Galderma R&D

158 total trials 7 currently recruiting 142 completed

Galderma R&D sponsors 158 registered US clinical trials on ClinicalTrials.gov, 7 of them currently recruiting, and 142 completed. 90 of these trials are in Phase 3-4 (later-stage) and 28 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Acne Vulgaris, with 7 trials.

Trial Pipeline

158 total, page 1 of 4

RECRUITING Phase 2

A Study of Nemolizumab for the Treatment of Adults With Systemic Sclerosis

NCT07047690

RECRUITING NA

A Study to Characterize Human Skin Changes From Biostimulator Treatments Via Non-invasive Imaging

NCT07399028

RECRUITING Phase 2

Proof of Concept Study to Assess the Pharmacokinetics/Pharmacodynamics of Nemolizumab in Adults With Chronic Pruritus of Unknown Origin (CPUO)

NCT07074977

RECRUITING Phase 4

A Clinical Study to Assess Efficacy and Tolerability of a Topical Skincare Product on Adults With Mature, Crepey Skin

NCT07398989

RECRUITING NA

A Clinical Study to Assess Histological Changes From Treatment of Poly L-lactic Acid Biostimulator on Women at Various Menopausal Stages

NCT07342400

RECRUITING

Real-world Experience on Using Nemolizumab in the Treatment of Moderate-to- Severe Prurigo Nodularis in Adults

NCT06988618

RECRUITING

Real-world Experience Using Nemolizumab in the Treatment of Moderate-to-Severe Atopic Dermatitis in Adolescents & Adults

NCT06988605

ACTIVE NOT RECRUITING NA

Evaluation of the Effects of a Biostimulator and Dermal Fillers for Cheek Augmentation and Contour Deficiencies

NCT06351358

ACTIVE NOT RECRUITING NA

Study to Evaluate the Safety and Effectiveness of GP0116

NCT05987163

ACTIVE NOT RECRUITING Phase 3

A Long-term Study of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)

NCT04204616

ACTIVE NOT RECRUITING Phase 3

Long-term Safety and Efficacy of Nemolizumab With Moderate-to-severe Atopic Dermatitis

NCT03989206

NOT YET RECRUITING NA

Study to Evaluate the Safety of Retreatment With Restylane® Lyft With Lidocaine for Augmentation of the Chin Region

NCT07566286

COMPLETED NA

Main Study: A Study to Evaluate the Effectiveness and Safety of GAL1906 for Correction of Wrinkles in the décolletage Area Sub-study: A Follow-up Study to Evaluate the Analysis of Mammograms Following Treatment for Correction of Wrinkles in Décolletage Area in the Investigational Study 43USRV1906

NCT04717934

COMPLETED Phase 4

A Study to Assess Efficacy and Tolerability of Topical Skincare Products on Psoriasis Patients

NCT06357221

COMPLETED NA

A Comparative Analysis of Two Hyaluronic Acid Fillers for Nasolabial Fold Correction

NCT06351293

COMPLETED Phase 4

A Controlled Study on Pain Management With Injection of Botulinum Toxin for Glabellar Line Correction

NCT06161246

COMPLETED Phase 4

A Clinical Study to Assess the Efficacy and Safety of a Healing Ointment on Diaper Rash

NCT06015217

COMPLETED NA

A Study to Evaluate the Effects for Midface Improvement When Pairing a Biostimulator with a Skincare Regimen

NCT05963204

COMPLETED NA

Safety and Effectiveness of Restylane Lyft With Lidocaine for Augmentation of the Chin Region to Improve the Chin Profile

NCT05777759

COMPLETED NA

Effectiveness and Safety of Restylane Contour in the Treatment of Temple Hollowing

NCT05691972

COMPLETED Phase 3

Assess Aesthetic Improvement With QM1114-DP in Subjects With Moderate to Severe Lateral Canthal Lines and Glabellar Lines

NCT05148000

COMPLETED NA

Gene Expression Study Between Two Dermal Injectables Hydroxylapatite Semi-permanent Filler

NCT05620043

COMPLETED NA

An Open-label Study of Poly-l-lactic Acid for Correction of Wrinkles in the décolletage Area

NCT05538728

COMPLETED Phase 4

Healing Ointment Usage Post-surgical Procedure

NCT05686928

COMPLETED Phase 1

Study to Access the Relative Bioavailability of Subcutaneous Dose of Nemolizumab When Administered Via Auto-Injector Versus Dual-Chamber Syringe

NCT05405985

COMPLETED

Sculptra Chart Review

NCT05463978

COMPLETED NA

Comparative Ultrasound Analysis of Two Hyaluronic Acid Dermal Fillers

NCT05622851

COMPLETED NA

Safety and Effectiveness of Restylane® Kysse for Lip Augmentation in Chinese Subjects

NCT05342753

COMPLETED Phase 3

Assess Aesthetic Improvement and Onset of QM1114-DP in Subjects With Moderate to Severe Glabellar Lines

NCT05146999

COMPLETED Phase 2

To Evaluate the Efficacy and Safety of Nemolizumab for 12 Weeks in Participants With Chronic Kidney Disease With Associated Moderate to Severe Pruritus

NCT05075408

COMPLETED Phase 3

A Study to Evaluate the Durability of Response and Safety of Nemolizumab for 24 Weeks in Participants With Prurigo Nodularis

NCT05052983

COMPLETED Phase 4

AkLief Evaluation in Acne-induced Post-Inflammatory Hyperpigmentation

NCT05089708

COMPLETED Phase 2

A Study to Assess the Effects of Nemolizumab on Cytochrome P450 Substrates in Participants With Moderate-to-Severe Atopic Dermatitis

NCT04562116

COMPLETED Phase 2

Pharmacokinetics, Safety and Efficacy of Nemolizumab in Participants With Moderate-to-Severe Atopic Dermatitis

NCT04921345

COMPLETED Phase 4

Study of Trifarotene Cream to Assess Risk of a Trophic Acne Scar Formation

NCT04856904

COMPLETED NA

Restylane Defyne in a Stepwise Treatment Approach

NCT04520997

COMPLETED Phase 3

Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)

NCT04501666

COMPLETED Phase 3

A Study to Assess the Efficacy and Safety of Nemolizumab (CD14152) in Participants With Prurigo Nodularis (PN)

NCT04501679

COMPLETED Phase 4

A Study to Compare Efficacy and Safety of Trifarotene Cream When Used With an Oral Antibiotic for the Treatment of Severe Acne Vulgaris (AV)

NCT04451330

TERMINATED Phase 3

A Study to Assess Recurrence of Actinic Keratosis in Participants Treated With Methyl Aminolevulinate Hydrochloride Cream or Vehicle Cream Who Achieved Complete Response to Treated Lesions in Earlier Study

NCT04269395

COMPLETED Phase 2

A Study to Assess Immunization Responses in Adult and Adolescent Participants With Moderate-to-Severe Atopic Dermatitis Treated With Nemolizumab

NCT04365387

COMPLETED Phase 3

Treatment of Moderate to Severe Lateral Canthal Lines

NCT04249687

COMPLETED Phase 3

Treatment of Moderate to Severe Glabellar Lines

NCT04249583

COMPLETED Phase 3

Treatment of Moderate to Severe Lateral Canthal Lines and Glabellar Lines Alone or in Combination

NCT04247074

COMPLETED Phase 3

Long-term Treatment of Moderate to Severe Glabellar Lines and Lateral Canthal Lines

NCT04225260

COMPLETED NA

Extension Study for 43USSA1705

NCT04225273

COMPLETED NA

Safety and Effectiveness of Sculptra Aesthetic for Correction of Cheek Wrinkles

NCT04124692

COMPLETED NA

Open Label Extension for 43USSA1812

NCT04595331

COMPLETED NA

Restylane-L for Correction of Infraorbital Hollows

NCT04154930

COMPLETED Phase 3

Multicenter Study to Assess the Efficacy and Safety of Methyl Aminolevulinate Hydrochloride (MAL) 16.8% Cream (CD06809-41) Versus Vehicle Cream for Actinic Keratosis of the Face

NCT04085367

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Phase Distribution

PhaseTrial count
Phase 1 4
Phase 2 24
Phase 3 41
Phase 4 49

What the Pipeline for Galderma R&D Shows

According to the ClinicalTrials.gov registry, Galderma R&D is linked to 158 US clinical trials across every stage of research activity. Of those, 7 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 142 are already marked complete, representing roughly 90% of the total.

The phase mix for Galderma R&D reports 90 late-stage studies (Phase 3 and Phase 4 combined) and 28 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Galderma R&D is Acne Vulgaris with 7 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.