This page shows the latest CRISPR Therapeutics news and features for those working in and with pharma, biotech and healthcare.
Following the amended agreement, Vertex will now lead the global development, manufacturing and commercialisation of the gene therapy CTX001, with support from CRISPR Therapeutics. ... Along with Vertex/CRISPR Therapeutics, bluebird bio is also seeking
Scribe Therapeutics has completed an oversubscribed $100m Series B financing round to advance the development of its CRISPR platform and pipeline. ... of patients,” said Jennifer Doudna, co-inventor of CRISPR technology, Nobel Laureate and co-founder
Vertex gained VX-880 from its previous acquisition of Semma Therapeutics for $950m in September 2019. ... Vertex is also looking to develop a CRISPR/Cas9 gene-editing therapy for the treatment of severe haemoglobinopathies in partnership with CRISPR
The initial areas of focus for the ATN are neurodegeneration, CRISPR-based therapeutics, protein degradation, functional genomics in human brain cells and sleep mechanisms and circuits. ... disorders; and developing therapeutics for brain diseases based
Collaboration will utilise KSQ’s CRISPR-screening technology. Japanese pharma company Takeda has signed a collaboration agreement with KSQ Therapeutics to develop and market novel immune-based cancer therapies using its ... technology. KSQ’s
Vertex/CRISPR Therapeutics make headway in sickle cell and beta thalassaemia. Also presenting data at ASH were Vertex and CRISPR Therapeutics, whose gene-editing therapy CTX001 scored some promising results in ... These are the first published results
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In late March, Vertex was boosted further when its main challenger in the field, Proteostatis Therapeutics, reported disappointing results for its rival triple therapy candidate. ... These include alpha-1 antitrypsin deficiency and focal segmental
The green light came after a delay of around a year caused by manufacturing issues, which allowed another candidate from CRISPR Therapeutics and Vertex Pharma - CTX001 for the rare blood disease ... Meanwhile, CRISPR isn’t the only gene-editing
drugs, Novartis’ Kymriah and Gilead/Kite’s Yescarta and Spark Therapeutics’ gene therapy Luxturna all reaching the market last year. ... CRISPR Therapeutics, one of the companies working with the exciting cutting-edge CRISPR/Cas9 gene editing
New CRISPR tech deals. After investing $335m in research support for a JV with CRISPR Therapeutics to discover, develop and commercialize new therapeutics to cure blood disorders, blindness, and congenital heart ... Financial details were not disclosed.
440. Pieris (US). Roche. Collaboration, licence. Bispecific Anticalin-based protein therapeutics platform to discover immuno-oncology targets. ... 350. CRISPR Therapeutics (CH). Bayer Lifescience. Joint venture. Combining gene editing technology and
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Lundberg most recently served as chief scientific officer of CRISPR Therapeutics, where he lead the development of the company’s first clinical trial application. ... Prior to CRISPR, he worked as head of translational medicine at Alexion
He becomes chief financial officer. CRISPR Therapeutics has appointed Marc Becker as its new chief financial officer with remit to drive development of its gene-editing technology platform. ... Becker said: “I am excited to join the CRISPR Therapeutics
Swiss biopharma company CRISPR Therapeutics has appointed Dr Tony Coles to its board of directors. ... Rodger Novak, chief executive officer of CRISPR Therapeutics, said: “Dr Coles is a venerated leader in the biotech industry with a strong track
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With transformative treatments that leverage CRISPR technology, there are many challenges to overcome throughout the journey of development through to patient access. ... Several manufacturers are developing novel treatments for the disease, including
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