Gilead's second HIV pre exposure prophylaxis (PrEP) medication has been approved for marketing
JESUS60
发表于 2024-1-8 20:29:13
1279
0
0
On January 8th, according to the official WeChat account of Geely Technology, DaKeWei& Reg; Enqutabine Propenofovir Tablets (II), Enqutabine 200mg/Propenofovir 25mg, F/TAF) have been approved by the National Medical Products Administration (NMPA) for pre exposure prophylaxis (PrEP) for adults and adolescents at least 35kg in weight at risk of human immunodeficiency virus type 1 (HIV-1) infection, to reduce the risk of HIV-1 infection due to high-risk sexual behavior. Previously, Gilead Entratabine Propenofovir Tablets had been approved in China for use in combination with other antiretroviral drugs in the treatment of HIV-1 infections in adults and adolescents (aged 12 years and above and weighing at least 35kg).
Pre exposure prevention refers to the use of specific antiviral drugs by individuals who have not yet been infected with HIV before engaging in behaviors that are susceptible to HIV infection, in order to prevent HIV infection. It is an important biomedical measure for HIV prevention. In August 2020, Gilead Scientific Enqutabine Tenofovir tablets were approved, becoming the first drug in China approved for pre exposure prevention of HIV in uninfected populations.
At present, sexual transmission has become the main route of HIV transmission in China. More than 95% of newly diagnosed HIV infected individuals in our country are infected through sexual means, and unsafe sexual behavior is the main cause of HIV sexual transmission. Unsafe sexual behaviors with a high risk of HIV infection include unprotected male same-sex sex, non fixed sexual partners, and paid sex.
CandyLake.com 系信息发布平台,仅提供信息存储空间服务。
声明:该文观点仅代表作者本人,本文不代表CandyLake.com立场,且不构成建议,请谨慎对待。
声明:该文观点仅代表作者本人,本文不代表CandyLake.com立场,且不构成建议,请谨慎对待。
猜你喜欢
- Eli Lilly and Predator Peptide Approved for Long term Weight Management Indications in China
- Tesla Musk: Expected FSD to be approved and implemented in China before the end of the year
- The Class 1 new drug introduced by Anjin with over 1 billion US dollars has been approved for clinical use
- JD Allianz Equity Transfer Approved: Allianz Insurance Group to Transfer 53.33% Equity of the Company to Allianz China Holdings
- Sanofi: Targeted therapy drug for chronic obstructive pulmonary disease (COPD), Dabitou, approved in China
- Intel Technology is expected to complete $8.5 billion in financing by the end of the year; A total of 109 domestic online games were approved in September
- Johnson&Johnson's drug Zebaike has been approved in China
- Lilly's Alzheimer's disease drug Kisunla approved for sale in the UK
- Lilly's Alzheimer's disease drug Kisunla approved for sale in the UK
- The third quarter reports of Geely and Jike have been released! What are the reasons for the integration of internal resources or the acquisition of controlling stakes?
-
南方財経は11月12日、百済神州が2024年第3四半期の報告書を発表し、同社の第3四半期の営業収入は71.39億元で、前年同期比26.9%増加した。上場企業の株主に帰属する純利益は-8.09億元で、主に前年同期に百時米施貴宝 ...
- 1900_后
- 3 天前
- 支持
- 反对
- 回复
- 收藏
-
北京商報(何倩記者)は11月14日、「チャトンと野菜を買ってサウジに出航した」との情報に対し、チャトンと野菜を買った関係責任者は北京商報記者に対し、関連業務はまだ初歩的な模索にすぎず、しばらく詳細な情報 ...
- 柔柔树呆熊呆j
- 昨天 16:39
- 支持
- 反对
- 回复
- 收藏
-
黄仁勲が最新発表! 11月13日、英偉達の黄仁勲CEOは英偉達日本サミットで、日本最大のAI工場を含むソフトバンクと協力して日本にAIインフラを構築すると発表した。ソフトバンクの孫正義元会長兼社長は、「ソフトバ ...
- tomy123123
- 前天 14:57
- 支持
- 反对
- 回复
- 收藏
-
【世界市場】1、ダウは0.11%、スタンダードは0.02%、ナノ指は0.26%下落した。2、大型科学技術株の多くが上昇し、アマゾンは2%超上昇し、株価は過去最高を記録した。3、国際金価格は4日連続で下落し、2600ドルの関門 ...
- 就放荡不羁就h
- 昨天 14:54
- 支持
- 反对
- 回复
- 收藏