Pacira Pharmaceuticals

88 total trials 5 currently recruiting 65 completed

Pacira Pharmaceuticals sponsors 88 registered US clinical trials on ClinicalTrials.gov, 5 of them currently recruiting, and 65 completed. 38 of these trials are in Phase 3-4 (later-stage) and 35 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Osteoarthritis of the Knee, with 4 trials.

Trial Pipeline

88 total, page 2 of 2

COMPLETED

Prospective Study Evaluating the Treatment of Hyperdynamic Forehead Wrinkles

NCT01984619

COMPLETED NA

Effectiveness and Safety Study of the Iovera Device for the Temporary Reduction in the Appearance of Forehead Wrinkles

NCT01950065

TERMINATED Phase 4

EXPAREL Administered by Infiltration Into the TAP for Prolonged Postsurgical Analgesia in Lower Abdominal Surgeries

NCT01919190

COMPLETED NA

Study Evaluating Treatment of Upper Limb Spasticity Using the Cryo-Touch III Device

NCT01863901

COMPLETED

A Prospective Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the Cryo-Touch IV Device

NCT01801826

COMPLETED Phase 3

Intercostal Nerve Block With Liposome Bupivacaine in Subjects Undergoing Posterolateral Thoracotomy

NCT01802411

COMPLETED

Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the CRYO-TOUCH III Device

NCT01808742

COMPLETED Phase 4

Pain Control in Bariatric Patients: EXPAREL(R) vs. the On-Q(R) Pain Ball

NCT02142829

COMPLETED NA

Study Evaluating Treatment of Forefoot Pain Related to Nerve Entrapment Using the Cryo-Touch III Device

NCT01753778

COMPLETED NA

Study Evaluating the Treatment of Occipital Neuralgia

NCT01753765

COMPLETED Phase 2

Femoral Nerve Block With Liposome Bupivacaine for Postsurgical Analgesia Following Total Knee Arthroplasty

NCT01683071

COMPLETED NA

A Prospective Study Evaluating the Treatment of Knee Osteoarthritis With the Cryo-Touch III Device

NCT01704157

COMPLETED NA

Probe Configuration and Time-Temperature Dose Ranging for Understanding of Skin Lesion Effects

NCT01681745

COMPLETED Phase 2

Study of FX006 in Patients With Osteoarthritis of the Knee

NCT01487161

TERMINATED Phase 4

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B302

NCT01507233

COMPLETED Phase 4

Study of EXPAREL in Patients Undergoing Breast Augmentation

NCT01582490

COMPLETED Phase 4

EXPAREL Infiltrated Into the TAP for Postoperative Analgesia in Unilateral Abdominal Hernia Repair

NCT01801124

COMPLETED Phase 4

TAP-patients With Robotic Assisted Lap Prostatectomy

NCT01582477

COMPLETED Phase 4

A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B501

NCT01509638

TERMINATED Phase 4

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B301

NCT01507220

COMPLETED Phase 4

A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B504

NCT01509807

COMPLETED Phase 4

Adult Patients Undergoing Open Colectomy MA402S23B303

NCT01507246

TERMINATED Phase 4

A Health Economic Trial in Adult Patients Undergoing Laparoscopic Colectomy

NCT02058290

COMPLETED Phase 2

A Study to Evaluate the Safety and Effectiveness of the Cryo-Touch II Device for the Treatment of Forehead and/or Glabellar Lines

NCT01447342

COMPLETED Phase 2

Cryo-Touch III Refinement Study Investigational Plan

NCT01379365

COMPLETED Phase 2

Cryo-Touch II for the Treatment of Wrinkles

NCT01167140

COMPLETED Phase 3

Study of Postoperative Analgesia in Bunionectomy

NCT00890682

COMPLETED Phase 1

Study of the MyoScience Tissue Remodeling Device for Facial Rejuvenation

NCT00842062

TERMINATED Phase 2

Dose Finding Posterolateral Thoracotomy Study

NCT00807209

TERMINATED Phase 3

Phase 3 Study of Local Administration of SKY0402 for Postoperative Analgesia in Subject Undergoing Breast Augmentation

NCT00813111

COMPLETED Phase 1

Evaluate the Onset of Action of SKY0402 Following Local Infiltration in Healthy Volunteers

NCT00806806

COMPLETED Phase 3

A Phase 3 Study to Evaluate the Safety and Efficacy of SKY0402 in Subjects Undergoing Total Knee Arthroplasty

NCT00745290

COMPLETED Phase 3

Study to Evaluate Postoperative Analgesia in Subjects Undergoing Hemorrhoidectomy

NCT00744848

COMPLETED Phase 2

Evaluation of the Safety and Efficacy of a Single Dose of SKY0402 in Subjects Undergoing Augmentation Mammoplasty

NCT01206608

COMPLETED Phase 2

Phase 2 Dose-Ranging Study of SKY0402 for Prolonged Postoperative Analgesia in Subject Undergoing Hemorrhoidectomy

NCT00529126

COMPLETED Phase 2

Dose-Ranging Study for Prolonged Postoperative Analgesia in Subject Undergoing Total Knee Arthroplasty

NCT00485693

COMPLETED Phase 2

Dose-ranging Study for Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia Repair

NCT00485433

COMPLETED Phase 4

DepoCyt Therapy in Patients With Neoplastic Meningitis From Lymphoma or a Solid Tumor

NCT00029523

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Phase Distribution

PhaseTrial count
Phase 1 13
Phase 2 22
Phase 3 17
Phase 4 21

What the Pipeline for Pacira Pharmaceuticals Shows

According to the ClinicalTrials.gov registry, Pacira Pharmaceuticals is linked to 88 US clinical trials across every stage of research activity. Of those, 5 studies are currently recruiting, about 6% of the sponsor's indexed portfolio, and 65 are already marked complete, representing roughly 74% of the total.

The phase mix for Pacira Pharmaceuticals reports 38 late-stage studies (Phase 3 and Phase 4 combined) and 35 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Pacira Pharmaceuticals is Osteoarthritis of the Knee with 4 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.