Egis Gyogyszergyar Nyrt

Egis Gyogyszergyar Rt.

Egis Gyogyszergyar Zrt.

Egis Gyogyszergyar

Egis Gyogyszergyar Nyilvanosan Mukodo Reszvenytarsasag

Gábor Gigler

Gyula Simig

József Barkóczy

György Lévay

Krisztina Móricz

László Gábor Hársing

Tibor Mezei

Balázs Volk

Gábor Szénási

Katalin Pallagi

István Gacsályi

András Egyed

Csilla Leveleki

Rita Kapillerné Dezsöfi

Nóra Sziray

Zoltán Greff

Szabolcs Kertesz

Hajnalka Kompagne

Miklós Végh

István Ling

Bernadett Martonné Markó

Zoltán Varga

Ferenc Bertha

Edit Pap

Adrienn Pálvölgyi

Attila Bóta

András Ferenc Wacha

Anita Gulyás

György Levay

Géza Szabó

Zoltán Rátkai

Endréné Flórian

Dániel Ulej

Gábor Szenasi

József Barkoczy

István Gacsalyi

Márta Agoston

László Gábor Harsing

Péter Kiricsi

Bernadett Markó

Balázs Molnar

József Fetter

József Schindler

Ildikó Nagyné Gyönös

Katalin Nagy

The present invention relates to a topical pharmaceutical composition comprising pregabalin and a reduced micellar phospholipid as an active ingredient, which results in a prolonged analgesic effect of pregabalin. The product can reduce neuropathic pain by at least 5 hours.

Topical pharmaceutical composition containing phospholipids

The present invention is concerned with new indol-2-one derivatives of Formula (I), which have favorable activity profile for the prophylaxis and treatment of disorders in the central nervous or in the cadiovascular system. 

Piperazine derivatives of alkyl oxindoles

The present invention is concerned with new 3,3-disubstituted indol-2-one derivatives of the general Formula (I), wherein Rstands for hydrogen, halogen, alkyl having 1-7 carbon atom(s) or sulfonamido; Rrepresents hydrogen or halogen; Rdenotes hydrogen, alkyl having 1-7 carbon atom(s) optionally carrying an aryl substituent or aryl optionally carrying one or two halogen substituent(s); Rstands for alkyl having 1-7 carbon atom(s); Rrepresents a group of the general Formula (II a) or (II b), wherein Q and W each represents nitrogen or CH; R, Rand Reach stands for hydrogen, halogen, trifluoromethyl, alkyl or alkoxy having 1-7 carbon atom(s), or Rand Rtogether represent ethylenedioxy; m is 0, 1, or 2; a is a single, double or triple bond; n is 0, 1 or 2; and pharmaceutically acceptable acid addition salts thereof which are useful in the treatment or prophylaxis of diseases of the central nervous system, the gastrointestinal system and the cardiovascular system. 

Piperazine derivatives of dialkyl oxindoles

The invention refers to novel 2,3-benzodiazepine derivatives of formula (I) and pharmaceutical compositions containing the same as the active ingredient. The novel compounds antipasmodic, muscle relaxant and neuroprotective activities. In formula I; X represents a hydrogen atom, a chloro atom or a methoxy group; Y stands for a hydrogen atom or a halo atom; Z means a methyl group or a chloro atom; R is a Calkyl group or a group of the formula &#x2014;NRR, wherein Rand Rrepresent, independently, a hydrogen atom, a Calkyl group, a Calkoxy group or a Ccycloalkyl group. 

2, 3-benzodiazepine derivatives and pharmaceutical compositions containing the same as the active ingredient

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Budapest, Hungary

Gábor Gigler