Indication Expansion Dynamics and Trial Characteristics of Novel Multi-Indication Anti-Cancer Drugs in China (2000-2024): A Cross-Sectional Study

中国新型多适应症抗癌药物适应症扩展动态及试验特征(2000-2024):一项横断面研究

阅读:3

Abstract

PURPOSE: To perform a cross-sectional analysis of the indication expansion trends and pivotal trial features of novel multi-indication anti-cancer drugs approved in China from 2000 to 2024. METHODS: We conducted a cross‑sectional review of 74 novel multi-indication anti-cancer drugs approved by the National Medical Products Administration (NMPA) in China from 2000 to 2024, encompassing 265 total indications. Data were collected from multiple sources, including the NMPA, the Center for Drug Evaluation (CDE) of the NMPA, the National Healthcare Security Administration (NHSA), ClinicalTrials.gov, and drug package inserts. Descriptive statistics and Fisher's exact test (two-tailed) or the χ(2) -test with Monte Carlo simulation, were used to analyze indication and clinical trial characteristics across indication approval sequence. RESULTS: Of the 74 drugs, 32 (43%) held two indications, 23 (31%) held three, and 19 (26%) held four or more. Solid tumors accounted for 80% of all indications, most commonly non-small cell lung cancer. Immune checkpoint inhibitors (ICIs) exhibited the greatest expansion, with the most extensively approved drug reaching 14 indications. However, the inclusion of these drugs in the National Reimbursement Drug List (NRDL) did not keep pace with their market approval. Sequential approvals across indications showed significant differences in treatment type (P<0.001), NMPA approval type (P=0.008), trial arms (P=0.009), trial design (P=0.030), and single-arm endpoints (P<0.001). CONCLUSION: Regulatory reforms facilitated the approval of novel multi-indication anti-cancer drugs, although NRDL inclusion has not kept pace. Targeted therapies dominate, while ICIs, though fewer, show the broadest indication expansion. Most drugs are approved for two to three indications, mainly in solid tumors, and later approvals were associated with different regulatory pathways than earlier ones.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。