Cynosure
Trial Pipeline
Feasibility Study to Collect and Assess Safety Data for a Radiofrequency Microneedling Device for Electrocoagulation and Hemostasis of Soft Tissues for Dermatologic Conditions
NCT05987319
Clinical Study to Evaluate Alexandrite Laser for the Treatment of Acne Scars
NCT04807179
Prospective Clinical Study to Assess Safety and to Collect Data on Radiofrequency Microneedling Device(s) For the Purpose of Evaluating Treatment on Skin
NCT06023303
Post Market Usability Evaluation Of The PicoSure Pro Device
NCT05102617
Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging
NCT04880070
Study for the RevLite Laser System for Facial Solar Lentigines
NCT02110108
Picosure Alexandrite Laser and Revlite Nd:Yag Laser for the Treatment of Unwanted Tattoos
NCT02110121
A Study of the RevLite Laser System for the Treatment of Refractory Mixed Type Melasma
NCT02110134
Clinical Evaluation of the Picosure Laser for the Treatment of Unwanted Tattoos
NCT02103153
Evaluating the Safety and Efficacy of the Pico Laser With a Specialized Lens Array for the Treatment of Wrinkles
NCT02091102
Evaluation of the Safety and Precursors of Efficacy
NCT02098811
Evaluation of the 755nm Alexandrite for the Treatment of Epidermal and Dermal Pigmented Lesions
NCT01754233
Evaluation of the 755nm Alexandrite Laser for Skin Toning and Epidermal Pigmented Lesions in Asian Skin Types
NCT01754246
Clinical Investigation of Non Invasive Fat Reduction
NCT01842802
Evaluation of the 755nm Alexandrite Laser for the Treatment of Tattoos
NCT01754207
What the Pipeline for Cynosure Shows
According to the ClinicalTrials.gov registry, Cynosure is linked to 15 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting — about 7% of the sponsor's indexed portfolio — and 13 are already marked complete, representing roughly 87% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for Cynosure reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for Cynosure is Acne Scars with 3 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.