Molecular Partners AG: Actavis confirms timeline for the start of phase III development of abicipar Montag, 11. Mai 2015 - 13:09
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Actavis confirms timeline for the start of phase III development of abicipar
Zurich-Schlieren, May 11, 2015. Molecular Partners AG (ticker: MOLN) today announced that the new Actavis/Allergan management team has confirmed the abicipar phase IIIclinical program is on track to be initiated by the end of Q2 2015 or early in the third quarter. Abicipar is an investigational drug for wet AMD, a leading cause of blindness in the western world. Current treatments require monthly or bi-monthly injections into the eye. The phase III study program will evaluate the safety and efficacy of abicipar and its potential to improve vision gains whilst reducing the number of treatment injections versus ranibizumab (Lucentis®), addressing two significant unmet medical needs for patients with wet AMD.
This is the first official announcement from Actavis/Allergan on abicipar following the companies’ merger in March, underlining the commitment to the DARPin™ program and to the timeline proposed by Allergan prior to the merger.
“We welcome Actavis’ high commitment to advancing abicipar through a strong phase III ophthalmology development program. We appreciate the Actavis/Allergan management team’s decision to prioritize the development program for abicipar, despite ongoing integration,“ said Patrick Amstutz, Chief Operating Officer at Molecular Partners. “We are looking forward to continuing to support our partner progress abicipar through to rapid commercial launch.”

