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Primary RegistryProtocol numberPublic titleScientific titleType of studyRecruitment statusLast updated
LBCTR2019121309CQAW039A2315Study of Safety of QAW039 in Patients With Asthma Inadequately Controlled on Standard-of-care Asthma Treatment A 2-treatment Period, Randomized, Placebo-controlled, Multicenter Parallel-group Study to Assess the Safety of QAW039 When Added to Existing Asthma Therapy in GINA Steps 3, 4 and 5 Patients With Uncontrolled Asthma. InterventionalComplete01/11/2019
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
LBCTR2019060240AMG334A2302Study of Efficacy and Safety of AMG 334 in Adult Episodic Migraine Patients A 12-week Double-blind, Randomized, Multi-center Study Comparing the Efficacy and Safety of Once Monthly Subcutaneous AMG 334 Against Placebo in Adult Episodic Migraine Patients (EMPOwER) InterventionalComplete28/05/2019
LBCTR2023115474LAU.SOP.HM3.13/Sep/2023“Surgical Site Infections Occurrence and Associated Risk Factors: a Matched Case-Control Study”“Surgical Site Infections Occurrence and Associated Risk Factors: a Matched Case-Control Study”ObservationalRecruiting28/11/2023
LBCTR2020063508WIL-31 CLINICAL STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF WILATE DURING PROPHYLAXIS IN PREVIOUSLY TREATED PATIENTS WITH VON WILLEBRAND DISEASE (VWD) CLINICAL STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF WILATE DURING PROPHYLAXIS IN PREVIOUSLY TREATED PATIENTS WITH VON WILLEBRAND DISEASE (VWD)InterventionalPending09/06/2020
LBCTR2019010183CLBH589D2222A multicenter, randomized, open-label Phase 2 study evaluating the safety and efficacy of three different regimens of oral panobinostat in combination with subcutaneous bortezomib and oral dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma who have been previously exposed to immunomodulatory agents “A multicenter, randomized, open-label Phase 2 study evaluating the safety and efficacy of three different regimens of oral panobinostat in combination with subcutaneous bortezomib and oral dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma who have been previously exposed to immunomodulatory agents”InterventionalComplete12/11/2018
LBCTR2019100038asdasdasdsadsd    30/11/2017
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