Printer Friendly
The Free Library
14,678,926 articles and books
Member login
User name  
Password 
 
Join us Forgot password?

IDDS to Host Conference Call to Discuss Positive Pivotal Phase II/III Dyloject(TM) Results.


NEW YORK -- Intrac, Inc. (OTC OTC

See: Over-the-counter.


OTC

See over-the-counter market (OTC).
 BB: ITRD ITRD Information Technology Research and Development
ITRD Innovative Treatment Remediation Demonstration (EPA) 
.OB) and its wholly-owned subsidiary Innovative Drug Delivery Systems (IDDS IDDS Institute for Defense and Disarmament Studies
IDDS Integrated Data Distribution System
IDDS Internet Document Distribution System
IDDS Insat Data Distribution System
IDDS Insoft Distributed Directory Server
) will host a conference call on Tuesday, July 26, 2005 beginning at 10:00 AM EDT EDT
abbr.
Eastern Daylight Time


EDT Eastern Daylight Time

EDT n abbr (US) (= Eastern Daylight Time) → hora de verano de Nueva York

EDT 
 to discuss the recently reported pivotal European Phase II/III study of Dyloject(TM) (diclofenac sodium injection). Results from the study demonstrated that Dyloject provided superior pain relief over 4 hours compared to placebo and therapeutic non-inferiority to Voltarol(R). These findings were the primary endpoints necessary to meet requirements for the Marketing Authorization Approval of Dyloject(TM). Additionally, preliminary analysis of the data did not reveal any unexpected safety signals and reported incidents of phlebitis phlebitis (fləbī`tĭs), inflammation of a vein. Phlebitis is almost always accompanied by a blood clot, or thrombus, in the affected vein, a condition known as thrombophlebitis (see thrombosis).  in patients receiving Dyloject were half the rate of Voltarol.

IDDS invites all those interested in hearing management's discussion of the Phase II/III study results to join the call by dialing (877) 407-9210 for domestic participants or (201) 689-8049 for international participants. Participants are asked to call the above numbers 5-10 minutes prior to the starting time.

A telephonic replay of this call will be available until 11:59 PM on Wednesday, July 27, 2005. To hear the replay, please call (877) 660-6853 for domestic participants or (201) 612-7415 for international participants. The account number for the replay is 286 and the conference ID is 162152.

Interested parties can also access a webcast of the conference call through the investor relations section of IDDS' website, www.idds.com. The webcast will be archived for 90 days following the call.

About Dyloject(TM)

Dyloject(TM) is an injectable non-steroidal anti-inflammatory drug Non-steroidal anti-inflammatory drugs, usually abbreviated to NSAIDs, are drugs with analgesic, antipyretic and anti-inflammatory effects - they reduce pain, fever and inflammation.  (NSAID NSAID: see nonsteroidal anti-inflammatory drug. ) that has analgesic, anti-inflammatory and antipyretic antipyretic /an·ti·py·ret·ic/ (-pi-ret´ik)
1. relieving or reducing fever.

2. an agent that so acts.


an·ti·py·ret·ic
n.
An agent that reduces or prevents fever.
 activity. Diclofenac, the same active ingredient in Dyloject(TM), Voltaren(R), Cataflam(R) and Voltarol(R), is a leading analgesic, with a demonstrated history of efficacy and safety since its approval in 1981. Historically, diclofenac has been used to treat pain from inflammatory and degenerative forms of osteoarthritis, musculoskeletal conditions, acute attacks of gout gout, condition that manifests itself as recurrent attacks of acute arthritis, which may become chronic and deforming. It results from deposits of uric acid crystals in connective tissue or joints. , kidney stones, and pain after operations or trauma. Currently, the only injectable form of diclofenac in Europe and other parts of the world is Voltarol(R). However, Voltarol(R) requires either injection into the very large gluteal gluteal /glu·te·al/ (gloo´te-al) pertaining to the buttocks.

glu·te·al
adj.
Of or relating to the buttocks.



gluteal

pertaining to the buttocks.
 muscle, or a slow (30 minutes or longer) infusion that must be freshly prepared for each patient. Voltarol(R) is not available in the United States. Dyloject(TM) is a new IDDS formulation utilizing the same active ingredient as Voltarol(R), but dissolved in a very small volume, stabilized for a long shelf life, and given as a single, brief injection. Worldwide, no comparable formulation of diclofenac has been available previously.

About IDDS

IDDS is a specialty pharmaceutical company, applying innovative proprietary technologies to develop new drugs and improved formulations of existing drugs to target unmet and underserved medical needs in the pain management market. For additional information please visit our website, www.idds.com.

Forward-Looking Statements

This news release contains forward-looking statements. Such statements are valid only as of today, and we disclaim any obligation to update this information. These statements are subject to known and unknown risks and uncertainties that may cause actual future experience and results to differ materially from the statements made. These statements are based on our current beliefs and expectations as to such future outcomes. Drug discovery and development involve a high degree of risk. Factors that might cause such a material difference include, among others, uncertainties related to the ability to attract and retain partners for our technologies, the identification of lead compounds, the successful preclinical development thereof, the completion of clinical trials, the 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.
 review process and other governmental regulation, our ability to obtain working capital, our ability to successfully develop and commercialize drug candidates, and competition from other pharmaceutical companies.
COPYRIGHT 2005 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2005, 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
Date:Jul 25, 2005
Words:617
Previous Article:Aperio Adds Scanner Patent to Growing Portfolio; Company Receives Additional Patent on Use of Line Scanning in Virtual Microscopy.
Next Article:Redland Brick Commences Construction of Expansion in Maryland, an Advisory from Industrialinfo.com.



Related Articles
Pivotal Phase II/III Study Shows Dyloject(TM) Significantly Reduces Moderate-to-Severe Post-Operative Pain.
Final Results of Phase II/III Study Show Dyloject(TM) Has Superior Pain Relief, Faster Onset and Less Thrombophlebitis Compared to Voltarol(R) in...
Javelin Announces Acceptance of Marketing Authorization Application (MAA) for European Regulatory Approval of Dyloject(TM).
Medicure Reports Positive Results From Phase II MEND-CABG Study.
Javelin's Phase 2B Study Successful: Final Analysis Demonstrates Low Doses of Dyloject(TM) Rapidly Relieve Postoperative Pain.
New, Favorable US and EU Assessments of NSAID Safety Bode Well For Javelin's Dyloject(TM).
Javelin Pharmaceuticals To Present Recent Clinical Results of Its Lead Product Dyloject(TM) at UBS Global Life Sciences Conference.
Javelin Pharmaceuticals Reports Third Quarter 2006 Results.
FDA CLEARS BIOMS MEDICAL FOR PHASE III MULTIPLE SCLEROSIS.
Javelin Pharmaceuticals Reports Results for The Year Ended 2006.(Financial report)

Terms of use | Copyright © 2009 Farlex, Inc. | Feedback | For webmasters | Submit articles