Precigen Announces First Patient Dosed For PRGN-2012 AdenoVerse Immunotherapy In Patients With Recurrent Respiratory Papillomatosis
Precigen Announces First Patient Dosed For PRGN-2012 AdenoVerse Immunotherapy In Patients With Recurrent Respiratory Papillomatosis
Precigen, Inc., a biopharmaceutical company specializing in the development of innovative gene and cell therapies to improve the lives of patients, today announced that the first patient has been dosed in the Phase I study of PRGN-2012, a first-in-class, investigational off-the-shelf (OTS) AdenoVerse™ immunotherapy in adult patients with recurrent respiratory papillomatosis (RRP) (clinical trial identifier: NCT04724980). The US Food and Drug Administration recently granted Orphan Drug Designation for PRGN-2012 in RRP in March 2021.
Precigen, Inc., a biopharmaceutical company specializing in the development of innovative gene and cell therapies to improve the lives of patients, today announced that the first patient has been dosed in the Phase I study of PRGN-2012, a first-in-class, investigational off-the-shelf (OTS) AdenoVerse™ immunotherapy in adult patients with recurrent respiratory papillomatosis (RRP) (clinical trial identifier: NCT04724980). The US Food and Drug Administration recently granted Orphan Drug Designation for PRGN-2012 in RRP in March 2021.
致力于开发创新的基因和细胞疗法以改善患者生活的生物制药公司Precigen,Inc.今天宣布,PRGN-2012年的第一阶段研究已经给第一名患者服用了剂量,这是一种针对成人复发性呼吸道乳头状瘤病患者的一流的研究现成的AdenoVerse™免疫疗法(临床试验标识符:NCT04724980)。美国食品和药物管理局最近批准RRP中PRGN-2012的孤儿药物命名2021年3月。
译文内容由第三方软件翻译。
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