a Laboratory UMRS 1138 "Cancer, Immune Control and Escape" , Cordeliers Research Centre , Paris , France.
b The Antibody Society , Framingham , MA , USA.
MAbs. 2018 Feb/Mar;10(2):183-203. doi: 10.1080/19420862.2018.1415671. Epub 2018 Jan 16.
The pace of antibody therapeutics development accelerated in 2017, and this faster pace is projected to continue through 2018. Notably, the annual number of antibody therapeutics granted a first approval in either the European Union (EU) or United States (US) reached double-digits (total of 10) for the first time in 2017. The 10 antibodies granted approvals are: brodalumab, dupilumab, sarilumab, guselkumab, benralizumab, ocrelizumab, inotuzumab ozogamicin, avelumab, duvalumab, and emicizumab. Brodalumab, however, had already been approved in Japan in 2016. As of December 1, 2017, nine antibody therapeutics (ibalizumab, burosumab, tildrakizumab, caplacizumab, erenumab, fremanezumab, galcanezumab, romosozumab, mogamulizumab) were in regulatory review in the EU or US, and regulatory actions on their marketing applications are expected by the end of 2018. Based on company announcements and estimated clinical study primary completion dates, and assuming the study results are positive, marketing applications for at least 12 antibody therapeutics that are now being evaluated in late-stage clinical studies may be submitted by the end of 2018. Of the 12 candidates, 8 are for non-cancer indications (lanadelumab, crizanlizumab, ravulizumab, eptinezumab, risankizumab, satralizumab, brolucizumab, PRO140) and 4 are for cancer (sacituzumab govitecan, moxetumomab pasudotox, cemiplimab, ublituximab). Additional antibody therapeutics to watch in 2018 include 19 mAbs undergoing evaluation in late-stage studies with primary completion dates in late 2017 or during 2018. Of these mAbs, 9 are for non-cancer indications (lampalizumab, roledumab, emapalumab, fasinumab, tanezumab, etrolizumab, NEOD001, gantenerumab, anifrolumab) and 10 are for cancer indications (tremelimumab, isatuximab, BCD-100, carotuximab, camrelizumab, IBI308, glembatumumab vedotin, mirvetuximab soravtansine, oportuzumab monatox, L19IL2/L19TNF). Positive clinical study results may enable marketing application submissions in 2018. Brief summaries of these antibody therapeutics are provided in this installment of the 'Antibodies to watch' article series.
2017 年,抗体治疗药物的研发步伐加快,预计这种更快的步伐将持续到 2018 年。值得注意的是,2017 年,在欧盟(EU)或美国(US)首次获得批准的抗体治疗药物数量首次达到两位数(共 10 种)。这 10 种获得批准的抗体分别是:brodalumab、dupilumab、sarilumab、guselkumab、benralizumab、ocrelizumab、inotuzumab ozogamicin、avelumab、duvalumab 和 emicizumab。然而,brodalumab 已于 2016 年在日本获得批准。截至 2017 年 12 月 1 日,9 种抗体治疗药物(ibalizumab、burosumab、tildrakizumab、caplacizumab、erenumab、fremanezumab、galcanezumab、romosozumab、mogamulizumab)正在欧盟或美国接受监管审查,预计 2018 年底前将对其营销申请采取监管行动。基于公司公告和估计的临床研究主要完成日期,并假设研究结果为阳性,至少有 12 种目前正在进行后期临床研究评估的抗体治疗药物的营销申请可能会在 2018 年底前提交。在这 12 个候选药物中,有 8 个是非癌症适应症(lanadelumab、crizanlizumab、ravulizumab、eptinezumab、risankizumab、satralizumab、brolucizumab、PRO140),4 个是癌症适应症(sacituzumab govitecan、moxetumomab pasudotox、cemiplimab、ublituximab)。2018 年还需要关注其他抗体治疗药物,包括正在进行后期研究的 19 种 mAb,这些 mAb 的主要完成日期为 2017 年底或 2018 年。在这些 mAb 中,有 9 种是非癌症适应症(lampalizumab、roledumab、emapalumab、fasinumab、tanezumab、etrolizumab、NEOD001、gantenerumab、anifrolumab),10 种是癌症适应症(tremelimumab、isatuximab、BCD-100、carotuximab、camrelizumab、IBI308、glembatumumab vedotin、mirvetuximab soravtansine、oportuzumab monatox、L19IL2/L19TNF)。阳性的临床研究结果可能使营销申请在 2018 年提交。本系列文章的“值得关注的抗体”部分提供了这些抗体治疗药物的简要总结。