Our profound expertise in neuroscience and more than a
decade of experience in contract research results in a sustainable advantage for our customers. We offer you a sophisticated range of validated transgenic and non-transgenic in vivo and in vitro models in order to make sure that your new chemical or biological entities get profiled in depth using both novel and established drug targets that may play a role in the complex etiology of neuro-degenerative disease.
QPS provides global DMPK services to support drug development from discovery through regulatory filing. Their team has extensive experience in pharmacokinetics, drug metabolism, radiolabeled studies, and other assays required for candidate selection and regulatory submission. Their Delaware facility has all necessary equipment for in vivo and in vitro DMPK studies on site to enable rapid study execution.
Recent Advances in Immune Monitoring Presentation Slides Covance
The human immune system plays a pivotal role in conferring protective immunity to pathogenic microorganisms and cancer while its hyper-activation can result in serious inflammatory conditions such as autoimmunity. Immune monitoring is critical to determine the efficacy of therapeutic approaches such as the administration of a vaccine or to ascertain the safety of an administered agent such as a biologic that targets the immune system. Immune monitoring can involve the measurement of soluble immune mediators including cytokines and chemokines, as well as the analysis of phenotypic and functional status of immune cells. There is a plethora of platforms that offer highly sensitive and specific assays to monitor the immune system. These include simple immunoassays to complex multiplex assays that measure soluble biomarkers in various biological fluids and cell-based assays using a variety of platforms such as flow cytometry and enzyme-linked immunospot (ELISPOT) assay. In order to generate reliable immune monitoring data that will help us determine the safety and efficacy of the therapeutic intervention approach from a global study, highly standardized methods to collect, process and prepare patient samples need to be implemented. These slides focus on the recent advances in immune monitoring.
Dr. Gabriel López-Berestein- Simposio Internacional 'Terapias oncológicas ava...Fundación Ramón Areces
Los días 15 y 16 de octubre de 2014, la Fundación Ramón Areces y la Real Academia Nacional de Farmacia, en colaboración con la Fundación de la Innovación Bankinter, reunieron en Madrid a algunos de los mayores expertos mundiales en nuevas terapias contra el cáncer. El Simposio Internacional, coordinado por la profesora y académica María José Alonso, analizó el momento actual de la lucha contra esta enfermedad. También fue un punto de encuentro para científicos de los más innovadores institutos de investigación en oncología, quienes debatieron sobre tres grandes temas: la Medicina Personalizada contra el cáncer, los nanomedicamentos en la terapia del cáncer y las terapias basadas en la inmunomodulación.
How to Make Awesome SlideShares: Tips & TricksSlideShare
Turbocharge your online presence with SlideShare. We provide the best tips and tricks for succeeding on SlideShare. Get ideas for what to upload, tips for designing your deck and more.
SlideShare is a global platform for sharing presentations, infographics, videos and documents. It has over 18 million pieces of professional content uploaded by experts like Eric Schmidt and Guy Kawasaki. The document provides tips for setting up an account on SlideShare, uploading content, optimizing it for searchability, and sharing it on social media to build an audience and reputation as a subject matter expert.
Our profound expertise in Neuroscience and two decades of experience in contract research result in a sustainable advantage for our customers. QPS offers you a sophisticated range of validated transgenic and non-transgenic in vivo and in vitro models to guarantee that your new chemical or biological compounds are profiled in depth.
Creative Biolabs' dedicated team of neuroscience CRO scientists want the same thing as you do: to find a cure for the devastating diseases of the central nervous system. Learn more, please visit https://neuros.creative-biolabs.com/antibody-discovery-services.htm.
This document provides information about Enzo Life Sciences, a company that provides products and services for life sciences research, drug development, and clinical research. It summarizes Enzo's product offerings which include reagents, assays, cell analysis tools, small molecule libraries, and genomics products. It also describes Enzo's mission to develop novel platforms that enable researchers to find better solutions for disease research and drug development.
QPS provides global DMPK services to support drug development from discovery through regulatory filing. Their team has extensive experience in pharmacokinetics, drug metabolism, radiolabeled studies, and other assays required for candidate selection and regulatory submission. Their Delaware facility has all necessary equipment for in vivo and in vitro DMPK studies on site to enable rapid study execution.
Recent Advances in Immune Monitoring Presentation Slides Covance
The human immune system plays a pivotal role in conferring protective immunity to pathogenic microorganisms and cancer while its hyper-activation can result in serious inflammatory conditions such as autoimmunity. Immune monitoring is critical to determine the efficacy of therapeutic approaches such as the administration of a vaccine or to ascertain the safety of an administered agent such as a biologic that targets the immune system. Immune monitoring can involve the measurement of soluble immune mediators including cytokines and chemokines, as well as the analysis of phenotypic and functional status of immune cells. There is a plethora of platforms that offer highly sensitive and specific assays to monitor the immune system. These include simple immunoassays to complex multiplex assays that measure soluble biomarkers in various biological fluids and cell-based assays using a variety of platforms such as flow cytometry and enzyme-linked immunospot (ELISPOT) assay. In order to generate reliable immune monitoring data that will help us determine the safety and efficacy of the therapeutic intervention approach from a global study, highly standardized methods to collect, process and prepare patient samples need to be implemented. These slides focus on the recent advances in immune monitoring.
Dr. Gabriel López-Berestein- Simposio Internacional 'Terapias oncológicas ava...Fundación Ramón Areces
Los días 15 y 16 de octubre de 2014, la Fundación Ramón Areces y la Real Academia Nacional de Farmacia, en colaboración con la Fundación de la Innovación Bankinter, reunieron en Madrid a algunos de los mayores expertos mundiales en nuevas terapias contra el cáncer. El Simposio Internacional, coordinado por la profesora y académica María José Alonso, analizó el momento actual de la lucha contra esta enfermedad. También fue un punto de encuentro para científicos de los más innovadores institutos de investigación en oncología, quienes debatieron sobre tres grandes temas: la Medicina Personalizada contra el cáncer, los nanomedicamentos en la terapia del cáncer y las terapias basadas en la inmunomodulación.
How to Make Awesome SlideShares: Tips & TricksSlideShare
Turbocharge your online presence with SlideShare. We provide the best tips and tricks for succeeding on SlideShare. Get ideas for what to upload, tips for designing your deck and more.
SlideShare is a global platform for sharing presentations, infographics, videos and documents. It has over 18 million pieces of professional content uploaded by experts like Eric Schmidt and Guy Kawasaki. The document provides tips for setting up an account on SlideShare, uploading content, optimizing it for searchability, and sharing it on social media to build an audience and reputation as a subject matter expert.
Our profound expertise in Neuroscience and two decades of experience in contract research result in a sustainable advantage for our customers. QPS offers you a sophisticated range of validated transgenic and non-transgenic in vivo and in vitro models to guarantee that your new chemical or biological compounds are profiled in depth.
Creative Biolabs' dedicated team of neuroscience CRO scientists want the same thing as you do: to find a cure for the devastating diseases of the central nervous system. Learn more, please visit https://neuros.creative-biolabs.com/antibody-discovery-services.htm.
This document provides information about Enzo Life Sciences, a company that provides products and services for life sciences research, drug development, and clinical research. It summarizes Enzo's product offerings which include reagents, assays, cell analysis tools, small molecule libraries, and genomics products. It also describes Enzo's mission to develop novel platforms that enable researchers to find better solutions for disease research and drug development.
Safety pharmacology aims to identify potential adverse effects of new drugs prior to clinical trials. It involves evaluating a drug's effects on major organ systems like the cardiovascular, central nervous, and respiratory systems. Biomarkers and newer approaches can provide mechanistic insight. Renal safety assessment is important and may involve in vivo, in vitro, and in silico models. Biomarkers of kidney injury like KIM-1 and clusterin are being used. Safety pharmacology helps predict hazards, identify risks, and facilitate risk management of new drugs.
Presentation generale mars Syncrosome_JPJulie Pitrat
Syncrosome focuses on preclinical in vivo efficacy studies to improve drug development success rates. With 15 validated disease models and customized experimental protocols, their team of experts help customers evaluate compound potential. Their services include drug efficacy studies, pharmacokinetics studies, and functional biomarker exploration using advanced techniques on appropriate animal models. Syncrosome has over 350 completed studies for 180 customers since 2000.
Jianying Xiao has over 16 years of experience in pharmaceutical research. She has expertise in in vivo and in vitro drug discovery techniques related to drug metabolism, infectious diseases, immunology, and cardio-metabolic disorders. She is proficient in various research techniques including animal handling, molecular biology, cell culture, and data analysis software. Jianying has worked at Merck & Co. for over 18 years, leading numerous projects that resulted in publications, patents, and awards. Her work has advanced drug programs from research through clinical trials.
This study evaluated urinary neutrophil gelatinase-associated lipocalin-2 (uNGAL) as a biomarker for lupus nephritis in 44 systemic lupus erythematosus patients. The patients were divided into two groups: 22 with lupus nephritis and 22 without. Urinary lipocalin-2 levels were measured using ELISA and compared between the two patient groups and 30 healthy controls. Urinary lipocalin-2 levels were significantly higher in patients with lupus nephritis compared to those without and the controls. A cutoff value of 13.2 ng/dl for urinary lipocalin-2 showed a sensitivity of 85% and specificity of 100
This study evaluated urinary neutrophil gelatinase-associated lipocalin-2 (uNGAL) as a biomarker for lupus nephritis in 44 systemic lupus erythematosus patients. The patients were divided into two groups: 22 with lupus nephritis and 22 without. Urinary lipocalin-2 levels were measured using ELISA and compared between the two patient groups and 30 healthy controls. Urinary lipocalin-2 levels were significantly higher in patients with lupus nephritis compared to those without and the controls. A cutoff value of 13.2 ng/dl for urinary lipocalin-2 showed a sensitivity of 85% and specificity of 100
Cambridge Bioscience_ ACEA User Group Meeting2014Jay Champaneri
This document provides an agenda and abstracts for the ACEA xCELLigence User Group Meeting taking place on June 24, 2014 at the Radisson Blu Hotel in London Stansted. The agenda outlines the schedule for presentations and talks on using the xCELLigence technology. Presentation abstracts provide more detail on several talks, including investigating cancer cell invasion and migration, using the technology to monitor cellular processes in drug development, and evaluating potential cardiac side effects of cancer drugs. The document promotes sharing of experiences using the xCELLigence impedance-based cell analysis system.
Overcoming the challenges of molecular diagnostics in government health insti...Yakubu Sunday Bot
overcoming the challenges of molecular diagnostics in government owned health institution in nigeria.Several challenges abound in the Nigerian health sector ranging from financial,political and lack of commitment.Its obvious and no wonder the state of health care deliveryy, vis a vis its quality of care to its citizenry.
Seventh Wave was established in 2003 and has grown from 5 to over 50 employees. It established a bioanalytical laboratory in 2006 to support drug discovery clients with LC-MS/MS analysis, method development and validation, pharmacokinetic studies, and in vitro assays. The bioanalytical lab has over 60 years of combined industry experience and state-of-the-art instrumentation to provide fast, high-quality service and respond to client challenges.
Seventh Wave was established in 2003 and has grown from 5 to over 50 employees. It established a bioanalytical laboratory in 2006 to support drug discovery clients with LC-MS/MS analysis, method development and validation, pharmacokinetic studies, and in vitro assays. The bioanalytical lab has over 60 years of combined industry experience and state-of-the-art instrumentation to provide fast, high-quality service and respond to client challenges.
2017 09-20 HUPO2017, Dublin, Alain van Gool withsupplAlain van Gool
Keynote lecture at the HUPO 2017 in Dublin, focussing on our innovations in translational omics for applications in our personalized healthcare at Radboudumc.
Validation of an Off-the-Shelf, Diet-Induced NASH Mouse Model using Digital Whole Slide Scanning of Liver Tissue and Artificial Intelligence-Enabled, Quantitative Histopathological Analysis
The document describes the activities of Biopra, a contract research organization serving the drug discovery industry. Biopra was founded by three experts in Alpha technologies who previously worked at PerkinElmer. Biopra offers assay development services focusing on Alpha technologies like AlphaScreen and AlphaLISA. Their services include developing biochemical and cellular assays for targets like kinases, epigenetic enzymes, and biomarkers. They have expertise in areas like epigenetics, biomarker detection, protein interactions, and kinase profiling. Biopra aims to provide high quality services executed by technology pioneers with quick turnaround times through a collaborative approach.
Medical technology encompasses healthcare products that diagnose, monitor, or treat diseases. Medical technologists, also called clinical laboratory technologists, perform complex scientific tests on blood and body fluids to analyze results. Nucleic acids like DNA and RNA are the building blocks of living organisms and work together to help cells replicate and build proteins. Medical technologists perform nucleic acid testing for conditions like Bloom syndrome, Lesch-Nyhan syndrome, and Fanconi anemia. Nucleic acid testing screens blood donations for transfusion-transmitted infections and can also detect other pathogens. Bloom syndrome causes short stature, sun-sensitive skin changes, and increased cancer risk. Lesch-Nyhan syndrome involves uric acid overproduction, neurological issues
This study analyzed the expression and clinical significance of serum biomarkers AFP, P-selectin (P-sel), and MMP-9 in patients with hepatic sclerosis combined with portal vein thrombosis (PVT). The study found that levels of all three biomarkers were significantly higher in patients with hepatic sclerosis and PVT compared to patients with hepatic sclerosis alone. Furthermore, AFP, P-sel, and MMP-9 were identified as main risk factors for PVT. The expression of AFP was also found to be positively correlated with the expression of P-sel and MMP-9 in patients with hepatic sclerosis and PVT.
Whether your focus is on small molecules, proteins, bio-therapeutics, vaccines, or gene therapy, QPS provides a full range of bioanalytical solutions to support drug development from discovery through clinical development and filing.
The document discusses how French clinical networks can accelerate the discovery of new treatments for cardiovascular and metabolic diseases. It describes the network of Clinical Investigation Centers in France and their resources like biobanks, databases, and cohorts. It provides examples of successes like discoveries of new medications and biomarkers. It discusses opportunities for industry-academic collaboration on multicenter clinical trials through an proposed European Drug Development Hub.
mRNA rather than DNA may become the nucleotide framework for new classes of drugs and vaccines. Exciting preclinical results in prophylaxis and initial clinical data in oncology suggest that mRNA technology could be translated into improvements in lung cancer and other diseases.
QPS DMPK provides a dedicated team of senior scientists to help select, design and conduct the appropriate ADME studies
for your specific compounds and therapeutic targets.
Working with QPS DMPK is a collaborative and consultative
endeavor that also incorporates our operational effectiveness
and dedication to customer service.
Safety pharmacology aims to identify potential adverse effects of new drugs prior to clinical trials. It involves evaluating a drug's effects on major organ systems like the cardiovascular, central nervous, and respiratory systems. Biomarkers and newer approaches can provide mechanistic insight. Renal safety assessment is important and may involve in vivo, in vitro, and in silico models. Biomarkers of kidney injury like KIM-1 and clusterin are being used. Safety pharmacology helps predict hazards, identify risks, and facilitate risk management of new drugs.
Presentation generale mars Syncrosome_JPJulie Pitrat
Syncrosome focuses on preclinical in vivo efficacy studies to improve drug development success rates. With 15 validated disease models and customized experimental protocols, their team of experts help customers evaluate compound potential. Their services include drug efficacy studies, pharmacokinetics studies, and functional biomarker exploration using advanced techniques on appropriate animal models. Syncrosome has over 350 completed studies for 180 customers since 2000.
Jianying Xiao has over 16 years of experience in pharmaceutical research. She has expertise in in vivo and in vitro drug discovery techniques related to drug metabolism, infectious diseases, immunology, and cardio-metabolic disorders. She is proficient in various research techniques including animal handling, molecular biology, cell culture, and data analysis software. Jianying has worked at Merck & Co. for over 18 years, leading numerous projects that resulted in publications, patents, and awards. Her work has advanced drug programs from research through clinical trials.
This study evaluated urinary neutrophil gelatinase-associated lipocalin-2 (uNGAL) as a biomarker for lupus nephritis in 44 systemic lupus erythematosus patients. The patients were divided into two groups: 22 with lupus nephritis and 22 without. Urinary lipocalin-2 levels were measured using ELISA and compared between the two patient groups and 30 healthy controls. Urinary lipocalin-2 levels were significantly higher in patients with lupus nephritis compared to those without and the controls. A cutoff value of 13.2 ng/dl for urinary lipocalin-2 showed a sensitivity of 85% and specificity of 100
This study evaluated urinary neutrophil gelatinase-associated lipocalin-2 (uNGAL) as a biomarker for lupus nephritis in 44 systemic lupus erythematosus patients. The patients were divided into two groups: 22 with lupus nephritis and 22 without. Urinary lipocalin-2 levels were measured using ELISA and compared between the two patient groups and 30 healthy controls. Urinary lipocalin-2 levels were significantly higher in patients with lupus nephritis compared to those without and the controls. A cutoff value of 13.2 ng/dl for urinary lipocalin-2 showed a sensitivity of 85% and specificity of 100
Cambridge Bioscience_ ACEA User Group Meeting2014Jay Champaneri
This document provides an agenda and abstracts for the ACEA xCELLigence User Group Meeting taking place on June 24, 2014 at the Radisson Blu Hotel in London Stansted. The agenda outlines the schedule for presentations and talks on using the xCELLigence technology. Presentation abstracts provide more detail on several talks, including investigating cancer cell invasion and migration, using the technology to monitor cellular processes in drug development, and evaluating potential cardiac side effects of cancer drugs. The document promotes sharing of experiences using the xCELLigence impedance-based cell analysis system.
Overcoming the challenges of molecular diagnostics in government health insti...Yakubu Sunday Bot
overcoming the challenges of molecular diagnostics in government owned health institution in nigeria.Several challenges abound in the Nigerian health sector ranging from financial,political and lack of commitment.Its obvious and no wonder the state of health care deliveryy, vis a vis its quality of care to its citizenry.
Seventh Wave was established in 2003 and has grown from 5 to over 50 employees. It established a bioanalytical laboratory in 2006 to support drug discovery clients with LC-MS/MS analysis, method development and validation, pharmacokinetic studies, and in vitro assays. The bioanalytical lab has over 60 years of combined industry experience and state-of-the-art instrumentation to provide fast, high-quality service and respond to client challenges.
Seventh Wave was established in 2003 and has grown from 5 to over 50 employees. It established a bioanalytical laboratory in 2006 to support drug discovery clients with LC-MS/MS analysis, method development and validation, pharmacokinetic studies, and in vitro assays. The bioanalytical lab has over 60 years of combined industry experience and state-of-the-art instrumentation to provide fast, high-quality service and respond to client challenges.
2017 09-20 HUPO2017, Dublin, Alain van Gool withsupplAlain van Gool
Keynote lecture at the HUPO 2017 in Dublin, focussing on our innovations in translational omics for applications in our personalized healthcare at Radboudumc.
Validation of an Off-the-Shelf, Diet-Induced NASH Mouse Model using Digital Whole Slide Scanning of Liver Tissue and Artificial Intelligence-Enabled, Quantitative Histopathological Analysis
The document describes the activities of Biopra, a contract research organization serving the drug discovery industry. Biopra was founded by three experts in Alpha technologies who previously worked at PerkinElmer. Biopra offers assay development services focusing on Alpha technologies like AlphaScreen and AlphaLISA. Their services include developing biochemical and cellular assays for targets like kinases, epigenetic enzymes, and biomarkers. They have expertise in areas like epigenetics, biomarker detection, protein interactions, and kinase profiling. Biopra aims to provide high quality services executed by technology pioneers with quick turnaround times through a collaborative approach.
Medical technology encompasses healthcare products that diagnose, monitor, or treat diseases. Medical technologists, also called clinical laboratory technologists, perform complex scientific tests on blood and body fluids to analyze results. Nucleic acids like DNA and RNA are the building blocks of living organisms and work together to help cells replicate and build proteins. Medical technologists perform nucleic acid testing for conditions like Bloom syndrome, Lesch-Nyhan syndrome, and Fanconi anemia. Nucleic acid testing screens blood donations for transfusion-transmitted infections and can also detect other pathogens. Bloom syndrome causes short stature, sun-sensitive skin changes, and increased cancer risk. Lesch-Nyhan syndrome involves uric acid overproduction, neurological issues
This study analyzed the expression and clinical significance of serum biomarkers AFP, P-selectin (P-sel), and MMP-9 in patients with hepatic sclerosis combined with portal vein thrombosis (PVT). The study found that levels of all three biomarkers were significantly higher in patients with hepatic sclerosis and PVT compared to patients with hepatic sclerosis alone. Furthermore, AFP, P-sel, and MMP-9 were identified as main risk factors for PVT. The expression of AFP was also found to be positively correlated with the expression of P-sel and MMP-9 in patients with hepatic sclerosis and PVT.
Whether your focus is on small molecules, proteins, bio-therapeutics, vaccines, or gene therapy, QPS provides a full range of bioanalytical solutions to support drug development from discovery through clinical development and filing.
The document discusses how French clinical networks can accelerate the discovery of new treatments for cardiovascular and metabolic diseases. It describes the network of Clinical Investigation Centers in France and their resources like biobanks, databases, and cohorts. It provides examples of successes like discoveries of new medications and biomarkers. It discusses opportunities for industry-academic collaboration on multicenter clinical trials through an proposed European Drug Development Hub.
mRNA rather than DNA may become the nucleotide framework for new classes of drugs and vaccines. Exciting preclinical results in prophylaxis and initial clinical data in oncology suggest that mRNA technology could be translated into improvements in lung cancer and other diseases.
QPS DMPK provides a dedicated team of senior scientists to help select, design and conduct the appropriate ADME studies
for your specific compounds and therapeutic targets.
Working with QPS DMPK is a collaborative and consultative
endeavor that also incorporates our operational effectiveness
and dedication to customer service.
At QPS, translational medicine brings together leading-edge technologies and pharmaceutical research and development experience to create a business service unit that works efficiently to advance your drug development program.
The QPS Bioanalysis General presentation is a summary of our capabilities in Neuropharmacology, Toxicology, DMPK, Bioanalytical, Translational Medicine, and Dermal and Transdermal Preclinical services.
This document discusses cerebrospinal fluid (CSF) sampling services provided by QPS Netherlands. CSF sampling can provide pharmacokinetic data about drug concentrations in the central nervous system. QPS Netherlands has the capability to perform CSF sampling procedures under clinical trial conditions in compliance with regulations. Their proximity to a university medical center allows for efficient CSF sample collection and analysis of biomarkers to support drug development studies.
When your focus is Biotherapeutics, QPS’ Global Laboratories provide a full range of bioanalytical solutions to support immunogenicity evaluations during drug development from discovery through clinical development and filing.
Partnering with QPS for a well-conceived and executed IND-enabling preclinical program will provide you with a detailed
assessment of your drug candidate and the most agile, flexible and timely pathway to filing an IND.
QPS Missouri's Negative Pressure Room.
A negative pressure room uses lower air pressure than the
rooms surrounding it to allow outside air into the facility.
This traps and keeps harmful particles from leaving the
potentially contaminated area.
A well-conceived and executed preclinical and clinical
radiolabeled ADME program will provide you with a detailed
assessment of the total fate (mass balance, route, and rate of excretion,
tissue distribution, metabolic pathways, and identity and quantity of
metabolites) of your drug candidate to support regulatory submissions.
QPS Regulated Bioanalysis of Antibody Drug ConjugatesQPS Holdings, LLC
PK profiling reflects molecular complexity. Since 2001 QPS’ bioanalytical teams have contributed to ADC drug development,
supporting the filing of one of the first drug targeting
programs and continue to develop customized
strategies for novel conjugate molecules.
To support research and development in different stages of biopharmaceutical compounds and products, QPS offers biomarker services in different global competence centers using
a wide range of technology platforms to support programs in any therapeutic area. QPS biomarker capabilities range from small molecule analysis to whole cell characterization.
When your focus is small molecules, biomarkers, or protein biotherapeutics,
QPS’ LC-MS/MS laboratories provide a full range of
bioanalytical solutions to support drug development
from discovery through clinical development.
This document outlines key milestones in the development and approval of gene therapy products from 1998 to 2020. It shows the year of important bioanalytical methods being applied to oligonucleotides and vectors used in gene therapy, as well as the year of approval for several gene therapy products that work via different mechanisms such as gene interference using antisense oligonucleotides, aptamers, or small interfering RNA, and gene insertion using viral vectors like adeno-associated virus or lentivirus. The most recent approvals in 2019-2020 include gene therapies to treat spinal muscular atrophy and beta-thalassemia.
This document provides an overview of assay technologies and milestones for a biopharmaceutical company from 1996 to 2020. It includes information on cytokine release assays, GLP, GMP, and CLIA compliance as well as platforms for analyzing biomarkers, genetics, small molecules, proteins, gene therapy, and more with techniques such as QPCR, flow cytometry, mass spectrometry, and immunoassays. Key developments include new assays for peptides, oligonucleotides, antibodies, and viral detection.
This white paper focuses on overcoming the challenges of participating in a pediatric trial. One of the biggest issues is that it is difficult to enroll participants in pediatric trials. Read these 5 strategies to help make it easier to enroll trial participants and complete successful trials.
QPS is a contract research organization that specializes in developing close relationships with clients based on trust and mutual respect. They offer flexible and nimble clinical work to improve outsourced work quality and reduce oversight needs. Their biosimilar drug development expertise can help clients advance their biosimilar portfolios in a timely manner for the benefit of patients worldwide.
Three Lessons to Help Accelerate Pharmaceutical Breakthroughs for CNS DisordersQPS Holdings, LLC
"Developing therapies for diseases of the central nervous system (CNS) presents special challenges directly related to the complexity of the human brain and its function of integrating our communications with the outside world. Animal models of human neurological and psychiatric disorders are scarce, because many of these human diseases do not naturally occur in animals, and their study necessitates either specific manipulation (induced models) or the production of genetically modified rodents (transgenic and KO models). Even with these models, it remains unclear, what behavioral domain really resembles higher brain function in humans, and how we can interpret animal data on cognition, emotion, social interaction or activities of daily living.
Furthermore, in contrast with other organs, the CNS is sequestered from the general circulation by the blood brain barrier (BBB), potentially preventing many compounds from reaching their intended target. Quantifying how much of and how long a compound resides in the CNS is difficult and indirect. Therefore, the assessment of target engagement calls for specific techniques and know-how. While animal models provide some information as to how well a given compound accesses the brain, this data cannot always be translated directly to humans. Insufficient knowledge of target-compound interaction may be a major cause of failure in drug development for CNS disorders.
QPS understands the specific challenges of translation from animal models to human clinical application. Our extensive experience in CNS affords us a clear view of its complexities and its current global clinical study environment. Our direct links with the international scientific community and close relationships with key opinion leaders worldwide, together with our dedicated experts, original strategies and operational transparency, are keys to the effective execution of CNS programs for our clients."
The Nobel Prize for the discovery that double-stranded RNAs (dsRNAs) can trigger silencing of complementary messenger RNA sequences was awarded in 1998 and the term ‘RNA interference’ (RNAi) was born, opening the door to a completely novel and untapped market within the pharmaceutical industry. Shortly thereafter, short dsRNAs — or short interfering RNAs (siRNAs) — were generated artificially and used to demonstrate that this process also occurs in mammalian cells. The knowledge that small strands of RNAs can affect gene expression has had a tremendous impact on basic and applied research, and RNAi is currently one of the most promising new approaches for disease therapy. In 2004, only six years after the discovery of RNAi, the first siRNA-based human therapeutics — developed to treat wet age-related macular degeneration — entered phase I clinical trials. RNAi is one of the fastest advancing fields in biology, and the flow of discovery gives true meaning to the expression ‘from the bench to the bedside'.
Sometimes practical or ethical considerations dictate whether healthy volunteers or patients should be recruited for a particular study. But there are usually sound scientific arguments for collecting PK data from actual patients, to supplement or substitute for PK data obtained from human healthy volunteers during the first phases of drug development. Knowing to what extent the results obtained in healthy volunteers – if available - can be extrapolated to the intended treatment population is critical. The US FDA has recognized the importance of PK studies for determining drug concentration-time profiles in target patient populations.
This white paper focuses on the 505(b)(2) New Drug Approval (NDA) regulatory pathway, which relies on the public literature of clinical studies and/or the FDA's filing of safety and efficacy data for a previously approved drug.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
3. QPS AUSTRIA
THE COMPANY
3
broschüre 2011.indd 3 05.07.11 20:10
QPS helps you navigate
Our profound expertise in
neuroscience and more than a
decade of experience in contract
research results in a sustainable
advantage for our customers.
We offer you a sophisticated range
of validated transgenic and non-
transgenic in vivo and in vitro
models in order to make sure
that your new chemical or biological
entities get profiled in depth using
both novel and established drug
targets that may play a role in the
complex etiology of neuro-
degenerative disease
5. QPS AUSTRIA
MISSION STATEMENT
5
broschüre 2011.indd 5 05.07.11 20:10
QPS helps you navigate 5
We are committed to combine
scientific experience, state of the art
techniques and excellent
communication to deliver superior
support in drug development.
Our mission is to accelerate the
development of medicines
worldwide by enabling cost effective
breakthroughs in pharmaceutical
innovation.
QPS is a global leader in contract
research.
We are known for our quality,
technical expertise, efficiency and
customer focus.
Our passionate and productive work
creates value for patients and
customers while creating
opportunities for employees to grow
and thrive.
7. EXPERIENCED PARTNER
IN DRUG DEVELOPMENTT
QPS Austria has developed
multiple methods for testing and
evaluating new potential treatment
approaches for neurological and
psychiatric indications.
The close link to state of the art
science enables us to reliably
assess the potential of new
compounds.
The wide range of assays and
evaluation methods allows our
customers to gain the most
comprehensive information about
their drug candidates.
Outstanding quality and reliable
timelines are our dedication.
QPS Austria can help to
significantly reduce the time to
approval.
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9. CELL BASED
DRUG TESTING
QPS Austria provides
a comprehensive portfolio of
standardized cell culture systems,
including primary neurons from
rat, mouse and chicken as well as
transgenic & non transgenic cell
Cultures can be analysed for a wide
spectrum of parameters:
Cell viability, apoptosis, necrosis
Mitochondrial impairment
Inflammation related parameters
Neurite growth
Disease related markers
Secretase inhibition or modulation
Tau phosphorylation
Broad range of analytes on a
multiplex platform
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We continuously establish new
models and perform validations on
request.
lines.
11. DISEASE RELATED IN VITRO
DRUG TESTING OPTIONS
At QPS Austria the effects of your
compounds on the most well-known
hallmarks of neurodegenerative
diseases can be tested in validated
assays.
Amyloid pathology can be
investigated using several different
aggregation, toxicity and secretase
assays. Drug mediated alteration of
Tau phosphorylation can be studied
using cells overexpressing human
mutant Tau441 or primary cultured
neurons.
Parkinson drug development
projects can be supported
by performing studies with
dopaminergic neuroblastoma cells,
MPP+ lesions and other disease
specific models.
Inflammation represents a major
topic in several neurodegenera-
tive diseases. Consequently QPS
established a range of assays to
study cytokines, NO release and
others.
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13. BIOANALYTICAL
SERVICES
QPS Austria is a GLP certified CRO
and experienced in high quality
performance of various bioanalytical
tasks within mono- or multicentral
clinical studies and other projects.
Covering the entire drug
development process, biomarker
and numerous other analyses are
performed by an experienced team.
Synucleins
Cellular aggregates (TDP-43, SOD1)
Neurotransmitters
Beyond the established assays we
provide customized development
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Tau & pTau species
Amyloid peptides (all Aβ species &
aggregation states)
Inflammation markers
and validation assays.
Lipid profile
Neurotrophic factors
15. GENERATION AND
CHARACTERIZATION
OF TRANSGENIC ANIMALS
New drug targets opening
effective pathways to treat neuro-
degenerative diseases represent
an interesting challenge and new
opportunities in drug development.
QPS Austria is experienced
in creating and validating new
transgenic animals. Custom tailored
transgenic mouse and rat models
are perfect tools to perform proof of
concept studies.
Beyond the generation of the
desired animal model we routinely
run breeding programs using
any rat or mouse model available.
As a further option we can apply
viral vectors carrying the genetic
information to be expressed.
The genetic, behavioral,
histological and biochemical
characterisation and validation
of the newly created models is
performed by our experienced
team at QPS Austria.
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17. QPS Austria provides a wide range of
transgenic mouse and rat models.
The most requested models are the
following:
Alzheimer’s disease
APPSL
APP x hQCSL
5 x FAD
TAU441
tg2576
Parkinson’s disease
human wt alpha-synuclein D-line
human wt alpha-synuclein Line 61
human alpha-synuclein A53T
Huntington’s disease
R6/2 mouse
Others
SOD1-G93A mouse (ALS)
TDP43-TARDBP (ALS & FTD)
TRANSGENIC
MOUSE AND RAT MODELS
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NPC1 -/- (Niemann Pick Disease)
APP x ApoB100SL
19. Test compounds are applied via
validated routes like ip, iv, in, po, im,
sc but also intrathecally, intraventri-
cularly or with devices like osmotic
mini pumps or implantable pellets.
Drug application via drinking water
or diet is also always an option.
Moreover, we apply viruses (e.g. LV
or AAV) for gene therapeutic or other
approaches.
Skilled personnel is able to sample
blood as well as cerebrospinal fluid
in vivo.
At the end of a drug application
period any organ as well as blood
and cerebrospinal fluid can be
sampled in sufficient amounts and
processed further for histological
and / or biochemical investigations
made in house or at any facility
defined by the sponsor.
SUPERIOR DRUG
APPLICATION & SAMPLING
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21. In many of the transgenic and
non-transgenic disease models
drug mediated behavioral changes
belong to the most important
experimental outcomes.
All behavioral paradigms are perfor-
med, recorded and evaluated using
automated up to date equipment.
Beyond experimental paradigms as
listed below we perform high level
techniques for drug testing and
phenotyping including homecage
phenotyping and others.
Poke hole activity
Rota rod
Two choice swim test
New object recognition
Social interaction
Prepulse inhibition
Ultrasound vocalisation
DRUG TESTING SERVICES
BEHAVIOR
Active and passive avoidance
Beam walk
Challenging beam walk
Pole test
Y – maze
T – maze
Elevated plus maze
Contextual fear conditioning
Fear conditioning
Cylinder test
Forced swim test
Morris water maze
Buried food test
Open field
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23. Studies at QPS Austria GmbH
provide quantitative and
qualitative histological readouts.
In the scope of neurodegenerative
diseases pathological hallmark
detection is highly standardized
like:
Plaque quantification (e.g.
6E10, ThioflavinS, Congo red)
Inflammation markers (e.g
Mac-1, Iba-1, GFAP)
α-synuclein: quantification of
Lewy body counts (e.g. α-syn,
phospho-α-syn, Campbell Switzer)
Neuron and synaptic counts
(e.g. TH, NeuN, Synaptophysin)
Tau pathology (e.g. AT180, HT7,
AT270)
Microbleeding and BBB
permeability (e.g. Prussian blue,
HRP)
Ischemic damage (e.g. TTC and
NBT staining)
Beyond standard evaluations
our team will be happy to help
with expertise in development
of appropriate study setups and
protocols. As special services we
are able to offer unbiased
stereology and electron micro -
scopy beside standard brightfield
and fluorescence microscopy.
DRUG TESTING SERVICES
HISTOLOGICAL EVALUATION
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QPS' reputation in neuro-
pharmacology and the
acknowledged bioanalytical
experience in all phases of drug
discovery and development create a
unique combination of services to
study pharmacokinetics, and
pharmacodynamics of discovery
candidates developed specifically for
neurological indications.
These services combine:
Administration of candidates in
various tissues (incl. intrathecal)
Usage of transgenic animals
Behavioral studies
Various sampling techniques
(including brain, CSF, spinal cord)
Wide range of bioanalytical
methods for PK and biomarker
assessments.
RAPID IN VIVO PK/PD/EFFICACY
SCREENING
IN TG & NTG ANIMALS
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Our regional facilities and ofces are located in:
USA, China, Japan, Taiwan, India, Netherlands, Austria, Czech Republic, Croatia, Israel, Serbia, Bosnia, Hungary, Spain, Germany,
United Kingdom, Slovakia, Bulgaria, Romania, Lithuania, Ukraine, Poland, France and South Korea
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27QPS helps you navigate
QPS is a reputable and profitable
provider of world-class pharma-
ceutical development services,
possessing unparalleled scientific
expertise within our
core competencies:
Neuropharmacology
DMPK
Toxicology
Bioanalysis
Translational Medicine
Early Stage Clinical
Phase II - IV Clinical
Program Management
QPS WORLDWIDE
OUR CORE COMPETENCIES