All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Not reported | 2004-004586-14 | Double-blind, randomised, placebo-controlled, phase III study comparing the efficacy and safety of bilastine 20 mg once daily and cetirizine 10 mg for the treatment of allergic allergic rhinitis | 2005-08-19 | due-trials |
Not reported | 2006-001245-33 | Double-blind, randomised, placebo-controlled, phase III study comparing the efficacy and safety of bilastine 20 mg once daily and levocetirizine 5 mg for the treatment of chronic idiopathic urticaria. | 2007-08-07 | due-trials |
Reported results | 2006-003004-19 | A randomised, double-blind, four way cross-over, placebo controlled trial to evaluate the clinical efficacy, onset of action and drug activity at 22-26 hours following the drug intake of Bilastne 20 m... | 2007-01-18 | due-trials |
Reported results | 2009-012013-22 | A Multicentre, International, Adaptive, Open-label, Repeated Administration Pharmacokinetic Study of Bilastine in Children from 2 to <12 Years of Age with Allergic Rhinoconjunctivitis or Chronic Urtic... | 2012-09-28 | due-trials |
Ongoing | 2011-004830-32 | Effects of bilastine on nasal volume after allergen-induced rhinitis in patients with allergic rhinitis Eficacia de bilastina sobre la obstrucción nasal en un modelo clínico de provocación nasal co... | not-yet-due | |
Listed as ongoing, but also has a completion date | 2012-003506-27 | A multicenter, double-blind, randomized, placebo-controlled, parallel group study to evaluate the safety and tolerability of 10 mg once daily bilastine in children from 2 to 11 years of age with eith... | 2014-07-11 | bad-data |
Completed, but no date, and reported results | 2015-000790-13 | A single-centre, randomized, double-blind, crossover, single-dose clinical trial to compare bilastine, desloratadine, rupatadine and placebo in the suppression of wheal and flare induced by intraderma... | bad-data | |
Reported results | 2016-001505-17 | An exploratory study to evaluate the efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases. Estudio exploratorio para evaluar ... | 2017-03-30 | due-trials |
Ongoing | 2017-004028-31 | Effect of the administration of different Hidroferol® Soft Gelatine Capsules (calcifediol) and cholecalciferol (Dibase®) regimens on 25(OH)D levels and markers of bone remodelling in postmenopausal wo... | not-yet-due | |
Reported results | 2018-000913-19 | Phase IV, single centre, randomised, open-label, two-period, two-way crossover clinical trial to assess the efficacy of Bilastine 20mg in the suppression of wheal and flare induced by intradermal hist... | 2018-06-30 | due-trials |
Reported results | 2018-002248-95 | Multi-centre, randomised, double blind, placebo-controlled, parallel, phase III study to assess the safety, tolerability and efficacy of bilastine ophthalmic solution 0.6% in adults | 2019-12-19 | due-trials |
Reported results | 2018-003940-21 | A pilot, multicentre, single-blind, randomized, placebo-controlled, parallel-group clinical trial, to assess the safety of Bilastine treatment regarding psychomotor performance using a virtual reality... | 2019-07-18 | due-trials |
Completed, but no date Terminated | 2019-003024-20 | Multicenter, double-blind, randomized clinical trial to evaluate and compare the efficacy and safety of Hemorrane® Plus (Hemorrane® + benzocaine) with Hemorrane® and with placebo in patients with grad... | bad-data | |
Listed as ongoing, but also has a completion date and reported results | 2020-001099-14 | Randomised, double-blind, double-dummy, multicentre trial to evaluate the efficacy and safety of three different weekly dosages of calcifediol versus placebo in subjects with either vitamin D deficien... | 2023-04-25 | bad-data |
Reported results | 2020-002098-86 | Multi-centre, randomised, double blind, placebo-controlled, parallel, phase III study to assess the safety, tolerability and efficacy of Bilastine ophthalmic solution 0.6% in children Ensayo fase I... | 2022-11-30 | due-trials |
Reported results Terminated | 2021-000316-31 | Multicenter, double-blind, randomized clinical trial to evaluate the efficacy of calcifediol soft capsules versus placebo in reducing hospital admissions in patients with a positive diagnostic test fo... | 2021-08-30 | due-trials |
Reported results | 2021-003011-26 | A multicentre, open-label clinical trial to assess plasma levels and safety of bilastine in children from 2 to 5 years of age with seasonal and/or perennial allergic rhinoconjunctivitis or urticaria | 2022-04-21 | due-trials |