Samyang Biopharmaceuticals Corporation

Samyang Holdings Corporation

Sa Won Lee

Min Hyo Seo

Bong Oh Kim

Do Hoon Kim

Sang Yeob Park

Hye Jung Lim

Seong Yun Jeong

Eun Kyung Choi

Joong Woong Cho

In Ja Choi

Yil Woong Yi

Hye Rim Kim

Bum Chan Min

Ji Yeong Kim

Gyeong Hae Kim

Jae Young Lee

Kyu Jin Kyung

Hye Won Kang

Ha Na Woo

Disclosed are an oral solid dosage form composition comprising an active ingredient and a solubilizing carrier wherein a foaming ingredient is used to improve disintegration, dispersion or dissolution, and a preparation method therefor.

Oral solid dosage form composition having improved disintegration and preparation method therefor

A pharmaceutical composition containing a specific related compound within a specified limit and a method for preparing the same are provided.

Pharmaceutical composition with improved storage stability and method for preparing the same

The present invention relates to an amphiphilic block copolymer composition which provides enhanced stability to a micelle formed by an amphiphilic block copolymer in an aqueous phase.

Amphiphilic block copolymer composition having enhanced micelle stability, and pharmaceutical composition comprising same

The present disclosure relates to an oral tablet composition comprising lenalidomide and a method for preparing the same. More particularly, the present disclosure relates to a tablet-type composition and a method for preparing the same wherein the composition exhibits physicochemical equivalence with lenalidomide preparations of hard capsules, has the same pharmacological, therapeutic effect in non-clinical studies and bioequivalence studies, and also has improved ease of taking, handling, safety and the like.

Oral tablet formulation of lenalidomide

The present invention relates to a polymer nanoparticle freeze-dried product, and a preparation method therefor, the polymer nanoparticle freeze-dried product being obtainable by treating, through a freeze-drying process comprising an annealing step, a polymer nanoparticle aqueous solution comprising an amphiphilic block copolymer, a polylactic acid derivative having a carboxyl terminal group, and a freeze-drying adjuvant, wherein the polymer nanoparticle freeze-dried product is reconstituted within five minutes upon reconstitution by means of an aqueous solvent under atmospheric pressure.

Polymer nanoparticle freeze-dried product, and preparation method therefor

Provided is a composition for preventing nausea or vomiting, including a 5-HTreceptor antagonist and a corticosteroid, and having a pH adjusted to 3.0-6.0. Provided also is a method for preparing a composition for preventing nausea or vomiting, including: mixing a 5-HTreceptor antagonist with a corticosteroid; and adjusting pH of the mixture obtained from the preceding operation to 3.0-6.0.

Composition for prevention of nausea or vomiting

The present invention relates to a polymer nanoparticle injection formulation composition containing rapamycin with improved water solubility, and more specifically, to an injection formulation composition containing rapamycin wherein water solubility is improved by solubilizing rapamycin having low water solubility with polymer nanoparticles, a preparation method thereof, and an anticancer composition for a combined use with radiotherapy.

Polymer nanoparticle injection formulation composition containing rapamycin with improved water solubility, preparation method thereof, and anticancer composition for combined use with radiotherapy

A sustained-release microparticle containing a poorly water-soluble drug is disclosed. The sustained-release microparticle containing a poorly water-soluble drug has a multivalent metal ion salt of polylactic acid having at least one terminal carboxyl group or a derivative thereof. The poorly water-soluble drug is entrapped in the multivalent metal ion salt of polylactic acid or a derivative thereof The polylactic acid has at least one terminal carboxyl group or a derivative thereof has an average molecular weight number from 500 to 5,000 daltons. A method for preparing a sustained-release polymeric microparticles containing a poorly water-soluble drug is provided.

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Daejeon, South Korea

Sa Won Lee