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Clinical non-inferiority study between Daflon 1000 mg, one oral suspension in a sachet per day and Daflon 500 mg, 2 tablets daily after eight weeks of treatment in patients suffering from symptomatic Chronic Venous Disease (CVD). International, multicenter, double-blind, randomized, parallel group study

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Study Phase

Phase 3

Therapeutic Area

Cardiovascular Diseases

Indicationvenous disease
SponsorInstitut de Recherches Internationales Servier (I.R.I.S)
Active substance/
Medical device


Active Substance CodeS005682
Protocol CodeCL3-05682-105
EudraCT Code2012-003559-13

Documents and links

Lay summary
Results summary READ MORE
Scientific publication READ MORE

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