2
Sponsors
Galecto Biotech AB, Narodowy Instytut Kardiologii Stefana Kardynala Wyszynskiego Panstwowy Instytut Badawczy, Synact Pharma ApS, Medical University Of Gdansk, Instytut Hematologii I Transfuzjologii
Conditions
000 people may be affected by HCM3) and all-cause mortality (RR 2.5; 95% CI 1.8-3.4) with a mean follow-up of 7 years.
HenceAF occurence is even higherAdvanced liver Fibrosis and CirrhosisArthritisAsthmaDiffuse large B-cell lymphoma) and aggressive B-cell lymphomas (HGBCLDiffuse large B-cell lymphomas (DLBCL
Phase 1
Aquatic Exercise and Efficacy Enhancement to Decrease Fall Risk in Older Adults With Hip Osteoarthritis
CompletedNCT00289458
Start: 2005-10-31End: 2008-04-30Updated: 2010-08-03
An Open-label, Randomized, Three-period, Crossover Study to compare the Pharmacokinetics of GB1211 upon dosing a capsule under fasting condition and a tablet under fasting and fed conditions in healthy volunteers.
CompletedCTIS2022-502200-67-00
Start: 2022-12-27End: 2023-04-10Target: 12Updated: 2023-04-04
An open label study followed by a randomised, double-blind, placebo-controlled, parallel group and an extension study to investigate the safety and efficacy of GB1211 (a galectin-3 inhibitor) in combination with atezolizumab in patients with Non-Small Cell Lung Cancer (NSCLC).
CompletedCTIS2024-514419-93-00
Start: 2022-05-19End: 2025-11-20Target: 49Updated: 2025-03-05
Phase 2
A randomized, double blind, placebo-controlled, dose response, phase II, multicentre trial to evaluate the efficacy and safety of oral AP1189 administered at the doses of 40, 70, or 100 mg for 12 weeks in combination with methotrexate, in DMARD-naïve participants with early rheumatoid arthritis and active inflammation.
RecruitingCTIS2024-514981-37-00
Start: 2024-12-05Target: 172Updated: 2025-12-12
A phase II efficacy and safety study of cell-free circulating tumor DNA-guided commencement of second-line treatment in patients with DLBCL/HGBCL relapse
Not yet recruitingCTIS2024-518275-64-00
Target: 340Updated: 2025-11-24
Phase 3
Phase 4
Multicenter, Randomized, Open-label Study to Assess Whether Treatment With Mycophenolate Sodium (MPS) Allows Higher Dose Optimization Versus Mycophenolate Mofetil (MMF) Leading to a Dose Reduction of Tacrolimus. Maximiza Study.
CompletedNCT01056822
Start: 2010-05-31End: 2013-04-30Updated: 2014-12-03
Early ablation of atrial fibrillation in patients with hypertrophic cardiomyopathy
CompletedCTIS2023-508743-43-00
End: 2025-09-16Target: 725Updated: 2024-09-16
Diagnosing Vesicoureteric Reflux in Children by Direct Isotope Cystography and Contrast Enhanced Voiding Ultrasonography
Not yet recruitingCTIS2024-518974-15-01
Target: 100Updated: 2024-11-18
Unknown Phase
Nutrition Study for School Age Children
CompletedNCT00620152
Start: 2008-04-30Target: 40Updated: 2010-08-24
Effect of a Pharmaceutical Intervention on the Level of Control of the Asthmatic Patient
CompletedNCT01085474
Start: 2010-04-30End: 2011-07-31Updated: 2013-01-28
Verify the Effectiveness rTMS Using MEG
NCT01874444
Start: 2013-05-31End: 2015-12-31Target: 28Updated: 2014-11-19