Galderma R&D
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 2 of 4
Safety and Efficacy of AbobotulinumtoxinA for the Treatment of Platysmal Bands
NCT04080882
Efficacy & Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis
NCT03989349
Efficacy and Safety of Nemolizumab in Subjects With Moderate-to-Severe Atopic Dermatitis
NCT03985943
Efficacy and Safety of a New Dilution and Injection Volume of AbobotulinumtoxinA for the Treatment of Glabellar Lines
NCT03960957
A Pharmacokinetics and Safety Study of Nemolizumab in Adolescent Participants With Atopic Dermatitis (AD)
NCT03921411
Participant Reported Outcomes With Use of Trifarotene 50 μg/g Cream in the Treatment of Moderate Facial and Truncal Acne Vulgaris
NCT03915860
Safety and Effectiveness of Sculptra Aesthetic for Correction of Nasolabial Folds.
NCT03780244
Safety and Efficacy of AbobotulinumtoxinA for the Treatment of Glabellar Lines
NCT03736928
GAL1704 for Cheek Augmentation and Correction of Midface Contour Deficiencies
NCT03700047
Subject Satisfaction With AbobutulinumtoxinA Treatment
NCT03687736
A Study to Evaluate the Safety and Efficacy of Restylane Defyne for Chin Augmentation and Correction of Chin Retrusion
NCT03624816
A Safety, Efficacy and Pharmacokinetics Study of CD11301 for the Treatment of Cutaneous T-Cell Lymphoma (CTCL)
NCT03292406
New Dermal Filler for Lip Augmentation
NCT03320824
Oracea Soolantra Association in Participants With Severe Rosacea
NCT03075891
Dose-ranging Study of Nemolizumab in Atopic Dermatitis
NCT03100344
Injection Technique Assessment of Restylane Lyft With Lidocaine for Cheek Augmentation
NCT03160716
Subject Reported Outcomes With Use of Adapalene 0.3% - Benzoyl Peroxide (BPO) 2.5% in Dark Skin Acne
NCT02932267
A Treatment for Severe Inflammatory Acne Subjects
NCT02899000
A Clinical Trial to Evaluate the Efficacy of Two Acne Treatments
NCT02755545
Comparison of Dysport Reconstitution at 1.5 mL and 2.5 mL for the Treatment of Moderate to Severe Glabellar Lines
NCT02718118
Injection Technique Assessment of Restylane Silk With Lidocaine for Lip Augmentation
NCT02703948
MirvasO Soolantra Association In the Treatment of Moderate to Severe rosaCea.
NCT02616250
Effectiveness and Safety of Restylane Lyft With Lidocaine in the Dorsal Hand
NCT02650921
Efficacy and Safety of CD5789 (Trifarotene) 50μg/g Cream Versus Vehicle Cream in Acne Vulgaris
NCT02566369
Double-Blind Efficacy and Safety of CD5789 (Trifarotene) 50µg/g Cream Versus Vehicle Cream in Acne Vulgaris
NCT02556788
Minoxidil 2% Solution and Botanical Hair Regimen in Women With Thinning Hair and Female Pattern Hair Loss/Androgenic Alopecia
NCT02460497
Sculptra Aesthetic Post-Approval Study
NCT02425943
Minoxidil 5% / Botanical Hair Regimen in Men With Thinning Hair and Male Pattern Hair Loss/Androgenic Alopecia
NCT02460289
CD5789 (Trifarotene) Long Term Safety Study on Acne Vulgaris
NCT02189629
Mirvaso in Use Study
NCT02249065
Safety and Efficacy Study of Botulinum Toxin for the Treatment of Glabellar Frown Lines
NCT02236312
A Treatment Regimen for Student Athletes With Mild to Moderate Acne Vulgaris
NCT02249104
Plaque Psoriasis Study in Pediatric Subjects
NCT02186665
Long Term Safety and Efficacy Study of Calcitriol 3 mcg/g Ointment in Pediatric Subjects With Plaque Psoriasis
NCT02125279
Adapalene BPO Gel Pump, Moisturizer SPF 30 and Foam Wash in Patients With Mild to Moderate Acne Vulgaris
NCT01951417
Subject Reported Target-lesion Numeric Rating Scale Evaluation by Subjects With Plaque Psoriasis Treated With Clobex® (Clobetasol Propionate) Spray 0.05%
NCT01893567
Multi-center, Randomized, Double-blind Efficacy and Safety of CD0271 0.3%/CD1579 2.5 % Topical Gel in Acne Vulgaris
NCT01880320
Tolerability of a Foaming Facial Cleanser and Moisturizer SPF 30 in a Pediatric Population (7-11) With Acne Prone Skin.
NCT01909713
Patient Centered Outcomes in Rosacea: An Exploratory Multi-media Analysis of the Patient Experience on Oracea
NCT01872715
PK and PD Study of Calcitriol 3 mcg/g Ointment in Pediatric Subjects With Plaque Psoriasis
NCT01766440
Repeat Insult Patch Test of Skin Irritation/Sensitization for Cetaphil Daily Facial Cleanser
NCT01888887
Patch Test Skin Irritation/Sensitization of Cetaphil Restoraderm Skin Restoring Body Wash
NCT01892410
Patch Test Skin Irritation/Sensitization of Cetaphil Daily Facial Moisturizer SPF 50
NCT01887860
Durolane Versus Phosphate Buffered Saline (PBS) in Knee Osteoarthritis
NCT01753830
Efficacy and Safety Study Comparing CD07805/47 Gel 0.5% to Azelaic Acid Gel 15% in Subjects With Erythema of Rosacea
NCT01659853
Dose Range Study of CD5789 in Acne Vulgaris
NCT01616654
Anesthetic Effect Duration Assessment
NCT01545765
Split-face Tolerability Comparison Between Adapalene-Benzoyl Peroxide Gel Versus Tretinoin Gel
NCT01522456
Phase 3 Papulopustular Rosacea Study
NCT01494467
Phase 3 Papulopustular Rosacea Study
NCT01493687
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 4 |
| Phase 2 | 24 |
| Phase 3 | 41 |
| Phase 4 | 49 |
Therapeutic Areas
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.