Safety and effectiveness of NOA LIFT vs VOLIFT for correcting nasolabial folds in adults
Official title: A Prospective Multi-Center, Evaluator- and Subject- Blinded, Randomized Study to Evaluate the Safety and Effectiveness of NOA LIFT Compared to JUVÉDERM VOLIFT With Lidocaine for the Correction of Nasolabial Folds
Run by AbbVie · NCT07794878 · Data updated 2026-11-12
This study tests whether NOA LIFT works as well as JUVÉDERM VOLIFT with lidocaine for correcting moderate to severe nasolabial folds in adults.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 288 (estimated) |
| Sponsor | AbbVie Industry-sponsored |
| Locations | 6 sites (Beijing, Beijing Municipality and 5 other locations) |
| Status | Recruiting |
| Started | August 19, 2026 |
| Main results expected | August 2028 |
| Study ends | August 2028 |
| Registry record updated | August 31, 2026 |
| Trial ID | NCT07794878 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with moderate (2) to severe (3) nasolabial folds on both sides, as assessed by evaluator live assessment.
✕Probably not a fit
Participants whose condition does not respond to treatment or who experience unacceptable safety risks may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this Phase 3 trial, adults with moderate to severe nasolabial folds are randomized to receive either NOA LIFT or JUVÉDERM VOLIFT with lidocaine. The study compares safety and effectiveness over about 12 months after treatment. Participants receive deep dermal injections at multiple sites in China and are followed to monitor adverse events and treatment outcomes. Approximately 288 participants will be enrolled across three Beijing/Guangzhou/Shenzhen centers. The trial uses a 2:1 randomization in favor of NOA LIFT.
Why it matters
Potential benefit: If successful, NOA LIFT could provide an effective alternative for correcting nasolabial folds.
How similar studies have gone: Similar HA filler comparisons have shown meaningful improvements in nasolabial folds, supporting this head-to-head approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Moderate (2) or Severe (3) on the 5-point Nasolabial Fold Severity Scale (NLFSS) for each nasolabial fold (NLF) on evaluator live assessment (both sides must qualify and have the same score) Exclusion Criteria: * Current cutaneous or mucosal inflammatory or infectious processes, abscess, unhealed wound, or cancerous or precancerous lesion in the treatment area(s). * Current enrollment in an investigational drug or device study or participation in such a study within 30 days before enrollment.
Where it's running
-
Peking Union Medical College Hospital (West) - Xidan Campus /ID# 267457
Beijing, Beijing Municipality, China Recruiting -
Zhujiang Hospital /ID# 276566
Guangzhou, Guangdong, China Recruiting -
Peking University Shenzhen Hospital /ID# 268255
Shenzhen, Guangdong, China Recruiting -
Nanjing Drum Tower Hospital /ID# 267555
Nanjing, Jiangsu, China Recruiting -
Zhongda Hospital Of Southeast University /ID# 276571
Nanjing, Jiangsu, China Recruiting -
Xianyang Hospital of Yanan University /ID# 267936
Xianyang, Shaanxi, China Recruiting
Study contacts
- Study coordinator: Abbvie Call Center
- Email: abbvieclinicaltrials@abbvie.com
- Phone: 844-663-3742
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.