| Completed | Open-Label, Safety Study Evaluating the Use of Dexmedetomidine in Pediatric Subjects Undergoing Procedure-Type Ultrasound, CT Scans, MRIs | Phase 4 | 2012-10-01 |
| Completed | Biosimilar Retacrit® in the Treatment of Chemotherapy-induced Anaemia in Oncology and Haematology Chemotherapy-induced Anemia | — | 2012-06-01 |
| Completed | Open-Label, Safety, and Efficacy Study of Dexmedetomidine in Preterm Subjects Ages ≥28 Weeks to <36 Weeks Gest Anesthesia | Phase 2 / Phase 3 | 2012-03-01 |
| Completed | Nivestim® (Filgrastim) Tolerance in Patients Treated by Toxic Chemotherapeutic Agents Solid Tumors, Malignant Hemopathy, Chemotherapy-induced Febrile Neutropenia (FN) | — | 2011-10-01 |
| Completed | Clinical Study to Investigate the Efficacy and the Safety of DA-9501 in Sedation During the Surgery or Medical Sedation | Phase 3 | 2011-07-01 |
| Completed | Phase II Pharmacokinetic and Pharmacodynamic Study of DEX in Subjects Aged 12 Months Through <24 Months Sedation, Pain | Phase 2 | 2011-06-01 |
| Completed | Nivestim™ in Treatment of Malignant Diseases Solid Tumour, Malignant Haematological Tumour, Primary or Secondary Prophylactic Treatment | — | 2011-06-01 |
| Completed | Biosimilar Retacrit™ (Epoetin Zeta) in the Treatment of Chemotherapy-Induced Symptomatic Anaemia in Haematolog Chemotherapy-induced Symptomatic Anaemia, Solid Tumours, Malignant Lymphomas | — | 2010-12-01 |
| Completed | Study to Evaluate Hemodynamic Effect of Different Loading Doses of Precedex in Post-surgical Intensive Care Un Intensive Care Unit | — | 2010-09-01 |
| Completed | Safety, Efficacy and Pharmacokinetic Study of Dexmedetomidine in Pediatrics Ages ≥28 Weeks to ≤44 Weeks Gestat Sedation | Phase 2 / Phase 3 | 2010-07-01 |
| Completed | A Study Comparing the Effects of Epoetin Hospira and Epogen/Epoetin Alfa (Amgen) When Administered IV in Patie Chronic Renal Failure | Phase 1 | 2010-07-01 |
| Completed | Study Evaluating Safety and Efficacy of Dexmedetomidine (DEX) in Intubated and Mechanically Ventilated Pediatr Sedation | Phase 3 | 2010-01-01 |
| Completed | Epoetin Alfa Biosimilar in the Management of Chemotherapy-Induced Symptomatic Anemia in Haematology and Oncolo Chemotherapy-induced Symptomatic Anemia, Solid Tumors, Malignant Hemopathies | — | 2009-09-01 |
| Completed | Pharmacokinetic/Pharmacodynamic (PK/PD) Study Evaluating Pegfilgrastim Hospira Compared to Neulasta (Amgen) in Healthy | Phase 1 | 2009-06-01 |
| Completed | A Randomized, Single-Dose, Comparative, Positive and Placebo Controlled, Four-Way, Four Period, Cross-Over Stu Ventricular Repolarization | Phase 1 | 2009-05-01 |
| Completed | Pharmacokinetics and Pharmacodynamics of Dexmedetomidine in Pediatrics Subjects Intubated and Mechanically Ventilated Pediatric Subjects | Phase 2 | 2008-11-01 |
| Completed | Bioequivalency Study Comparing Hospira's Generic Iron Sucrose Injection to Venofer Healthy Volunteers | Phase 1 | 2008-06-01 |
| Completed | Safety and Efficacy of Repeated Doses of PMI-150 (Intranasal Ketamine) in Acute Post-operative Pain Following Pain, Postoperative | Phase 3 | 2008-06-01 |
| Completed | Long-term Clinical Study Evaluating the Safety and Efficacy of Dexmedetomidine in ICU Subjects Sedation | Phase 3 | 2007-10-01 |
| Completed | Pharmacokinetics (PK) and Pharmacodynamics (PD) of Mayne Glucagon for Injection Compared With Glucagen® (Novo Hypoglycemia | Phase 1 | 2007-08-01 |
| Completed | The Pharmacokinetics and Safety Characteristics of Docetaxel in Patients With Cancer Cancer | Phase 1 | 2007-08-01 |
| Terminated | Safety and Efficacy of PMI-150 (Intranasal Ketamine) for the Treatment of Breakthrough Pain in Cancer Patients Pain, Cancer | Phase 3 | 2007-06-01 |
| Terminated | A Research Study to Evaluate the Effectiveness of Dexmedetomidine in Preventing Delirium After Hip Fracture Re Delirium | Phase 3 | 2007-04-01 |
| Withdrawn | A Research Study to Evaluate the Effectiveness of Dexmedetomidine in Preventing Delirium After Heart Surgery Delirium | Phase 3 | 2007-04-01 |
| Completed | A Safety and Efficacy Study of Dexmedetomidine in Patients Requiring Sedation During Monitored Anesthesia Care Anesthesia, Surgical Procedures, Elective | Phase 3 | 2006-12-01 |
| Completed | A Safety and Efficacy Study of Dexmedetomidine in Patients Requiring Sedation for Elective Awake Fiberoptic In Awake Fiberoptic Intubation | Phase 3 | 2006-08-01 |
| Completed | Post-Marketing Clinical Study to Assess Efficacy and Safety of Dexmedetomidine in Post-Operative Patients Conscious Sedation | Phase 4 | 2005-11-01 |
| Completed | A Safety and Efficacy Study of Dexmedetomidine in ICU Patients Requiring Continuous Sedation Mechanically Ventilated and Intubated Subjects | Phase 4 | 2005-03-01 |