Solu Therapeutics received FDA Fast Track designation.
The designation is for their lead CyTAC program targeting relapsed or refractory CMML.
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Clinical-stage biotechnology company
solutherapeutics.comLast updated
In short: Solu Therapeutics advanced its STX-0712 program for leukemia through FDA Fast Track designation, clinical trials, and $41M in Series A funding.
The designation is for their lead CyTAC program targeting relapsed or refractory CMML.
The investigational therapy targets chronic myelomonocytic leukemia, an aggressive blood cancer with limited options.
The funding supports clinical evaluation of STX-0712, a novel CCR2-CyTAC therapy for CMML and other hematologic malignancies.
He succeeds co-founder David Donabedian and brings over 30 years of biopharma experience to lead development of CyTaC platform.
BOSTON, Dec. 2, 2025 /PRNewswire/ -- Solu Therapeutics, a biotechnology company pioneering novel therapies to eliminate disease-driving cells in cancer, immunology, and other therapeutic areas...
Solu Therapeutics Inc. has identified heterobifunctional cotinine-containing compounds acting as sodium channel protein type 10 subunit α (SCN10A; Nav1.8) blockers or sodium channel protein type...
Funding to support clinical evaluation of STX-0712, drive additional pipeline programs, and target new applications of company's proprietary CyTAC™ and TicTAC™ platforms. Phase 1 trial...
Six years ago, Brandon Turunen, PhD, answered a call from his employer, GSK, for proposals to develop new medicines. "They would oftentimes do calls for...
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