Abnormal Vaginal Bleeding Breast Disorders Female Infertility Genital HPV Candidiasis of Vulva and Vagina
Languages:
English Polish Spanish
Description:
Dr. Foley graduated from the Wayne State University School of Medicine in 2002. She works in Troy, MI and specializes in Obstetrics & Gynecology. Dr. Foley is affiliated with William Beaumont Hospital.
Dr. Foley graduated from the University of Florida College of Medicine at Gainesville in 1997. She works in Naples, FL and specializes in Pediatrics and Adolescent Medicine. Dr. Foley is affiliated with NCH North Naples Hospital.
SriSai PC 7972 W Jefferson Blvd, Fort Wayne, IN 46804 2604592840 (phone), 2604592779 (fax)
Languages:
English Spanish
Description:
Ms. Foley works in Fort Wayne, IN and specializes in Internal Medicine. Ms. Foley is affiliated with Lutheran Hospital Of Indiana, Parkview Hospital Randallia and Saint Vincent Kokomo.
2010 to 2000 Medical AssistantBergen Community Blood Center Paramus, NJ 2008 to 2010 PhlebotomistPulmonary Associates of Northern New Jersey Englewood, NJ 1998 to 2000 Medical Assistant
Education:
The HoHoKus School of Medical Sciences Ramsey, NJ 1998 MedicalParamus High School Paramus, NJ 1992 Diploma
License Records
Jennifer Foley
License #:
3009-S - Expired
Issued Date:
Nov 8, 2000
Expiration Date:
Jun 30, 2002
Type:
Licensed Social Worker
License #:
370P-S - Expired
Issued Date:
Sep 15, 2000
Type:
Licensed Social Worker
Us Patents
Pharmaceutically Acceptable Salts Of 2-{4-[(3)-Piperidin-3-Yl]Phenyl}-2-Indazole-7-Carboxamide
Jennifer R. Foley - Garwood NJ, US Robert Darrin Wilson - Hoddesdon Herts, GB
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07D 211/32 A61K 31/445
US Classification:
546199, 514322
Abstract:
The present invention relates to pharmaceutically acceptable salts of an amide substituted indazole which are inhibitors of the enzyme poly(ADP-ribose)polymerase (PARP), previously known as poly(ADP-ribose)synthase and poly(ADP-ribosyl) transferase. The compounds of the present invention are useful as mono-therapies in tumors with specific defects in DNA-repair pathways and as enhancers of certain DNA-damaging agents such as anticancer agents and radiotherapy. Further, the compounds of the present invention are useful for reducing cell necrosis (in stroke and myocardial infarction), down regulating inflammation and tissue injury, treating retroviral infections and protecting against the toxicity of chemotherapy.
Synthesis And Crystalline Forms Of Melanocortin-4 Receptor Agonist
Alex M. Chen - Edison NJ, US Jennifer R. Foley - Garwood NJ, US John Limanto - Rahway NJ, US Robert M. Wenslow - Cream Ridge NJ, US Karen C. Thompson - Lansdale PA, US Andrey V. Peresypkin - Cambridge MA, US
The present invention relates to a process for producing crystalline N-[1-((3R)-1′-{[(3S,4R)-1-tert-butyl-4-(2,4-difluorophenyl)pyrrolidine-3-yl]carbonyl}-6-chloro-5-methyl-2,3-dihydrospiro[indene-1,4′-piperidine]-3-yl)-1-methylethyl]acetamide, and novel salts, solvates, hydrates and polymorphs thereof.
Paolo Avalle - Hertford, GB Jennifer R. Foley - Garwood NJ, US Peter Mullens - Welwyn Garden City, GB Yaling Wang - Westfield NJ, US Peter Yehl - Cranbury NJ, US
International Classification:
A61K 31/435 C07D 221/16 A61P 35/00
US Classification:
514290, 546 93
Abstract:
This invention relates to salt forms of the compound N-[(2R)-1,4-dioxan-2-ylmethyl]-N-methyl-N′-[3-(1-methyl-H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]sulfamide, an inhibitor of tyrosine kinases, in particular the receptor tyrosine kinase MET, that are useful in the treatment of cellular proliferative diseases, for example cancer, hyperplasias, restenosis, cardiac hypertrophy, immune disorders and inflammation. in particular, the invention relates to the sodium salt of N-[(2R)-1,4-dioxan-2-ylmethyl]-N-methyl-N′-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]sulfamide.
Synthesis And Crystalline Forms Of Cb-1 Antagonist/Inverse Agonist
Kevin R. Campos - Berkeley Heights NJ, US Cheng-Yi Chen - Plainsboro NJ, US Jennifer R. Foley - Garwood NJ, US Michael Hillier - Libertyville IL, US Wendy S. Jen - Fanwood NJ, US Amude M. Kassim - Monmouth Junction NJ, US Artis Klapars - Edison NJ, US Andrey V. Peresypkin - Cambridge MA, US Thorsten Rosner - Berkeley Heights NJ, US Cecile G. Savarin - Newbury Park CA, US Matthew Tudge - Chatham NJ, US Narayan Variankaval - Plainsboro NJ, US Vicky Vydra - Tinton Falls NJ, US Dalian Zhao - Fanwood NJ, US
The present invention relates to a process for producing crystalline 3-[(1S)-1-(1-{(S)-(4-chlorophenyl)[3-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]methyl}azetidin-3-yl)-2-fluoro-2-methyl-propyl]-5-fluorobenzonitrile, and novel salts, solvates, hydrates and polymorphs thereof.