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use of pegylated variants of igf-i for the treatment of neuromuscular disorders

机译:igf-i的聚乙二醇化变体在治疗神经肌肉疾病中的应用

摘要

use of pegylated variants of igf-i for the treatment of neuromuscular disorders. the present invention relates to the pharmaceutical use of igf-i polyethylene glycol (peg) variants for the treatment, prevention and / or delaying the progression of neuromuscular disorders, in particular amyotrophic lateral sclerosis (als). more specifically, the present invention relates to the use of a pegylated variant of igf-i for the production of a pharmaceutical composition for the treatment, prevention and / or delay of neuromuscular disorders, in particular where the pegylated variant of igf- i is characterized by the fact that it is derived from the amino acid sequence of wild-type human igf-i (seq id no: 1) and carries one or two amino acid changes at amino acid positions 27, 65 and 68 so that one or two amino acids at positions 27, 65 and 68 is / are a poiar amino acid but not lysine and peg is attached to at least one lysine residue.
机译:igf-i的聚乙二醇化变体在神经肌肉疾病治疗中的应用。本发明涉及igf-i聚乙二醇(peg)变体在治疗,预防和/或延缓神经肌肉疾病,特别是肌萎缩性侧索硬化(al)的进展中的药物用途。更具体地,本发明涉及igf-i的聚乙二醇化变体在制备用于治疗,预防和/或延迟神经肌肉疾病的药物组合物中的用途,特别是在igf-i的聚乙二醇化变体的特征在于因为它是从野生型人igf-i(seq id no:1)的氨基酸序列衍生而来,并且在第27、65和68位氨基酸位置带有一个或两个氨基酸变化,因此一个或两个氨基酸在27、65和68位上的氨基酸是p氨基酸,但不是赖氨酸,且peg连接至至少一个赖氨酸残基。

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