Challenges in anticancer drug R&D in China
[...]29 (16%) phase 1 studies targeted the PD-1/PD-L1 pathway. [...]far, there are 12 PD-1 inhibitors and eight PD-L1 inhibitors being developed by 15 Chinese biopharmaceutical companies. To deal with the shortage of clinical trial sites, the China Food and Drug Administration (CFDA) plans to abolis...
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Published in: | The lancet oncology Vol. 20; no. 2; pp. 183 - 186 |
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Abstract | [...]29 (16%) phase 1 studies targeted the PD-1/PD-L1 pathway. [...]far, there are 12 PD-1 inhibitors and eight PD-L1 inhibitors being developed by 15 Chinese biopharmaceutical companies. To deal with the shortage of clinical trial sites, the China Food and Drug Administration (CFDA) plans to abolish the current clinical trial agency accreditation system.3,5 Under the new record management system, medical facilities can avoid the lengthy certification process of registering a new trial, and only need to register on the CFDA's website to get approval for doing clinical trials.5 To cultivate a more innovation-friendly drug R&D ecosystem, the CFDA shifted their clinical trial regulatory policy from strict entry, tolerant exit, to tolerant entry, strict exit.3,5 Instead of overemphasising the approval of clinical trial applications, current policies focus more on the quality control of trials and post-marketing pharmacovigilance.5 Clinical trial data falsification is now a felony with at least 3 years in prison. According to the previous definition, novel molecular entities and drugs modified from existing molecular entities were both classified as innovative drugs and received the same treatment. [...]unlike phase 1 studies of other EGFR T790M tyrosine kinase inhibitors, the first-in-human study of ML007 (CTR20180977) includes patients with untreated, symptomatic brain metastasis. |
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AbstractList | [...]29 (16%) phase 1 studies targeted the PD-1/PD-L1 pathway. [...]far, there are 12 PD-1 inhibitors and eight PD-L1 inhibitors being developed by 15 Chinese biopharmaceutical companies. To deal with the shortage of clinical trial sites, the China Food and Drug Administration (CFDA) plans to abolish the current clinical trial agency accreditation system.3,5 Under the new record management system, medical facilities can avoid the lengthy certification process of registering a new trial, and only need to register on the CFDA's website to get approval for doing clinical trials.5 To cultivate a more innovation-friendly drug R&D ecosystem, the CFDA shifted their clinical trial regulatory policy from strict entry, tolerant exit, to tolerant entry, strict exit.3,5 Instead of overemphasising the approval of clinical trial applications, current policies focus more on the quality control of trials and post-marketing pharmacovigilance.5 Clinical trial data falsification is now a felony with at least 3 years in prison. According to the previous definition, novel molecular entities and drugs modified from existing molecular entities were both classified as innovative drugs and received the same treatment. [...]unlike phase 1 studies of other EGFR T790M tyrosine kinase inhibitors, the first-in-human study of ML007 (CTR20180977) includes patients with untreated, symptomatic brain metastasis. |
Author | Wenfeng, Fang Lv, Cheng Xiaoyuan, Chen Gong, Jifang Zhimin, Yang Zhang, Li Ba, Yi Zhao, Shen Hu, Xichun Shen, Lin |
Author_xml | – sequence: 1 givenname: Shen surname: Zhao fullname: Zhao, Shen organization: Department of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China – sequence: 2 givenname: Cheng surname: Lv fullname: Lv, Cheng organization: Covance, Shanghai, China – sequence: 3 givenname: Jifang surname: Gong fullname: Gong, Jifang organization: Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Haidian, Beijing, 100142, China – sequence: 4 givenname: Fang surname: Wenfeng fullname: Wenfeng, Fang organization: Department of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China – sequence: 5 givenname: Xichun surname: Hu fullname: Hu, Xichun organization: Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China – sequence: 6 givenname: Yi surname: Ba fullname: Ba, Yi organization: Department of Medical Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China – sequence: 7 givenname: Chen surname: Xiaoyuan fullname: Xiaoyuan, Chen organization: National Center for Drug Evaluation, China Food and Drug Administration, Beijing, China – sequence: 8 givenname: Yang surname: Zhimin fullname: Zhimin, Yang organization: National Center for Drug Evaluation, China Food and Drug Administration, Beijing, China – sequence: 9 givenname: Lin surname: Shen fullname: Shen, Lin organization: Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Haidian, Beijing, 100142, China – sequence: 10 givenname: Li surname: Zhang fullname: Zhang, Li email: zhangli6@mail.sysu.edu.cn organization: Department of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China |
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Cites_doi | 10.1016/S1470-2045(12)70117-1 10.1016/S1470-2045(18)30495-9 10.1016/S1470-2045(11)70184-X 10.1001/jamaoncol.2016.2129 10.1038/nrd.2018.167 10.1038/nrd.2016.200 10.1038/nrd.2017.94 |
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References | (bib6) 2017 Zhou, Wu, Chen (bib8) 2011; 12 (bib5) 2017 Schwaederle, Zhao, Lee (bib11) 2016; 2 (bib3) 2017 (bib4) 2016 Fang, Yang, Ma (bib10) 2018; 19 Zhang, Ma, Song (bib9) 2012; 13 Tang, Pearce, O'Donnell-Tormey, Hubbard-Lucey (bib12) 2018 (bib7) 2017 Mullard (bib2) 2017; 16 Shao, Xu, Li, Chakravarthy, Yang, Kaitin (bib1) 2016; 15 Shao (10.1016/S1470-2045(18)30865-9_bib1) 2016; 15 Schwaederle (10.1016/S1470-2045(18)30865-9_bib11) 2016; 2 Mullard (10.1016/S1470-2045(18)30865-9_bib2) 2017; 16 Fang (10.1016/S1470-2045(18)30865-9_bib10) 2018; 19 Tang (10.1016/S1470-2045(18)30865-9_bib12) 2018 Zhang (10.1016/S1470-2045(18)30865-9_bib9) 2012; 13 Zhou (10.1016/S1470-2045(18)30865-9_bib8) 2011; 12 |
References_xml | – volume: 2 start-page: 1452 year: 2016 end-page: 1459 ident: bib11 article-title: Association of biomarker-based treatment strategies with response rates and progression-free survival in refractory malignant neoplasms: a meta-analysis publication-title: JAMA Oncol contributor: fullname: Lee – volume: 15 start-page: 739 year: 2016 end-page: 740 ident: bib1 article-title: Regulatory watch: innovative drug availability in China publication-title: Nat Rev Drug Discov contributor: fullname: Kaitin – volume: 12 start-page: 735 year: 2011 end-page: 742 ident: bib8 article-title: Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study publication-title: Lancet Oncol contributor: fullname: Chen – volume: 19 start-page: 1338 year: 2018 end-page: 1350 ident: bib10 article-title: Camrelizumab (SHR-1210) alone or in combination with gemcitabine plus cisplatin for nasopharyngeal carcinoma: results from two single-arm, phase 1 trials publication-title: Lancet Oncol contributor: fullname: Ma – year: 2017 ident: bib5 article-title: Opinions of the state council regarding deepening reforms on the examination and approval system, encouraging drug and medical device innovations – year: 2017 ident: bib3 article-title: Policies on reforming clinical trial administrations and encouraging drug and medical device innovations – year: 2016 ident: bib4 article-title: Notice of the general administration of the people's republic of China on releasing the work program for the reform of the classification of chemical drugs registration – year: 2017 ident: bib6 article-title: Decisions about adjustments of regulations on import drug registration and management – year: 2018 ident: bib12 article-title: Trends in the global immuno-oncology landscape publication-title: Nat Rev Drug Discov contributor: fullname: Hubbard-Lucey – volume: 16 start-page: 443 year: 2017 end-page: 446 ident: bib2 article-title: Chinese biopharma starts feeding the global pipeline publication-title: Nat Rev Drug Discov contributor: fullname: Mullard – year: 2017 ident: bib7 article-title: Policies on accelerating reviews and approvals of new drugs and medical devices to encourage drug and medical device innovations – volume: 13 start-page: 466 year: 2012 end-page: 475 ident: bib9 article-title: Gefitinib versus placebo as maintenance therapy in patients with locally advanced or metastatic non-small-cell lung cancer (INFORM; C-TONG 0804): a multicentre, double-blind randomised phase 3 trial publication-title: Lancet Oncol contributor: fullname: Song – volume: 13 start-page: 466 year: 2012 ident: 10.1016/S1470-2045(18)30865-9_bib9 article-title: Gefitinib versus placebo as maintenance therapy in patients with locally advanced or metastatic non-small-cell lung cancer (INFORM; C-TONG 0804): a multicentre, double-blind randomised phase 3 trial publication-title: Lancet Oncol doi: 10.1016/S1470-2045(12)70117-1 contributor: fullname: Zhang – volume: 19 start-page: 1338 year: 2018 ident: 10.1016/S1470-2045(18)30865-9_bib10 article-title: Camrelizumab (SHR-1210) alone or in combination with gemcitabine plus cisplatin for nasopharyngeal carcinoma: results from two single-arm, phase 1 trials publication-title: Lancet Oncol doi: 10.1016/S1470-2045(18)30495-9 contributor: fullname: Fang – volume: 12 start-page: 735 year: 2011 ident: 10.1016/S1470-2045(18)30865-9_bib8 article-title: Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study publication-title: Lancet Oncol doi: 10.1016/S1470-2045(11)70184-X contributor: fullname: Zhou – volume: 2 start-page: 1452 year: 2016 ident: 10.1016/S1470-2045(18)30865-9_bib11 article-title: Association of biomarker-based treatment strategies with response rates and progression-free survival in refractory malignant neoplasms: a meta-analysis publication-title: JAMA Oncol doi: 10.1001/jamaoncol.2016.2129 contributor: fullname: Schwaederle – year: 2018 ident: 10.1016/S1470-2045(18)30865-9_bib12 article-title: Trends in the global immuno-oncology landscape publication-title: Nat Rev Drug Discov doi: 10.1038/nrd.2018.167 contributor: fullname: Tang – volume: 15 start-page: 739 year: 2016 ident: 10.1016/S1470-2045(18)30865-9_bib1 article-title: Regulatory watch: innovative drug availability in China publication-title: Nat Rev Drug Discov doi: 10.1038/nrd.2016.200 contributor: fullname: Shao – volume: 16 start-page: 443 year: 2017 ident: 10.1016/S1470-2045(18)30865-9_bib2 article-title: Chinese biopharma starts feeding the global pipeline publication-title: Nat Rev Drug Discov doi: 10.1038/nrd.2017.94 contributor: fullname: Mullard |
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SubjectTerms | Biopharmaceuticals Clinical trials Epidermal growth factor receptors Generic drugs Innovations Metastases Mutation PD-1 protein PD-L1 protein Pharmacovigilance Protein-tyrosine kinase Quality control Regulatory reform Studies |
Title | Challenges in anticancer drug R&D in China |
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