Friday, 20 November 2009

Lansoprazole (Prevacid) ODT tablets: Teva Receives Favorable Court Decision; Innovator appeled in CAFC

Innovator Takeda has appealed against the U.S. District Court for the District of Delaware decision, wherein, court found no infringement by Teva in a patent dispute on Lansoprazole (Prevacid) ODT tablets.

Earlier, generic player Teva Pharma announced (in a press release Here ) that the U.S. District Court for the District of Delaware has issued a decision in its litigation over the Company's Abbreviated New Drug Application (ANDA) to market its generic version of Takeda Pharmaceuticals North America, Inc.'s Prevacid® (Lansoprazole) SoluTab.



The Court found that Teva's generic Lansoprazole orally disintegrating tablets do not infringe the following disputed patent:



US5464632 (Assignee: Laboratoires Prographarm ; Date of Filing: November 29, 1994; Date of expiry: May 7, 2013) The patent covers a rapidly disintegratable tablet for oral administration with or without the use of water, said tablet comprising an active substance and a mixture of excipients, wherein said active substance is multiparticulate and in the form of coated microcrystals, coated microgranules or uncoated microgranules and wherein said mixture of excipients comprises excipients which are responsible for the disintegration, said tablet being intended to be swallowed said disintegration occurring in less than sixty seconds under the action of the excipients which are responsible for the disintegration and which are selected from the group consisting at least one disintegrating agent and at least one swelling agent.



To overcome above claim, Teva used Starlac (a coprocessed excipients with 85% of Lactose and 15% of corn starch). The generic company and innovator provided testimony in the court w.r.t mechanism of disintegration of Starlac, however, opposing party could not prove convincingly that either lactose or corn starch was responsible for the rapid disintegration of generic product. In the light of above findings, court concluded that Teva’s generic version would not be covered under the scope of ‘632 patent.

As per press release, Teva intends to complete an analysis of the decision before deciding upon its next course of action.

Annual sales of the brand product were approximately $500 million in the United States for the twelve months that ended June 30, 2009 based on IMS sales data.

Friday, 13 November 2009

New Paragraph IV certifications reported by USFDA From Oct, 2009 to 5th November, 2009

1) Diclofenac Sodium and Misoprostol (Arthrotec) 50 mg + 0.2 mg DR Tablets : Paragraph IV filed on June 29, 2009

2) Fluvoxamine Maleate 100 mg Capsules (Luvox CR) 5 mg ad 10 mg Tablets: Para IV filed on April 20, 2009

3) Glycopyrrolate (Robinul Forte) 1.5 mg Tablets : Para IV filed on May 6, 2009

4) Vardenafil (Levitra) 5 mg ad 10 mg Tablets: Para IV filed on July 10, 2009

5) Amoxicillin and Clavulanate Potassium (Augmentin XR) 1000 mg + 62.5 mg ER tablets : Para IV filed on Jan 21, 2009

6) Armodafinil (Nuvigil) 50 mg, 150 mg and 250 mg: Para IV filed on July 24, 2009; for the other stregths like 100 mg and 200 mg, Para IV filed on Sep 11, 2009

7) Atazanavir Sulfate (Reyataz) 300 mg Capsules: Para IV filed on July 20, 2009

8) Caspofungin Acetate (Cancidas) 50 mg and 70 mg vial for injection: Para IV filed on June 26, 2009

9) Cisatracurium Besylate (Nimbex) 2 mg/mL, 5 mL vial and 10 mg/mL, 20 mL vial: Para IV filed on Aug 4, 2009; 2 mg/mL, 10 mL vial Para IV filed on Aug 12, 2009

10) Ezetimibe and Simvastatin (Vytorin) 10 mg + 10 mg, 10 mg + 20 mg, 10 mg + 40 mg and 10 mg + 80 mg Tablets: Para IV filed on July 27, 2009

11) Olopatadine Hydrochloride (Patanase) 0.665 mg/Spray (Nasal Spray): Para IV filed on June 29, 2009

12) Metformin Hydrochloride (Glumetza) 500 mg and 1000 mg ER tablets: Para IV filed on July 27, 2009

13) Mometasone Furoate (Nasonex ) 50 mcg/nasal spray: Para IV filed on Aug 7, 2009

14) Morphine Sulfate (Avinza) 45 mg and 75 mg ER capsules: Para IV filed on July 30, 2009

15) Ramelteon 8 mg Tablets (Rozerem): Para IV filed on July 22, 2009

16) Sibutramine Hydrochloride (Meridia) 10 mg and 15 mg: Para IV filed on Aug 14, 2009


17) Tigecycline (Tygacil) For Injection 50 mg per vial: Para IV filed on June 15, 2009

18) Tobramycin (Tobi) 300 mg/5 ml Inhalation Solution: Para IV filed on June 29, 2009

19) Linezolid (Zyvox) 100 mg/5 ml Oral Suspension: Para IV filed on Aug 3, 2009

Source: USFDA Para IV list Here

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Disclaimer: "IP Pharma Doc" blog is published for information purpose only. "IP Pharma Doc" blog contains no legal advice. I assume no legal responsibility for the views/information expressed here. “IP Pharma Doc” blog is my personal website and not edited by my employer, accordingly, no part of my blog should be attributed to my employer. All information on the present blog should be double checked for its accuracy and applicability. © Dr. Sarwal (2007)
 
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