The dose-escalating trial is aimed at validating the safety profile of ERY-ASP in 12 to 18 patients with ALL. The trial was approved by the US FDA last year and the University of Chicago, Duke University Medical Center and Ohio State University are now open for patient accrual.
ERY-ASP, also known as Graspa in Europe, is an L-asparaginase product, with a safer and broader range of clinical use compared with existing forms due to the entrapment and protection of the enzyme inside red blood cells. In Europe, the therapy is being investigated in a Phase III study in relapsing ALL, in Phase IIb in acute myeloid leukemia (AML) and in Phase II in pancreas cancer.
Perrigo to acquire United States rights for Entocort from AstraZeneca
US FDA approves Boehringer Ingelheim's Pradaxa
Phase II clinical trial for potential treatment of androgenetic alopecia completed by Samumed
Life Sciences Partners collaborates on immuno-oncology with Bristol-Myers Squibb
Arsanis initiates first cohort in Phase one clinical trial of ASN100
Impax introduces generic Avodart (Dutasteride) Capsules, 0.5 mg
Mylan unveils generic FazaClo orally disintegrating tablets for treating schizophrenia