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DRUG11 trials

Sponsors

Centre Hospitalier Regional Et Universitaire De Brest, Hospices Civils De Lyon, University Medical Center Utrecht, Chiesi Farmaceutici S.p.A., Genetic S.p.A.

Conditions

AsthmaBipolar disorder- depressive episodeChronic Open-angle GlaucomaChronic postchirurgical or post-traumatic neuropathic painMajor Depressive DisorderMild to moderate asthmaModerate to severe controlled asthma according to Step 4 and Step 5 of the Global Initiative for Asthma (GINA) 2022 Guidelines.Ocular Hypertension

Phase 2

Phase 3

A randomised, controlled trial to investigate the effect of a four/six week intensified pharmacological treatment for schizophrenia, major depressive disorder and bipolar depression compared to treatment as usual in subjects who had a first-time treatment failure on their first-line treatment.
WithdrawnCTIS2022-502185-24-00
University Medical Center Utrechtmajor depressive disorder or bipolar disorder type I and II (currently in a depressive episode), schizoaffective disorder, Schizophrenia +1
Target: 945Updated: 2023-06-19
Analgesic effectiveness of capsaicin 8% cutaneous patch for the treatment of chronic postsurgical or post-traumatic neuropathic pain: a randomized placebo controlled study in children aged 12 to 17-y
RecruitingCTIS2022-500265-27-00
Centre Hospitalier Regional Et Universitaire De BrestChronic postchirurgical or post-traumatic neuropathic pain
Start: 2024-03-05Target: 46Updated: 2025-02-24
A 12-week double-blind, multicentre, randomised, active-controlled, 2-arm, parallel-group clinical trial to evaluate the safety of CHF5993 pMDI 200/6/12.5 µg HFA-152a, compared to CHF5993 pMDI 200/6/12.5 µg HFA-134a, in subjects with asthma
CompletedCTIS2023-503333-22-00
Chiesi Farmaceutici S.p.A.Moderate to severe controlled asthma according to Step 4 and Step 5 of the Global Initiative for Asthma (GINA) 2022 Guidelines.
Start: 2024-01-15End: 2025-02-24Target: 677Updated: 2025-09-25
RANDOMIZED, OPEN LABEL, PARALLEL-GROUP, TWO-ARM, MULTICENTER STUDY WITH CLINICAL ENDPOINT COMPARING PRESERVATIVE FREE BIMATOPROST OPHTHALMIC SOLUTION 0.1 MG/ML AND LUMIGAN® (BIMATOPROST OPHTHALMIC SOLUTION) 0.1 MG/ML IN PATIENTS WITH CHRONIC OPEN-ANGLE GLAUCOMA OR OCULAR HYPERTENSION IN ONE OR BOTH EYES.
RecruitingCTIS2023-504759-28-00
Genetic S.p.A.Chronic Open-angle Glaucoma, Ocular Hypertension
Start: 2024-04-05Target: 124Updated: 2024-05-10
A prospective, randomized, double-blind placebo-controlled multicentre trial with mannan-conjugated birch pollen allergoids administered subcutaneously to adolescents and adults with birch pollen-induced allergic rhinitis or rhinoconjunctivitis.
CompletedCTIS2024-515717-17-00
Inmunotek S.L.birch pollen-induced allergic rhinitis birch pollen-induced allergic rhinoconjunctivitis
Start: 2024-10-28End: 2025-06-27Target: 360Updated: 2025-08-07
Low-dose AtropIne for Myopia control in children
Active, not recruitingCTIS2024-513091-17-00
Medical Center - University Of FreiburgProgressive myopia
Start: 2021-09-29Target: 300Updated: 2024-10-24
A Double-blind, Randomized, Psychoactive Placebo-controlled Study to Evaluate the Efficacy and Safety of Intranasal Esketamine 84 mg in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder in Adolescent Participants with Acute Suicidal Ideation or Behavior
Not yet recruitingCTIS2024-518615-19-00
Janssen Cilag InternationalMajor Depressive Disorder
Target: 96Updated: 2025-11-24

Phase 4