Patrick Englebienne - Zingem, BE Kenny De Meirleir - Mechelen, BE Charles Vincent Herst - Oakland CA, US
Assignee:
R.E.D. Laboratories N.V. - Zellik
International Classification:
A61K 49/00
US Classification:
424 91
Abstract:
Methods are provided for diagnosing and/or characterizing disease involving abnormal levels of cellular apoptosis activity in a subject. In the subject methods, a sample is obtained from a subject suspected of having or known to have a disease involving abnormal levels of cellular apoptosis. The sample is then assayed for the presence of low molecular weight Actin protein fragments. The assay results are used to diagnose the presence of disease involving abnormal levels of cellular apoptosis activity and/or characterize disease involving abnormal levels of cellular apoptosis activity in the subject, e. g. to confirm an initial disease involving abnormal levels of cellular apoptosis diagnosis, to determine the stage of the disease, to monitor disease progression, to predict disease attacks, and the like. Also provided by the subject invention are kits for practicing the methods.
Karim El Bakkouri - Anderlecht, BE Patrick Englebienne - Zingem, BE Kenny De Meirleir - Mechelen, BE Charles Vincent Herst - Oakland CA, US
Assignee:
R.E.D. Laboratories, N.V./S.A. - Zellik
International Classification:
A61K 31/545
US Classification:
514206, 514200, 514202, 514203, 514204
Abstract:
Methods for treating a host suffering from a chronic immune disease, e. g. , MS or CFS, are provided. In practicing the subject methods, an effective amount of an elastase inhibitory agent, e. g. , a β-lactam containing compound, is administered to the host. Also provided are compositions for use in practicing the subject methods.
Diagnostic Method For Chronic Fatigue Syndrome By Measuring Elastase
Patrick Englebienne - Zingem, BE Kenny De Meirleir - Mechelen, BE Charles Vincent Herst - Oakland CA, US
Assignee:
R.E.D. Laboratories, N.V. - Zellik
International Classification:
C12Q 1/34
US Classification:
435 18
Abstract:
The present invention relates to methods and kits for the diagnosis and confirmation of Chronic Fatigue Syndrome (CFS) by measuring elastase activity in a patient sample, preferably a PBMC sample. The assays of the invention can also be used to characterize CFS, to determine the disease stage, the disease progression, the efficiency of a therapeutic regime and/or to predict the recurrence of possible attacks. The assays of the invention advantageously allow CFS to be distinguished from other CICIDs like MS or RA.
Methods And Compositions For Use In The Diagnosis And Treatment Of Chronic Immune Disease
Patrick Englebienne - Zingem, BE Kenny De Meirleir - Mechelen, BE Charles Herst - Oakland CA, US
International Classification:
G01N033/564
US Classification:
436506000
Abstract:
Methods and compositions are provided for use in the diagnosis and treatment of a host suffering from a chronic immune disease. In the diagnostic methods of the subject invention, a host derived sample, typically PBMC or a derivative thereof, is assayed for the presence of low molecular weight fragments of RNase L, typically in conjunction with an evaluation of caspase activity. The results of this assay are then employed to diagnose and/or characterize a chronic immune disease in the host. In the treatment methods of the subject invention, an effective amount of agent capable of enhancing RNase L homodimer activity in the host, e.g., in host PBMC, is administered to the host. Also provided are methods for identifying agents having RNase L cleavage-inhibitory activity or RNase L fragment antagonist activity.
Methods And Compositions For Use In The Diagnosis And Treatment Of Chronic Immune Disease
Patrick Englebienne - Zingem, BE Kenny Leo De Meirleir - Mechelen, BE Charles Vincent Herst - Oakland CA
Assignee:
R.E.D. Laboratories, N.V. - Zellik
International Classification:
G01N 33564
US Classification:
436506, 435 4, 435 71, 435 29
Abstract:
Methods and compositions are provided for use in the diagnosis and treatment of a host suffering from a chronic immune disease. In the diagnostic methods of the subject invention, a host derived sample, typically PBMC or a derivative thereof is assayed for the presence of low molecular weight fragments of RNase L, typically in conjunction with an evaluation of caspase activity. The results of this assay are then employed to diagnose and/or characterize a chronic immune disease in the host. In the treatment methods of the subject invention, an effective amount of agent capable of enhancing RNase L homodimer activity in the host, e. g. , in host PBMC, is administered to the host. Also provided are methods for identifying agents having RNase L cleavage-inhibitory activity or RNase L fragment antagonist activity.
Controlled Release Of Antibodies To Modulate Cytokines
- Redwood City CA, US Scott Burkholtz - Redwood City CA, US Charles V. Herst - Oakland CA, US Tom Hodge - Redwood City CA, US Lu Wang - San Jose CA, US
Assignee:
Flow Pharma, Inc. - Redwood City CA
International Classification:
C07K 16/24 G01N 33/68 C07K 16/28 A61K 47/68
Abstract:
An injectable formulation, comprising: poly(lactic-co-glycolic (PLGA) microsphere encapsulating siltuximab, wherein microspheres are sized to release siltuximab over a period of hours, days and weeks, where the biocompatible polymer releases antibody at an absorption rate which is characterized by an absorption rate constant (Ka (h) in the range of (0.001 to 2.048)+/−20%, or +/−10%, or +/−5%. for use and treating human patients with infections. The invention includes treating patients with viral infections of SARS-Cov-2 using siltuximab.
- Redwood City CA, US CHARLES V. HERST - Oakland CA, US LU WANG - San Jose CA, US SCOTT R. BURKHOLZ - Greer SC, US
Assignee:
FLOW PHARMA, INC. - Redwood City CA
International Classification:
A61K 39/00 G16B 40/00 G06F 17/18 G16B 5/00
Abstract:
A method of making a personalized cancer vaccine is disclosed. The method includes predicting whether a first neoantigen or a second neoantigen of an individual cancer patient has a stronger binding affinity for a human leukocyte antigen (HLA) complex of the patient and creating a particle containing the neoantigen with the stronger predicted binding affinity. The predicting step can be implemented using artificial intelligence, statistical modeling, or a combination thereof. Particles are created by encapsulating the neoantigen with the stronger predicted binding affinity for the HLA complex of the patient in a biocompatible material. Placing the antigen in a particular sized particle is referred to here as Size Exclusion Antigen Presentation Control, (SEAPAC) used in methods of treating the patient using such a personalized cancer vaccine.
- Redwood City CA, US CHARLES V. HERST - Oakland CA, US LU WANG - San Jose CA, US SCOTT R. BURKHOLZ - Greer SC, US SERBAN I. CIOTIOS - San Jose CA, US
Assignee:
FLOW PHARMA, INC. - Redwood City CA
International Classification:
A61K 39/00 C12Q 1/6886
Abstract:
A personalized cancer vaccine is disclosed. The vaccine is comprised of particles encapsulating neoantigens. The neoantigens are chosen by predicting whether a first neoantigen or a second neoantigen of an individual cancer patient has a stronger binding affinity for a human leukocyte antigen (HLA) complex of the patient and using the neoantigen with the stronger predicted binding affinity. Such a predicting step includes artificial intelligence, statistical modeling, or a combination thereof. Placing the antigen in a particular sized particle is referred to here as Size Exclusion Antigen Presentation Control, (SEAPAC) used in methods of treating the patient using such a personalized cancer vaccine.
Emery Pharma
Consultant Scientist
Aradigm Corporation Sep 2016 - Jan 2018
Regulatory Affairs Consultant
Chronix Biomedical Corporation Aug 2015 - Apr 2017
Director of Clinical Trials at Chronix Biomedical
White Rabbit Pictures Aug 2015 - Apr 2017
Managing Partner
The Maestro the Movie Aug 2015 - Apr 2017
Managing Partner
Education:
Golden Gate University 1994 - 1996
Master of Business Administration, Masters, Finance
University of California, Riverside 1986 - 1990
Master of Fine Arts, Masters, Fine Arts, Performing Arts, Creative Writing
Northwestern University 1984 - 1989
Doctorates, Doctor of Philosophy, Biology
University of California, Berkeley 1979 - 1980
Master of Public Health, Masters
University of California, Berkeley 1974 - 1978
Bachelors, Bachelor of Arts
Skills:
Fda Infectious Diseases Biotechnology Pharmaceutical Industry Lifesciences Medical Devices Oncology Drug Delivery Vaccines Immunology Cell R&D Life Sciences Glp Cancer Molecular Biology Drug Discovery Gmp Clinical Research Laboratory Validation Assay Development Cell Biology Film Creative Writing Screenwriting Film Production Feature Films Short Films Biochemistry In Vivo Genetics Formulation Drug Development Regulatory Affairs Analytical Chemistry Iso 13485 V&V Managed Care Cardiology Sop Commercialization Regulatory Submissions Hardware Diagnostics Neuroscience Gcp Process Simulation Neurology Change Control 21 Cfr Part 11
Certifications:
State of Nevada Clinical Laboratory General Supervisor License 16736Tgs-3 State of Nevada - Health and Human Resources, License 16736Tgs-3
May 2013 to 2000 ConsultantFlow Pharma Corporation
Feb 2011 to 2000 ScientistZogenix Corporation Emeryville, CA Nov 2006 to Jan 2011 Laboratory ManagerChronix Corporation San Jose, CA Jan 2004 to Dec 2007 ConsultantR.E.D. Laboratories Reno, NV Jan 2005 to Dec 2006 General SupervisorR.E.D. Laboratories Brussels, IL Feb 1998 to Dec 2006 Lab DirectorPharmaDiagnostics, Zingem, Belgium
Apr 2004 to Nov 2006 ConsultantAradigm Corporation Hayward, CA Jul 1994 to Jun 1997 Laboratory ManagerONCORE Analytics, Inc Houston, TX Jan 1990 to May 1994 Laboratory DirectorM.D. Anderson Cancer Center Houston, TX 1989 to 1990 Post-doctoral FellowCetus Corporation Emeryville, CA 1980 to 1984 Research AssociateNaval Biosciences Laboratory Oakland, CA 1978 to 1980 Research Assistant
Education:
Golden Gate University San Francisco, CA 1996 M.B.A. in FinanceNorthwestern University Chicago, IL 1989 Ph.D. in BiologyU.C. Berkeley Berkeley, CA 1980 M.P.H. in Biomedical Lab SciencesU.C. Berkeley Berkeley, CA 1978 B.A.