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美国FDA第三个胰酶药物Pancreaze获批上市

2010-04-25 16:46:06  作者:新特药房  来源:互联网  浏览次数:109  文字大小:【】【】【
简介: 4月12日,美国食品药品监督管理局批准了Johnson & Johnson公司的胰酶药物Pancreaze缓释胶囊上市。这也是第三个获得FDA批准的该类药物,其活性组分为胰脂肪酶。 胰酶药物可帮助胰美产生不足而引起的消化 ...

4月12日,美国食品药品监督管理局批准了Johnson & Johnson公司的胰酶药物Pancreaze缓释胶囊上市。这也是第三个获得FDA批准的该类药物,其活性组分为胰脂肪酶。

胰酶药物可帮助胰美产生不足而引起的消化不良,比如囊胞性纤维症、慢性胰腺炎、胰腺肿瘤、全部或部分胰腺切除等。这之前,FDA批准上市的胰酶类药物有Abbott Products公司的Creon,和Eurand Pharmaceuticals公司的的Zenpep。Pancreaze的上市为美国20多万患者提供了满足FDA标准的安全、有效并且有品质保证的胰酶药物新选择.
FDA Approves Pancreatic Enzyme Product, Pancreaze

The U.S. Food and Drug Administration today approved Pancreaze Delayed Release Capsules, a pancreatic enzyme product (PEP). It is the third such product to receive FDA approval.

Pancreatic enzyme products improve food digestion in patients whose bodies do not produce enough pancreatic enzymes. This includes people who have conditions such as cystic fibrosis, chronic pancreatitis, pancreatic tumors, or removal of all or a part of the pancreas.

Until today, Creon, manufactured by Abbott Products, Inc. (formerly Solvay Pharmaceuticals), and Zenpep, manufactured by Eurand Pharmaceuticals, were the only FDA-approved pancreatic enzyme products on the market.

Today’s approval of Pancreaze, manufactured by Johnson & Johnson, increases the supply of FDA-approved PEPs for the estimated 200,000 or more patients in the United States who need these products. Approved pancreatic enzyme products meet FDA standards for safety, efficacy, and product quality.

“The approval of Pancreaze, along with Creon and Zenpep, allows patients and healthcare professionals to choose the approved pancreatic enzyme product that is appropriate for them,” said Donna Griebel, M.D., director of the FDA’s Division of Gastroenterology Products.

Unapproved versions of pancreatic enzyme products have been available for many years. In October 2007, FDA established a date of April 28, 2010 for the makers of unapproved pancreatic enzyme products to stop manufacturing and distributing unapproved products. Supplies of approved PEPs are expected to meet demand.

Currently, the FDA is working with approved PEPs manufacturers, patient advocacy groups, and health care professional organizations to make the public aware of the availability of pancreatic enzyme products. Patients with questions about their current PEP or making a switch to a different pancreatic enzyme product should consult with their healthcare provider.

For more information:

Questions and Answers for Healthcare Professionals and the Public: Switching to an Approved Pancreatic Enzyme Product (PEP)


 

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