No Carolina / NY / Florida
Ph: 561.316.3330

Metrion Biosciences Launches Good Laboratory Practice hERG Screening Service

Summation

  • Metrion Biosciences Limited (“Metrion”), the specialist ion channel contract research and drug discovery company, today announced it has received notification from the UK's Medicines and Healthcare products Regulatory Agency (MHRA) that the Company is now a member of the UK GLP (Good Laboratory Practice) Compliance Monitoring Programme, and is therefore able to offer GLP compliant hERG ion channel screening services to the global life sciences community.
  • Metrion's expanding portfolio of ion channel services now includes the new GLP hERG assays in addition to high throughput screening (HTS) in both automated electrophysiology and fluorescence formats, a comprehensive ion channel cell biology capability, translational assays, and significant expertise for neuroscience drug discovery research.
  • The addition of the new GLP hERG service further strengthens the Company's suite of cardiac safety screening assays, providing a substantial range of options to assess potential cardiac liabilities as preclinical discovery research programmes are progressed.

Metrion Biosciences Limited (“Metrion”), the specialist ion channel contract research and drug discovery company, today announced it has received notification from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) that the Company is now a member of the UK GLP (Good Laboratory Practice) Compliance Monitoring Programme, and is therefore able to offer GLP compliant hERG ion channel screening services to the global life sciences community.

GLP hERG screening is a vital step in the transition from preclinical research to Phase 1 clinical trials in humans, regardless of therapeutic target class. Pharmacological assessments against the human ether-à-go-go related gene (hERG) potassium channel, conducted in compliance with GLP principles and adhering to ICH S7A and ICH S7B guidelines, is an important step in the Investigational New Drug (IND) application process for potential small molecule therapeutics.

Metrion Biosciences has offered hERG profiling services since the Company was founded in 2015 and has since expanded its cardiac safety offer to include a full panel of Comprehensive in Vitro Proarrhythmia Assay (CiPA) services. The addition of the new GLP hERG service further strengthens the Company’s suite of cardiac safety screening assays, providing a substantial range of options to assess potential cardiac liabilities as preclinical discovery research programmes are progressed.

Metrion’s expanding portfolio of ion channel services now includes the new GLP hERG assays in addition to high throughput screening (HTS) in both automated electrophysiology and fluorescence formats, a comprehensive ion channel cell biology capability, translational assays, and significant expertise for neuroscience drug discovery research.

Dr. Andrew Southan, Chief Executive of Metrion Biosciences, said: “The launch of our GLP hERG screening capability adds further depth to our ion channel drug discovery services and complements our existing cardiac safety service portfolio. Our team is pleased to be able to offer GLP quality services to new and existing clients globally as we continue to develop Metrion as a leading ion channel focused CRO.”

More News

Seek Labs Announces Successful Completion of African Swine Fever Virus In Vivo Trial Utilizing CRISPR-based Treatments

The trial, which aimed to replicate and expand an earlier trial, demonstrated pigs infected with ASFV and treated with Seek Labs’ CRISPR-based systems survived longer than untreated infected pigs. Over half of the CRISPR-treated pigs survived beyond the duration of the trial. Observations and data from both studies reveal compelling outcomes where treatment prolonged lifespans of infected pigs compared to control groups.

Gyros Protein Technologies Introduces Gyrolab Generic Rodent ADA Kit Reagents to Support Preclinical Immunogenicity Assessment

The new Roden ADA Kit expedites bioanalysis by removing the need for assay development and optimization across molecules to provide robust, reproducible, reliable data from nanoliter sample volumes. This is beneficial when ADA assessment is evaluated in preclinical animal models where sample volume may be limited.

Unleashing Biotech Potential: ATLATL Scientific & Miltenyi Biotec Partnership

Since the inception of their partnership five years ago, ATLATL Scientific and Miltenyi Biotec have worked closely together to leverage their respective expertise and resources.

spot_img

By using this website you agree to accept Medical Device News Magazine Privacy Policy