It appears that Galderma S.A.’s long-acting wrinkle-reducing injectable relabotulinumtoxinA will be well positioned to compete in the highly competitive neurotoxin category – if it gets approved by the US Food and Drug Administration.
Key Takeaways
- Galderma announced topline results from two Phase IIIb studies, investigating relabotulinumtoxinA for the treatment of glabellar lines and lateral canthal lines.
- The company ran the extra studies to further characterize the rapid onset of action and durability of the novel liquid formulation of botulinum toxin A
The Swiss dermatology specialist announced topline results from two Phase IIIb studies on 30 November, investigating relabotulinumtoxinA for the treatment of glabellar lines (frown lines) and lateral canthal lines (crow’s feet)
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