Allergan

52 total trials 51 completed

Trial Pipeline

ACTIVE NOT RECRUITING

Safety Follow-up Study in Subjects With Silicone Gel-filled Breast Implants as Compared Both to Saline-filled Breast Implants and to National Norms

NCT00443274

COMPLETED Phase 2

A Study To Assess the Adverse Effects and Change in Condition of OnabotulinumtoxinA X Injection in Adult Participants With Forehead Lines

NCT05152576

COMPLETED Phase 4

CoolSculpting® Elite for Non-Invasive Fat Reduction

NCT04897867

COMPLETED

18 Month Prospective Efficacy and Safety Study of Bimatoprost Intracameral Implant (DURYSTA)

NCT04647214

COMPLETED Phase 1

Intradermal (ID) BOTOX in the Treatment of Facial Fine Lines

NCT04631588

COMPLETED Phase 3

Efficacy and Safety of a New Artificial Tear Formulation Compared With Systane Ultra Multidose in Participants With Dry Eye Disease

NCT04393441

COMPLETED Phase 1

Safety, Tolerability and Drug- Drug Interaction Study of Ubrogepant With Erenumab or Galcanezumab in Participants With Migraine

NCT04179474

COMPLETED Phase 2

BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence

NCT03861936

COMPLETED

Chart Review of XEN 45 Gel Stent: Long Term Performance and Safety Assessment (XEN LT)

NCT03868254

COMPLETED

Dynamic Optical Coherence Tomography(D-OCT) Aging Study: A Preliminary Evaluation of Structural Differences Between Young and Aged Skin, Cellulite and Atrophic Acne Scars in Female Caucasian Subjects With Fitzpatrick Skin Types I-III Utilizing Non-invasive in Vivo D-OCT.

NCT03767400

COMPLETED NA

JUVÉDERM® VOLITE™ XC for Cheek Skin Smoothness

NCT03728309

COMPLETED Phase 3

Efficacy, Safety, and Tolerability of Levomilnacipran ER in Pediatric Patients (7-17 Years) With Major Depressive Disorder

NCT03569475

COMPLETED NA

Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topical Products in Participants With Moderate Facial Melasma

NCT02977507

COMPLETED NA

Evaluation of Dry Eye Symptoms in CAE With Application of Intranasal Neurostimulation

NCT02910713

COMPLETED Phase 4

Evaluation of Maintaining Visual Performance in Participants Who Engage in Electronic Visual Tasking While Using Restasis®

NCT02554981

COMPLETED Phase 3

Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants With Open-angle Glaucoma or Ocular Hypertension

NCT02247804

COMPLETED Phase 4

Efficacy and Safety Study of BOTOX® Compared to Topiramate for the Prevention of Chronic Migraine in Adults

NCT02191579

COMPLETED Phase 2

A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Degeneration

NCT02181517

COMPLETED Phase 4

Patient Satisfaction Study of Combined Facial Treatment With BOTOX® Cosmetic, JUVÉDERM® and LATISSE® (HARMONY Study)

NCT02176356

COMPLETED Phase 2

OnabotulinumtoxinA as Treatment for Major Depressive Disorder in Adult Females

NCT02116361

COMPLETED Phase 3

A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

NCT02147197

COMPLETED Phase 4

A Study of Dapsone Gel in Females With Skin of Color and Acne Vulgaris

NCT02032407

COMPLETED

Characterization of Signs and Symptoms of Participants With and Without Meibomian Gland Dysfunction

NCT01979887

COMPLETED Phase 4

OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With Overactive Bladder

NCT01945489

COMPLETED Phase 2

A Safety and Efficacy Study of Bimatoprost in Men With Androgenic Alopecia (AGA)

NCT01904721

COMPLETED Phase 1

A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women With Interstitial Cystitis (IC) and Hunner's Lesions

NCT01879683

COMPLETED Phase 2

A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in Chronic Glaucoma or Ocular Hypertension

NCT01863953

COMPLETED Phase 2

AGN-199201 for the Treatment of Erythema With Rosacea

NCT01735201

COMPLETED Phase 1

Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With Rosacea

NCT01579084

COMPLETED Phase 3

Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease

NCT01459588

COMPLETED Phase 4

Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Prominence

NCT01448525

COMPLETED Phase 4

Ocular Surface Tolerability Study of Prostaglandin Analogues in Patients With Open-Angle Glaucoma or Ocular Hypertension

NCT01253902

COMPLETED Phase 1

QT Intervals Study to Compare the Acute Effects of Orally Inhaled Dihydroergotamine (DHE), Oral Moxifloxacin, and Placebo

NCT01191723

COMPLETED Phase 2

Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension

NCT01110499

COMPLETED

Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal Sensation and Dry Eye

NCT01161771

COMPLETED Phase 1

Pharmacodynamic Study to Compare Acute Effects of Dihydroergotamine Mesylate (DHE) on Pulmonary Arterial Pressure

NCT01089062

COMPLETED Phase 3

Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic Overactive Bladder With Urinary Incontinence

NCT00910845

COMPLETED NA

Safety and Effectiveness of Juvéderm® VOLUMA XC Injectable Gel for Cheek Augmentation

NCT00978042

COMPLETED Phase 1

A Study Evaluating the Effect of Botulinum Toxin Type A on Semen Quality in Patients With Benign Prostatic Hyperplasia

NCT00894517

COMPLETED Phase 4

Trospium Chloride XR in Obese Female Patients With Overactive Bladder

NCT00932022

COMPLETED Phase 4

A Clinical Study to Evaluate if Benzalkonium Chloride (BAK) in a Quinolone Eyedrop Reduces the Likelihood of Developing Resistant Organisms

NCT00874887

COMPLETED Phase 4

Efficacy of Ketorolac 0.4% in Prostaglandin Suppression

NCT00791323

COMPLETED Phase 3

Phase 3 Study of MAP0004 in Adult Migraineurs

NCT00623636

COMPLETED Phase 2

Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear

NCT00691197

COMPLETED Phase 2

A Study of 2 Doses of MAP0010 in Adult Asthmatics

NCT00554970

COMPLETED Phase 3

A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With Cataract Surgery

NCT00524264

COMPLETED Phase 4

Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost 0.005%

NCT00440011

COMPLETED Phase 2

Study of MAP0010 in Asthmatic Children and Adolescents

NCT00697801

COMPLETED Phase 2

Safety and Efficacy Study of Gatifloxacin Compared With Ciprofloxacin in Patients With Acute Bacterial Corneal Ulcers

NCT00651586

COMPLETED Phase 3

Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension

NCT00652106

COMPLETED Phase 3

Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients Wtih Glaucoma or Ocular Hypertension

NCT00332072

COMPLETED Phase 3

Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension

NCT00332436

Phase Distribution

PhaseTrial count
Phase 1 7
Phase 2 12
Phase 3 11
Phase 4 12

What the Pipeline for Allergan Shows

According to the ClinicalTrials.gov registry, Allergan is linked to 52 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting — about 0% of the sponsor's indexed portfolio — and 51 are already marked complete, representing roughly 98% 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 Allergan reports 23 late-stage studies (Phase 3 and Phase 4 combined) and 19 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 Allergan is Ocular Hypertension with 9 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.

Related

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