Product
NT 201
Aliases
Botulinum toxin type A (150 kiloDalton), free from complexing proteins, IncobotulinumtoxinA, Incobotulinumtoxin A, NT 201 Placebo (3 other aliases)
Name
DAXXIFY
INN Name
Botulinum Toxin Type A
FDA Approved
Yes
6 clinical trials
3 organizations
8 indications
2 documents
Indication
Essential TremorIndication
Platysmal BandIndication
Horizontal Forehead LinesIndication
Glabellar Frown LinesIndication
Lateral Canthal LinesIndication
Enlarged PoresIndication
Sebum HypersecretionClinical trial
Prospective, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial With an Open-label Period to Investigate the Efficacy and Safety of NT 201 in the Unilateral and Bilateral Treatment of Essential Tremor of the Upper LimbStatus: Completed, Estimated PCD: 2023-04-26
Clinical trial
Prospective, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Investigate the Efficacy and Safety of NT 201 in the Treatment of Lower Limb Spasticity Caused by Stroke or Traumatic Brain Injury in Adult Subjects, Followed by an Open Label Extension With or Without Combined Upper Limb TreatmentStatus: Recruiting, Estimated PCD: 2025-08-01
Clinical trial
A Prospective, Double-blind, Randomized, Placebo-controlled, Multicenter Study to Investigate the Efficacy and Safety of NT 201 Doses in the Treatment of Platysma ProminenceStatus: Completed, Estimated PCD: 2023-10-19
Clinical trial
A Prospective, Randomized, Double-blind, Placebo-controlled, Multicenter Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Simultaneous Treatment of Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines, and Lateral Canthal Lines)Status: Completed, Estimated PCD: 2021-04-15
Clinical trial
A Prospective, Randomized, Double-blind, Multicenter Study to Investigate the Safety and Duration of Effect of Different NT 201 Dose Groups Following the Treatment of Glabellar Frown LinesStatus: Completed, Estimated PCD: 2020-09-10
Clinical trial
A Prospective, Randomized, Double-blind, Placebo-controlled, Multi-center Exploratory Study to Investigate NT 201 in the Treatment of Enlarged Pores and Excessive Sebum Production in the FaceStatus: Active (not recruiting), Estimated PCD: 2024-06-01
Document
DailyMed Label: DAXXIFYOrganization
Revance Therapeutics, Inc.Document
DailyMed Label: Dysport Organization
Galderma Laboratories, L.P.Organization
Ipsen Biopharmaceuticals, Inc.