The company is re-dosing the product in patients with Duchenne muscular dystrophy. The re-dosing programme in North America will include up to 72 patients across 14 sites who had participated in the drisapersen DEMAND V (Phase II) & DEMAND III (Phase III) studies.
The company regained the rights to drisapersen from its previous partner, GSK, in January 2014. The product is administered subcutaneously, with once weekly dosing. The firm aims to allow home-dosing where feasible, and cost-free transport with straightforward logistics for clinical centres, through collaboration with Greenphire and the Medical Research Network.
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