Galderma has initiated a Phase II clinical trial of a novel muscle relaxant in the US. The Phase II clinical trial is a multicenter, dose-ranging study designed to evaluate the safety and effectiveness of Galderma's internally developed liquid form of botulinum toxin for the treatment of glabellar lines, and follows successful completion of a Phase I study earlier this year. Currently, all commercially available botulinum toxins come in powder form and have to be reconstituted with saline before use. The development of a liquid formulation has the potential to present healthcare professionals with a ready-to-use product that may result in a better patient experience and improved outcomes, according to Galderma.

“This trial initiation demonstrates Galderma's commitment to innovation in the aesthetic market and is designed to strengthen and complement our current neurotoxin franchise,” said Humberto C. Antunes, President and CEO of Galderma. “Our current neurotoxin business, which includes Dysport and Azzalure, continues its strong performance in key markets around the world. The development of a liquid neurotoxin represents a significant advancement over existing commercial products and would allow us to further strengthen our position in the aesthetic category by better meeting physician and patient needs.”

In July 2014, Galderma acquired the US and Canadian rights to a portfolio of injectable aesthetic medicine products, completing its global footprint and extending its leadership in aesthetic medicine. Galderma also announced it had strengthened its collaboration with Ipsen focused on the development and commercialization of new neurotoxins, increasing the scope of their R&D collaboration to further enhance their capabilities to meet the needs of patients and physicians worldwide.