Mode
Text Size
Log in / Sign up

BoNTA injection reduces axillary sweat in Chinese patients with primary hyperhidrosis.

BoNTA injection reduces axillary sweat in Chinese patients with primary hyperhidrosis.
Photo by Navy Medicine / Unsplash
Key Takeaway
Consider BoNTA injection for axillary hyperhidrosis in Chinese patients, noting the 16-week efficacy and limited safety data.

This was a Phase 3, multicenter, randomized, double-blind, placebo-controlled study in 344 Chinese patients with primary axillary hyperhidrosis. The intervention was a single intradermal injection of botulinum toxin type A (BoNTA), compared to placebo.

The primary outcome was the proportion of patients with over 50% reduction in axillary sweat weight at Week 4 posttreatment. In the experimental group, 83.72% (216/258) achieved this, versus 55.81% (48/86) in the control group, an absolute difference of 27.91% (P < .001).

Secondary outcomes included percentage changes in sweat weight at Weeks 1, 4, 8, and 16, reductions in sweat weight, hyperhidrotic area, HDSS scores, bromhidrosis grade, and satisfaction scores. The study had a 16-week follow-up. Safety data, including adverse events, serious adverse events, and discontinuations, were not reported; tolerability was described as well tolerated.

Key limitations include the lack of reported safety data and the specific population (Chinese patients). The practice relevance was not reported. Given the evidence, a single BoNTA injection appears effective for reducing axillary sweat in this population over 16 weeks, but clinicians should consider the study's scope and missing safety details.

Study Details

Study typeRct
Sample sizen = 258
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: The efficacy and safety of botulinum toxin type A (BoNTA) treatment for primary axillary hyperhidrosis (PAH) have not been explored in the Chinese population. OBJECTIVES: The objective was to evaluate efficacy and safety of 1 intradermal BoNTA injection in Chinese PAH cases. METHODS: This was a Phase 3, multicenter, randomized, double-blind, placebo-controlled study. Patients were randomized to an experimental group or the control group at a ratio of 3:1 and received either BoNTA or a placebo once. The primary efficacy endpoint was the proportion of patients who experienced an over 50% reduction in axillary sweat weight at Week 4 posttreatment compared to baseline. The key secondary efficacy endpoints were the percentage changes in axillary sweat weight at Weeks 1, 4, 8, and 16 posttreatment. RESULTS: A total of 344 patients were randomized to the experimental group (n = 258) or the control group (n = 86). The proportions of patients who experienced an over 50% reduction in axillary sweat weight at Week 4 posttreatment were 83.72% (216/258) in the experimental group and 55.81% (48/86) in the control group, respectively. The between-group difference was 27.91% (P < .001). BoNTA treatment yielded a significant reduction in axillary sweat weight, hyperhidrotic area, hyperhidrosis disease severity scale (HDSS) scores, and grade of bromhidrosis. The patients in the experimental group reported significantly higher satisfaction scores than those in the control group. BoNTA treatment was well tolerated. Neither group experienced suspected unexpected serious adverse reactions, or adverse events or adverse drug reactions leading to withdrawal or death. CONCLUSIONS: One intradermal 50-U BoNTA treatment led to a significant reduction in axillary sweat weight, axillary hyperhidrotic area, HDSS scores, and axillary bromhidrosis grades in Chinese PAH patients. The therapeutic effect was maintained for 16 weeks posttreatment, with a favorable safety profile.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.