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The Cam­bridge, MA biotech’s two clin­i­cal-stage as­sets are in on­col­o­gy: pe­riph­er­al T cell lym­phoma and glioblas­toma. With the market for biotech stocks constrained, Genocea Biosciences plans to. He was mum on which in­di­ca­tions the pair will go af­ter, but Myeloid did note that the part­ner­ship em­pha­sizes the broad reach of its R&D ca­pa­bil­i­ties “to in­di­ca­tions be­yond can­cer” in its press re­lease. Hell lead Tessera Therapeutics, a well-funded genetic medicine startup.

Pair­ing the two par­ties’ tech could lead to sim­pli­fied de­liv­ery of ex vi­vo and in vi­vo cell ther­a­pies, the com­pa­nies said. The goal is to work with Prime for “many years” on “mul­ti­ple prod­ucts,” Getts said. Our focus is to bring intelligent solutions to prescribers and patients who need better solutions. Tessera Therapeutics is a life sciences company developing Gene Writing, a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Our mission is to market products which truly make a difference for patients. Healthcare Founded: 2018 Funding to Date: 558.91MM. Tessara utilises the RealBrain 3D micro-tissue platform to accelerate neural drug discovery and regenerative medicine projects both in house and with our partners. And be­cause we’re us­ing some­thing that’s with­in our hu­man genome, we be­lieve that im­muno­genic­i­ty is go­ing to be sig­nif­i­cant­ly less, too.” TerSera Therapeutics LLC acquires and develops specialty pharmaceutical products with a focus on select therapeutic areas.

Tessera Therapeutics, a biotechnology company pioneering a new approach in genetic medicine known as Gene Writing, announced today the appointment of Howard Liang, Ph.D., as President and Chief Financial Officer. “You can de­liv­er much larg­er car­goes - it’s all on one RNA con­struct - and the cost of goods ob­vi­ous­ly is in the world of what an RNA costs ver­sus what some of these vi­ral-based mech­a­nisms are. Expanded Team Will Accelerate Development of Breakthrough ‘Gene Writing’ Platform A New Approach in Genetic Medicine. “Why we’re ex­cit­ed about work­ing with Prime, this re­al­ly over­comes pret­ty much, not all, but al­most all, of the lim­i­ta­tions as­so­ci­at­ed with AAV de­liv­ery, lentivi­ral de­liv­ery,” Getts told End­points. With lessons learned from Vor, Sid­dhartha Mukher­jee takes a dif­fer­ent route to tar­get sol­id tu­mors with start­up Myeloid