BioSpace Collaborative

Academic/Biomedical Research
News & Jobs
Biotechnology and Pharmaceutical Channel Medical Device and Diagnostics Channel Clinical Research Channel BioSpace Collaborative    Job Seekers:  Register | Login          Employers:  Register | Login  

NEWSLETTERS
Free Newsletters
Archive
My Subscriptions

NEWS
News by Subject
News by Disease
News by Date
PLoS
Search News
Post Your News
JoVE

CAREER NETWORK
Job Seeker Login
Most Recent Jobs
Search Jobs
Post Resume
Career Fairs
Career Resources
For Employers

HOTBEDS
Regional News
US & Canada
  Biotech Bay
  Biotech Beach
  Genetown
  Pharm Country
  BioCapital
  BioMidwest
  Bio NC
  BioForest
  Southern Pharm
  BioCanada East
  C2C Services & Suppliers™
Europe
Asia

DIVERSITY

PROFILES
Company Profiles

INTELLIGENCE
Research Store

INDUSTRY EVENTS
Research Events
Post an Event
RESOURCES
Real Estate
Business Opportunities

 News | News By Subject | News by Disease News By Date | Search News
Get Our Industry eNewsletter FREE email:    
   

ZARS Pharma Announces FDA Approval Of A Topical Local Anesthetic Peel


7/7/2006 10:38:25 AM

SALT LAKE CITY, July 6 /PRNewswire-FirstCall/ -- ZARS Pharma announced today that the U.S. Food and Drug Administration (FDA) has approved a topical local anesthetic peel developed under the name of S-Caine(TM) Peel (Lidocaine and Tetracaine) 7%/7% Cream.

The approved product will be used to locally anesthetize intact skin before various superficial dermatological procedures such as dermal filler procedures, pulsed dye laser therapy, facial laser resurfacing, and laser- assisted tattoo removal. The product is indicated for use in adults.

The Lidocaine and Tetracaine 7%/7% Cream is a topical local anesthetic cream that forms a pliable peel on the skin when exposed to air. The approved product is applied for 20-30 minutes prior to procedures such as dermal filler injections or facial laser ablation, and for 60 minutes for procedures such as laser-assisted tattoo removal.

Robert Lippert, President and Chief Executive Office of ZARS Pharma, stated, "We are thrilled with the FDA approval. This product will provide physicians with a new option in reducing patients' pain associated with common cosmetic and aesthetic procedures. I am also very proud of the ZARS organization since this approval represents the second NDA approval in the last 12 months."

In clinical trials, the most common side effects were local skin reactions, such as erythema, blanching and edema. The Lidocaine and Tetracaine 7%/7% Cream should not be used for a duration longer than recommended, and is contraindicated in patients with a known history of sensitivity to lidocaine, tetracaine, or local anesthetics of the amide or ester type. The FDA has not approved a proprietary name yet; a proprietary name will have to receive FDA approval prior to the U.S. launch of the product.

About ZARS Pharma: ZARS Pharma is a specialty pharmaceutical company focused on the development and commercialization of patented technologies that deliver drugs into and across the skin. The Company's primary therapeutic targets are pain management and dermatology. ZARS possesses a rich product pipeline of late-stage products that includes ThermoProfen(TM) and Titragesia(TM). Furthermore the Company will be filing additional INDs within the year.

More information about the Company and its technology can be found on its web site at http://www.zars.com.

Contacts: Gregory S. Ayers

Chief Financial Officer Tel: 801-350-0202

Source: ZARS Pharma


Read at BioSpace.com


   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES
 

//-->