Caribou Biosciences Announces Oral Presentation on In Vivo Cas12a chRDNA Genome Editing at the 27th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT)
15 Avril 2024 - 3:00PM
Caribou Biosciences, Inc. (Nasdaq: CRBU), a leading clinical-stage
CRISPR genome-editing biopharmaceutical company, today announced an
abstract on the efficient use of Cas12a chRDNA genome-editing
technology for in vivo hepatic gene disruption has been accepted
for an oral presentation at the 27th annual meeting of the American
Society of Gene and Cell Therapy (ASGCT), which is being held May
7-11, 2024, in Baltimore, Maryland.
Details of the oral presentation are as follows:
Title: Cas12a CRISPR hybrid RNA-DNA
(chRDNA)-mediated in vivo genome-editing technology for efficient
and functional hepatic gene disruptionPresenter:
Meghdad Rahdar, PhD, director of technology development, Caribou
BiosciencesDate and time: Friday, May 10, 2024 at
4:30 pm ETSession: Advancements in Technologies
for In Vivo Gene TherapiesLocation:
324-326Abstract number: 278
Accepted abstracts will be available on the ASGCT Annual Meeting
website on April 22, 2024 at 4:30 pm ET. The presentation will be
available on the Scientific Publications page of Caribou’s website
on Friday, May 10, 2024 at 6:00 am ET.
About Caribou’s novel next-generation CRISPR
platformCRISPR genome editing uses easily designed,
modular biological tools to make DNA changes in living cells. There
are two basic components of Class 2 CRISPR systems: the nuclease
protein that cuts DNA and the RNA molecule(s) that guide the
nuclease to generate a site-specific, double-stranded break,
leading to an edit at the targeted genomic site. CRISPR systems are
capable of editing unintended genomic sites, known as off-target
editing, which may lead to harmful effects on cellular function and
phenotype. In response to this challenge, Caribou has developed
CRISPR hybrid RNA-DNA guides (chRDNAs; pronounced “chardonnays”)
that direct substantially more precise genome editing compared to
all-RNA guides. Caribou is deploying the power of its chRDNA
technology to carry out high efficiency multiple edits, to develop
CRISPR-edited therapies.
About Caribou Biosciences, Inc.Caribou
Biosciences is a clinical-stage CRISPR genome-editing
biopharmaceutical company dedicated to developing transformative
therapies for patients with devastating diseases. The company’s
genome-editing platform, including its Cas12a chRDNA technology,
enables superior precision to develop cell therapies that are
armored to potentially improve activity against diseases. Caribou
is advancing a pipeline of clinical-stage off-the-shelf cell
therapies from its CAR-T cell platform as readily available
treatments for patients with hematologic malignancies and
autoimmune diseases. Follow us @CaribouBio and visit
www.cariboubio.com.
Caribou Biosciences, Inc.
contacts:Investors:Amy Figueroa,
CFAinvestor.relations@cariboubio.com
Media:Peggy Vorwald,
PhDmedia@cariboubio.com
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