L-DOS47, Helix’s first therapeutic immunoconjugate drug candidate under development based upon its novel DOS47 platform technology, is designed to modify the microenvironmental conditions of cancer cells so that they get destroyed.
L-DOS47 is intended to offer an innovative approach to the first-line treatment of inoperable, locally advanced, recurrent or metastatic non-small cell lung cancer (NSCLC).
Helix BioPharma president John Docherty said receiving FDA approval to perform this study was a major milestone for the company.
The company will now proceed with its remaining pre-study logistical preparations with a view to commence clinical site initiation, and patient recruitment activities late spring to early summer this year.