Dermata and Revance: Revolutionizing Botulinum Toxin Delivery
Generated by AI AgentWesley Park
Tuesday, Jan 21, 2025 8:16 am ET1min read
DRMA--
In the ever-evolving world of aesthetics and medical treatments, Dermata Therapeutics and Revance Therapeutics have joined forces to potentially disrupt the botulinum toxin market. The two companies have entered into a clinical trial collaboration agreement to evaluate the topical application of Dermata's Xyngari™ with Revance's Daxxify® for the treatment of primary axillary hyperhidrosis. This innovative approach could pave the way for a needle-free, intradermal delivery of botulinum toxin, offering patients a more convenient and less invasive treatment option.

The collaboration between Dermata and Revance brings together Dermata's unique Spongilla powder technology, Xyngari™, and Revance's long-lasting botulinum toxin, Daxxify®. Xyngari™, a topical product derived from a freshwater sponge, has shown promising results in clinical trials for the treatment of primary axillary hyperhidrosis and multiple aesthetic skin conditions. Daxxify®, on the other hand, is a long-acting botulinum toxin that has received approval in the United States for treating moderate to severe glabellar lines and cervical dystonia. By combining these two innovative technologies, Dermata and Revance aim to create a superior treatment option for patients seeking a needle-free, intradermal delivery of botulinum toxin.
The Phase 2a clinical trial will evaluate the efficacy, safety, and tolerability of Xyngari™ and Daxxify® versus Xyngari™ and placebo in patients with moderate-to-severe axillary hyperhidrosis for 16 weeks. The trial will be randomized, double-blind, and placebo-controlled, enrolling approximately 48 patients across sites in the United States. The endpoints will focus on the percent of patients with greater than 50% reduction in gravimetrically measured sweat production from baseline, the percent of patients with gravimetric sweat production less than 50mg, and the mean absolute change from baseline in gravimetrically measured sweat production.
If successful, this collaboration could expand the opportunities for Daxxify® beyond injections, further strengthening Revance's position in the botulinum toxin market. Additionally, the needle-free delivery system could attract patients seeking a more convenient and less painful treatment option, potentially capturing a significant share of the market. As the clinical trial progresses, investors will be watching closely to see if this innovative approach can live up to its promise.

In conclusion, the collaboration between Dermata and Revance to develop a needle-free, intradermal delivery of botulinum toxin using Xyngari™ and Daxxify® has the potential to revolutionize the botulinum toxin market. By combining Dermata's unique Spongilla powder technology with Revance's long-lasting botulinum toxin, the companies aim to create a superior treatment option for patients with primary axillary hyperhidrosis and potentially other medical and aesthetic indications. As the Phase 2a clinical trial progresses, investors should keep a close eye on this promising development.
RVNC--
In the ever-evolving world of aesthetics and medical treatments, Dermata Therapeutics and Revance Therapeutics have joined forces to potentially disrupt the botulinum toxin market. The two companies have entered into a clinical trial collaboration agreement to evaluate the topical application of Dermata's Xyngari™ with Revance's Daxxify® for the treatment of primary axillary hyperhidrosis. This innovative approach could pave the way for a needle-free, intradermal delivery of botulinum toxin, offering patients a more convenient and less invasive treatment option.

The collaboration between Dermata and Revance brings together Dermata's unique Spongilla powder technology, Xyngari™, and Revance's long-lasting botulinum toxin, Daxxify®. Xyngari™, a topical product derived from a freshwater sponge, has shown promising results in clinical trials for the treatment of primary axillary hyperhidrosis and multiple aesthetic skin conditions. Daxxify®, on the other hand, is a long-acting botulinum toxin that has received approval in the United States for treating moderate to severe glabellar lines and cervical dystonia. By combining these two innovative technologies, Dermata and Revance aim to create a superior treatment option for patients seeking a needle-free, intradermal delivery of botulinum toxin.
The Phase 2a clinical trial will evaluate the efficacy, safety, and tolerability of Xyngari™ and Daxxify® versus Xyngari™ and placebo in patients with moderate-to-severe axillary hyperhidrosis for 16 weeks. The trial will be randomized, double-blind, and placebo-controlled, enrolling approximately 48 patients across sites in the United States. The endpoints will focus on the percent of patients with greater than 50% reduction in gravimetrically measured sweat production from baseline, the percent of patients with gravimetric sweat production less than 50mg, and the mean absolute change from baseline in gravimetrically measured sweat production.
If successful, this collaboration could expand the opportunities for Daxxify® beyond injections, further strengthening Revance's position in the botulinum toxin market. Additionally, the needle-free delivery system could attract patients seeking a more convenient and less painful treatment option, potentially capturing a significant share of the market. As the clinical trial progresses, investors will be watching closely to see if this innovative approach can live up to its promise.

In conclusion, the collaboration between Dermata and Revance to develop a needle-free, intradermal delivery of botulinum toxin using Xyngari™ and Daxxify® has the potential to revolutionize the botulinum toxin market. By combining Dermata's unique Spongilla powder technology with Revance's long-lasting botulinum toxin, the companies aim to create a superior treatment option for patients with primary axillary hyperhidrosis and potentially other medical and aesthetic indications. As the Phase 2a clinical trial progresses, investors should keep a close eye on this promising development.
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