Printer Friendly
The Free Library
19,595,263 articles and books
Member login
User name  
Password 
 
Join us Forgot password?

American Pharmaceutical Partners Adds to Its Broad Oncology Portfolio with the Approval of Mitoxantrone Injection, USP.


SCHAUMBURG, Ill. -- American Pharmaceutical Partners, Inc. (NASDAQ NASDAQ
 in full National Association of Securities Dealers Automated Quotations

U.S. market for over-the-counter securities. Established in 1971 by the National Association of Securities Dealers (NASD), NASDAQ is an automated quotation system that reports on
:APPX APPX Appendix
APPX Application eXcellence (4GL software development tool) 
) (APP), a leading specialty injectable pharmaceutical company, today announced that it has received approval from the U.S. Food and Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) for its Abbreviated New Drug Application abbreviated new drug application Pharmacology An application made in the US by a pharmaceutical company requesting authority to market a 'new' drug for which both its therapeutic indications and formulation were previously approved by the FDA in another similar  (ANDA) for Mitoxantrone Injection, USP USP - unique sales point  (Concentrate), the generic equivalent of Serono Labs' Novantrone(R). According to IMS (1) See IP Multimedia Subsystem.

(2) (Information Management System) An early IBM hierarchical DBMS for IBM mainframes. IMS was widely implemented throughout the 1970s under MVS and continues to be used under z/OS.
, sales in 2005 of mitoxantrone in the United States exceeded $76 million. APP expects to commence marketing mitoxantrone immediately. APP will sell mitoxantrone in AP-rated bar coded, latex-free vials with TALL man lettering.

Mitoxantrone Injection, USP in combination with corticosteroids is indicated as initial chemotherapy for the treatment of patients with pain related to advanced hormone-refractory prostate cancer. Mitoxantrone Injection, USP in combination with other approved drug(s) is indicated in the initial therapy of acute nonlymphocytic leukemia acute non·lym·pho·cyt·ic leukemia
n.
See acute myelogenous leukemia.
 (ANLL ANLL Acute nonlymphocytic leukemia ) in adults. This category includes myelogenous, promyelocytic, monocytic, and erythroid erythroid /er·y·throid/ (er´i-throid)
1. of a red color; reddish.

2. pertaining to the cells of the erythrocytic series.


er·y·throid
adj.
1.
 acute leukemias.

This approval increases APP's oncology product offerings to seventeen and brings the total number of FDA approvals received by APP this year to eight. APP markets and manufactures one of the broadest portfolios of oncology products and, combined with the 23 ANDA's currently under review by the FDA, is positioned to be one of the largest manufacturers of injectable pharmaceutical products for the critically ill patient.

About American Pharmaceutical Partners, Inc.

American Pharmaceutical Partners, Inc. is a specialty drug company that develops, manufactures and markets injectable pharmaceutical products, focusing on the oncology, anti-infective and critical care markets. Abraxis(TM) Oncology, the proprietary division of APP, is devoted entirely to developing and promoting innovative, next-generation cancer therapies such as ABRAXANE(R) for Injectable Suspension (paclitaxel protein-bound particles for injectable suspension) (albumin-bound). At the close of the merger between American Pharmaceutical Partners (APP) and American BioScience (ABI Abi (ā`bī) [short for Abijah], in the Bible, King Hezekiah's mother.


(Application Binary Interface) A specification for a specific hardware platform combined with the operating system.
) in the second quarter of this year, APP will become a division of Abraxis BioScience, a fully integrated global biopharmaceutical company. For more information, visit APP's website at www.appdrugs.com and www.abraxisoncology.com.

FORWARD-LOOKING STATEMENT

The statements contained in this press release that are not purely historical are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements, whether expressed or implied, involve risks and uncertainties, There are important factors that could cause actual results to differ materially from those in the forward-looking statements. These factors include, without limitation, successfully commercializing mitoxantrone, the difficulty in predicting the timing or outcome of other product research and development efforts, potential product characteristics and indications, marketing approvals and launches of other products, the impact of pharmaceutical industry regulation, the impact of competitive products and pricing, the availability and pricing of ingredients used in the manufacture of pharmaceutical products, the ability to successfully manufacture products in a time-sensitive and cost effective manner, the acceptance and demand of new pharmaceutical products, the impact of patents and other proprietary rights held by competitors and other third parties. Additional relevant information concerning risks can be found in APP's Form 10-K for the year ended December 31, 2005, APP's information statement filed on March 13, 2006 and other documents it has filed with the Securities and Exchange Commission.

NOVANTRONE(R) is a registered trademark of Immunex Corporation. This product is now marketed by Serono, Inc.
COPYRIGHT 2006 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2006, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

 Reader Opinion

Title:

Comment:



 

Article Details
Printer friendly Cite/link Email Feedback
Publication:Business Wire
Geographic Code:1USA
Date:Apr 11, 2006
Words:538
Previous Article:RailAmerica Reports March Carloads.
Next Article:American Pacific Financial Corporation Acquires US Plastic Lumber, Inc. Assets Forms Trimax Building Products, Inc.
Topics:



Related Articles
Bigmar, Inc. receives IKS approval for pharmaceutical manufacturing at new Swiss plant.
Bigmar, Inc. Receives Suitability Petition Approval From FDA to File ANDA for Methotrexate for Injection, 500 Mg.
BIGMAR Receives FDA Approval for Fluorouracil Injection; Sixth ANDA Approval in 1999.
OSI Reiterates Confidence in Tarceva.
FDA Approves Tarceva(R) in Combination with Gemcitabine Chemotherapy for Treatment of Locally Advanced, Inoperable or Metastatic Pancreatic Cancer;...
Teva Announces Tentative Approval of Ondansetron Injection USP.
Teva Announces Approval of Mitoxantrone Hydrochloride Injection USP.
FDA APPROVES TEVA'S ANDA TO MARKET GENERIC VERSION OF ZOCOR.
Study Showed Significant and Sustained Efficacy Of COPAXONE(R) Alone Following Short-Term Combination Therapy With IV Steroids in Multiple Sclerosis...

Terms of use | Copyright © 2012 Farlex, Inc. | Feedback | For webmasters | Submit articles