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    • 88. 发明公开
    • FcεRI 특이적 인간 항체 및 이를 포함하는 알레르기 질환 치료 또는 진단용 조성물
    • FcεRI特异性人体抗体及其组合物,用于治疗或诊断包含其的过敏性疾病
    • KR1020120135868A
    • 2012-12-17
    • KR1020120057081
    • 2012-05-30
    • (주)네오팜
    • 박병덕윤선주배종환박은혜김욱동김민희강현정유경숙
    • C07K16/28C12N15/13A61K39/395A61P37/08
    • PURPOSE: A Fc epsilon RI-specific human antibody with high affinity to Fc region of IgE and a method for preparing the same are provided to effectively conjugation of IgE and Fc epsilon RI and to treat or diagnose allergic rhinitis, asthma, atopic dermatitis, and contact dermatitis. CONSTITUTION: A heavy chain variable region of a Fc epsilon RI-specific antibody contains CDR1, CDR2, and CDR3. The heave chain variable region has an amino acid of sequence number 2, 4, 6, 8, 10, 12, 14, or 16. A light chain variable region of the Fc epsilon RI-specific antibody contains CDR1, CDR2 and CDR3. The light chain variable region has an amino acid of sequence number 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, or 40. A pharmaceutical composition for treating allergic diseases contains the Fc epsilon-specific antibody, a fragment thereof, and one or more pharmaceutically acceptable carriers.
    • 目的:提供对IgE Fc区具有高亲和力的FcεRI特异性人抗体及其制备方法,以有效地缀合IgE和FcεRI并治疗或诊断过敏性鼻炎,哮喘,特应性皮炎和 接触性皮炎。 构成:FcεRI特异性抗体的重链可变区含有CDR1,CDR2和CDR3。 起始链可变区具有序列号为2,4,6,8,10,12,14或16的氨基酸。FcεRI特异性抗体的轻链可变区含有CDR1,CDR2和CDR3。 轻链可变区具有序列号18,20,22,24,26,28,30,32,34,36,38或40的氨基酸。用于治疗过敏性疾病的药物组合物含有Fcε特异性 抗体,其片段和一种或多种药学上可接受的载体。
    • 90. 发明公开
    • HGF 활성을 가지는 c-Met에 대한 인간항체 및 이의 용도
    • C-MET定位具有HGF活性的全身激动人体抗体及其用途
    • KR1020120134938A
    • 2012-12-12
    • KR1020110054177
    • 2011-06-03
    • 한국생명공학연구원주식회사 와이바이오로직스
    • 박영우조기원박찬웅유석호장명희김혜난윤선하조규원박미라
    • C07K16/22C12N15/13A61K39/395A61P25/28
    • C07K16/2863A61K2039/505C07K2317/21C07K2317/622C07K2317/75C07K2317/92C07K2317/94
    • PURPOSE: A human antibody which is derived from human body and specifically binds to c-Met is provided to treat neuronal infarction, progressive nephropathy, liver cirrhosis, lung fibrosis, kidney, liver, lung injury, and ulcerative wound which are cured by HGF or c-Met activation. CONSTITUTION: A human antibody contains a complementarity determining region (CDR) and framework region(FR) which are derived from human and specifically binds to c-Met. The human antibody contains: a heavy chain variable region containing heavy chain CDR1 of sequence number 1, heavy chain CDR2 of sequence number 2, and heavy chain CDR3 of sequence number 3; and a light chain variable region containing light chain CDR1 of sequence number 4, light chain CDR2 of sequence number 5, and light chain CDR3 of sequence number 6. The antibody contains a heavy chain variable region amino acid of sequence number 7 and a light chain variable region amino acid of sequence number 8. The human antibody is glycosylated or/and PEGylated. A composition for wound healing contains the human antibody as an active ingredient and pharmaceutically acceptable carrier. A composition for treating neurodegenerative diseases contains the human antibody as an active ingredient and pharmaceutically acceptable carrier.
    • 目的:提供从人体衍生并特异性结合c-Met的人类抗体,用于治疗由HGF或其他物质固化的神经元梗死,进行性肾病,肝硬化,肺纤维化,肾脏,肝脏,肺损伤和溃疡性伤口 c-Met激活。 构成:人抗体含有衍生自人体并且特异性结合c-Met的互补决定区(CDR)和框架区(FR)。 人抗体包含:含有序列号1的重链CDR1,序列号2的重链CDR2和序列号3的重链CDR3的重链可变区; 和含有序列号4的轻链CDR1,序列号5的轻链CDR2和序列号6的轻链CDR3的轻链可变区。抗体含有序列号7的重链可变区氨基酸和轻链 可变区氨基酸序列号8.人抗体是糖基化的或/和聚乙二醇化的。 用于伤口愈合的组合物包含人抗体作为活性成分和药学上可接受的载体。 用于治疗神经变性疾病的组合物含有人抗体作为活性成分和药学上可接受的载体。