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"Weekly Highlights"
"Weekly Highlights" is a column launched by Siqi Club to summarize the major events in the pharmaceutical industry over the week, covering the latest policy updates, news, pharmaceutical finance, and drug approval progress.
Personnel Changes
HUMAN RESOURCES
Zai Lab President Harald Reinhart Retires
On June 11, Zai Lab announced that Harald Reinhart, President of the company and Global Development Head of the Central Nervous System, Autoimmune and Infectious Diseases (NSAiID) fields, will retire on June 30.
Head of Bayer's Global Biotechnology Departs
According to Fierce Biotech, Jens Vogel, Senior Vice President and Global Head of Biotechnology at Bayer, will leave the company.
Policy Brief
POLICY
2024 National Medical Insurance Catalog Adjustment Launched
On June 13, the National Healthcare Security Administration (NHSA) opened a public consultation on the "2024 Work Plan for Adjusting the National Basic Medical Insurance, Work-related Injury Insurance, and Maternity Insurance Drug Catalog" and related documents. The 2024 adjustment of the medical insurance catalog is imminent.
Pharmaceutical News Updates
PHARMA
Novartis' Capmatinib Approved for Marketing in China
On June 12, Novartis announced the launch of Capmatinib Hydrochloride Tablets (Toreada).®) has been approved by the China National Medical Products Administration (NMPA) for marketing, indicated for adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring MET exon 14 skipping mutations who have not received prior systemic treatment.
Lilly's Alzheimer's Treatment Receives Support from FDA Advisory Committee
On June 11, the Peripheral and Central Nervous System Drugs Advisory Committee (PCNS) of the U.S. FDA voted 11 to 0, unanimously determining that Eli Lilly's Alzheimer's disease (AD) antibody therapy donanemab has benefits that outweigh the risks for treating patients with early symptomatic Alzheimer’s disease. In a simultaneous 11 to 0 vote, the committee also concluded that the data submitted by Eli Lilly demonstrated the drug’s efficacy.
Lilly's New Diabetes Drug Approved for Marketing
On June 12, the latest announcement on the official website of China's National Medical Products Administration (NMPA) showed that the marketing application for the glucagon intranasal powder, a Category 5.1 new drug submitted by Eli Lilly and Company, has been approved.
Pharmaceutical Finance
BUSINESS
Price of Hong Kong Version of Angong Niuhuang Pill Increases by Over 20%, with One Pill Costing Nearly 1200 RMB
Recently, the official website of Beijing Tongrentang Chinese Medicine Co., Ltd. (hereinafter referred to as Tongrentang Chinese Medicine) showed that the price of the Hong Kong version of one-pill Angong Niuhuang Pill is 1,280 Hong Kong dollars (approximately 1,189 yuan), and the price of the six-pill Angong Niuhuang Pill is 7,680 Hong Kong dollars (approximately 7,133 yuan), with each pill weighing 3 grams. Previously, the price of one pill of the Hong Kong version of Beijing Tongrentang's Angong Niuhuang Pill was 1,060 Hong Kong dollars (approximately 985 yuan), which means that the price increase this time exceeds 20%.
The First AI Drug Discovery Stock is Born! XtalPi Successfully Listed
On June 13, XtalPi was officially listed on the Hong Kong Stock Exchange in China. Currently, only Black Sesame Technologies and XtalPi have submitted listing applications under the new "Chapter 18C" regulations. This time, XtalPi has fired the first shot, not only becoming the first AI pharmaceutical stock in China but also the first Specialized Technology stock in Hong Kong.
Over $1.7 Billion! AbbVie Partners with a Chinese Biotech Company
On June 13, AbbVie and Mingji Biopharmaceutical (Beijing) Co., Ltd. announced the signing of a licensing agreement to jointly develop FG-M701.
Under the terms of the agreement, AbbVie will obtain the exclusive global license for the development, manufacturing, and commercialization of FG-M701. MabGenesis will receive $150 million as an upfront payment and near-term milestone payments, and is eligible to receive up to an additional $1.56 billion in clinical development, regulatory registration, and commercialization milestone payments, as well as tiered royalties of up to a low double-digit percentage of net sales.

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