XTalks

SEPTEMBER 15, 2020

Specifically, the vaccine contains human recombinant glutamate decarboxylase 65 (GAD65) protein conjugated to aluminum hydroxide (GAD-alum). The vaccine triggers an immune response against pro-inflammatory processes resulting from autoimmune attack of the pancreas – the inflammation helps to destroy the insulin-producing ?-islet

Vaccination 103

Vaccination Vaccine Insulin Trials 103

The Pharma Data

MARCH 7, 2022

The IGA results in the equivalent genotype (genetic make-up) and short-hair coat trait seen in some conventionally bred cattle, known as a “slick” coat. This is the FDA’s first low-risk determination for enforcement discretion for an IGA in an animal for food use. Solomon, D.V.M., director of the FDA’s Center for Veterinary Medicine.

Genome 52

Genome Genomics Production Marketing 52

XTalks

APRIL 15, 2021

For example, the sequence environment around the ADRA2B gene contains many other nearby genes, so a simple approach to SNP selection would generate spurious results. Though the HERMES, and the related 2010 CHARGE study, performed large heart failure genomic association analysis, both consortia relied on genotyping and self-reported data.

Development 98

Development Drugs Genomics Genome 98

XTalks

NOVEMBER 10, 2020

We know that users don’t want to report false negatives caused by poor-quality data, which is why we’ve also introduced a genotyping feature for all curated variants contained within any gene panels of interest. HS: At Congenica, we understand the importance of quality.

Genome 98

Genome Genomics Medicine Genetic Disease 98

Roots Analysis

AUGUST 31, 2023

For example, people affected by phenylketonuria must avoid consuming food containing phenylalanine amino acid. It is worth highlighting that nutrigenomics can be used for the treatment of inborn errors of metabolism by manipulating diet. Similarly, people suffering from lactose intolerance must avoid milk products.

Genomics 40

Genomics Genome Genetics Gene 40

XTalks

APRIL 24, 2023

These are, in my view, the most valid comparisons, particularly in inherited diseases where the genotype is obviously the same in each individual patient, and as a consequence, the difference in phenotype after gene therapy is a true difference,” he adds. As a result, there are several EU regulations and directives to follow.

Gene Therapy 95

Gene Therapy Gene Trials Clinical Trials 95

Roots Analysis

SEPTEMBER 20, 2023

In fact, owing to the various therapeutic applications, the government in different nations have legalized various pharmaceutical compositions containing cannabis for medical use. Cannabis-infused products primarily contain the cannabinoids cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC).

Laboratory Information Management System 40

Laboratory Information Management System Production Contamination Containment 40

XTalks

FEBRUARY 4, 2021

Through these collaborations, cohort research dataset sharing programs allow for whole-genome sequence and genotype data to be made available for independent research. Now, if all you’ve already got is a bioresource of 20,000 people that have already been genotyped, you can choose those from that sample and focus your effort.”.

Research 98

Research Biobanking Drugs Genome 98

The Pharma Data

SEPTEMBER 2, 2021

Durvalumab ± Tremelimumab + Platinum-Etoposide in 1L ES-SCLC: Exploratory Analysis of HLA Genotype and Survival in CASPIAN. Lead author. Abstract title. Presentation details. Immuno-Oncology. Garassino, MC. Abstract #MA16.06. Mini Oral Session: MA16 – SCLC: New Targets, Biomarkers, and Systemic Therapies. 13 September 2021. 20:35 – 20:40 MDT.

Trials 52

Trials Medicine Antibody Clinical Trials 52

The Pharma Data

APRIL 14, 2021

Accelerated Approval Granted for Locally Advanced or Metastatic Urothelial Cancer Following a Platinum-Containing Chemotherapy and a PD-1/PD-L1 Inhibitor –. – New Indication Marks Second FDA Approval for Trodelvy in 2021 –. TRODELVY contains a genotoxic component, SN-38, and targets rapidly dividing cells. FOSTER CITY, Calif.–(BUSINESS

Genotype 52

Genotype Containment FDA Approval Genotoxicity 52

The Pharma Data

APRIL 7, 2021

The incidence of Grade 3-4 neutropenia in genotyped patients was 69% in patients homozygous for the UGT1A1*28, 48% in patients heterozygous for the UGT1A1*28 allele and 46% in patients homozygous for the wild-type allele. TRODELVY contains a genotoxic component, SN-38, and targets rapidly dividing cells.

HR 52

HR Genotype FDA Approval Genotoxicity 52

The Pharma Data

MARCH 25, 2021

SG contains a genotoxic component and can cause teratogenicity and/or embryo-fetal lethality when administered to a pregnant woman. In addition to the European Union, regulatory reviews of SG in metastatic TNBC are currently underway in the U.K., Embryo-Fetal Toxicity.

Genotoxicity 52

Genotoxicity Genotype Containment Protein 52