Elicera Therapeutics

The dose escalation study, which is carried out in collaboration with Uppsala University as sponsor, has previously been able to report signals of clinical activity in two of eight evaluable patients in the ELC-100 study, where a total of 12 patients are planned to be treated in four dose levels/cohorts. After the DSMB’s recommendation to continue the trial, recruitment of the remaining three patients in the last cohort can commence.

About the ELC-100 clinical phase I/IIa dose escalation study

The ELC-100 study is conducted in two phases. Phase I, which is now underway, has the primary goal of investigating the safety of the treatment and determining the maximum tolerable dose. The first phase of the study has four dose levels with three patients at each level. In addition to determining the maximum tolerable dose, efficacy is also evaluated for example in the form of tumor response.

So far, no dose-limiting adverse events have been reported. Full efficacy reporting from the ELC-100 study is expected when the study is fully completed.

About ELC-100

ELC-100 is an oncolytic virus based on a genetically modified adenovirus that has been optimized for its ability to selectively enter and replicate in neuroendocrine cancer cells but not healthy cells. Tumor cell death is achieved via so-called oncolysis when the virus particles have replicated to a sufficient extent in the tumor cell that it explodes and dies. ELC-100 is currently being used in an ongoing phase I/IIa clinical trial in the treatment of neuroendocrine tumors.