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BioWorld - Wednesday, January 21, 2026
Home » Topics » Regulatory » NMPA

NMPA
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Tislelizumab approved in China for first-line advanced squamous NSCLC

Jan. 14, 2021

Phase III trial of sacituzumab govitecan in metastatic urothelial cancer cleared to begin in China

Jan. 7, 2021

Chi-Med wins China approval for first in-house oncology drug

Jan. 5, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs).
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Sinopharm CNBG's COVID-19 vaccine approved in China

Jan. 5, 2021

Chi-Med wins China approval for first in-house oncology drug

Jan. 4, 2021
By David Ho
HONG KONG – Hutchison China Meditech Ltd. (Chi-Med) earned approval from China’s National Medical Products Administration (NMPA) for Sulanda (surufatinib) for the treatment of non-pancreatic neuroendocrine tumors (NETs), marking what CEO Christian Hogg called a “major milestone” as the first drug to be discovered and developed by Chi-Med without the support of a development partner.
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Sulanda approved in China for non-pancreatic NETs

Dec. 31, 2020

Arctic Vision obtains IND approval for ARVN-001 in China

Dec. 28, 2020

Byvasda approved in China the treatment of recurrent glioblastoma

Dec. 28, 2020

Orelabrutinib approved in China for two cancer indications

Dec. 28, 2020

Chinese clearance for phase III trial of APL-1202 for first-line nonmuscle invasive bladder cancer

Nov. 5, 2020
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