
Pacira BioSciences Inc
PCRXHealthcare|Drug Manufacturers - Specialty & Generic|USA
$25.47
-0.01 (-0.04%)
DCF (FCF)
$43.62
Tangible Book
$7.15
Graham Number
$18.67
Earnings Power
$19.49
Clinical Trials (152)
| Trial | Conditions | Phase | Status | Enrollment | Design | Drug |
|---|---|---|---|---|---|---|
| NCT06269705 ZILRETTA in Subjects With Shoulder Osteoarthritis | Glenohumeral Osteoarthritis | P3 | Active | 150 | RCT, Single-blind | ZILRETTA |
| NCT07212114 Efficacy of EXPAREL vs. Bupivacaine | Total Ankle Arthroplasty, Postsurgical Analgesia | P3 | Recruiting | 104 | RCT, Double-blind | EXPAREL, 0.25% bupivacaine (HCl): 50 ml, 0.25% bupivacaine (HCl): 30 ml |
| NCT06884865 A Study to Assess Safety and Tolerability of PCRX-201 in Subjects With Painful Osteoarthritis of the Knee | Osteoarthritis (OA) of the Knee | P2 | Active | 135 | RCT, Double-blind | Enekinragene Inzadenovec (PCRX-201), Placebo |
| NCT04119687 Study to Evaluate the Safety and Tolerability of FX201 in Patients with Osteoarthritis of the Knee | Osteoarthritis, Knee | P1 | Active | 72 | Open-label | FX201 |
| NCT06271265 Study to Evaluate the Pharmacokinetics and Safety of EXPAREL for Postoperative Analgesia in Subjects Undergoing Cardiac Surgery | Postoperative Pain | P1 | Recruiting | 48 | RCT, Open-label | EXPAREL, bupivacaine |
| NCT06340451 Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity | Spasticity, Cerebral or Spinal Condition | N/A | Active | 132 | RCT, Double-blind | — |
| NCT07125833 Cryoneurolysis of the Suprascapular Nerve for Perioperative Pain Control After Receiving a Reverse Total Shoulder Arthroplasty (RTSA) | Degenerative Joint Disease of Shoulder | N/A | Recruiting | 20 | RCT, Open-label | — |
| NCT06603051 The Effect of Pre-Operative Cryoneurolysis on Post-Operative Narcotic Consumption in Patients Undergoing Autograft ACL Reconstruction | ACL Repair | N/A | Recruiting | 20 | RCT, Open-label | — |
| NCT06958289 Cryoneurolysis for Spasticity Treatment: Long-term Clinical Outcomes and Mechanisms in the Central Nervous System | Spasticity as Sequela of Stroke | N/A | Recruiting | 25 | Open-label | — |
| NCT07214844 A Prospective Study to Evaluate the Efficacy of Iovera Lumbar Medial Branch Cryoneurolysis Versus Radiofrequency Ablation for the Treatment of Chronic Low Back Pain | Low Back Pain, Chronic | N/A | Recruiting | 110 | RCT, Double-blind | — |
| NCT06946368 Effectiveness of Exparel Anesthetic Administered by the Surgeon During Knee Surgery | Total Knee Arthroplasty | N/A | Recruiting | 60 | RCT, Open-label | — |
| NCT05495334 Innovations in Genicular Outcomes Registry | Knee Osteoarthritis | Recruiting | 10,000 | — | — | |
| NCT02142829 Pain Control in Bariatric Patients: EXPAREL(R) vs. the On-Q(R) Pain Ball | Obesity | P4 | Completed | 101 | Open-label | EXPAREL, On-Q Pain Ball |
| NCT02353754 Evaluation of the Safety and Efficacy of EXPAREL When Administered Into the TAP in Subjects Undergoing Cesarean Section | Pain | P4 | Terminated | 12 | Open-label | Intrathecal morphine injection, EXPAREL |
| NCT01919190 EXPAREL Administered by Infiltration Into the TAP for Prolonged Postsurgical Analgesia in Lower Abdominal Surgeries | Pain | P4 | Terminated | 67 | RCT, Single-blind | EXPAREL, Placebo |
| NCT00029523 DepoCyt Therapy in Patients With Neoplastic Meningitis From Lymphoma or a Solid Tumor | Meningeal Neoplasms | P4 | Completed | 100 | RCT, Open-label | Intrathecal (injected into the spinal fluid) DepoCyt, Intrathecal methotrexate, Intrathecal cytarabine (also known as ara-C) |
| NCT02787226 Liposomal Bupivacaine Infiltration vs Continuous Perineural Ropivacaine Infusion for Post-operative Pain After Total Shoulder Arthroplasty | Postoperative Pain, Shoulder Arthritis | P4 | Terminated | 100 | RCT, Open-label | Liposomal Bupivacaine Infiltration, Continuous Perineural Ropivicaine Infusion |
| NCT01509807 A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B504 | Retraction of Colostomy | P4 | Completed | 33 | Open-label | IV morphine sulfate or Sponsor-approved equivalent, EXPAREL |
| NCT06995352 Liposomal Bupivacaine Versus Continuous Peripheral Nerve Blocks for Analgesia Following Ankle Surgery | Moderate-to-severely Painful Ankle Surgery | P4 | By Invite | 140 | RCT, Double-blind | Popliteal nerve block including liposomal bupivacaine, Adductor canal nerve block including liposomal bupivacaine, Continuous popliteal nerve block with normal saline, Popliteal nerve block with exclusively unencapsulated bupivacaine, Adductor canal nerve block with exclusively unencapsulated bupivacaine, Continuous popliteal nerve block with unencapsulated bupivacaine |
| NCT01582490 Study of EXPAREL in Patients Undergoing Breast Augmentation | Mammoplasty, Postoperative Pain | P4 | Completed | 19 | Open-label | Instillation - EXPAREL, Infiltration - EXPAREL |
| NCT07584915 Pilot Study on EXPAREL as an Intra-articular Posteromedial Surgeon Administered (IPSA) Block vs. Local Infiltration Analgesia in Knee Replacement Surgery | Total Knee Arthroplasty, Total Knee Arthroplasty Recovery | P4 | By Invite | 40 | RCT, Single-blind | Bupivacaine liposome injectable suspension (IPSA block), Bupivacaine liposome injectable suspension (LIA) |
| NCT01507246 Adult Patients Undergoing Open Colectomy MA402S23B303 | Bowel Obstruction | P4 | Completed | 42 | Open-label | IV morphine sulfate, EXPAREL (bupivacaine liposome injectable suspension) |
| NCT03927911 Phase 4 Study in Adult Subjects Undergoing Posterior Lumbar Spine Surgeries | Postoperative Pain Management | P4 | Terminated | 65 | Open-label | EXPAREL and Bupivacaine, Standard of Care |
| NCT02199574 Pharmacokinetic Evaluation of EXPAREL in Adults Undergoing Tonsillectomy | Pain | P4 | Completed | 12 | Open-label | EXPAREL |
| NCT01801124 EXPAREL Infiltrated Into the TAP for Postoperative Analgesia in Unilateral Abdominal Hernia Repair | Hernia | P4 | Completed | 13 | Open-label | EXPAREL |
| NCT03975283 Use of Exparel for Postoperative Analgesia Following Bariatric Surgery | Post Operative Pain | P4 | Unknown | 80 | RCT, Double-blind | Exparel 266 MG Per 20 ML Injection, Bupivacaine Hcl 0.25% Inj |
| NCT02255500 EXPAREL Infiltration in Subjects Undergoing Femoral Nerve Block With Bupivacaine HCl for Total Knee Arthroplasty | Pain | P4 | Completed | 23 | Open-label | Bupivacaine FNB, EXPAREL Infiltration |
| NCT03149887 Liposomal Bupivacaine After Arthroscopic Rotator Cuff Repair | Rotator Cuff Tear | P4 | Completed | 54 | RCT, Double-blind | Liposomal bupivacaine, Placebo |
| NCT00134979 Formoterol Certihaler, Tiotropium HandiHaler and Tiotropium HandiHaler in Combination With Formoterol Certihaler in Patients With Stable Chronic Obstructive Pulmonary Disease | Chronic Obstructive Pulmonary Disease | P4 | Completed | 847 | RCT, Double-blind | Formoterol |
| NCT03827291 QL Block With Exparel in Colectomy | Laparotomy, Colectomy | P4 | Completed | 35 | Open-label | Exparel |
| NCT02058290 A Health Economic Trial in Adult Patients Undergoing Laparoscopic Colectomy | Bowel Obstruction | P4 | Terminated | 122 | Open-label | IV morphine sulfate or Sponsor-approved equivalent, EXPAREL |
| NCT02586077 Foot and Ankle Clinic Application for Liposomal Related Anesthetic | Ankle Arthrodesis, Hindfoot Arthrodesis | P4 | Completed | 36 | Open-label | Exparel |
| NCT03290196 The Effect of EXPAREL® on Postsurgical Pain, and the Use of Narcotics | Rotator Cuff Tear | P4 | Terminated | 13 | Open-label | EXPAREL 1.3 % in 20 ML Injection |
| NCT03853694 Efficacy and Safety of EXPAREL Versus Standard of Care (SoC) in Subjects Undergoing Elective Cesarean Section | Elective Cesarean Section, Pain Management | P4 | Completed | 167 | RCT, Open-label | 50 mcg Duramorph+ EXPAREL + multi-modal pain regimen, 150 mcg Duramorph + multi-modal pain regimen, Exparel TAP + multi-modal pain regimen |
| NCT02713490 Local Infiltration Analgesia With and Without EXPAREL Following Total Knee Arthroplasty | Pain | P4 | Completed | 140 | RCT, Double-blind | EXPAREL, Bupivacaine |
| NCT01507233 A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B302 | Bowel Obstruction | P4 | Terminated | 5 | Open-label | IV morphine sulfate, EXPAREL (bupivacaine liposome injectable suspension) |
| NCT03015961 Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion Surgery | Postoperative Pain Management | P4 | Terminated | 38 | RCT, Double-blind | EXPAREL and bupivacaine HCl, Bupivacaine HCl |
| NCT01507220 A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B301 | Bowel Obstruction | P4 | Terminated | 2 | Open-label | morphine sulfate, bupivacaine liposome extended-release injectable suspension |
| NCT04278846 Efficacy of Liposomal Bupivacaine for Prolonged Postoperative Analgesia in Patient Undergoing Breast Reconstruction With Tissue Expander | Pain, Postoperative, Mammaplasty | P4 | Completed | 50 | RCT, Open-label | Depofoam bupivacaine, Bupivacaine hydrochloride (HCl) |
| NCT01582477 TAP-patients With Robotic Assisted Lap Prostatectomy | Postsurgical Pain, Analgesia | P4 | Completed | 24 | Open-label | EXPAREL 20 mL, EXPAREL 40 mL |
| NCT03541941 Exparel vs. Bupivacaine Hydrochloride vs. Placebo for Hernia Repair | Analgesia, Postoperative | P4 | Completed | 164 | RCT, Double-blind | Exparel, Bupivacaine Hcl 0.25% Inj, Placebo |
| NCT05730920 IV Methadone Vs EXPAREL Erector Spinae Plane Blockade in Pediatric Subjects Undergoing Idiopathic Scoliosis Correction | Adolescent Idiopathic Scoliosis, Juvenile Idiopathic Scoliosis | P4 | Completed | 30 | RCT, Double-blind | Methadone, Liposomal bupivacaine (LB, Exparel) |
| NCT03907033 Liposomal Bupivacaine in Vaginal Hysterectomy | Vaginal Hysterectomy | P4 | Terminated | 28 | RCT, Double-blind | Liposomal bupivacaine, Bupivacaine Hydrochloride |
| NCT01919606 EXPAREL Administered Into the TAP for Analgesia in Subjects Undergoing Open Total Abdominal Hysterectomy | Postoperative Pain | P4 | Terminated | 1 | Open-label | EXPAREL |
| NCT01509638 A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B501 | Retraction of Colostomy | P4 | Completed | 47 | Open-label | Group 1 Standard of Care, Group 2 EXPAREL |
| NCT02128646 Liposomal Bupivacaine (Exparel) for Postoperative Pain Control for Open and Laparoscopic Abdominal Hernia Repair | Pain | P4 | Completed | 19 | RCT, Open-label | EXPAREL, Ketorolac |
| NCT02058303 Study of A Long Lasting Local Anesthestic for Hand, Wrist or Finger Surgery | Hand Injuries, Wrist Injuries | P4 | Terminated | 37 | RCT, Double-blind | Exparel Forearm block, Bupivacaine supraclavicular block |
| NCT03955458 EXPAREL Facia Iliaca Compartment Block for Intertrochanteric Hip Fracture | Hip Fractures, Intertrochanteric Fractures | P4 | Withdrawn | — | RCT, Open-label | EXPAREL, Ropivacaine, Bupivacaine Hydrochloride |
| NCT03176459 Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-Sections | C-Section, Pain Management | P4 | Completed | 186 | RCT, Double-blind | Exparel + Bupivacaine, Bupivacaine |
| NCT02284386 Pharmacokinetics and Safety of Bupivacaine HCl Spinal Block and EXPAREL Local Infiltration in Total Knee Arthroplasty | Pain | P4 | Completed | 15 | Open-label | Bupivacaine SNB, EXPAREL Infiltration |
| NCT03738696 Liposomal Bupivacaine in Rotator Cuff Repair | Rotator Cuff Injury | P4 | Completed | 64 | RCT, Open-label | Exparel, Ropivacaine |
| NCT03802864 Post-operative Pain Control of Testicular Sperm Extraction Using Liposomal Bupivacaine | Male Infertility | P4 | Completed | 50 | RCT, Double-blind | Liposomal Bupivacaine, Standard Bupivacaine |
| NCT04504812 A Sequenced Strategy for Improving Outcomes in People With Knee Osteoarthritis Pain | Knee Osteoarthritis | P3 | Completed | 1,937 | RCT, Single-blind | Duloxetine |
| NCT05139030 Phase 3 Adductor Canal Block With EXPAREL in Subjects Undergoing Primary Unilateral Total Knee Arthroplasty | Knee Osteoarthritis, Pain Management | P3 | Completed | 167 | RCT, Double-blind | bupivacaine liposome injectable suspension, Bupivacaine Hydrochloride |
| NCT00813111 Phase 3 Study of Local Administration of SKY0402 for Postoperative Analgesia in Subject Undergoing Breast Augmentation | Pain | P3 | Terminated | 136 | RCT, Double-blind | SKY0402, Bupivacaine HCl |
| NCT00130351 A 3-week Study Investigating Patient Use and Functionality of Formoterol in a Novel Inhalation Device in Patients With Asthma | Asthma | P3 | Completed | 155 | Open-label | — |
| NCT01379365 Cryo-Touch III Refinement Study Investigational Plan | Facial Wrinkles, Skin Aging | P2P3 | Completed | 88 | Open-label | — |
| NCT05171179 The Use of Pecs Blocks in Combination With Exparel in Breast Reconstruction Surgery | Mammaplasty | P3 | Completed | 60 | RCT, Single-blind | Exparel, Bupivacaine |
| NCT01683071 Femoral Nerve Block With Liposome Bupivacaine for Postsurgical Analgesia Following Total Knee Arthroplasty | Postoperative Pain | P2P3 | Completed | 297 | RCT, Double-blind | Placebo, EXPAREL 67 mg, EXPAREL 133 mg, EXPAREL 266 mg |
| NCT02357459 Study of FX006 for the Treatment of Pain in Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P3 | Completed | 486 | RCT, Double-blind | FX006, Placebo, TCA IR 40 |
| NCT03793010 Study to Evaluate the Efficacy and Safety of FX006 in Patients With Hip Osteoarthritis | Osteoarthritis, Hip | P3 | Terminated | 70 | RCT, Double-blind | FX006, Normal saline |
| NCT03739021 Exparel for Total Shoulder Pain | Chronic Shoulder Pain | P2P3 | Not Yet Recruiting | 60 | RCT, Open-label | Exparel, Ropivacaine |
| NCT04117074 Thoracic Epidural Analgesia vs Surgical Site Infiltration With Liposomal Bupivacaine Following Open Gynecologic Surgery | Surgery, Analgesia | P3 | Completed | 106 | RCT, Open-label | Liposomal bupivacaine |
| NCT03046446 Study to Assess the Safety of Repeat Administration of FX006 Administered to Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P3 | Completed | 208 | Open-label | FX006 32 mg |
| NCT01447342 A Study to Evaluate the Safety and Effectiveness of the Cryo-Touch II Device for the Treatment of Forehead and/or Glabellar Lines | Facial Wrinkles, Skin Aging | P2P3 | Completed | 54 | Open-label | — |
| NCT02713178 Efficacy, Safety, and Pharmacokinetics of Femoral Nerve Block With EXPAREL in Total Knee Arthroplasty | Pain | P3 | Completed | 232 | RCT, Double-blind | bupivacaine liposome injectable suspension, Placebo |
| NCT03529942 Study to Evaluate the Effect of FX006 on Synovial Inflammation in Patients With OA of the Knee | Osteoarthritis, Knee | P3 | Completed | 129 | Open-label | FX006 32 mg |
| NCT00890721 Study of Pain Control in Hemorrhoidectomy | Hemorrhoid | P3 | Completed | 189 | RCT, Double-blind | SKY0402, Placebo |
| NCT03270514 Comparison of Sternal Wound Infiltration With Liposomal Bupivacaine v. Bupivacaine Hydrochloride | Coronary Artery Disease, Coronary Artery Stenoses | P3 | Completed | 60 | RCT, Double-blind | Exparel Injectable Product, Bupivacaine Hydrochloride |
| NCT02740114 Wound Infiltration With Liposomal Bupivacaine vs. Standard Wound Infiltration With Bupivacaine in Patient's Undergoing Open Gynecologic Surgery on an Enhanced Recovery Pathway | Malignant Neoplasms of Female Genital Organs, Gynecologic Cancer | P3 | Terminated | 105 | RCT, Single-blind | Bupivacaine, Liposomal Bupivacaine, Oxycodone |
| NCT01167140 Cryo-Touch II for the Treatment of Wrinkles | Facial Wrinkles | P2P3 | Completed | 42 | Open-label | — |
| NCT00744848 Study to Evaluate Postoperative Analgesia in Subjects Undergoing Hemorrhoidectomy | Hemorrhoids | P3 | Completed | 204 | RCT, Double-blind | Bupivacaine HCl, SKY0402 |
| NCT02517905 Evaluation of EXPAREL for Prolonged Postsurgical Analgesia in Subjects Undergoing Third Molar Extraction | Dental Pain | P3 | Completed | 166 | RCT, Double-blind | Bupivacaine liposome, Placebo |
| NCT00745290 A Phase 3 Study to Evaluate the Safety and Efficacy of SKY0402 in Subjects Undergoing Total Knee Arthroplasty | Postoperative Pain | P3 | Completed | 245 | RCT, Double-blind | Bupivacaine HCl, SKY0402 |
| NCT04518462 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 | Lower Extremity Surgery, Bunion | P3 | Completed | 121 | RCT, Double-blind | Exparel, Bupivacaine Hydrochloride |
| NCT06350981 Analgesic Requirement for Post-Operative Pain Control in TLIP Interbody Fusion | Back Pain, Surgery-Complications | P2P3 | By Invite | 76 | RCT, Double-blind | Exparel, Bupivacain |
| NCT03954639 Phase 3, Randomized, Double Blinded, Active Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of EXPAREL Admixed With Bupi vs. Bupi Only Administered as Combined Sciatic and Adductor Canal Nerve Block for Postsurgical Analgesia in Lower Extremity Surgeries | Bunion, Metatarsophalangeal Fusion | P3 | Withdrawn | — | RCT, Double-blind | EXPAREL 13.3Mg/mL Suspension for Injection, Bupivacaine Hydrochloride |
| NCT06077422 Exparel vs. Marcaine ESP Block for Post-cardiac Surgical Pain | Pain, Postoperative, Opioid Use | P2P3 | By Invite | 150 | RCT, Double-blind | bupivacaine liposome injectable suspension, Bupivacaine Hydrochloride |
| NCT02713230 Efficacy, Safety, and Pharmacokinetics of Brachial Plexus Block With EXPAREL in Shoulder Surgery | Pain | P3 | Completed | 156 | RCT, Double-blind | bupivacaine liposome injectable suspension, bupivacaine liposome injectable suspension, Placebo |
| NCT05157841 Phase 3, Sciatic Nerve Block With EXPAREL for Subjects Undergoing Bunionectomy | Bunionectomy, Hallux Valgus | P3 | Completed | 185 | RCT, Double-blind | Bupivacaine liposome injectable suspension 266 mg, Bupivacaine HCl, Bupivacaine liposome injectable suspension 133 mg |
| NCT00890682 Study of Postoperative Analgesia in Bunionectomy | Bunion, Hallux Valgus | P3 | Completed | 193 | RCT, Double-blind | SKY0402, Placebo |
| NCT01802411 Intercostal Nerve Block With Liposome Bupivacaine in Subjects Undergoing Posterolateral Thoracotomy | Posterolateral Thoracotomy, Postoperative Pain | P3 | Completed | 191 | RCT, Double-blind | EXPAREL 266 mg, Placebo |
| NCT03682302 Multicenter Study for Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPAREL | Postoperative Pain Management | P3 | Completed | 98 | RCT, Open-label | Exparel, 0.5% Bupivacaine HCl |
| NCT03382262 Study to Compare Exposure of TA Following Administration of FX006 or TAcs in Patients With OA of the Shoulder or Hip | Osteoarthritis of the Shoulder, Osteoarthritis of the Hip | P2 | Completed | 55 | RCT, Open-label | FX006 32 mg, TAcs 40 mg |
| NCT01487200 Pharmacokinetic and Pharmacodynamic Study of FX006 in Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P2 | Completed | 24 | RCT, Double-blind | FX006 10 mg, FX006 40 mg, FX006 60 mg, TCA IR 40 |
| NCT04065074 Study to Evaluate a Procedure for Intra-articular Injection of FX006 in Patients With Osteoarthritis of the Hip | Osteoarthritis, Hip | P2 | Completed | 16 | Open-label | FX006 32 mg |
| NCT03378076 Study to Compare Exposure of TA Following Administration of Either FX006 or TAcs in Patients With Bilateral Knee OA | Bilateral Knee Osteoarthritis | P2 | Completed | 24 | RCT, Open-label | FX006 32 mg, TAcs 40 mg |
| NCT01487161 Study of FX006 in Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P2 | Completed | 229 | RCT, Double-blind | FX006, TCA IR |
| NCT01203644 Evaluation of the Safety, Efficacy, and Pharmacokinetics of SKY0402 in Subjects Undergoing Inguinal Hernia Repair | Inguinal Hernia | P2 | Completed | 76 | RCT, Double-blind | SKY0402, Bupivacaine HCl |
| NCT00529126 Phase 2 Dose-Ranging Study of SKY0402 for Prolonged Postoperative Analgesia in Subject Undergoing Hemorrhoidectomy | Postoperative Pain | P2 | Completed | 100 | RCT, Double-blind | SKY0402, Bupivacaine HCl |
| NCT02468583 Proof of Concept Study Comparing FX006 to Kenalog®-40 in Patients With Post-Traumatic Osteoarthritis of the Knee | Post-traumatic Osteoarthritis of the Knee | P2 | Terminated | 6 | RCT, Double-blind | FX006 32 mg, TCA IR 40 mg |
| NCT02922582 Study of Local Administration of DepoTXA for Reduced Postsurgical Bleeding in Subjects Undergoing TKA | Total Knee Arthroplasty | P2 | Terminated | 16 | RCT, Single-blind | DepoTXA, Tranexamic Acid |
| NCT01291914 Study of FX005 for the Treatment of Pain in Patients With Osteoarthritis of the Knee | Osteoarthritis, Knee | P1P2 | Completed | 140 | RCT, Double-blind | FX005, Placebo 1 (Carrier), Placebo 2 (Diluent) |
| NCT03106545 Liposome Bupivacaine for ANKLE Blocks | Hallux Valgus (Bunions) | P2 | Completed | 40 | RCT, Double-blind | Liposome bupivacaine |
| NCT02762370 Study to Assess the Effects of FX006 on Blood Glucose in Patients With OA of the Knee and Type 2 Diabetes | Osteoarthritis of the Knee, Type 2 Diabetes Mellitus | P2 | Completed | 33 | RCT, Double-blind | FX006 32 mg, TCA IR 40 mg |
| NCT00842062 Study of the MyoScience Tissue Remodeling Device for Facial Rejuvenation | Facial Rhytides | P1P2 | Completed | 380 | Open-label | — |
| NCT02116972 Study of FX006 vs Normal Saline in Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P2 | Completed | 310 | RCT, Double-blind | FX006 32 mg, Placebo, FX006 16 mg |
| NCT06977568 A Study to Evaluate an Intra-Articular Injection of ZILRETTA Versus Triamcinolone Acetonide, Immediate Release in Subjects With Osteoarthritis of the Hip | Osteoarthritis of Hip | P2 | Terminated | 1 | RCT, Open-label | Zilretta, Triamcinolone Acetonide |
| NCT04160091 Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive Capsulitis | Osteoarthritis of the Shoulder, Adhesive Capsulitis | P2 | Terminated | 19 | RCT, Double-blind | FX006, Normal Saline |
| NCT00485433 Dose-ranging Study for Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia Repair | Postoperative Pain | P2 | Completed | 98 | RCT, Double-blind | Bupivacaine HCl, SKY0402 |
| NCT01206608 Evaluation of the Safety and Efficacy of a Single Dose of SKY0402 in Subjects Undergoing Augmentation Mammoplasty | Postoperative Pain | P2 | Completed | 40 | RCT, Double-blind | SKY0402 + bupivacaine HCl, Mid-dose SKY0402 + bupivacaine HCl |
| NCT02637323 Study to Characterize the PK and Local Extent and Duration of Exposure From FX006 in Patients With OA of the Knee | Osteoarthritis of the Knee | P2 | Completed | 81 | Open-label | FX006 32 mg, TCA IR 40 |
| NCT00807209 Dose Finding Posterolateral Thoracotomy Study | Postoperative Pain | P2 | Terminated | 3 | RCT, Open-label | Low Dose SKY0402, High Dose SKY0402, Placebo, Fentanyl via PCA, Bupivacaine via epidural |
| NCT03106519 Liposome Bupivacaine for WRIST Blocks | Dupuytren's Contracture of the Hand (Viking's Disease) | P2 | Completed | 32 | RCT, Double-blind | Liposome bupivacaine + bupivacaine |
| NCT00485693 Dose-Ranging Study for Prolonged Postoperative Analgesia in Subject Undergoing Total Knee Arthroplasty | Postoperative Pain | P2 | Completed | 138 | RCT, Double-blind | Bupivacaine HCl, SKY0402 |
| NCT02003365 Study to Characterize the Local Duration of Exposure From FX006 in Patients With Osteoarthritis of the Knee | Osteoarthritis of the Knee | P2 | Completed | 50 | Open-label | FX006 10 mg, FX006 40 mg, TCA IR 40 mg |
| NCT04182672 Study to Assess the Safety and Efficacy of FX006 Administered to Patients With Greater Trochanteric Bursitis | Trochanteric Bursitis | P2 | Completed | 22 | Open-label | FX006 |
| NCT01206595 Safety, Efficacy, and Pharmacokinetics of SKY0402 Administered as a Nerve Block in Subjects Undergoing Bunionectomy | Postoperative Pain | P2 | Completed | 58 | RCT, Double-blind | SKY0402, Bupivacaine HCl |
| NCT02985762 PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery | Spinal Fusion, Pain Management | P1 | Completed | 15 | Open-label | EXPAREL |
| NCT05456490 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 | Healthy | P1 | Completed | 54 | RCT, Double-blind | Liposomal Bupivacaine 13.3, Bupivacaine |
| NCT00812305 Hepatic Impairment Study: Pharmacokinetics in Healthy and Hepatically Impaired Subjects | Pain, Hepatic Impairment | P1 | Completed | 16 | Open-label | SKY0402 300mg in healthy patients, SKY0402 300mg in hepatically impaired patients |
| NCT01349140 EXPAREL Dose-Response for Single-Injection Femoral Nerve Blocks | Healthy Volunteers | P1 | Completed | 14 | Double-blind | SKY0402 |
| NCT00806806 Evaluate the Onset of Action of SKY0402 Following Local Infiltration in Healthy Volunteers | Postoperative Pain Management | P1 | Completed | 128 | RCT, Single-blind | SKY0402, Placebo |
| NCT04826328 Study to Evaluate the Safety and Tolerability of FX301 in Patients Undergoing Bunionectomy | Pain, Postoperative, Bunion | P1 | Completed | 85 | RCT, Double-blind | FX301, Normal Saline |
| NCT04002089 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 | Bunion | P1 | Completed | 45 | Open-label | Exparel Injectable Product, Bupivacaine |
| NCT00003073 Chemotherapy in Treating Young Patients With Recurrent or Refractory Meningeal Leukemia, Lymphoma, or Solid Tumors | Brain and Central Nervous System Tumors, Leukemia | P1 | Unknown | 15 | — | liposomal cytarabine |
| NCT03485014 Study in Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPAREL | Postoperative Pain Management | P1 | Completed | 15 | Open-label | Exparel |
| NCT00728832 A Pharmacokinetic (PK) Study of Extended-Release Epidural Morphine in Upper Abdominal Surgery | Postoperative Pain | P1 | Completed | 39 | RCT, Open-label | DepoDur (extended-release epidural morphine) |
| NCT04261049 Effect of Zilretta Injection | Osteoarthritis, Knee | P1 | Completed | 35 | Open-label | Triamcinolone Acetonide Extended-Release Injectable Suspension |
| NCT02210247 Safety and Pharmacokinetics Study of Redosing EXPAREL in Healthy Volunteers | Healthy Volunteers | P1 | Completed | 60 | Open-label | EXPAREL |
| NCT04173611 Evaluation of Safety, Pharmacokinetics and Pharmacodynamics of EXPAREL® Administered Via a Single Intrathecal Injection to Healthy Volunteers | Healthy | P1 | Terminated | 20 | RCT, Double-blind | EXPAREL, Bupivacaine Hydrochloride |
| NCT03428984 Study in Adult Subjects Undergoing Posterolateral Thoracotomy | Postoperative Pain Management | P1 | Terminated | 5 | RCT, Open-label | EXPAREL |
| NCT04293809 Study to Evaluate the Pharmacokinetics and Safety of EXPAREL Administered as a Pectoral Plane Block in Women Undergoing Breast Augmentation | Breast Augmentation | P1 | Completed | 30 | RCT, Open-label | Exparel Injectable Product, Bupivacaine Hydrochloride |
| NCT00485667 Phase 1 Thorough QT Study in Young Healthy Volunteers | Postoperative Pain | P1 | Completed | 48 | RCT, Double-blind | SKY0402, Moxifloxacin 400mg, Placebo injection, Placebo tablet |
| NCT06284109 Preoperative (Pre-amputation) Cryoanalgesia to Improve Post-amputation Phantom Limb Pain | Postoperative Pain | N/A | Withdrawn | — | RCT, Double-blind | — |
| NCT03327220 Treatment With Iovera° for Total Knee Arthroplasty (TKA) Post-Operative Pain | Total Knee Arthroplasty | N/A | Completed | 124 | RCT, Open-label | — |
| NCT01681745 Probe Configuration and Time-Temperature Dose Ranging for Understanding of Skin Lesion Effects | Histological Response of Tissue to Cold | N/A | Completed | 30 | Open-label | — |
| NCT06093776 Rib Fracture Cryoanalgesia | Pain Management Improvement | Completed | 5 | — | — | |
| NCT06935539 Cryoneurolysis vs Radiofrequency Ablation for Chronic Sacroiliac Joint Pain | Chronic Sacroiliac Joint Pain | N/A | Not Yet Recruiting | 30 | RCT, Open-label | — |
| NCT02821325 Intra-articular Volumetric Assessment After Total Knee Arthroplasty | Hematoma | Completed | 10 | — | — | |
| NCT01863901 Study Evaluating Treatment of Upper Limb Spasticity Using the Cryo-Touch III Device | Upper Limb Spasticity | N/A | Completed | 19 | Open-label | — |
| NCT01950065 Effectiveness and Safety Study of the Iovera Device for the Temporary Reduction in the Appearance of Forehead Wrinkles | Forehead Wrinkles | N/A | Completed | 85 | RCT, Single-blind | — |
| NCT01753778 Study Evaluating Treatment of Forefoot Pain Related to Nerve Entrapment Using the Cryo-Touch III Device | Entrapment Neuropathy | N/A | Completed | 7 | Open-label | — |
| NCT03578237 Cryoanalgesia to Prevent Acute and Chronic Pain Following Surgery: A Randomized, Double-Masked, Sham-Controlled Study | Mastectomy, Upper Limb Amputation Below Elbow | N/A | Completed | 99 | RCT, Double-blind | — |
| NCT03076710 Post-Operative Pain Management Following Spine Surgery | Pain Management, Analgesia | Withdrawn | — | — | Opioids delivered through PCA, EXPAREL® infiltration | |
| NCT02284113 A Randomized, Study to Evaluate the Iovera° Device in Treating Pain Associated With Total Knee Arthroplasty | Arthritis of the Knee | N/A | Completed | 150 | RCT, Double-blind | — |
| NCT03836313 Assessing if Cryoneurolysis Improves Prehabilitation and Decreases Pain After Surgery With Less Opioid Use in TKA Patients | Arthropathy of Knee, Pain, Joint | N/A | Withdrawn | — | RCT, Double-blind | — |
| NCT05604144 Cryoanalgesia for the Treatment of Pain in Subjects With Morton's Neuroma | Morton's Neuroma, Pain Management | N/A | Unknown | 5 | Open-label | — |
| NCT02260921 Study to Evaluate the Iovera° Device for Temporary Relief From Knee Pain | Knee Osteoarthritis | N/A | Completed | 180 | RCT, Double-blind | — |
| NCT03909516 Evaluate the Iovera° Device in Treating Pain Associated With Anterior Cruciate Ligament Reconstruction | ACL Reconstruction | N/A | Withdrawn | — | RCT, Open-label | — |
| NCT01801826 A Prospective Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the Cryo-Touch IV Device | Frown Lines, Glabellar Frown Lines | Completed | 61 | — | — | |
| NCT01704157 A Prospective Study Evaluating the Treatment of Knee Osteoarthritis With the Cryo-Touch III Device | Osteoarthritis of the Knee | N/A | Completed | 33 | Open-label | — |
| NCT04191031 Study to Evaluate Iovera®° in Adult Patients Undergoing Total Knee Arthroplasty | Post-Operative Pain Management | N/A | Terminated | 79 | RCT, Double-blind | — |
| NCT06016127 Cryoneurolysis for Facet Mediated Chronic Low Back Pain | Low Back Pain, Facet Joint Pain | N/A | Completed | 30 | RCT, Open-label | — |
| NCT01984619 Prospective Study Evaluating the Treatment of Hyperdynamic Forehead Wrinkles | Wrinkles | Completed | 47 | — | — | |
| NCT06340932 Impact of Opioid Avoidance Protocol for ACL Reconstruction | ACL Tear, Post Operative Pain | Completed | 32 | — | Celecoxib, Acetaminophen, Oxycodone, Tramadol, Bupivacaine Hydrochloride, Acetaminophen 500Mg Cap | |
| NCT03081299 Characterization of Bio-psychosocial Pain Profiles in the Perioperative Period | Pain, Postoperative | Completed | 471 | — | — | |
| NCT02554357 Quality of Analgesia After Interscalene Block After Arthroscopic Shoulder Surgery | Injury of Shoulder Region | N/A | Completed | 50 | RCT, Double-blind | Exparel block in arthroscopic shoulder surgery, Bupivacaine block in shoulder surgery |
| NCT01808742 Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the CRYO-TOUCH III Device | Frown Lines, Glabellar Frown Lines | Completed | 17 | — | — | |
| NCT01076686 Observational Study to Assess Long-Term Follow-Up of Breast Augmentation Subjects | Postoperative Pain | Completed | 94 | — | Questionnaire and Physical Exam | |
| NCT03688477 Iovera° to Treat Pain Associated With ACL Reconstruction and Rehabilitation | Anterior Cruciate Ligament Reconstruction | N/A | Withdrawn | — | RCT, Single-blind | — |
| NCT01753765 Study Evaluating the Treatment of Occipital Neuralgia | Occipital Neuralgia | N/A | Completed | 26 | Open-label | — |