solution
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
Esketamine nasal spray (Spravato) for the treatment of therapy-resistant bipolar depression. An open-label pilot trial.
RecruitingCTIS2023-508125-27-00
Start: 2025-04-01Target: 20Updated: 2024-11-26
A Phase II, multinational, multicentre, double-blind, randomised, active-controlled, 3-way cross-over study to evaluate the therapeutic equivalence of CHF5993 pMDI 100/6/12.5 µg HFA-152a versus CHF5993 pMDI 100/6/12.5 µg HFA-134a in subjects with mild to moderate asthma. [TRECONY]
Not yet recruitingCTIS2025-521456-35-00
Target: 42Updated: 2026-03-11
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
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
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
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
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
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
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
Target: 96Updated: 2025-11-24
Phase 4
Symptoms control and adhErenCe assessment during treatment with mepolizUmab new pREfilled devices. SECURE
CompletedCTIS2022-501029-19-00
Start: 2022-12-13End: 2025-03-27Target: 130Updated: 2024-01-15
"SAFE DISCONTINUATION OF ANTIDEPRESSANTS IN INDIVIDUALS WITH CLINICALLY REMITTED DEPRESSIVE DISORDERS"
Not yet recruitingCTIS2023-509377-23-00
Target: 150Updated: 2024-10-08