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Home » CRISPR

Articles Tagged with ''CRISPR''

Arsenal adds to its storehouse with a $220M series B

Sep. 7, 2022
By Lee Landenberger
Arsenal Biosciences Inc. closed on an oversubscribed $220 million series B financing so it could continue developing its programmable cell therapy research programs and its candidates for treating solid tumor malignancies. Arsenal’s lead program is AB-1015 for treating ovarian cancer.
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Neuron

New screening platform reveals neurodegeneration drug targets in microglia

Aug. 12, 2022
By Nuala Moran
As the resident innate immune cells of the brain, microglia are emerging as key drivers of neurological diseases, but as yet there is no systematic way of exploring their potential as drug targets.
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Gene editing illustration
Newco news

CRISPR co-inventor’s Epic Bio launches with $55M series A

July 15, 2022
By Lee Landenberger
Controlling the epigenetics of a patient, figuring out what genes are expressed and understanding their level of expression, is at the center of Epic Bio, a new company founded by Stanley Qi, co-inventor on the CRISPR patent held by the University of California.
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Macrophage and cancer cell

Go ask Alice: Eat me and don’t eat me signals at the heart of DEM Biopharma

June 23, 2022
By Lee Landenberger
Despite a huge amount of progress in the hot space CD47, there’s a large space beyond it to explore, according to DEM Biopharma Inc.’s CEO David Donabedian. The new company just raised $70 million to develop therapies targeting don’t eat me, hence DEM, and eat me signals on cancer cells and macrophages.
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Spotlight raises $36.5M to advance non-viral gene editing tech, lead I-O program

March 22, 2022
By Michael Fitzhugh
Spotlight Therapeutics Inc., a company developing cell-targeted in vivo CRISPR gene editing biologics, has raised $36.5 million in series B financing to support advancement of its first-in-class immuno-oncology program and further applications of its in-house technology platform. The financing round was co-led by new investors GordonMD Global Investments and Epiq Capital Group, with participation from Magnetic Ventures, as well as existing investors GV, Emerson Collective and others.
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US PTAB may have spoken, but CRISPR patent battle wages on

March 1, 2022
By Mari Serebrov
The U.S. Patent Trial and Appeal Board’s (PTAB) decision Feb. 28 that Broad Institute scientists were the first to invent the use of CRISPR/Cas9 genome editing in eukaryotic cells is just another chapter in the ongoing saga of who has patent rights to various elements of the CRISPR platform.
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Petri dish and capsules

Phages help to combat bacteria, reduce antibiotic use

Dec. 27, 2021
By John Fox
An international study led by scientists at the University of Exeter in the U.K. suggests how to combine antibiotic and bacteriophage therapy optimally, in order to reduce antibiotic use and potentially prevent multidrug resistance in bacteria.
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CRISPR Cas9 illustration

Ers Genomics granted CRISPR-Cas9 patent in China

Nov. 23, 2021
By Doris Yu
A Chinese patent covering methods and compositions for the use of CRISPR-Cas9 in eukaryotes has been granted to Dublin-based Ers Genomics Ltd., making what Michael Arciero, vice president of intellectual property and commercial development at the company, called “a strong but not surprising statement by China,” which has made the biotechnology industry one of its top national priorities.
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Ers Genomics granted CRISPR-Cas9 patent in China

Nov. 18, 2021
By Doris Yu
A Chinese patent covering methods and compositions for the use of CRISPR-Cas9 in eukaryotes has been granted to Dublin-based Ers Genomics Ltd., making what Michael Arciero, vice president of intellectual property and commercial development at the company, called “a strong but not surprising statement by China,” which has made the biotechnology industry one of its top national priorities.
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Chroma Medicine closes $125M A round for epigenetic editing platform

Nov. 17, 2021
By Cormac Sheridan
Chroma Medicine Inc. emerged from stealth with $125 million in series A financing and high ambitions to rewrite the rules of genomic medicine by modulating the epigenetic status of target genes in order to switch expression on or off and thereby achieve therapeutic outcomes.
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