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 therapeutic platform biotechnology company
solutherapeutics.comLast updated
In short: Solu debuted with significant seed and Series A funding and initiated clinical trials for its lead cancer therapy, STX-0712.
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--(BUSINESS WIRE)--Solu Therapeutics, a precision-medicine company developing therapeutics to eliminate disease-driving cells, founded by Longwood Fund, today announced the closing of an oversubscribed $31 million...
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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