Abstract: The present invention relates to a long-acting conjugate of a triple agonist having activities to all of glucagon, GLP-1, and GIP receptors and uses thereof.
Type:
Grant
Filed:
June 29, 2018
Date of Patent:
September 3, 2019
Assignee:
HANMI PHARM. CO., LTD.
Inventors:
Euh Lim Oh, Jong Suk Lee, Young Jin Park, Chang Ki Lim, Sung Youb Jung, Se Chang Kwon
Abstract: The present invention relates to a novel method for preparing thienopyrimidine compound having an activity of selectively inhibiting tyrosine kinase, specifically the mutant epidermal growth factor receptor tyrosine kinase; and a novel intermediate used therein. According to the method of the present invention, the industrial mass-production of the compound of Formula 1, which is useful as a therapeutic agent for non-small cell lung cancer induced by the mutant epidermal growth factor receptor tyrosine kinase, can be implemented more conveniently and efficiently than the conventional technology.
Type:
Grant
Filed:
October 31, 2016
Date of Patent:
August 27, 2019
Assignee:
HANMI PHARM. CO., LTD.
Inventors:
Wook Jang, Young Ho Moon, Tae Hee Ha, Kwee Hyun Suh
Abstract: Provided are a composite capsule and a method of preparing the composite capsule. The composite capsule includes a first dissolving part including a core, an inner coating layer on the core, and a first enteric coating layer on the inner coating layer, wherein core contains, as an active ingredient, esomeprazole or a pharmaceutically acceptable salt thereof. The composite capsule further includes a second dissolving part including a core, which contains, as an active ingredient, esomeprazole or a pharmaceutically acceptable salt thereof, an inner coating layer on the core, and a second enteric coating layer on the inner coating layer.
Type:
Application
Filed:
October 19, 2017
Publication date:
August 15, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Taek Kwan KWON, Seung Hun CHANG, Ho Taek IM, Yong ll KIM, Jae Hyun PARK, Jong Soo WOO
Abstract: Provided are a pyrimidine compound represented by Formula 1, a method of preparing the same, and a pharmaceutical use of the pyrimidine compound for the prevention or treatment of cancer.
Type:
Grant
Filed:
September 11, 2018
Date of Patent:
May 7, 2019
Assignee:
HANMI PHARM. CO., LTD.
Inventors:
Young Jin Ham, Seok Jong Kang, Jae Yul Choi, Seo Hee Kim, Tae Woo Kim, In Hwan Bae, Young Gil Ahn, Kwee Hyun Suh
Abstract: The present invention relates to an albumin-free liquid formulation comprising a long-lasting oxyntomodulin conjugate in which an oxyntomodulin peptide comprising a derivative, variant, precursor or fragment of oxyntomodulin is linked to an immunoglobulin Fc region, which can increase the duration of physiological activity of the long-lasting oxyntomodulin conjugate and maintain the in vivo stability thereof for an extended period of time, as compared to native oxyntomodulin, as well as a method for preparing the liquid formulation. The liquid formulation comprises a buffer, a sugar alcohol and a nonionic surfactant and does not contain a human serum albumin and factors that are potentially harmful to the human body, and thus is not susceptible to viral infection.
Type:
Grant
Filed:
June 29, 2017
Date of Patent:
May 7, 2019
Assignee:
Hanmi Pharm Co. Ltd.
Inventors:
Hyun Uk Kim, Hyung Kyu Lim, Myung Hyun Jang, Sang Yun Kim, Sung Min Bae, Se Chang Kwon
Abstract: Provided are a pyrimidine compound represented by Formula 1, a method of preparing the same, and a pharmaceutical use of the pyrimidine compound for the prevention or treatment of cancer.
Type:
Application
Filed:
December 19, 2018
Publication date:
May 2, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Young Jin HAM, Seok Jong Kang, Jae Yul Choi, Seo Hee Kim, Tae Woo Kim, In Hwan Bae, Young Gil Ahn, Kwee Hyun Suh
Abstract: One aspect of the present invention provides: a composite capsule preparation containing tadalafil or a pharmaceutically acceptable salt thereof and tamsulosin or a pharmaceutically acceptable salt thereof, wherein the composite capsule preparation comprises, on the surface thereof, a film coating layer comprising, as a film coating material, polyvinyl alcohol (PVA) or a copolymer comprising PVA; and a preparation method therefor.
Type:
Application
Filed:
March 31, 2017
Publication date:
May 2, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Jin Wook TAK, Jung Hyun CHO, Jin Cheul KIM, Yong Il KIM, Jae Hyun PARK, Jong Soo WOO
Abstract: The present invention relates to a glucagon derivative, a conjugate thereof, and a composition comprising the same, and a therapeutic use thereof, and in particular, for metabolic syndrome, hypoglycemia, and congenital hyperinsulinism.
Type:
Application
Filed:
December 27, 2018
Publication date:
April 25, 2019
Applicant:
HANMI PHARM. CO., LTD
Inventors:
Jung Kuk KIM, Young Jin Park, In Young Choi, Sung Youb Jung
Abstract: The present invention relates to an insulin analog that has reduced insulin receptor binding affinity for the purpose of increasing the blood half-life of insulin, and long-acting insulin, a conjugate, and a method of preparing long-acting insulin using the same.
Type:
Grant
Filed:
January 20, 2015
Date of Patent:
April 9, 2019
Assignee:
HANMI PHARM. CO., LTD
Inventors:
Sung Youb Jung, Sang Youn Hwang, Euh Lim Oh, Sung Hee Park, Hyun Uk Kim, Chang Ki Lim, Se Chang Kwon
Abstract: The present invention relates to a pharmaceutical composition for the prevention or treatment of non-alcoholic fatty liver disease including a long-acting GLP-1/glucagon receptor dual agonist, and a method for preventing or treatment of non-alcoholic fatty liver disease including administering the composition. The composition of the present invention either has no side effect of weight gain or reduces the side effect of weight gain, which is a side-effect of conventional therapeutic agents for non-alcoholic fatty liver disease, and reduces the amount of administrations of a long-acting GLP-1/glucagon receptor dual agonist, thus greatly improving patient's convenience. In addition, the long-acting GLP-1/glucagon receptor dual agonist of the present invention improves in vivo sustainability and stability.
Type:
Grant
Filed:
September 16, 2015
Date of Patent:
March 19, 2019
Assignee:
Hanmi Pharm. Co., Ltd.
Inventors:
Sang Youn Hwang, Jin Young Kim, Seung Su Kim, In Young Choi, Sung Youb Jung, Se Chang Kwon
Abstract: The present invention relates to a conjugate in which an immunoglobulin Fc region is linked to therapeutic enzymes through a non-peptide polymer linkage moiety, and more specifically, to a conjugate in which a non-peptide polymer linkage moiety is specifically linked to an immunoglobulin Fc, a method of preparing the same, and a composition comprising the same.
Type:
Application
Filed:
January 31, 2017
Publication date:
February 14, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Dae Jin KIM, Jung Kuk KIM, Sung Youb JUNG, Se Chang KWON
Abstract: Provided are a pyrimidine compound represented by Formula 1, a method of preparing the same, and a pharmaceutical use of the pyrimidine compound for the prevention or treatment of cancer.
Type:
Application
Filed:
September 11, 2018
Publication date:
January 31, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Young Jin HAM, Seok Jong KANG, Jae Yul CHOI, Seo Hee KIM, Tae Woo KIM, In Hwan BAE, Young Gil AHN, Kwee Hyun SUH
Abstract: A composition for preventing or treating diabetes mellitus includes insulin and a GLP-1/glucagon dual agonist. The composition can inhibit the weight gain and reduce the danger of hypoglycemia due to the administration of insulin, lower the administration dose and greatly improve the compliance of drugs through a combined administration of a long-acting insulin conjugate and a long-acting GLP-1/glucagon dual agonist conjugate. In addition, the long-acting insulin conjugate and the long-acting GLP-1/glucagon dual agonist conjugate can improve the in vivo sustainability and stability because an insulin and a GLP-1/glucagon dual agonist are linked to the immunoglobulin Fc region via a non-peptidyl linker. A method for preventing or treat diabetes mellitus includes administration of the insulin and a GLP-1/glucagon dual agonist.
Type:
Grant
Filed:
June 1, 2015
Date of Patent:
January 29, 2019
Assignee:
HANMI PHARM. CO., LTD.
Inventors:
Sung Youb Jung, Sang Youn Hwang, Seung Su Kim, In Young Choi, Se Chang Kwon
Abstract: The present invention relates to crystalline forms of N-(3-(2-(4-(4-methylpiperazin-1-yl)phenylamino)thieno[3,2-d]pyrimidin-4-yloxy)phenyl)acrylamide, and pharmaceutical compositions containing the same. The crystalline forms can be easily used for the preparation of a pharmaceutical composition containing the same as an active ingredient.
Type:
Application
Filed:
December 30, 2016
Publication date:
January 17, 2019
Applicant:
HANMI PHARM. CO., LTD.
Inventors:
Jae Hyuk JUNG, Jong Ouk BAEK, Sun Young JUNG, Eun Joo KWAK, Hee Cheol KIM, Tae Hee HA
Abstract: Provided are a thieno[3,2-d]pyrimidine derivative of formula (I) or a pharmaceutically acceptable salt thereof having inhibitory activity for protein kinase, and a pharmaceutical composition comprising same for prevention and treatment of abnormal cell growth diseases.
Type:
Grant
Filed:
October 13, 2017
Date of Patent:
June 25, 2019
Assignee:
Hanmi Pharm. Co. Ltd.
Inventors:
In Hwan Bae, Jung Beom Son, Sang Mi Han, Eun Joo Kwak, Ho Seok Kim, Ji Young Song, Eun Young Byun, Seung Ah Jun, Young Gil Ahn, Kwee Hyun Suh