Pacira Pharmaceuticals
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 1 of 2
A Study to Assess Safety and Tolerability of PCRX-201 in Subjects With Painful Osteoarthritis of the Knee
NCT06884865
Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity
NCT06340451
Study to Evaluate the Pharmacokinetics and Safety of EXPAREL for Postoperative Analgesia in Subjects Undergoing Cardiac Surgery
NCT06271265
ZILRETTA in Subjects With Shoulder Osteoarthritis
NCT06269705
Innovations in Genicular Outcomes Registry
NCT05495334
Study to Evaluate the Safety and Tolerability of FX201 in Patients with Osteoarthritis of the Knee
NCT04119687
A Study to Evaluate an Intra-Articular Injection of ZILRETTA Versus Triamcinolone Acetonide, Immediate Release in Subjects With Osteoarthritis of the Hip
NCT06977568
Phase 1, Dose Escalation Study to Evaluate of Safety, Pharmacokinetics and Pharmacodynamics of Liposomal Bupivacaine 13.3 Administered Via a Single Intrathecal Injection to Healthy Volunteers
NCT05456490
Phase 3, Sciatic Nerve Block With EXPAREL for Subjects Undergoing Bunionectomy
NCT05157841
Phase 3 Adductor Canal Block With EXPAREL in Subjects Undergoing Primary Unilateral Total Knee Arthroplasty
NCT05139030
Study to Evaluate the Safety and Tolerability of FX301 in Patients Undergoing Bunionectomy
NCT04826328
Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of EXPAREL, EXPAREL Admixed With Bupivacaine HCl vs. Bupivacaine HCl Administered as Combined Sciatic and Saphenous Nerve Blocks for Postsurgical Analgesia in Subjects Undergoing Lower Extremity Surgeries
NCT04518462
Study to Evaluate Iovera®° in Adult Patients Undergoing Total Knee Arthroplasty
NCT04191031
Evaluation of Safety, Pharmacokinetics and Pharmacodynamics of EXPAREL® Administered Via a Single Intrathecal Injection to Healthy Volunteers
NCT04173611
Study to Evaluate the Pharmacokinetics and Safety of EXPAREL Administered as a Pectoral Plane Block in Women Undergoing Breast Augmentation
NCT04293809
Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis
NCT04160091
Phase 4 Study in Adult Subjects Undergoing Posterior Lumbar Spine Surgeries
NCT03927911
Study to Evaluate a Procedure for Intra-articular Injection of FX006 in Patients With Osteoarthritis of the Hip
NCT04065074
Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety, of EXPAREL Administered as Sciatic Nerve Block (In Popliteal Fossa), for Postsurgical Analgesia in Subjects Undergoing Bunionectomy
NCT04002089
Multicenter Study for Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPAREL
NCT03682302
Efficacy and Safety of EXPAREL Versus Standard of Care (SoC) in Subjects Undergoing Elective Cesarean Section
NCT03853694
Study to Evaluate the Efficacy and Safety of FX006 in Patients With Hip Osteoarthritis
NCT03793010
Study in Adult Subjects Undergoing Posterolateral Thoracotomy
NCT03428984
Study to Evaluate the Effect of FX006 on Synovial Inflammation in Patients With OA of the Knee
NCT03529942
Study in Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPAREL
NCT03485014
Study to Compare Exposure of TA Following Administration of FX006 or TAcs in Patients With OA of the Shoulder or Hip
NCT03382262
Study to Compare Exposure of TA Following Administration of Either FX006 or TAcs in Patients With Bilateral Knee OA
NCT03378076
Treatment With Iovera° for Total Knee Arthroplasty (TKA) Post-Operative Pain
NCT03327220
Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-Sections
NCT03176459
Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion Surgery
NCT03015961
Study to Assess the Safety of Repeat Administration of FX006 Administered to Patients With Osteoarthritis of the Knee
NCT03046446
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
NCT02985762
Study of Local Administration of DepoTXA for Reduced Postsurgical Bleeding in Subjects Undergoing TKA
NCT02922582
Efficacy, Safety, and Pharmacokinetics of Femoral Nerve Block With EXPAREL in Total Knee Arthroplasty
NCT02713178
Efficacy, Safety, and Pharmacokinetics of Brachial Plexus Block With EXPAREL in Shoulder Surgery
NCT02713230
Local Infiltration Analgesia With and Without EXPAREL Following Total Knee Arthroplasty
NCT02713490
Study to Assess the Effects of FX006 on Blood Glucose in Patients With OA of the Knee and Type 2 Diabetes
NCT02762370
Study to Characterize the PK and Local Extent and Duration of Exposure From FX006 in Patients With OA of the Knee
NCT02637323
Evaluation of EXPAREL for Prolonged Postsurgical Analgesia in Subjects Undergoing Third Molar Extraction
NCT02517905
Evaluation of the Safety and Efficacy of EXPAREL When Administered Into the TAP in Subjects Undergoing Cesarean Section
NCT02353754
Proof of Concept Study Comparing FX006 to Kenalog®-40 in Patients With Post-Traumatic Osteoarthritis of the Knee
NCT02468583
Study of FX006 for the Treatment of Pain in Patients With Osteoarthritis of the Knee
NCT02357459
Pharmacokinetics and Safety of Bupivacaine HCl Spinal Block and EXPAREL Local Infiltration in Total Knee Arthroplasty
NCT02284386
A Randomized, Study to Evaluate the Iovera° Device in Treating Pain Associated With Total Knee Arthroplasty
NCT02284113
Study to Evaluate the Iovera° Device for Temporary Relief From Knee Pain
NCT02260921
EXPAREL Infiltration in Subjects Undergoing Femoral Nerve Block With Bupivacaine HCl for Total Knee Arthroplasty
NCT02255500
Pharmacokinetic Evaluation of EXPAREL in Adults Undergoing Tonsillectomy
NCT02199574
Safety and Pharmacokinetics Study of Redosing EXPAREL in Healthy Volunteers
NCT02210247
Study of FX006 vs Normal Saline in Patients With Osteoarthritis of the Knee
NCT02116972
Study to Characterize the Local Duration of Exposure From FX006 in Patients With Osteoarthritis of the Knee
NCT02003365
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 13 |
| Phase 2 | 22 |
| Phase 3 | 17 |
| Phase 4 | 21 |
Therapeutic Areas
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.
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.