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IntelGenx Technologies Corp. (IGXT)

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  • Dec. 1, 2014, 8:43 AM
    • The German Federal Institute for Drugs and Medical Devices has validated the European Marketing Authorization Application (MAA) from RedHill Biopharma Ltd. (NASDAQ:RDHL) and IntelGenx Corp. (OTCQX:IGXT) for Rizaport, an oral thin film formulation of rizatriptan, for the treatment of acute migraines. The German regulator's formal review of the application is now underway with feedback expected in 2H 2015.
    • The MAA was submitted under the European Mutual Recognition Procedure with Germay as the reference member state and Luxemburg as the concerned member state.
    • The companies submitted an NDA to the FDA in March 2013 but are still working on the issues cited in a Complete Response Letter (CRL) received in February 2014.
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  • Nov. 19, 2014, 7:45 AM
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  • Nov. 12, 2014, 10:19 AM
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  • Oct. 1, 2014, 11:31 AM
    • RedHill Biopharma (RDHL -1.6%) and IntelGenx (OTCQX:IGXT -3%) submit a Marketing Authorization Application to the German Federal Institute for Drugs and Medical Devices seeking European marketing clearance for RHB-103, an oral thin film formulation of rizatriptan for the treatment of acute migraines, under the brand name Rizaport.
    • Rizatriptan benzoate is a 5-HT1 receptor agonist. It is the active drug in Merck's Maxalt. Rizaport utilizes IntelGenx's VersaFilm technology.
    • The MAA was submitted under the European Mutual Recognition Procedure with Germany as the reference member state.
    • The companies submitted an NDA to the FDA in March 2013. The agency responded with a CRL in February 2014 raising questions about chemistry, manufacturing and controls. The firms' efforts to address the issues are ongoing.
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  • Sep. 18, 2014, 12:25 PM
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  • Jul. 18, 2014, 1:09 PM
    • IntelGenx (OTCQX:IGXT +6.5%) CEO Dr. Horst G. Zerbe will host a conference call on July 23, 2014 at 10:00 am EDT to update investors on its business and recent management changes.
    • The FDA sent the firm a CRL in February stating that it could not approve VersaFilm due to issues pertaining to third party manufacturing, packaging and labeling.
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  • Feb. 4, 2014, 8:44 AM
    • The FDA has told IntelGenx (IGXT) and RedHill Biopharma (RDHL -2.8%) that it won't yet approve their VersaFilm oral film treatment for acute migraines, due to issues over third party manufacturing, packaging and labeling.
    • However, in a complete response letter, the FDA said it accepted the bioequivalence study and safety information submitted, and that it requires no additional studies.
    • IntelGenx and RedHill intend to address the FDA's concerns within weeks, and to advance discussion with potential partners for the commercialization of VersaFilm.
    • In addition to seeking FDA approval for the product, IntelGenx and RedHill intend to file for European authorization later this year. (PR)
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Company Description
IntelGenx, through its cutting edge formulation platforms, has developed a broad and diverse product portfolio, including products for the treatment of indications such as severe depression, hypertension, erectile dysfunction, migraine, insomnia, CNS indications, idiopathic pulmonary fibrosis,... More
Sector: Services
Country: Canada