IntelliPharmaCeutics

IntelliPharmaCeutics International Inc.
Type Public
(
Traded as TSXI NASDAQIPCI
Industry Biotechnology
Pharmaceutical
Founded 1998
Founder(s) Isa Odidi, Amina Odidi
Headquarters Toronto, Ontario, Canada
Area served North America
Products Medicine
Drugs
Controlled Release Drugs
Website www.intellipharmaceutics.com

IntelliPharmaCeutics (TSXI) is a Canadian specialty pharmaceutical company, operating internationally and primarily engaged in the research, development, and commercialization of controlled-release and targeted pharmaceutical products.

Contents

Disclosed product pipeline

Focalin XR

Dexmethylphenidate XR is a generic version of the marketed drug Focalin XR, which is partnered with Par Pharmaceutical (5, 10, 15, 20 mg strengths) and is currently the subject of an Abbreviated New Drug Application (ANDA) filing with the U.S. Food and Drug Administration (FDA).

Focalin XR is an extended-release formulation of dexmethylphenidate and is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in patients aged 6 years and older. ADHD is one of the most common childhood disorders and can continue through adolescence and adulthood.

In December 2010, IntelliPharmaCeutics filed an ANDA with the U.S. FDA for approval to market a generic of the 30 mg strength of Focalin XR.[1]

Venladaxine XR/Effexor XR

Venlafaxine XR is a generic version of the marketed drug Effexor XR. This product is currently the subject of an Abbreviated New Drug Application (ANDA) filing with the U.S. FDA.[2]

Effexor XR is an extended-release capsule for oral administration that contains venlafaxine hydrochloride. It is indicated for the treatment of symptoms of major depressive disorder, generalized anxiety disorder, social anxiety disorder, and panic disorder.

Pantoprozole XR/Protonix XR

IntelliPharmaCeutics' Pantoprozole XR is a delayed release pantoprazole sodium, a generic version of the marketed drug Protonix. This product is currently the subject of an Abbreviated New Drug Application (ANDA) filing with the U.S. FDA.

Protonix is a delayed-release capsule for oral administration that contains pantoprazole sodium. Protonix inhibits gastric acid secretion and is prescribed for the short-term treatment of conditions such as stomach ulcers associated with gastroesophageal reflux disease as well as the long term treatment of pathological hypersecretory conditions including Zollinger-Ellison syndrome.[2]

Rexista

Rexista is one of IntelliPharmaCeutics non-generic development products. It is an abuse- and alcohol-resistant, controlled-release oral oxycodone formulation. This product is covered by pending patent applications. Rexista is a unique dosage form, designed to be resistant to well-documented abuse that is experienced with current oxycodone products. This includes abuse by injection when combined with solvents and by nasal inhalation when crushed or powdered.[3] Rexista is also designed to resist release of the entire dose when consumed with alcohol, a significant problem with some opioid drugs, such as hydromorphone.[4]

The pilot clinical trial produced the following results:[5]

References

  1. ^ "Intellipharmaceutics Files ANDA with FDA " - BioTuesday.ca [1]
  2. ^ a b "Reuters Finance". Reuters.com. http://www.reuters.com/finance/stocks/keyDevelopments?symbol=IPCI.O. Retrieved 2010-12-13. 
  3. ^ "Rexista". Intellipharmaceutics.com. http://www.intellipharmaceutics.com/oxycodone.cfm. Retrieved 2010-12-13. 
  4. ^ "FDA on Opioids". Capc.org. http://www.capc.org/fda-opioids. Retrieved 2010-12-13. 
  5. ^ "Press Release, May 20, 2010". Intellipharmaceutics.com. http://www.intellipharmaceutics.com/releasedetail.cfm?ReleaseID=472169. Retrieved 2010-12-13. 

External links