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Obetix(Obeticholic)奥贝胆酸国内上市了吗

发布时间:2025-03-16 14:10:04 阅读:1125 来源:问药网
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奥贝胆酸

奥贝胆酸 生产厂家:印度西普拉(Cipla)制药公司 功能主治:治疗原发性胆汁性胆管炎,降低碱性磷酸酶和总胆红素 用法用量:用法用量  (1)成人患者每天服用5mg。  (2)三个月后,若患者ALP或总胆红素没有明显降低,且病人耐受情况尚可,增加剂量至每天口服10mg。
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Obetix(Obeticholic)奥贝胆酸国内上市了吗,Obetix(Obeticholic acid)在2016年5月27日获美国FDA批准上市。随后,2016年12月12日奥贝胆酸(Obeticholicacid)在获欧盟批准上市。目前奥贝胆酸(Obeticholicacid)原研药并未在中国上市。

Obetix (Obeticholic): Has it Been Launched in the Domestic Market?

Answer: As of my knowledge cutoff in September 2021, Obetix (Obeticholic) has not been officially launched in the domestic market in China. However, please note that the pharmaceutical market is dynamic, and there may have been updates since then. It is advisable to refer to the latest information or consult a healthcare professional for the most accurate and up-to-date details.

1. Introduction to Obetix (Obeticholic) and Primary Biliary Cholangitis (PBC)

Obetix, also known as Obeticholic acid, is a medication primarily used in the treatment of primary biliary cholangitis (PBC). PBC is a chronic liver disease characterized by the progressive destruction of small bile ducts in the liver, leading to the accumulation of toxic bile acids. If left untreated, PBC can cause liver damage and, eventually, liver failure. Obetix works by reducing the accumulated bile acids and slowing down the progression of PBC.

2. Global Availability and Approval Status

Obetix obtained approval from the U.S. Food and Drug Administration (FDA) in 2016 and the European Medicines Agency (EMA) in 2017 for the treatment of PBC. It has been commercialized in several countries, including the United States and various European countries. However, the availability and approval status of Obetix can vary from country to country.

3. Regulatory Process and Market Entry Challenges in China

The regulatory process for approving new drugs in China involves multiple stages and stringent requirements. Pharmaceutical companies must undergo clinical trials, submit comprehensive data, and obtain approval from the National Medical Products Administration (NMPA) before a medication can be launched in the domestic market. Additionally, regulatory authorities assess factors such as safety, efficacy, quality, and affordability to ensure patient welfare.

However, the market entry process in China can come with its own set of challenges. Domestically produced drugs and established medications may have a significant presence in the market, making it competitive for new entrants like Obetix. Pharmaceutical companies may need to tailor their drug development and marketing strategies to meet the specific demands and regulations of the Chinese market.

4. Future Prospects and Potential Launch in China

Considering the burden of liver diseases and the increasing awareness of innovative treatments, there is a possibility that Obetix may be launched in the domestic market in the future. Pharmaceutical companies may actively pursue regulatory approval and market entry, considering the potential demand for Obetix among patients with PBC in China. However, it is crucial to track official announcements and regulatory updates for the most accurate information regarding the availability of Obetix in the country.

In conclusion, as of my knowledge cutoff in September 2021, Obetix (Obeticholic) has not been launched in the domestic market in China. However, due to the dynamic nature of the pharmaceutical industry, it is important to refer to the latest information or consult healthcare professionals or official sources to obtain the most accurate and up-to-date details regarding the availability and regulatory status of Obetix in China.