Actuate Therapeutics, a Phase 2 biotech developing in-licensed inhibitor therapies for difficult to treat cancers, filed on Friday with...
Read moreActuate Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation for elraglusib...
Read moreTempus announced a brand-new multi-omics collaboration with Actuate Therapeutics to support its ongoing Phase 1/2 Study of elraglusib, formerly...
Read moreActuate Therapeutics and The University of Kansas Cancer Center announced the enrollment of the first patient on a Phase...
Read moreActuate Therapeutics, Inc. announced that their Phase 2 open-label single arm study of elraglusib (9-ING-41) plus gemcitabine/nab-paclitaxel treatment met...
Read moreActuate Therapeutics announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation for 9-ING-41 for...
Read moreActuate Therapeutics, Inc. announced enrollment of the first patients with first-line advanced pancreatic cancer in a phase 2 study...
Read moreActuate Therapeutics, Inc. has raised an additional $6.5M in a Series B-3 financing round led by Bios Partners with...
Read moreWe are delighted to announce that Actuate Therapeutics is the latest company to join the Kairos portfolio. Founded in...
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