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Primary RegistryProtocol numberPublic titleScientific titleType of studyRecruitment statusLast updated
LBCTR2020023394CLNP023X2203Study of Safety and Efficacy of LNP023 in Patients With Kidney Disease Caused by Inflammation An Adaptive Seamless Randomized, Double-blind, Placebo-controlled, Dose Ranging Study to Investigate the Efficacy and Safety of LNP023 in Primary IgA Nephropathy Patients InterventionalOther31/01/2020
LBCTR2021034759MRX-503An Open-label Extension Study to Evaluate the Long-term Safety and Efficacy of Maralixibat in the Treatment of Subjects With Progressive Familial Intrahepatic Cholestasis (PFIC)An Extension Study of Maralixibat in Patients With Progressive Familial Intrahepatic Cholestasis (PFIC)InterventionalOther03/03/2021
LBCTR2020104622BO40336ALINAA PHASE III, OPEN-LABEL, RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ADJUVANT ALECTINIB VERSUS ADJUVANT PLATINUM-BASED CHEMOTHERAPY IN PATIENTS WITH COMPLETELY RESECTED STAGE IB (TUMORS 4 CM) TO STAGE IIIA ANAPLASTIC LYMPHOMA KINASEPOSITIVE NONSMALL CELL LUNG CANCERInterventionalOther12/10/2020
LBCTR2023055223RLY5016-208pPatiromer for treatment of hyperkalaemia in children from birth to <6 years of ageA 2-Part, Open-Label, Phase 2, Multiple Dose Study to Evaluate the Pharmacodynamic Effects, Safety, and Tolerability of Patiromer in Children under 6 Years of Age with Hyperkalaemia (EMERALD 2)InterventionalOther14/12/2022
LBCTR2021074831GBT2104-132 (C5361002)A Randomized, Double-blind, Placebo-controlled, Multicenter Study of a Single Dose of Inclacumab to Reduce Re-admission in Participants With Sickle Cell Disease and Recurrent Vaso-occlusive CrisesGBT2104-132: A Randomized, Double-blind, Placebo-controlled, Multicenter Study of a Single Dose of Inclacumab to Reduce Re-admission in Participants With Sickle Cell Disease and Recurrent Vaso-occlusive CrisesInterventionalOther24/06/2021
LBCTR2020071296ISIS 702843-CS2A Phase 2a, Randomized, Open-Label Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ISIS 702843 Administered Subcutaneously to Patients with Non-Transfusion Dependent β-Thalassemia IntermediaA Phase 2a, Randomized, Open-Label Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ISIS 702843 Administered Subcutaneously to Patients with Non-Transfusion Dependent β-Thalassemia IntermediaInterventionalPending03/10/2019
LBCTR2019121361HD2305Preoperative Chlorhexidine Gluconate Bathing Could Prevent Post-obstetric and gynecologic Surgical-site Infections: A Pilot for a Randomized Controlled TrialPreoperative Chlorhexidine Gluconate Bathing Could Prevent Post-obstetric and gynecologic Surgical-site Infections: A Pilot for a Randomized Controlled TrialInterventionalPending24/12/2019
LBCTR2020023398LAUMCRH.RH2.4/Dec/2019The Efficacy of Octenidine in Sinusitis compared to standard of careThe Efficacy of Octenidine in Sinusitis compared to standard of careInterventionalPending18/02/2020
LBCTR2020093402IMR-BTL-201A Phase 2 Study to Evaluate the Safety and Tolerability of IMR-687 in Subjects with Beta ThalassemiaA Phase 2 Study to Evaluate the Safety and Tolerability of IMR-687 in Subjects with Beta ThalassemiaInterventionalPending24/02/2020
LBCTR2020083421IMR-SCD-301A Phase 2b Study to Evaluate the Safety and Efficacy of IMR-687 in Subjects with Sickle Cell DiseaseA Phase 2b Study to Evaluate the Safety and Efficacy of IMR-687 in Subjects with Sickle Cell DiseaseInterventionalPending26/08/2020
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