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180 Results

Protocol Code Study Title Active Substance Study Phase Therapeutic Area
CL1-64315-002 An International Phase Ib Multicentre Study to Characterize the Safety and Tolerability of Intravenously Administered… S064315 / Phase 1 Oncology
CL3-95008-002 Efficacy and safety of bumetanide oral liquid formulation in children aged from 2 to less… BUMETANIDE / S095008 / Phase 3 Neurosciences
CL3-95008-001 Efficacy and safety of bumetanide oral liquid formulation in children and adolescents aged from 7… BUMETANIDE / S095008 / Phase 3 Neurosciences
CL2-201086-002 Efficacy and safety of 3 doses of S201086/GLPG1972 administered orally once daily in patients with… S201086 / Phase 2 Rhumatology
Control-2 Efficacy of ivabradine in combination with beta-blockers vs up-titration of beta-blockers in daily practice IVABRADINE - S016257 / Phase 4 Cardiovascular
CL3-05153-008 A clinical study to test the safety and the efficacy of a single-pill combination of… AMLODIPINE / ATORVASTATIN / ATORVASTATIN - AMLODIPINE - PERINDOPRIL ARGININE - S005153 / PERINDOPRIL / S005153 / Phase 3 Cardiovascular
CL3-05682-109 Clinical non-inferiority study between Micronized purified flavonoid fraction 1000 mg, one chewable tablet per day… MICRONISED PURIFIED FLAVONOID FRACTION / S005682 / Phase 3 Cardiovascular
CL1-95010-001 Safety, Tolerability and Pharmacokinetics of S 95010 After Single Escalating Intravenous Doses in Young Healthy… S095010 / Phase 1 Cardiovascular
CL3-95005-006 An open-label, randomised, phase III Study cOmparing trifLuridine/tipiracil (S 95005) in combination with bevacizumab to… TIPIRACIL / TRIFLURIDINE / TRIFLURIDINE - TIPIRACIL / Phase 3 Oncology
CL1-81694-003 Phase I/II trial of S 81694 administered intravenously in combination with paclitaxel to evaluate the… S081694 / Phase 1-2 Oncology
CL1-49076-002 Phase I/II study of S49076, a multi-target inhibitor of c-MET, AXL, FGFR in combination with… S049076 / Phase 1-2 Oncology
CL1-80881-002 INES - Phase Ib dose allocation study of oral administration of lucitanib given in combination… LUCITANIB / Phase 1 Oncology
CL1-68587-001 A phase 1, open label, non-comparative, monocenter study to evaluate the safety and the ability… S068587 / S068587 - UCART19 / UCART19 / Phase 1 Oncology
IC4-95005-183-DEU Prospective, Multicenter, Open-label Phase IV trial of Trifluridine/Tipiracil to Evaluate the Health-related Quality of Life… TIPIRACIL / TRIFLURIDINE / TRIFLURIDINE - TIPIRACIL / Phase 4 Oncology
SC3-90049-001 Assessment of the acceptability of a sublingual formulation of piribedil (S90049), 10 to 30 mg… PIRIBEDIL / Phase 3 Neurosciences
SC2-90049-003 Effect of 3 doses (20, 40 and 60 mg) of a sublingual formulation of piribedil… PIRIBEDIL / Phase 2 Neurosciences
PKH-05720-001 A study to assess the release profiles from fixed combination tablets (gliclazide MR/metformin) GLICLAZIDE / GLICLAZIDE - METFORMINE - S005720 / METFORMINE / S005720 / Phase 1 Metabolism
MC3-06790-001 Study of the effect of trimetazidine MR 35 mg (2 tabs/day) on the emergence of… TRIMETAZIDINE / Phase 3 Cardiovascular
IC4-5702-205-CHN Study of Combination Therapy of Gliclazide MR and Basal Insulin Versus Insulin Monotherapy to Treat… Phase 4 Metabolism
IC4-20098-542 Efficacy and safety of Valdoxan® given orally once a day for 24 weeks in patients… AGOMELATINE / AGOMELATINE - S020098 / S020098 / Phase 4 Neurosciences
IC4-12911-098 PRotelos 2g in the OSteoporosis treatment, the Tolerability and Efficacy Profile - PROSTEP STRONTIUM / STRONTIUM RANELATE / Phase 4 Rhumatology
IC4-05682-099 Efficacy of Detralex® in Edema Treatment. An open, 6-month, multicentre study. EDET Study MICRONISED PURIFIED FLAVONOID FRACTION / Phase 4 Cardiovascular
IC4-05682-031 Detralex* versus placebo in the treatment of acute hemorrhoids in patients with acute hemorrhoidal attack.… MICRONISED PURIFIED FLAVONOID FRACTION / Phase 4 Cardiovascular
DM4-90652-001 Patient pREference and satisFaction for pErindopril oRodispersible vs convENtional tablets in daily Clinical practicE. PREFERENCE PERINDOPRIL / PERINDOPRIL ARGININE / Phase 4 Cardiovascular
DM4-20098-112 Clinical long-term effects of Valdoxan® (25 or 50 mg) in depressed patients. Clinical, national, interventional,… AGOMELATINE / AGOMELATINE - S020098 / S020098 / Phase 4 Neurosciences

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EU Clinical Trials Register

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ISRCTN registry

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