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Merck’s ethical gene editing considerations published in Bioethics Journal


The American Journal of Bioethics has accepted Merck’s publication on ethical issues in genome editing to be printed in its July issue. A summary version has been published in The American Journal of Bioethics blog.


By Team ABLE

Merck, a leading science and technology company and leader in genome editing, has announced that The American Journal of Bioethics has accepted a publication on ethical issues in genome editing to be printed in its July issue. A summary version has been published in The American Journal of Bioethics blog.

\"Publication of this work demonstrates that Merck is a true ethical innovator,\" said Udit Batra, member of the Merck Executive Board, and CEO, Life Science. \"Merck established a Bioethics Advisory Panel — a diverse group of global biomedical experts — to provide guidance for research in which its businesses are involved, including research on or using genome editing. We take this work very seriously.\"

Co-authored by colleagues from the company\'s Bioethics Advisory Panel and colleagues from the Life Science  and Healthcare business sectors of Merck and the company\'s Corporate Affairs function, the publication discusses critical ethical issues involved with the practical processes of discovery, development, manufacture, sale and distribution of genome-editing technology products such as Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR).

\"Our publication incorporates the critical responsibilities of suppliers such as Merck,\" said Dr. Jochen Taupitz, a renowned ethics expert and professor at the University of Mannheim, and co-author of the publication. Taupitz is also a member of the Bioethics Advisory Panel of Merck.

\"As a company that is leading the way in genome-editing innovation, Merck recognizes a need to develop and implement science-based bioethics,\" said Steven Hildemann, global chief medical officer at the Healthcare business sector of Merck, and senior author of the publication. \"This publication describes our novel approach to ensure our genome-editing products are developed and distributed adhering to the highest standards of rapidly evolving bioethical guidance.\"
Merck\'s Bioethics Advisory Panel has defined a clear operational position taking into account scientific and societal issues to inform promising therapeutic approaches for use in research and applications.

A popular method of editing genes, CRISPR acts as genetic scissors which can be used to remove or replace an existing gene, switch a gene on or off or insert a new gene with unprecedented accuracy. The publication leverages the experience of the company\'s Life Science business in developing and selling CRISPR genome-editing technology over the past 13 years. 

CRISPR patents are directed to chromosomal integration, or cutting of the sequence of eukaryotic cells and insertion of a synthetic exogenous DNA sequence to make a desired genomic change. Scientists can replace a disease-associated mutation with a beneficial or functional sequence — important for creating disease models and allowing new gene therapy solutions.

Merck has made significant contributions to the genome-editing field. It was the first company to offer custom biomolecules for genome editing globally (TargeTron RNA-guided group II introns and CompoZr zinc finger nucleases), driving adoption of these techniques by researchers all over the world. Merck was also the first company to manufacture arrayed CRISPR libraries covering the entire human genome, accelerating cures for diseases by allowing scientists to explore more questions about root causes.

An online preview of the genome-editing bioethics publication in The American Journal of Bioethics can be found at: http://www.bioethics.net/2018/05/ethical-considerations-in-the-manufacture-sale-and-distribution-of-genome-editing-technologies/