Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TrenibotulinumtoxinE (TrenibotE) is a first-in-class botulinum neurotoxin serotype E developed for the treatment of moderate to severe glabellar lines (frown lines between the eyebrows). Unlike traditional botulinum toxin type A products (such as onabotulinumtoxinA/BOTOX), TrenibotE is characterized by a rapid onset of action—clinical effects can be observed as early as 8 hours after administration—and a shorter duration of effect lasting approximately 2–3 weeks. This profile may address concerns among new patients about unnatural or prolonged results from aesthetic neurotoxins. The drug acts primarily by inhibiting acetylcholine release at neuromuscular junctions through SNARE protein antagonism and also exhibits glutamate antagonism and neuromuscular blocking activity. Developed originally by Bonti and further advanced by AbbVie/Allergan Aesthetics, TrenibotE has completed pivotal Phase 3 trials with positive results for efficacy and safety in over 2,100 patients[1][4][5][7][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on trenibotulinumtoxinE.