARATIVE, NON-INFERIORITY TRIAL EVALUATING THE EFFICACY AND TOLERABILITY OF GENERIC LATANOPROST 0.05 MG/ML EYE DROPS SOLUTIO... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001805-63 | Sponsor Protocol Number: EDP1815-207 | Start Date*: 2021-11-12 | |||||||||||
Sponsor Name:EVELO Biosciences Inc | |||||||||||||
Full Title: A phase 2, multicenter, double-blind, placebo-controlled, multiple-cohort study investigating the effect of EDP1815 in participants for the treatment of mild, moderate and severe atopic dermatitis | |||||||||||||
Medical condition: Mild, moderate and severe atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003150-86 | Sponsor Protocol Number: V1.0 | Start Date*: 2019-09-20 |
Sponsor Name:Royal Cornwall Hospitals NHS Trust | ||
Full Title: A Study to Investigate the Effect of Different Durations of Ameluz Application on Response to Treatment of Acral Actinic Keratoses | ||
Medical condition: Actinic keratoses | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003802-14 | Sponsor Protocol Number: CRC-PSO-SKINPEN-A-27 | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Skin penetration of anti-inflammatory compounds in lesional compared to non-lesional skin of psoriasis patients | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002563-18 | Sponsor Protocol Number: PC_RSV_003 | Start Date*: 2017-10-09 | |||||||||||
Sponsor Name:Pulmocide Ltd | |||||||||||||
Full Title: A single-blind, placebo controlled, randomised study to evaluate antiviral activity and safety and pharmacokinetics of inhaled PC786 against respiratory syncytial virus (RSV) in healthy adult subje... | |||||||||||||
Medical condition: Human Respiratory Syncytial Virus (RSV) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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