HOME ZACKS RESEARCH FUNDS PORTFOLIO BROKER RESEARCH MARKETS SCREENING EDUCATION SERVICES
Zacks Rank    Equity Research    Premium Home    My Account    Help    
Learn more
Self Investors Wanted Today

Few spots available. Master Zacks' market-tripling Stock Picking Method in your home at our cost.
Opportunity ends Saturday, Nov. 21 >>

Quote:
Login Free Membership
Search:

 
Analyst Blog  

Metozolv ODT Launch on Track

September 29, 2009 | Comments: 0
Recommended this article (1)
SLXP | AZN | WYE | JNJ | SNTS
Print    Share

Salix Pharmaceuticals, Ltd. (SLXP - Analyst Report) is on track to launch a new product, Metozolv ODT (metoclopramide HCl) 5mg and 10mg orally disintegrating tablets, in Nov 2009. Metozolv ODT recently received approval from the U.S. Food and Drug Administration (FDA) for the relief of symptoms in adults associated with acute and recurrent diabetic gastroparesis and for the treatment of short-term therapy (4-12 weeks) for adults with symptomatic documented gastroesophageal reflux disease (GERD) who fail to respond to conventional therapy. Metozolv ODT’s orally disintegrating formulation should make the product more convenient to use especially in the case of patients who have difficulty swallowing or do not have water available when treatment is needed. 

According to the company, gastroparesis is estimated to affect up to five million people in the United States , with females being at a higher risk.

Meanwhile, the GERD market is huge -- it is estimated that approximately one-third of the U.S. population suffer from GERD. The GERD market is dominated by players like AstraZeneca (AZN - Analyst Report), Wyeth (WYE), Johnson & Johnson (JNJ - Analyst Report) and Santarus (SNTS - Analyst Report) among others.

 

The approval of Metozolv ODT is a major positive for Salix which has faced several regulatory setbacks in the recent past. The company first faced a setback in 2008 when the FDA did not grant approval to Salix’s tablet formulation of Colazal (1100mg). Then, earlier this year, the company received a complete response letter from the FDA for Metozolv ODT. In addition to issues regarding the application, the agency asked the company to submit a Risk Evaluation and Mitigation Strategy (REMS) for the candidate. Another candidate, vapreotide acetate, received a disappointing feedback from an FDA advisory panel that voted against approving the product for the treatment of acute esophageal variceal bleeding (EVB).

 
With the pipeline failing to deliver over the past few quarters, the approval of Metozolv ODT should help restore investor confidence in Salix. Metozolv ODT should be available in November 2009. The company intends to promote the product aggressively and has plans to hire a second sales force of 64 sales representatives for the product. We have a Neutral rating on Salix.

Email

Print

Share

RSS

Rate Pos

Rate Neg

Comment
Read/Post Comments (0) | Recommended this article (1)
 Posting Comment...
There was a problem posting this this comment. Please try back later.
[CLICK TO CLOSE X]
Comments (Limit 1000 Characters - Used: 0)
Display Name: Email Address:  
 Loading Comments...
Be the first to comment on this article!
Best Stocks. Best Insight. Join Now...it's FREE!
Over 550,000 investors look forward to the timely insights in our email newsletter; Zacks Profit from the Pros. In each daily issue you will find:
  • Free  Four Zacks #1 Rank "Strong Buy" Stocks
  • Free  Timely Market Commentary
  • Free  Wealth Management Tips
  • Free  Profitable Strategy Screens
  • Free  Bull and Bear Stocks of the Day
Zacks FREE Registration

More Zacks Resources

Market Summary Nov 22, 2009 02:40 am ET
DJIA 10318.16  -14.28 -0.14%
NASD 2146.04  -10.78 -0.50%
S&P 500 1091.38  -3.52 -0.32%
Sponsored Links