智通财经APP讯，荃信生物-B(02509)发布公告，公司自主研发的长效双抗QX027N注射液获得国家药品监督管理局药品审评中心的临床试验默示许可(受理号： CXSL2500757，CXSL2500758)，拟用于治疗哮喘及特应性皮炎。该候选药物的临床许可标志着公司在自免及过敏疾病领域的创新双抗矩阵正式迈入临床阶段。
QX027N是公司双特异性抗体研发的重要成果，意味着公司在呼吸和皮肤两大疾病领域的协同布局取得进一步进展。面对全球数亿哮喘与特应性皮炎患者亟待解决的临床需求，公司将持续推进创新疗法的研发与临床转化，为患者提供更高效、更安全及更便利的治疗选择。
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