Pharmaceutical Business review

Helix begins enrolment for third dose level cohort of phase I/II study of L-DOS47

Three patients enrolled in the second dose level cohort completed the first treatment cycle and well tolerated the L-DOS47 therapy.

Patients to be enrolled in the third cohort will receive the next dose level 0.33 micrograms of L-DOS47 per kilogram of patient body weight.

Helix chief executive officer Robert Verhagen said, "L-DOS47 therapy continues to be well tolerated by the patients treated in our first two dose levels."

The immunoconjugate-based drug candidate, L-DOS47, is based on DOS47 technology designed to modify the microenvironmental conditions of cancer cells resulting in their destruction.