Irish pharmaceutical company Allergan plc (NYSE:AGN) said on Friday that it has agreed to acquire Bonti Inc for an upfront payment of USD195m as well as additional potential commercial milestone payments, subject to certain adjustments and other customary closing conditions.
Based in Newport Beach, CA, Bonti is a privately held clinical-stage biotechnology company focused on the development and commercialisation of novel, fast-acting neurotoxin programmess for aesthetic and therapeutic applications.
Upon closing of the acquisition, Allergan will acquire the global rights to Bonti's pipeline consisting of two botulinum neurotoxin serotype E (BoNT/E) programmes currently in Phase 2 development, EB-001A (aesthetic) and EB-001T (therapeutic). The active ingredient in both programmes, EB-001, is a novel botulinum neurotoxin serotype E (BoNT/E) with a unique clinical profile, characterized by a rapid onset of action within 24 hours and a two to four week duration of effect.
Recently, Bonti's topline results from the first clinical study of EB-001 in glabellar frown lines confirmed both the safety and efficacy of the differentiated profile. In the US, there are about 65 million consumers who are considering facial injectable treatments, including being treated with a faster acting shorter-duration product.
AstraZeneca's Fasenra misses primary endpoint in Phase III COPD trial
Hemogenyx reports positive safety and early efficacy data from third patient in CAR-T trial
Sanofi reports positive phase 2a results for brivekimig in hidradenitis suppurativa
GSK commits USD30bn to US R&D and manufacturing expansion
Neurocrine Biosciences announces presentation of Osavampator Phase 2 data at Psych Congress 2025
Ascletis presents ASC30 study results at EASD Annual Meeting
Three WuXi Biologics manufacturing facilities receive GMP certification from Turkish regulator
VarmX secures strategic collaboration and option agreement with CSL for novel coagulation therapy
Avidity Biosciences closes USD690m public offering of common stock
Akeso's ligufalimab (CD47 mAb) granted FDA Orphan Drug Designation for AML
Forte Biosciences highlights positive FB102 data in celiac disease at Tampere Symposium
SureSpace Launches in Dubai to Tackle Doomscrolling and Redefine Social Networking
Kodiak reports positive APEX data for KSI-101 in macular edema secondary to inflammation
Biophytis secures Brazilian funding and partnerships for obesity Phase 2 trial