Solu Therapeutics received FDA Fast Track designation.
The designation is for their lead CyTAC program targeting relapsed or refractory CMML.
See the latest news and media coverage for Solu. We track all announcements, press releases, and industry mentions in real time, all in one place.
Clinical-stage therapeutic platform biotechnology company
solutherapeutics.comLast updated
In short: Solu initiated STX-0712 dosing in its AML cohort and received FDA Fast Track designation for CMML.
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.
Solu Therapeutics, a biotechnology company pioneering novel therapies to eliminate disease-driving cells in cancer and immunology, today announced that initial results from its first-in-human Phase...
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...
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...
Solu Therapeutics has debuted with $31 million in seed financing to develop a small-molecule drug technology licensed from GSK. Called Cytotoxicity Targeting Chimera, or CyTaC...
Track Solu and your other target companies to get real-time alerts and weekly summaries delivered straight to your inbox.
Browse news for competitors to Solu and other trending companies.