| NCT05571059 | Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF) | RECRUITING | PHASE2 | 2024-01-31 | 2026-01 | 2026-01 |
| NCT03340675 | Oral Ifetroban in Subjects With Duchenne Muscular Dystrophy | ACTIVE_NOT_RECRUITING | PHASE2 | 2020-10-19 | 2025-12 | 2025-09 |
| NCT03611010 | Dose-ranging Efficacy and Pharmacokinetics Study of Intravenous Atorvastatin in Hypercholesterolemic Patients | COMPLETED | PHASE2 | 2018-08-07 | 2020-02-24 | 2020-02-17 |
| NCT02583399 | Safety and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients | COMPLETED | PHASE4 | 2017-08-08 | 2019-07-02 | 2019-07-02 |
| NCT03028350 | Oral Ifetroban to Treat Aspirin Exacerbated Respiratory Disease (AERD) | COMPLETED | PHASE2 | 2017-07-17 | 2023-04-25 | 2023-04-25 |
| NCT02802228 | Study to Assess Safety and Efficacy of Ifetroban for Treatment of Portal Hypertension in Cirrhotic Patients | COMPLETED | PHASE2 | 2017-03-06 | 2018-07-17 | 2018-07-17 |
| NCT02682511 | Oral Ifetroban to Treat Diffuse Cutaneous Systemic Sclerosis (SSc) or SSc-associated Pulmonary Arterial Hypertension | ACTIVE_NOT_RECRUITING | PHASE2 | 2017-01 | 2026-05 | 2026-02 |
| NCT02013141 | Telavancin Pediatric PK Study (Ages >12 Months to 17 Years) | TERMINATED | PHASE1 | 2014-12 | 2021-03 | 2021-03 |
| NCT02208063 | A Phase 3 Telavancin Staphylococcus Aureus (S. Aureus) Bacteremia Trial | TERMINATED | PHASE3 | 2014-12 | 2018-04-12 | 2018-04-12 |
| NCT02216357 | Trial to Determine the Safety of Oral Ifetroban in Patients With a History of Aspirin Exacerbated Respiratory Disease | COMPLETED | PHASE2 | 2014-08 | 2016-01 | 2016-01 |
| NCT02123017 | Efficacy and Safety of Bisacodyl and Lactulose as a Preparation for Colonoscopy | COMPLETED | PHASE2 | 2014-04 | 2014-08 | 2014-08 |
| NCT01901393 | Efficacy of Intravenous Ibuprofen Compared to Intravenous Ketorolac for Pain Control Following Arthroscopic Knee Surgery | COMPLETED | PHASE4 | 2013-07 | 2014-08 | 2014-08 |
| NCT01887470 | 2 Regimens of Lactulose for Colonoscopy Preparation in Adults | COMPLETED | PHASE2 | 2013-07 | 2013-10 | 2013-10 |
| NCT01650519 | A Pilot Study to Determine the Efficacy of Intravenous Ibuprofen for Pain Control Following Arthroscopic Knee Surgery | COMPLETED | PHASE4 | 2012-09 | 2013-01 | 2012-12 |
| NCT01451411 | A Study to Assess the Efficacy, Safety and Pharmacokinetics of Intravenous Conivaptan (Vaprisol®) in Pediatric Subjects With Euvolemic or Hypervolemic Hyponatremia | TERMINATED | PHASE3 | 2012-02 | 2014-01 | 2014-01 |
| NCT01436500 | Safety and Pharmacokinetics of Ifetroban in Hepatorenal Syndrome Patients | COMPLETED | PHASE2 | 2011-10 | 2015-07 | 2015-06 |
| NCT01332253 | Safety and Efficacy of Intravenous Ibuprofen for Treatment of Pain in Pediatric Patients Undergoing Tonsillectomy | COMPLETED | PHASE3 | 2011-07 | 2012-08 | 2012-07 |
| NCT01334957 | Surgical Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen | COMPLETED | PHASE4 | 2011-06 | 2013-01 | 2012-12 |
| NCT01334944 | Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen | COMPLETED | PHASE4 | 2011-06 | 2012-10 | 2012-09 |
| NCT01370148 | A Study to Assess the Effect of Severe Hepatic Impairment on the Pharmacokinetics of Intravenous Conivaptan | COMPLETED | PHASE1 | 2011-04 | 2014-02 | 2014-02 |
| NCT01238796 | A Study to Evaluate the Effect of Renal Function on the Biological Activity of Telavancin | COMPLETED | PHASE1 | 2010-12 | 2011-02 | 2011-02 |
| NCT01118663 | Safety and Efficacy Study of a New Formulation of Acetylcysteine Injection | TERMINATED | PHASE3 | 2010-09 | 2013-05 | 2012-11 |
| NCT01002573 | Safety, Efficacy, and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients | COMPLETED | PHASE3 | 2010-07 | 2013-06 | 2013-06 |
| NCT00712543 | A Preference Study Comparing Kristalose® and Liquid Lactulose | COMPLETED | PHASE4 | 2009-06 | 2009-09 | 2009-09 |
| NCT00843986 | Safety and Efficacy of Conivaptan in Hyponatremic Patients With Symptomatic Acute Decompensated Heart Failure (ADHF) | TERMINATED | PHASE3 | 2009-04 | 2009-08 | 2009-08 |
| NCT00887627 | Study to Compare Conivaptan Pharmacokinetics in Subjects With Mild & Moderate Kidney Function Impairment to Subjects With Normal Kidney Function | COMPLETED | PHASE1 | 2009-04 | 2010-07 | 2010-07 |
| NCT00867880 | Pharmacokinetic Study Of Ibuprofen Injection (IVIb) In Healthy Adult Subjects | COMPLETED | PHASE1 | 2009-03 | 2009-06 | 2009-05 |
| NCT00851227 | Study to Compare Conivaptan in Subjects With Mild & Moderate Liver Impairment Versus Subjects With Normal Liver Function | COMPLETED | PHASE1 | 2009-02 | 2010-01 | 2010-01 |
| NCT00592475 | A Study to Assess the Safety and Effects of Intravenous (IV) Conivaptan on the Hepatic Hemodynamic Response in Cirrhotic Patients | COMPLETED | PHASE2 | 2007-12 | 2008-11 | 2008-11 |
| NCT00606489 | Efficacy and Safety Study of Caldolor (Intravenous Ibuprofen) in Hospitalized Adult and Pediatric Burn Patients | COMPLETED | PHASE3 | 2007-11 | 2009-05 | 2009-05 |
| NCT00470600 | Efficacy and Safety Study of Caldolor (IV Ibuprofen) in Hospitalized Adult Orthopedic Patients | COMPLETED | PHASE3 | 2007-05 | 2008-09 | 2008-09 |
| NCT00478192 | Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia | COMPLETED | PHASE3 | 2007-04 | 2008-08 | 2008-08 |
| NCT00435591 | A Study of Multiple Dosing Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia | COMPLETED | PHASE4 | 2007-01 | 2008-09 | 2008-09 |
| NCT00225706 | A Study of Caldolor in Hospitalized Febrile Pediatric Patients | COMPLETED | PHASE3 | 2005-10 | 2007-08 | 2007-08 |
| NCT00107978 | Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus | COMPLETED | PHASE3 | 2005-02 | 2006-05 | 2006-05 |
| NCT00107952 | Comparison of Telavancin and Vancomycin for Hospital-acquired Pneumonia Due to Methicillin-resistant Staphylococcus Aureus | COMPLETED | PHASE3 | 2005-02 | 2007-07 | 2007-07 |
| NCT00091819 | Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus | COMPLETED | PHASE3 | 2005-01 | 2006-06 | 2006-06 |
| NCT00124020 | Comparison of Telavancin and Vancomycin for Hospital-acquired Pneumonia Due to Methicillin-resistant Staphylococcus Aureus | COMPLETED | PHASE3 | 2005-01 | 2007-05 | 2007-05 |
| NCT00225732 | Trial of Caldolor for Treatment of Pain in Post-Operative Adult Patients | COMPLETED | PHASE3 | 2005-01 | 2008-01 | 2008-01 |
| NCT00077675 | Phase 2 Trial of TD-6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI) | COMPLETED | PHASE2 | 2004-02 | 2004-09 | 2004-09 |
| NCT00379847 | An Open-Label Study of YM087 (Conivaptan) in Patients With Euvolemic or Hypervolemic Hyponatremia | COMPLETED | PHASE3 | 2004-02 | 2005-06 | 2005-06 |
| NCT00062647 | Telavancin for Treatment of Uncomplicated Staphylococcus Aureus Bacteremia | COMPLETED | PHASE2 | 2003-08 | 2006-08 | 2006-08 |
| NCT00061633 | Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI) | COMPLETED | PHASE2 | 2003-06 | 2004-01 | 2004-01 |
| NCT00057356 | Safety and Efficacy Study of YM087 (Conivaptan) in Patients With Acute Decompensated Heart Failure | COMPLETED | PHASE2 | 2002-11 | 2004-03 | 2004-03 |
| NCT01131000 | Efficacy, Safety, and Pharmacokinetics of Intravenous Ibuprofen in Adult Febrile Patients | COMPLETED | PHASE3 | 2002-06 | 2005-08 | 2005-08 |
| NCT00380575 | Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia | COMPLETED | PHASE3 | 2000-08 | 2003-02 | |
| NCT00492037 | Study of Efficacy & Safety of Oral YM087 in Subjects With Euvolemic or Hypervolemic Hyponatremia | COMPLETED | PHASE3 | 2000-01 | 2002-02 | |