Isofol has enrolled and dosed its first group of patients in the IND-study ISO-FF-001
Isofol Medical AB (publ) announced today that the first six patients were enrolled and dosed in the ISO-FF-001 study. The study, which is part of the regulatory documentation required for an oncology drug to be granted approval, investigates possible effects of Modufolin on heart rhythm (ECG). The ISO-FF-001 is performed under an IND at the CTC (clinical Trial Consultants) study facility in Uppsala, Sweden. The study is planned to be finalized in August 2017.Isofol Medical AB (publ), a clinical staged oncology company, announced today that the first six patients were enrolled and dosed in