CRISPR Therapeutics, a gene editing company, has signed an expanded clinical and commercial license agreement into oncology with MaxCyte, a cell-based medicines and life sciences company, it was reported yesterday.
Both firms have entered into a non-exclusive commercial license agreement that will enable CRISPR Therapeutics to deploy MaxCyte's Flow Electroporation Technology to develop CRISPR/Cas9-based therapies in immuno-oncology.
The expanded relationship is based on a present agreement announced in March 2017, which allowed for the development of commercial therapeutics for haemoglobin-related diseases. According to the terms of the new license agreement, CRISPR Therapeutics will receive non-exclusive development and commercial-use rights to MaxCyte's cell engineering platform to develop immuno-oncology cell therapies. MaxCyte will provide its technology to CRISPR Therapeutics as part of the enabling technology license agreement and will receive milestone and sales-based payments in addition to other licensing fees.
Medivir and Vetbiolix report positive results from VBX-1000 Proof-of-Concept clinical study
Norgine submits first marketing authorisation application submissions for approval of eflornithine
Innovent Biologics names new Oncology CMO
UroGen's UGN-103 IND accepted by FDA for bladder cancer treatment
Innate Pharma advances Sanofi-developed NK cell engager to Phase 2 for blood cancer patients
Precision Epigenomics partners with TruDiagnostic
Portage Biotech expands evaluation of strategic alternatives
Stamford Pharmaceuticals starts locally advanced basal cell carcinoma (laBCC) trial of SP-002
QST selects RayStation for advanced carbon ion therapy
Candel Therapeutics granted FDA Orphan Drug Designation for CAN-2409 in pancreatic cancer treatment
ELIAS Animal Health names new chief revenue officer
Innate Pharma reports preclinical efficacy of IPH45
Roche attains CE Mark for first companion diagnostic for HER2-low metastatic breast cancer
BioCity Biopharma's BC2027 Phase one study IND application receives US FDA approval
enGene Holdings names new senior vice president, Urologic Oncology and Clinical Development