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Clinical trial updates
Drug and device trials that companies register on ClinicalTrials.gov: newly completed phase 3 studies, changes of status and the dates a study is due to finish.
About this data
- What it is
- ClinicalTrials.gov is the US registry of clinical studies. Drug and device makers register their trials there and update the record as each study moves on. We list the studies that companies sponsor, and match the sponsor to a public company when the name lines up. The page opens on Phase 3 studies marked completed, the late-stage trials that come before a request for approval. Change View to see the changes of status we have noticed, or every recent update.
- Who files it
- The sponsor of the study, in its record on ClinicalTrials.gov. The registry is run by the US National Library of Medicine and does not check what sponsors report.
- How current
- We check the registry every day. Sponsors update records on their own schedule, from the same week to months later, so a change can appear in the registry well after it happened.
- Terms
- ClinicalTrials.govClinicalTrials.gov is the US government's registry of clinical studies, run by the National Library of Medicine. Sponsors register a study before it starts and update the record as it goes. The registry does not check what a sponsor reports.Phase 3The late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages.statusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time).completedThe sponsor has marked the study as finished. It says nothing about whether the treatment worked: results, if any, are reported separately and often later.status changesOur history of status changes starts the day we first stored each study, so a change made before that is not shown. The date is when we noticed the change, which can be later than when the sponsor made it.primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update.company matchWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private.
- Worth knowing
- A completed study is not a result: the registry says the study ended, not whether the treatment worked. Status changes start on the day we first stored each study, so earlier changes are not shown. Dates are the sponsor's own, and an estimated date can pass without an update. We match sponsors to companies automatically, with a hand-checked list for the large drugmakers, so a study with no ticker may still belong to a public company. This is information about studies, not a forecast of what they will show or of a stock's price.
- Not to be confused with
- FDA approvals and clearances: what the FDA decided, not what a sponsor reports about a study.
All of this comes from ClinicalTrials.gov, the US registry of clinical studies. We are not affiliated with it.
Source and freshness · Information, not investment advice (disclaimer).
Studies updated per day, last 30 days
All industry-sponsored studies Sponsor matched to a public company
By the day the sponsor last updated the study's record. A study updated twice counts once, on its latest day.
Latest clinical trial updates
Showing: ticker BAX · All recent updates
Studies by the date their record was last updated.
| Updated | Study | SponsorWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private. | PhaseThe late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages. | StatusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time). | Enrolled | Primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update. | Source |
|---|---|---|---|---|---|---|---|
| Sep 23, 2026 | Gen 2 Battrode Wear Study NCT07256951 · Adhesive Wear Time Adhesive | BAX Baxter Healthcare Corporation | Not applicable | Completed | 40 | Dec 23, 2025 | Registry ↗ |
| Mar 11, 2026 | Timmy3 Module Clinical Accuracy ISO 80601-2-56:2017 + A1 2018 NCT06056011 · Febrile Illness Connex CVSM with Timmy3 module | BAX Baxter Healthcare Corporation | Not applicable | Completed | 373 | Mar 18, 2025 | Registry ↗ |
| Nov 12, 2025 | Mobile Cardiac Telemetry (MCT) Study NCT07158333 · Healthy Mobile Cardiac Telemetry (MCT System) | BAX Baxter Healthcare Corporation | — | Completed | 15 | Sep 12, 2025 | Registry ↗ |
| Aug 3, 2025 | PMCF Study for COSEAL® in Gynecologic Surgery NCT05996809 · Adhesion Coseal | BAX Baxter Healthcare Corporation | — | Completed | 200 | May 8, 2025 | Registry ↗ |
| Jul 31, 2025 | Oscillation and Lung Expansion (OLE) Therapy for Treatment of Neuromuscular Disease (NMD) Patients NCT05366010 · Neuromuscular Diseases Oscillation and Lung Expansion (OLE) therapy | BAX Baxter Healthcare Corporation | Not applicable | Terminated | 41 | Feb 27, 2024 | Registry ↗ |
| Jun 29, 2025 | A Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Numeta G16%E NCT06842134 · Parenteral Nutrition Numeta G16%E, Sodium Glycerophosphate Injection | BAX Baxter Healthcare Corporation | Phase 1 | Completed | 16 | May 22, 2025 | Registry ↗ |
| Jun 29, 2025 | A Bioequivalence Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Inorganic… NCT06842121 · Parenteral Nutrition Sodium Glycerophosphate Injection, Sodium Phosphates Inject… | BAX Baxter Healthcare Corporation | Phase 1 | Completed | 42 | May 22, 2025 | Registry ↗ |
| Jun 5, 2025 | Doxil/Caelyx BE Study NCT05567601 · Ovarian Cancer, AIDS-related Kaposi Sarcoma DOXIL/CAELYX | BAX Baxter Healthcare Corporation | Phase 1 | Completed | 36 | Jun 21, 2024 | Registry ↗ |
| Apr 24, 2025 | Efficacy and Safety of Numeta G13%E Compared to Compounded Parenteral Nutrition in Preterm Neonates NCT06894446 · Malnutrition, Infant, Enteral Feeding Intolerance Numeta G13%E, Compounded Parenteral Nutrition (cPN) solution | BAX Baxter Healthcare Corporation | Phase 3 | Withdrawn | 0 | May 30, 2022 | Registry ↗ |
| Apr 22, 2025 | Evaluation of the Effectiveness of The Volara System Determined by Sputum Movement and Production NCT06937216 · Bronchiectasis Adult, COPD Volara therapy | BAX Baxter Healthcare Corporation | Not applicable | Not yet recruiting | 10 | Sep 2025 | Registry ↗ |
| Mar 21, 2025 | PMCF Study for ADEPT® in LaparoscopicGynecologic Surgery NCT05811585 · Adhesion ADEPT | BAX Baxter Healthcare Corporation | — | Completed | 153 | May 31, 2024 | Registry ↗ |
| Mar 21, 2025 | DermaClose DUKE Fasciotomy and Wound Study NCT05330767 · Wound of Skin DermaClose Continuous External Tissue Expander Device, Derm… | BAX Baxter Healthcare Corporation | — | Terminated | 7 | Nov 13, 2023 | Registry ↗ |
| Aug 16, 2024 | Tympanic Thermometer Study NCT06556628 · Body Temperature Changes, Fever Increased Body Temperatures | BAX Baxter Healthcare Corporation | — | Unknown | 1,000 | May 31, 2025 | Registry ↗ |
| Jul 22, 2024 | BAX602 in Preventing the Adhesion Around Great Cardiac Vessels in Pediatric Patients With Congenita… NCT05647161 · Congenital Heart Disease in Children BAX602, No Intervention | BAX Baxter Healthcare Corporation | Not applicable | Unknown | 34 | Oct 31, 2025 | Registry ↗ |
| Apr 16, 2024 | Starling Registry Study NCT04648293 · Hemodynamic Monitoring Starling | BAX Baxter Healthcare Corporation | — | Completed | 1,207 | Feb 21, 2024 | Registry ↗ |
| Dec 27, 2023 | Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clino… NCT04555044 · Essential Fatty Acid Deficiency (EFAD) Clinolipid, Intralipid | BAX Baxter Healthcare Corporation | Phase 4 | Completed | 101 | Oct 16, 2022 | Registry ↗ |
| Jul 14, 2023 | Starling/CRRT Observational Study NCT05729048 · Hemodynamic Monitoring Starling | BAX Baxter Healthcare Corporation | — | Withdrawn | 0 | Mar 14, 2025 | Registry ↗ |
| Nov 16, 2022 | Hemopatch Performance Evaluation: A Prospective Observational Registry NCT03392662 · Dura Mater Nick Cut or Tear, Hemostatis Hemopatch | BAX Baxter Healthcare Corporation | — | Completed | 621 | Jan 28, 2019 | Registry ↗ |
| Oct 12, 2022 | Cefazolin PK Study 3g vs 2g NCT05309304 · Healthy Cefazolin | BAX Baxter Healthcare Corporation | Phase 1 | Completed | 24 | Aug 30, 2022 | Registry ↗ |
| Jan 20, 2022 | Validation of a Sensor for Non-invasive Measurement of Stroke Volume and Cardiac Output NCT04255108 · Cardiac Failure Cova Patch | BAX Baxter Healthcare Corporation | — | Completed | 50 | Apr 9, 2020 | Registry ↗ |
| Jan 20, 2022 | Validation of a Sensor for Non-Invasive Measurements NCT03463148 · CHF, Renal Disease | BAX Baxter Healthcare Corporation | — | Completed | 136 | Apr 19, 2021 | Registry ↗ |
| Jul 21, 2021 | Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clino… NCT02476994 · Essential Fatty Acid Deficiency (EFAD) Clinolipid, Intralipid | BAX Baxter Healthcare Corporation | Phase 4 | Terminated | 1 | Oct 2016 | Registry ↗ |
| Apr 1, 2021 | Healthy Volunteer Study to Evaluate the Impact of Various Common Interventions on Venous Pressure S… NCT04324593 · Healthy Volunteers Peripheral intravenous analysis (PIVA) algorithm | BAX Baxter Healthcare Corporation | Not applicable | Terminated | 26 | Mar 21, 2020 | Registry ↗ |
| Aug 3, 2020 | Effectiveness and Safety of CELSTAT for Hemostasis in Intraoperative Tissue Bleeding NCT02640235 · Bleeding Active CELSTAT, Surgicel Original | BAX Baxter Healthcare Corporation | Not applicable | Completed | 260 | Jul 21, 2017 | Registry ↗ |
| Jul 31, 2020 | Bioequivalence Study Assessing Iron Sucrose or Venofer® in Healthy Adult Subjects NCT04155814 · Bioequivalance Iron Sucrose Injection, Venofer Injection | BAX Baxter Healthcare Corporation | Phase 1 | Completed | 196 | Dec 18, 2019 | Registry ↗ |
| Apr 6, 2020 | Hemopatch Compared to TachoSil in Postoperative Air Leak Duration After Pulmonary Resection NCT03450265 · Air Leak From Lung Hemopatch, Tachosil | BAX Baxter Healthcare Corporation | Not applicable | Completed | 279 | Jul 9, 2019 | Registry ↗ |
| Jan 29, 2020 | Observational Study Using the CoVa Monitoring System 3 NCT03884582 · Healthy Cova Monitoring System 3 | BAX Baxter Healthcare Corporation | — | Completed | 14 | May 1, 2019 | Registry ↗ |
| Dec 18, 2019 | The Mechanism of Action of the Unite Biomatrix in Diabetic Foot Ulcer NCT00958711 · Diabetic Foot Ulcers Unite Biomatrix, Saline and Gauze | BAX Baxter Healthcare Corporation | Not applicable | Terminated | 90 | May 2012 | Registry ↗ |
| Dec 6, 2019 | Efficacy and Safety of TISSEEL Lyo Compared to Manual Compression as an Adjunct to Haemostasis NCT04083807 · Adjunct to Hemostasis During Vascular Surgery TISSEEL Lyo, Manual compression with surgical gauze pads | BAX Baxter Healthcare Corporation | Phase 3 | Completed | 104 | Oct 22, 2019 | Registry ↗ |
| Sep 10, 2019 | Remotely Monitoring Patients With Chronic Conditions in Their Home NCT03207802 · CHF Discontinuation of using device | BAX Baxter Healthcare Corporation | — | Completed | 36 | Dec 17, 2017 | Registry ↗ |
| Sep 10, 2019 | Efficacy and Safety of FS VH S/D 500 S-apr (Tisseel) as an Adjunct to Sutured Dural Repair in Crani… NCT02891070 · Cerebrospinal Fluid Leak FS VH S/D 500 s-apr, DuraSeal Dural Sealant | BAX Baxter Healthcare Corporation | Phase 3 | Completed | 224 | Aug 22, 2018 | Registry ↗ |
| May 28, 2019 | Peritoneal Membrane Dysfunction in Peritoneal Dialysis Using Metabolomics NCT03964701 · End Stage Renal Disease, Dialysis no intervention | BAX Baxter (Hellas) Ltd | — | Unknown | 18 | Apr 22, 2020 | Registry ↗ |
| Mar 8, 2019 | Japan Phase 2/3 Clinical Study With BLM-240 (Desflurane) NCT00762372 · Anesthesia desflurane, desflurane/nitrous oxide | BAX Baxter Healthcare Corporation | Phase 2/3 | Completed | 216 | Aug 2008 | Registry ↗ |
| Jul 6, 2018 | Efficacy and Safety of ARTISS for Flap Adherence in Abdominoplasty NCT01112735 · Seroma, Hematoma FS VH S/D 4 s-apr (= two-component fibrin sealant, double v… | BAX Baxter Healthcare Corporation | Phase 2 | Completed | 40 | Dec 2010 | Registry ↗ |
| Apr 26, 2018 | Intravenous (IV) Solutions for Dehydration in Children With Gastroenteritis NCT01234883 · Dehydration, Gastroenteritis multiple electrolyte solution, saline | BAX Baxter Healthcare Corporation | Phase 4 | Terminated | 100 | Feb 2013 | Registry ↗ |
| Jan 23, 2018 | Veritas in Non-Bridging Ventral Hernia Repair NCT01426477 · Hernia | BAX Baxter Healthcare Corporation | — | Terminated | 20 | Aug 2017 | Registry ↗ |
| Aug 4, 2017 | Efficacy and Safety Study of Anti-Adhesion Product in the Prevention of Intraperitoneal Adhesions NCT00512356 · Intraperitoneal Adhesions Anti-Adhesion Product | BAX Baxter Healthcare Corporation | Phase 2 | Completed | 46 | Feb 25, 2003 | Registry ↗ |
| Jul 2, 2017 | Necklace-Shaped Sensor for Non-Invasive Monitoring of Stroke Volume and Cardiac Output NCT02719301 · Heart Failure | BAX Baxter Healthcare Corporation | — | Completed | 85 | Jan 2017 | Registry ↗ |
| Jun 21, 2017 | Effects of IV Chloride Content on Outcomes NCT02083198 · SIRS, Balanced Fluids | BAX Baxter Healthcare Corporation | — | Completed | 1,558 | Apr 1, 2014 | Registry ↗ |
| May 19, 2017 | Reinforcement of Surgical Staple Lines Using Peri-Strips Dry (PSD) With Veritas Collagen Matrix NCT00566943 · Obesity PSD Veritas Collagen Matrix, Roux-en-Y gastric by-pass surg… | BAX Baxter Healthcare Corporation | Not applicable | Completed | 101 | Dec 2008 | Registry ↗ |
| May 10, 2017 | Peri-Strips Dry (PSD) Veritas Collagen Matrix Staple Line Reinforcement for Colorectal Surgery NCT00559013 · Colorectal Cancer Staple line reinforcement | BAX Baxter Healthcare Corporation | Not applicable | Completed | 38 | Dec 2008 | Registry ↗ |
| May 8, 2017 | Efficacy and Time and Resources for Hylenex-facilitated SC Rehydration Versus ORT for Dehydrated Ch… NCT01120431 · Dehydration Oral rehydration fluid, Isotonic hydration fluid and recomb… | BAX Baxter Healthcare Corporation | Phase 4 | Withdrawn | 0 | May 2010 | Registry ↗ |
| Apr 20, 2017 | Safety and Efficacy Study of FS 4 IU VH S/D (Fibrin Sealant With 4IU/mL Thrombin, Vapor Heated, Sol… NCT00157131 · Deep Partial or Full Thickness Wounds Fibrin Sealant, ARTISS 4IU/ml VH SD, Staples | BAX Baxter Healthcare Corporation | Phase 3 | Completed | 150 | Feb 2007 | Registry ↗ |
| Apr 5, 2017 | Retrospective Analysis of Veritas in Breast Reconstruction NCT01454713 · Seroma, Necrosis | BAX Baxter Healthcare Corporation | — | Completed | 54 | Oct 2011 | Registry ↗ |
| Apr 5, 2017 | Performance of Inductigraft in Spinal Fusion NCT01452022 · Degenerative Disk Disease, Spinal Stenosis of Lumbar Region Inductigraft | BAX Baxter Healthcare Corporation | Not applicable | Completed | 125 | Aug 2015 | Registry ↗ |
| Apr 5, 2017 | Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion NCT01018771 · Degenerative Disc Disease Actifuse ABX, INFUSE, plus Mastergraft granules | BAX Baxter Healthcare Corporation | Not applicable | Completed | 100 | Dec 2012 | Registry ↗ |
| Apr 5, 2017 | Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion NCT01013389 · Degenerative Disc Disease Actifuse ABX, INFUSE, plus master granules (MGG) | BAX Baxter Healthcare Corporation | Not applicable | Completed | 20 | Dec 2012 | Registry ↗ |
| Apr 5, 2017 | Bone Graft Materials Observational Registry NCT00974623 · Degenerative Disc Disease, Herniated Disc Bone graft substitute, autograft or allograft | BAX Baxter Healthcare Corporation | — | Terminated | 329 | Jan 2013 | Registry ↗ |
| Apr 5, 2017 | Acute Achilles Repair With or Without OrthADAPT Augmentation NCT00962143 · Achilles Tendon Tear Achilles repair with OrthADAPT augmentation, Achilles repai… | BAX Baxter Healthcare Corporation | Not applicable | Withdrawn | 0 | Dec 2010 | Registry ↗ |
| Apr 5, 2017 | Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation NCT00957255 · Rotator Cuff Tear OrthoADAPT, Standard of care | BAX Baxter Healthcare Corporation | Not applicable | Withdrawn | 0 | Apr 2010 | Registry ↗ |
The newest 50 items, most recent first. Each row links to the study's page on ClinicalTrials.gov. Updated Nov 15, 2026, 6:42 PM EST.
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