SciTech Secures 2nd FDA IND Approval for ST-001 Targeting SCLC
Advancing Cancer Care with Innovative NanoTherapeutics for SCLC

SciTech Development is proud to announce a major breakthrough in the fight against cancer. The U.S. Food and Drug Administration (FDA) has approved their Investigational New Drug (IND) application for a Phase 1a/b clinical trial of ST-001 nanoFenretinide, a pioneering treatment targeting relapsed and refractory small cell lung cancer (SCLC). Known for its aggressive nature and limited treatment options, SCLC has long been a challenge in oncology. With its innovative nanoparticle design, ST-001 is poised to deliver fenretinide with enhanced safety and efficiency, bringing new hope to patients in need.
This FDA approval marks a key milestone for SciTech Development, enabling patient recruitment and the next phase of clinical trials to begin. Backed by promising results from earlier trials on T-cell non-Hodgkin lymphoma, the company believes ST-001 has the potential to revolutionize cancer therapy with its advanced drug delivery platform. Learn more about the significance of this achievement and how SciTech is pushing boundaries in oncology. Click here to read the full press release.
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