Merz North America

35 total trials 1 currently recruiting 31 completed

Merz North America sponsors 35 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 31 completed. 15 of these trials are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Volume Loss in the Dorsum of the Hand, with 2 trials.

Trial Pipeline

35 total, page 1 of 1

RECRUITING Phase 3

A Study of NT 201 in Adults With Moderate to Severe Platysma Prominence in the United States

NCT07122193

ACTIVE NOT RECRUITING NA

A Study to Determine if RADIESSE® Dilute Treatment in Décolleté of Adult Women Affects Radiographic Imaging Assessments

NCT07086248

TERMINATED

Longitudinal Evaluation and Real-world Evidence of NT201

NCT05222607

COMPLETED Phase 1

A Study of NT 201 in the Treatment of Enlarged Pores and Excessive Sebum Production in the Face

NCT05784363

COMPLETED NA

Evaluation of the Effectiveness and Safety of Diluted RADIESSE® in the Treatment of Décolleté Wrinkles

NCT05163353

COMPLETED NA

Effectiveness and Safety of the Octave System for Lifting the Eyebrow and Improving the Appearance of the Face and Neck

NCT05067504

COMPLETED NA

A Study of Octave System for Improving Lines and Wrinkles of the Décolleté

NCT04681352

COMPLETED Phase 3

Safety and Efficacy Study of the Simultaneous Treatment of Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines and Lateral Canthal Lines) in Subjects With Moderate to Severe Upper Facial Lines

NCT04594213

COMPLETED NA

Evaluation of Effectiveness and Safety of Belotero Balance® (+) Lidocaine for Volume Augmentation of the Infraorbital Hollow

NCT04594239

COMPLETED NA

A Pilot Study to Assess the Effectiveness and Safety of Belotero Balance® Injection for Volume Augmentation of the Infraorbital Hollow

NCT03777917

COMPLETED NA

Evaluation of Effectiveness and Safety of Radiesse (+) to Improve the Contour of Jawline by Adding Volume to the Jawline

NCT03583359

COMPLETED NA

Evaluation of Pain With Belotero® Balance With Integral Lidocaine for Correction of the Nasolabial Folds

NCT03319719

COMPLETED NA

Open-label, Prospective Evaluation of the Ulthera® System for Lifting Submental (Under the Chin) and Neck Tissue in Chinese Patients

NCT03351335

COMPLETED NA

Radiesse® Safety Study For the Treatment of Hands

NCT02904096

COMPLETED NA

Radiological Evaluation of Radiesse Implantation in the Hands

NCT02949921

TERMINATED

Neurogenic Dysphonia/Dysphagia Registry

NCT02493491

COMPLETED Phase 4

Pediatric Subjects With Tinea Corporis

NCT02227290

COMPLETED Phase 4

The Treatment of Glabellar Frown Lines

NCT02096081

COMPLETED Phase 4

An Open Label Pharmacokinetic Study of Naftin for Tinea Corporis

NCT02466867

COMPLETED NA

Evaluation of Radiesse® Dermal Filler for Hand Treatment

NCT01832090

COMPLETED Phase 4

Pharmacokinetic Study of Pediatric Subjects With Tinea Cruris and Tinea Pedis

NCT01712360

COMPLETED NA

Study of the Cabochon System for Improvement in the Appearance of Cellulite

NCT01671839

COMPLETED Phase 4

Belotero Post Approval Study

NCT01635855

COMPLETED NA

Mederma to Reduce Appearance of Post Surgical Scars

NCT01504061

COMPLETED Phase 3

Evaluation of the Efficacy and Safety of NAFT-600 in Subjects With Tinea Pedis

NCT01290341

COMPLETED Phase 3

Efficacy and Safety of NAFT-600 in Subjects With Tinea Pedis

NCT01289015

COMPLETED

Trial Evaluating Xeomin® (incobotulinumtoxinA) for Cervical Dystonia or Blepharospasm in the United States

NCT01287247

COMPLETED NA

Safety and Effectiveness of Belotero® in Subjects With Fitzpatrick Phototypes IV Through VI

NCT00922623

COMPLETED Phase 4

Evaluation of Pain With Lidocaine-Mixed Radiesse® Injectable Dermal Filler

NCT01012661

COMPLETED Phase 3

Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea Cruris

NCT00750152

COMPLETED Phase 3

Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea Pedis

NCT00750139

COMPLETED NA

This is a Post Approval Study of Coaptite® in the Treatment of Female Urinary Incontinence

NCT00996489

COMPLETED Phase 3

Multicenter Study of the Safety and Efficacy of Dermal Filler, Belotero® Soft

NCT00877279

COMPLETED Phase 4

Radiesse® Injectable Dermal Filler for the Treatment of Nasolabial Folds in Persons of Color

NCT01012388

COMPLETED Phase 3

Multicenter Study of the Safety and Effectiveness of Dermal Filler, Belotero®.

NCT00876265

What the Pipeline for Merz North America Shows

According to the ClinicalTrials.gov registry, Merz North America is linked to 35 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 3% of the sponsor's indexed portfolio, and 31 are already marked complete, representing roughly 89% of the total.

The phase mix for Merz North America reports 15 late-stage studies (Phase 3 and Phase 4 combined) and 1 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Merz North America is Volume Loss in the Dorsum of the Hand with 2 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

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.

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.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.