Ucb S.a.

Ucb Pharma, S.a.

Ucb Farchim Sa

Ucb Biopharma Sprl

Ucbbiopharma Srl

Ucb, Inc.

Domenico Fanara

Michel Deleers

Anthony Guichaux

Monique Berwaer

Henri Vranckx

Frédéric Eeckman

Frederic Eeckman

Guy Bodson

Charles Dogimont

Jacques Timmermans

Anne Bouquelle

Pierre Grognet

Valery Barillaro

Philippe Nolf

Claire Poulain

Jean Scouvart

Serge Cuypers

Martine Larbanoix

Eric Schenkel

Bertrand Dodelet

Frederic Dargelas

Frédéric Dargelas

The present invention relates to an immediate release formulation of pharmaceutical compounds.

Pharmaceutical compositions comprising 2-oxo-1-pyrrolidine derivatives

The present invention relates to a pharmaceutical composition comprising Levetiracetam, Brivaracetam or Seletracetam as active ingredient, the invention relates specifically to a prolonged release formulation.

Prolonged release formulations comprising an 2-oxo-1-pyrrolidine derivative

The present invention relates to pharmaceutical compositions for oral administration of active compounds.

Formulations

The present invention relates to a liquid composition containing an active substance belonging to the family of substituted benzhydryl piperazines with reduced amounts of preservatives.

Pharmaceutical composition of piperazine derivatives

The present invention relates to a pharmaceutical composition comprising brivaracetam as active ingredient, the invention relates specifically to a prolonged release formulation.

Pharmaceutical compositions comprising Brivaracetam

The present invention relates to a pharmaceutical composition comprising Brivaracetam or Seletracetam as active ingredient, the invention relates specifically to a prolonged release formulation made of granules containing the active ingredient in their inner core.

Prolonged release formulations comprising an 2-oxo-1-pyrrolidine derivate

Pharmaceutical compositions comprising brivaracetam

The present invention concerns a tablet comprising two distinct segments. More particularly, the invention relates to combinations of two pharmaceutical substances and methods of treatment of allergic disorders.

Tablet comprising cetirizine and pseudoephedrine

The invention relates to pharmaceutical compositions which can be administrated orally, allowing the controlled release of at least one active substance comprising

Pharmaceutical compositions for the controlled release of active substances

A method is described for preparing a fluid pharmaceutical composition which allows the controlled release of at least one active substance. The method involves mixing a therapeutically effective amount of at least one active substance, from 3 to 55% by weight of phospholipid, from 16 to 72% by weight of pharmaceutically acceptable solvent, and from 4 to 52% by weight of fatty acid. The composition has a property of gelling instantaneously in the presence of an aqueous phase.

Use of gellable pharmaceutical compositions in periodontology

The present invention is directed a pharmaceutical composition which can be administered orally, allowing for the controlled release of at least one active substance. The composition includes at least one active substance, between 5 and 60% by weight, relative to the total weight of the composition, of at least one excipient, selected from inert matrices, hydrophilic matrices, lipid matrices, mixtures of inert matrices and of lipid matrices, and mixtures of hydrophilic matrices and of inert matrices, with the exception of mixtures including a polyacrylic acid and at least one hydrophilic matrix of the cellulose type; and between 5 and 50% by weight, relative to the total weight of the composition, of at least one alkalinizing agent soluble in an aqueous phase under physiological pH conditions, selected from alkali or alkaline-earth metal hydroxides, carbonates, bicarbonates, phosphates, sodium borate and basic salts of organic acids. The invention further includes a process for preparation of the composition, multi-layered pharmaceutical compositions including at least one layer of the inventive composition, and processes for producing same.

Pharmaceutical compositions for controlled release of active substances

A method is described for preparing a fluid pharmaceutical composition which allows the controlled release of at least one active substance. The method involves mixing a therapeutically effective amount of at least one active substance, from 3 to 55% by weight of phospholipid, from 16 to 72% by weight of pharmaceutically acceptable solvent, and from 4 to 52 % by weight of fatty acid. The composition has a property of gelling instantaneously in the presence of an aqueous phase.

Use of pharmaceutical compositions capable of being gelled in periodontology

A fluid pharmaceutical composition is described which allows the controlled release of at least one active substance. The composition comprises a therapeutically effective amount of at least one active substance, from 3 to 55% by weight of phospholipid, from 16 to 72% by weight of pharmaceutically acceptable solvent, and from 4 to 52% by weight of fatty acid. The composition has a property of gelling instantaneously in the presence of an aqueous phase.

Pharmaceutical compositions capable of being gelled

The invention concerns pharmaceutical compositions for oral administration, comprising an active substance belonging to the family of substituted benzhydrylpiperazines and at least a cyclodextrin.

Growing community of inventors

Wanze, Belgium

Domenico Fanara