ABOUT SYNTHEGO
Synthego is a genome engineering company that enables life science research and therapy development with a mission of increased access to engineered therapies for all patients. With unparalleled CRISPR expertise, state-of-the-art GMP capabilities, and a continuum of product offerings, Synthego supports CRISPR-edited cell and gene therapeutic development at every step, from R&D through IND submission to first-in-human trials.
FEATURED CONTENT
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This article explores the details of Chemistry, Manufacturing, and Controls and Critical Quality Attributes, which play an important role in gene editing.
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CRISPR therapies are being developed for genetic disorders, cancer, and infectious diseases. Explore which CRISPR clinical trials are worth keeping an eye on this year.
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Review the fundamentals of CRISPR technology, development, and its use to manipulate genes in different ways, such as altering their nucleotide sequences or changing their expression.
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Navigate the intricate regulatory landscape with knowledge that can help you move your CRISPR therapies quickly and efficiently through clinical trials.
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A regulatory expert provides her insight on what regulatory experts do and how they can help you accelerate your path from bench to clinic.
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Disease modeling helps us understand disease and create therapies. Learn about the types of disease models, the impact of CRISPR, current challenges, and trends.
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The single guide RNA (sgRNA) is one of the key components of successful CRISPR gene editing. Here we cover all the important aspects of sgRNA and Synthego’s sgRNA products.
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Join a discussion surrounding cell and gene therapy products, specific FDA initiatives, broader regulatory trends, and the predicted growth of cell and gene therapy products in the coming years.
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What is cell and gene therapy and how has the invention of CRISPR revolutionized the industry? Learn about the history of these therapies and life-changing treatments on the horizon.
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CRISPR technology is revolutionizing cell and gene therapies, but how do CRISPR clinical trials work? Follow this explanation of CRISPR therapies from the discovery phase to FDA approval.
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Learn how to approach CRISPR cell and gene therapy development challenges, such as regulatory hurdles, ensuring consistency, finding qualified and experienced staff, and obtaining GMP-Grade reagents.
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Grow your understanding of how new developments in CRISPR gene therapy drugs and FDA guidance are affecting cell and gene therapy products.
VIDEOS
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How is the approval of the US' first CRISPR therapy reshaping the landscape of CRISPR regulations and ongoing clinical trials?
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In this insightful video, Lina Jamis, Associate Director of Regulatory Affairs at Synthego, shares key learnings and valuable perspectives on the latest developments in the field of CRISPR therapeutics.
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As CRISPR use continues to grow, so has the demand for clinical-grade guide RNA. Learn about GMP sgRNA and their stringent process and manufacturing controls.
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Professor Stephanie Cherqui shares her thoughts on taking CRISPR-based therapies from research to the clinic, the upcoming trials she is working on, and more.
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Explore a state-of-the-art GMP facility focused on CRISPR based Cell and Gene therapies with helping temperature controlled warehouse and multiple synthesis suites.
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Learn how to accelerate your clinical timeline for cell and gene therapies and improve next-generation GMP production facilities.
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Explore this video explaining a next-generation GMP sgRNA facility.
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Learn about the clinical trial for a new sickle cell disease treatment from an early clinical trial patient who has, at this time, experienced complete recovery from symptoms.
CONTACT INFORMATION
Synthego Corporation
3696 Haven Ave, Suite A
Redwood City, CA 94063
UNITED STATES
Phone: 888-622-6883
Contact: Meenakshi Prabhune
FEATURED PRODUCTS
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Explore regulatory support services that can help you successfully to navigate CRISPR-based therapeutic development and prepare you for a successful IND submission.
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Transition from early-phase research through process development into the clinic with these continuum sgRNA available in different grades.
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Seamlessly transition from discovery to delivery with INDe sgRNAs. These quality sgRNAs can be synthesized in quantities from milligrams to grams and follow high purity specifications.
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Consistently achieve high editing efficiency and quick turnaround time in as little as 7 days with synthetic sgRNA that pave your way to a successful CRISPR experiment.
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Move your CRISPR-based therapeutics from discovery to delivery in a seamless transition with IND-enabling (INDe) sgRNAs designed specifically for preclinical safety, toxicity, and efficacy studies.
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IND-enabling sgRNAs are high quality sgRNAs with increased quality oversight and documentation enabling comparability between reagents as you transition into clinical trials.
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A new state-of-the-art GMP facility has been created to accelerate the development of CRISPR-based cell and gene therapies, overcoming challenges such as procuring reliable GMP-grade sgRNA persist.
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Learn about three different grades of high-quality synthetic sgRNAs that will help support every step of your CRISPR-based therapy development process.