On this page, you will find different kinds of study results:
• A Lay summary which is a summary of clinical trial results written in an easy-to-understand way.
• A summary of results called synopsis which is written in scientific language. It is prepared for Medicines Agencies and Ethics Committees,
• A scientific publication which presents results for scientists and medical doctors.
218 Results
Protocol Code |
Study Title |
Active substance/Medical device |
Study Phase |
Therapeutic Area |
CL1-80881-002 |
INES - Phase Ib dose allocation study of oral administration of lucitanib given in combination…
|
LUCITANIB, S080881
|
Phase 1
|
Cancers
|
|
CL1-68587-001 |
A phase 1, open label, non-comparative, monocenter study to evaluate the safety and the ability…
|
UCART19, S068587
|
Phase 1
|
Cancers
|
|
IC4-95005-183-DEU |
Prospective, Multicenter, Open-label Phase IV trial of Trifluridine/Tipiracil to Evaluate the Health-related Quality of Life…
|
TIPIRACIL, TRIFLURIDINE, S095005
|
Phase 4
|
Cancers
|
|
SC3-90049-001 |
Assessment of the acceptability of a sublingual formulation of piribedil (S90049), 10 to 30 mg…
|
PIRIBEDIL, S090049
|
Phase 3
|
Neuropsychiatric Diseases
|
|
SC2-90049-003 |
Effect of 3 doses (20, 40 and 60 mg) of a sublingual formulation of piribedil…
|
PIRIBEDIL, S090049
|
Phase 2
|
Neuropsychiatric Diseases
|
|
PKH-05720-001 |
A study to assess the release profiles from fixed combination tablets (gliclazide MR/metformin)
|
GLICLAZIDE, 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, S006790
|
Phase 3
|
Other
|
|
IC4-5702-205-CHN |
Study of Combination Therapy of Gliclazide MR and Basal Insulin Versus Insulin Monotherapy to Treat…
|
GLICLAZIDE, S005702
|
Phase 4
|
Metabolism
|
|
IC4-20098-542 |
Efficacy and safety of Valdoxan® given orally once a day for 24 weeks in patients…
|
AGOMELATINE, S020098
|
Phase 4
|
Neuropsychiatric Diseases
|
|
IC4-12911-098 |
PRotelos 2g in the OSteoporosis treatment, the Tolerability and Efficacy Profile - PROSTEP
|
STRONTIUM RANELATE, S012911
|
Phase 4
|
Rheumatology
|
|
IC4-05682-099 |
Efficacy of Detralex® in Edema Treatment. An open, 6-month, multicentre study. EDET Study
|
MICRONISED PURIFIED FLAVONOID FRACTION, S005682
|
Phase 4
|
Cardiovascular Diseases
|
|
IC4-05682-031 |
Detralex* versus placebo in the treatment of acute hemorrhoids in patients with acute hemorrhoidal attack.…
|
MICRONISED PURIFIED FLAVONOID FRACTION, S005682
|
Phase 4
|
Cardiovascular Diseases
|
|
DM4-90652-001 |
Patient pREference and satisFaction for pErindopril oRodispersible vs convENtional tablets in daily Clinical practicE. PREFERENCE
|
PERINDOPRIL ARGININE, S090652
|
Phase 4
|
Cardiovascular Diseases
|
|
DM4-20098-112 |
Clinical long-term effects of Valdoxan® (25 or 50 mg) in depressed patients. Clinical, national, interventional,…
|
AGOMELATINE, S020098
|
Phase 4
|
Neuropsychiatric Diseases
|
|
DM4-20098-108 |
Clinical efficacy of VALDOXAN in everyday practice conditions (efficiency) in depressed patients, on a treatment-naive…
|
AGOMELATINE, S020098
|
Phase 4
|
Neuropsychiatric Diseases
|
|
DM4-20098-107 |
Response to VALDOXAN® and restoration of social rhythms in Major Depressive Disorder: VALDOXAN® D-Rhythm study.…
|
AGOMELATINE, S020098
|
Phase 4
|
Neuropsychiatric Diseases
|
|
CL3-95005-004 |
Update in progress An open-label early access phase IIIb study of trifluridine / tipiracil (S 95005/TAS-102) in patients… |
TIPIRACIL, TRIFLURIDINE, S095005
|
Phase 3
|
Cancers
|
|
CL3-90652-004 |
Evaluation of the effect of the oral administration of perindopril orodispersible at a dose of…
|
PERINDOPRIL ARGININE, S090652
|
Phase 3
|
Cardiovascular Diseases
|
|
CL3-78989-019 |
A safety open-label study of Gevokizumab in the treatment of patients with chronic non-infectious Uveitis…
|
GEVOKIZUMAB, S078989
|
Phase 3
|
Other
|
|
CL3-78989-002 |
A randomized, double-masked, placebo-controlled study of the efficacy of gevokizumab in the treatment of patients…
|
GEVOKIZUMAB, S078989
|
Phase 3
|
Other
|
|
CL3-20098-089 |
Efficacy and safety of agomelatine (25mg/day with blinded potential adjustment to 50mg/day) versus escitalopram (10mg/day…
|
AGOMELATINE, S020098
|
Phase 3
|
Neuropsychiatric Diseases
|
|
CL3-20098-087 |
Efficacy and safety of 2 doses of agomelatine (10 mg/day or 25 mg/day) versus placebo…
|
AGOMELATINE, S020098
|
Phase 3
|
Neuropsychiatric Diseases
|
|
CL3-20098-083 |
Early effect of agomelatine on general interest in outpatients with Major Depressive Disorder. A 12-week,…
|
AGOMELATINE, S020098
|
Phase 3
|
Neuropsychiatric Diseases
|
|
CL3-20098-080 |
Effects of agomelatine (25 to 50 mg/day) on circadian rhythms in patients with Major Depressive…
|
AGOMELATINE, S020098
|
Phase 3
|
Neuropsychiatric Diseases
|
|
CL3-20098-078 |
Efficacy and safety of agomelatine (25-50 mg/day) for 12 weeks in patients with Generalized Anxiety…
|
AGOMELATINE, S020098
|
Phase 3
|
Neuropsychiatric Diseases
|
|
Servier clinical trials are mainly registered on
EU Clinical Trials Register
The EU Clinical Trials Register contains information on interventional clinical trials on medicines carried out in Europe, which started after 1 May 2004.
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ClinicalTrials.gov
Clinicaltrials.gov is a registry that contains information on clinical studies of human participants carried out around the world.
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ISRCTN registry
The International Standard Randomized Controlled Trial Number (ISRCTN) registry is a primary clinical trial registry recognised by World Health Organization (WHO) and International Committee of Medical Journal Editor (ICMJE) that accepts all clinical research studies.
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