- Watertown MA, US Neal Green - Newton MA, US Gary Gustafson - Ridgefield CT, US Gary Marshall - Watertown MA, US Lorna Mitchell - Cambridge, NZ David Richard - Littleton MA, US Zhongguo Wang - Lexington MA, US Sanjeev Forsyth - Milton MA, US Patrick F. Kelly - Concord MA, US Madhu Mondal - Winchester MA, US Maria Ribadeneira - Cambridge MA, US Patricia Schroeder - Somerville MA, US
International Classification:
A61K 31/436 A61P 9/00
Abstract:
The compound (S)-1-(5-((2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-7-yl)sulfonyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-3-hydroxy-2-phenylpropan-1-one, or a pharmaceutically acceptable salt thereof, is useful to increase the affinity of hemoglobin for oxygen. Methods and compositions for the treatment of a hemoglobinopathies are provided herein, including certain pharmaceutical compositions for activating PKR.
Treating Sickle Cell Disease With A Pyruvate Kinase R Activating Compound
- Watertown MA, US Neal GREEN - Newton MA, US Gary GUSTAFSON - Ridgefield CT, US Gary MARSHALL - Watertown MA, US Lorna MITCHELL - West Beach, AU David RICHARD - Littleton MA, US Zhongguo WANG - Lexington MA, US Sanjeev FORSYTH - Milton MA, US Patrick F. KELLY - Concord MA, US Madhu MONDAL - Winchester MA, US Maria RIBADENEIRA - Cambridge MA, US Patricia SCHROEDER - Somerville MA, US
International Classification:
A61K 31/436 A61P 7/06 A61K 9/00
Abstract:
Compounds that activate pyruvate kinase R can be used for the treatment of sickle cell disease (SCD). Methods and compositions for the treatment of SCD are provided herein, including a therapeutic compound designated as Compound 1.
- Cambridge MA, US Thomas Wai-Ho Lee - Lexington MA, US Rajesh R. Iyengar - West Newton MA, US Nicholas Robert Perl - Somerville MA, US Peter Germano - Newton MA, US Maria D. Ribadeneira - Cambridge MA, US Kim Tang - Belmont MA, US
The present disclosure relates to the use of stimulators of soluble guanylate cyclase (sGC), pharmaceutically acceptable salts thereof and pharmaceutical formulations or dosage forms comprising them, alone or in combination with one or more additional agents, for the treatment of various CNS diseases, wherein an increase in sGC stimulation, or an increase in the concentration of nitric oxide (NO), or cyclic guanosine 3′,5′-monophosphate (cGMP) or both, or an upregulation of the NO pathway is desirable.
Resumes
Executive Director Of Dmpk And Clinical Pharmacology
Forma Therapeutics, Inc.
Executive Director of Dmpk and Clinical Pharmacology
Ironwood Pharmaceuticals
Director Dmpk
Boehringer Ingelheim Sep 2010 - Mar 2013
Associate Director
Astrazeneca 2001 - 2010
Principal Scientist Ii
Education:
Georgia State University 1994
Doctorates, Doctor of Philosophy, Physiology, Philosophy
George Brown College
Skills:
Drug Discovery Pharmaceutical Industry Adme Dmpk Drug Development Drug Metabolism In Vitro Pharmacology Pharmacokinetics Clinical Development Assay Development Biotechnology Lc Ms Bioanalysis Biomarkers In Vivo Medicinal Chemistry Hplc Ind High Throughput Screening Drug Design Glp Cell Culture Cro Pharmaceutical Research Pharmacodynamics Lifesciences
Reade Street Prep
Head Spanish Teacher
Green Ivy Schools Jul 2015 - Jun 2016
Spanish Preschool Teacher
New York Kids Club Jul 2015 - Jun 2016
Spanish Teacher
The Green Beetle Mar 2010 - Jan 2011
Account Manager
Geoscape Sep 2007 - Feb 2010
Client Solutions Specialist
Education:
Universidad Católica Boliviana 1996 - 2000
Skills:
Marketing Strategy Marketing Research Account Management Social Media Marketing Marketing Communications Market Research Advertising Direct Marketing Marketing Strategy Online Advertising Digital Marketing Social Media Competitive Analysis
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