Published on 3/9/2018 10:20:00 AM
Issue 37: March 2018
FDA BURST: EMAIL TO ASCPT MEMBERS
In cooperation with the Food and Drug Administration (FDA), and as a service to our members, ASCPT will periodically distribute information about newly approved therapies or significant changes to approved therapies. Dissemination of this information helps the FDA inform professionals in the patient care arena of recent approvals in a timely manner. Included in the email from the FDA is a link to the product label, which provides the relevant clinical pharmacology information on the indication, contraindications, dosing, and safety. In sending this information, ASCPT does not endorse any product or therapy and does not take any position on the safety or efficacy of the product or therapy described.
FDA Announces Availability of the Guidance, "E18 Genomic Sampling and Management of Genomic Data"
On March 2, 2018, the US Food and Drug Administration (FDA) announced the availability of the final guidance for industry entitled "E18 Genomic Sampling and Management of Genomic Data". The guidance was prepared under the auspices of the International Council for Harmonisation (ICH), formerly the International Conference on Harmonisation. FDA finalized the guidance after carefully reviewing comments received on the draft guidance with the same name published in June 2016. The final guidance contains the same basic principles from the draft guidance, and includes revisions to the guideline to address comments received and to provide greater clarity.
The guidance provides guidelines for genomic sampling and management of genomic data from interventional and non-interventional clinical studies. Awareness of, and interest in, genomic data obtained from clinical studies are growing. In particular, genomic research could be used in all phases of drug development to assess genomic correlates of drug response, and to understand mechanisms of disease or drug pharmacology. The identification of genomic biomarkers underlying variability in drug response may be valuable to optimize patient therapy, design more efficient studies, and inform drug labeling. Furthermore, the generation and interpretation of genomic data, both within and across clinical studies and drug development programs, allow for a better understanding of pharmacological and pathological mechanisms and enable the identification of new drug targets.
This guidance focuses on the general principles of collecting, processing, transporting, storing, and disposing of genomic samples or data in clinical studies. The guidance is intended to provide harmonized principles of genomic sampling and of management of genomic data in clinical studies to foster interactions amongst stakeholders, including drug developers, investigators, and regulators; and to encourage genomic research within clinical studies.
In general, FDA's guidance documents do not establish legally enforceable responsibilities. Instead, guidances describe the Agency's current thinking on a topic and should be viewed only as recommendations, unless specific regulatory or statutory requirements are cited.
The "E18 Genomic Sampling and Management of Genomic Data" guidance is available at https://go.usa.gov/xnzBY
. Please refer to the guidance for more details.
Instructions for submitting either electronic or written comments on Agency guidances at any time may be found in the federal register notice for this guidance (https://go.usa.gov/xnujv
We always welcome your thoughts regarding the format, content, and utility of the communication. Comments may be sent via email to firstname.lastname@example.org
This communication was prepared by Office of Clinical Pharmacology, Office of Translational Sciences, CDER, FDA.