Astex Pharmaceuticals
Lab Operations Manager
Protagonist Therapeutics Dec 2016 - Dec 2017
Consultant, Formulation Development
Nvs Technologies 2011 - Apr 2015
Research Scientist
Alza Corporation Jan 2004 - Dec 2008
Senior Research Associate Scientist
Alza Corporation Jan 2002 - Jan 2004
Chemist Iii
Education:
The National Hispanic University 2010 - 2011
Notre Dame De Namur University 1991 - 1995
Bachelors, Bachelor of Science, Biology
Skills:
Gmp Formulation Biotechnology Pharmaceutical Industry Fda Glp Sop Drug Delivery Drug Development Medical Devices Pharmaceutics Validation R&D
Alza Corporation Mountain View, CA Feb 1996 to Dec 2008 Senior Associate ScientistOral Product FormulationProcess DevelopmentCommunication and Coordination in cGMP EnvironmentLeadership and Administration
Education:
UCSC Extension Cupertino, CA Jan 2008 to Jan 2009 Certificate in Program and Project ManagementNotre Dame de Namur University Belmont, CA 1995 B.S. in Biology
Us Patents
Uniform Delivery Of Topiramate Over Prolonged Period Of Time With Enhanced Dispersion Formulation
Iran Reyes - San Jose CA, US Noymi Yam - Sunnyvale CA, US Padmaja Shivanand - Los Altos CA, US Shaoling Li - Sunnyvale CA, US Patrick Wong - Burlingame CA, US
International Classification:
A61K009/22 A61K009/24
US Classification:
424468000
Abstract:
Compositions and dosage forms for enhanced dispersion of topiramate in a controlled release dosage form delivered as a dry or substantially dry erodible solid at a uniform rate over a prolonged period of time are described.
Methods And Dosage Forms For Reducing Side Effects Of Benzisozazole Derivatives
Gayatri Sathyan - San Jose CA, US Suneel Gupta - Sunnyvale CA, US Noymi Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US Sonya Seroff - San Jose CA, US
International Classification:
A61K031/42 A61K009/22
US Classification:
424468000, 514379000
Abstract:
Disclosed are dosage forms and methods comprising benzisoxazole derivatives. More particularly, disclosed are dosage forms, methods, and new uses of benzisoxazole derivatives that substantially reduce or substantially eliminate certain side effects of the benzisoxazole derivatives when dosed to a patient.
Methods And Dosage Forms For Controlled Delivery Of Paliperidone And Risperidone
Nyomi Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US Sonya Seroff - San Jose CA, US Suneel Gupta - Sunnyvale CA, US Gayatri Sathyan - San Jose CA, US
International Classification:
A61K031/519 A61K009/24
US Classification:
424473000, 514259410
Abstract:
Dosage forms and methods for providing a substantially ascending rate of release of paliperidone or risperidone are provided. The sustained release dosage forms provide therapeutically effective average steady-state plasma paliperidone or risperidone concentrations when administered once per day. This once-a-day dosing regimen results in only one peak plasma paliperidone or risperidone concentration occurrence in each 24 hour period. In addition, the peak plasma paliperidone or risperidone concentration occurs at a later time following dose administration and exhibits a lesser magnitude than the peak plasma paliperidone or risperidone concentration that occurs following administration of paliperidone or risperidone in an immediate-release dosage form.
Osmotic Dosage Form With Controlled Release And Fast Release Aspects
Iran Reyes - San Jose CA, US Julie Lee - Sunnyvale CA, US Brian Barclay - Sunnyvale CA, US Iswadi Liejanto - Redwood City CA, US Nipun Davar - Fremont CA, US
International Classification:
A61K 9/24
US Classification:
424473000
Abstract:
Disclosed are osmotic dosage forms and methods that provide for fast release of drugs together with controlled release of drugs. In an aspect, disclosed are osmotic dosage forms including: a semi-permeable membrane; a lubricating subcoat located within the semi-permeable membrane; an orifice in the semi-permeable membrane located at an end of the semi-permeable membrane; a drug layer located adjacent to the orifice and within the lubricating subcoat; a push layer located within the lubricating subcoat and on a side of the drug layer opposite from the orifice; wherein an area of the orifice is greater than or equal to about 1,600 mil; and wherein the drug layer comprises from about 20 wt % to about 90 wt % microcrystalline cellulose, and less than or equal to about 10 wt % of a drug, based on the total weight of the drug layer. Also disclosed are methods of making osmotic dosage forms.
Methods And Dosage Forms For Controlled Delivery Of Paliperidone And Risperidone
Nyomi V. Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul D. Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US Sonya Seroff - San Jose CA, US Suneel K. Gupta - Sunnyvale CA, US Gayatri Sathyan - San Jose CA, US
International Classification:
A61K 31/519 A61K 9/20
US Classification:
424464, 51425941
Abstract:
Dosage forms and methods for providing a substantially ascending rate of release of paliperidone or risperidone are provided. The sustained release dosage forms provide therapeutically effective average steady-state plasma paliperidone or risperidone concentrations when administered once per day. This once-a-day dosing regimen results in only one peak plasma paliperidone or risperidone concentration occurrence in each 24 hour period. In addition, the peak plasma paliperidone or risperidone concentration occurs at a later time following dose administration and exhibits a lesser magnitude than the peak plasma paliperidone or risperidone concentration that occurs following administration of paliperidone or risperidone in an immediate-release dosage form.
Methods And Dosage Forms For Reducing Side Effects Of Benzisozazole Derivatives
Gayatri Sathyan - San Jose CA, US Suneel Gupta - Sunnyvale CA, US Noymi V. Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul D. Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US Sonya Seroff - San Jose CA, US
International Classification:
A61K 31/519 A61P 25/18
US Classification:
51425941
Abstract:
Disclosed are dosage forms and methods comprising benzisoxazole derivatives. More particularly, disclosed are dosage forms, methods, and new uses of benzisoxazole derivatives that substantially reduce or substantially eliminate certain side effects of the benzisoxazole derivatives when dosed to a patient.
Methods And Dosage Forms For Reducing Side Effects Of Benzisozazole Derivatives
Gayatri Sathyan - San Jose CA, US Suneel Gupta - Sunnyvale CA, US Noymi V. Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul D. Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US Sonya Seroff - San Jose CA, US
International Classification:
A61K 31/519 A61P 25/18
US Classification:
51425941
Abstract:
Disclosed are dosage forms and methods comprising benzisoxazole derivatives. More particularly, disclosed are dosage forms, methods, and new uses of benzisoxazole derivatives that substantially reduce or substantially eliminate certain side effects of the benzisoxazole derivatives when dosed to a patient.
Methods And Dosage Forms For Controlled Delivery Of Paliperidone
Nyomi Yam - Sunnyvale CA, US Iran Reyes - San Jose CA, US Nipun Davar - Fremont CA, US Atul Ayer - Palo Alto CA, US Julie Lee - Sunnyvale CA, US
International Classification:
A61K031/519
US Classification:
514/259410
Abstract:
Dosage forms and methods for providing a substantially ascending rate of release of paliperidone are provided. The sustained release dosage forms provide therapeutically effective average steady-state plasma paliperidone concentrations when administered once per day. This once-a-day dosing regimen results in only one peak plasma paliperidone concentration occurrence in each 24 hour period. In addition, the peak plasma paliperidone concentration occurs at a later time following dose administration and exhibits a lesser magnitude than the peak plasma paliperidone concentration that occurs following administration of paliperidone in an immediate-release dosage form.
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