Clinical Trials Directory

Trials / Sponsors / Alza Corporation, DE, USA

Alza Corporation, DE, USA

Industry · 37 registered clinical trials.

StatusTrialPhaseStarted
WithdrawnAn Evaluation of Safety of the Fentanyl Transdermal System for Management of Acute Post-Operative Pain in Pedi
Pain, Postoperative, Pediatrics
Phase 32008-10-01
CompletedBioequivalence Between Integrated E-TRANS (Fentanyl) System and Separated (Two-Part) E-TRANS (Fentanyl) System
Pain, Postoperative
Phase 12008-03-01
TerminatedA Prospective Safety Surveillance Study of Fentanyl Iontophoretic Transdermal System (40 Mcg)
Pain
2007-12-01
CompletedA Safety and Effectiveness Study of a Single Dose of JNJ-17216498 in Patients With Narcolepsy
Narcolepsy
Phase 22007-01-01
CompletedStudy to Investigate the Safety, Tolerability, Absorption, Distribution, Metabolism, and Elimination of RWJ-44
Chronic Small Plaque Psoriasis
Phase 22006-09-01
CompletedA Comparison of the Safety and Effectiveness of Two Forms of Patient-controlled Pain Medication Used After Sch
Pain, Postoperative
Phase 32004-04-01
CompletedA Comparison of the Safety and Effectiveness of Two Forms of Patient-controlled Pain Medication Used After Tot
Pain, Postoperative, Analgesia
Phase 32004-03-01
CompletedA Study to Evaluate the Effectiveness and Safety of Slow Release Hydromorphone HCL for Treatment of Patients W
Osteoarthritis, Hip, Osteoarthritis, Knee
Phase 32003-11-01
CompletedA Study of the Effectiveness and Safety of Dapoxetine in the Treatment of Men With Premature Ejaculation.
Ejaculation
Phase 32003-06-01
CompletedPharmacokinetics of Naltrexone Following Intravenous and Oral Routes of Administration in Healthy Volunteers
Biological Availability
Phase 12003-05-01
CompletedPharmacokinetics of Fentanyl Following Intravenous and Oral Routes of Administration in Healthy Volunteers
Biological Availability
Phase 12003-04-01
CompletedA Study to Evaluate the Safety of D-TRANS Fentanyl With Naltrexone in Adult Patients With Chronic Pain and Who
Chronic Pain
Phase 22003-01-01
CompletedAn Effectiveness and Safety Study Evaluating OROS Methylphenidate Hydrochloride (HCl), Ritalin (Methylphenidat
Attention Deficit Hyperactivity Disorder
Phase 31998-11-01
CompletedA Comparative Effectiveness Study Evaluating OROS Methylphenidate HCl, Ritalin (Methylphenidate HCl), and Plac
Attention Deficit Hyperactivity Disorder
Phase 31998-03-01
CompletedA Study to Evaluate the Safety and Efficacy of OROS® Oxybutynin Chloride for the Treatment of Urge Urinary Inc
Urinary Incontinence
Phase 31997-03-01
CompletedA Study Comparing the Efficacy and Safety of OROS® Oxybutynin to That of Ditropan® (Immediate-release Oxybutyn
Urge Incontinence
Phase 31996-07-01
CompletedEfficacy and Safety of OROS Oybutynin and TTS Oxybutynin in Middle-Aged and Elderly Women With Urinary Inconti
Urinary Incontinence
Phase 31995-12-01
CompletedClinical Use and Safety of the Fentanyl Transdermal Therapeutic System (TTS) in the Management of Pain in Pati
Pain, Cancer
Phase 31987-10-01
CompletedEfficacy of the Fentanyl Transdermal Therapeutic System (TTS) in the Management of Pain in Patients With Cance
Pain, Cancer
Phase 31986-05-01
CompletedStudy of the Effectiveness and Tolerability of OROS Hydromorphone HCI SR(Slow-release) Tablets and Immediate-R
Pain
Phase 3
CompletedAn Effectiveness, Safety and Quality of Life Measures With Hydromorphone HCL, Dilaudid CR (Controlled Release)
Osteoarthritis, Knee, Osteoarthritis, Hip
Phase 3
CompletedSafety, Effectiveness, and Impact on Quality of Life on Long-Term Administration of OROS Hydromorphone Slow-Re
Low Back Pain
Phase 3
CompletedA Study on Efficacy (Effectiveness), Safety, and Impact on Quality of Life Measures of Dilaudid CR (Controlled
Low Back Pain
Phase 2
CompletedA Study of OROS Hydromorphone HCL vs Morphine in Cancer Pain Patients.
Pain, Analgesics, Opioid
Phase 3
CompletedA Multicenter Study Comparing the Efficacy and Safety of OROS Methylphenidate HCl, Ritalin (Methylphenidate HC
Attention Deficit Hyperactivity Disorder
Phase 3
CompletedA Repeated Dose Study of the Metabolism and Action Evaluation of OROS Hydromorphone HCI (Slow Release) Tablets
Pain, Analgesics, Opioid
Phase 1
CompletedAn Open-Label Evaluation of the Dose Proportionality of OROS� Hydromorphone HCL Tablets 8mg, 16mg, 32mg, 64mg
Analgesia
Phase 1
CompletedAn Open-Label Evaluation of the Independent Effects of Coadministration of a High-Fat Meal and Naltrexone Bloc
Analgesia
Phase 1
CompletedSafety and Tolerability of Long-Term Administration of Hydromorphone HCI CR (Controlled Release)
Pain, Analgesics, Opioid
Phase 3
CompletedEfficacy and Tolerability of DITROPAN XL (Oxybutynin Chloride) Versus DETROL LA (Tolterodine Tartrate) in Trea
Urinary Incontinence
Phase 3
CompletedA Repeated-Dose Evaluation of Use of a Pain Relieving Drug and Safety of OROS Hydromorphone HCI in Patients Wi
Analgesics, Opioid, Pain
Phase 3
CompletedA Randomized, Open-Label, Single-Dose, Small Study to Evaluate the Safety and Effectiveness of Hydromorphone i
Pain, Postoperative, Orthopedic Procedures, Analgesia
Phase 2
CompletedA Study of the Effectiveness and Safety of Dapoxetine in the Treatment of Men With Premature Ejaculation
Ejaculation
Phase 3
CompletedA Repeated-Dose Evaluation of a Pain Relieving Drug Use and Safety of OROS Hydromorphone HCI in Patients With
Pain, Analgesics, Opioid
Phase 3
CompletedLong-term Safety and Effectiveness of OROS Methylphenidate HCl in Children With Attention Deficit Hyperactivit
Attention Deficit Hyperactivity Disorder
Phase 3
CompletedSafety and Tolerability of Long-term Administration of OROS Hydromorphone HCI (Slow Release) in Cancer Pain
Analgesics, Opioid, Pain
Phase 3
CompletedAn Open-Label Study of the Long-Term Safety of Dapoxetine HCl in the Treatment of Rapid Ejaculation
Ejaculation, Erectile Dysfunction, Sexual Dysfunction
Phase 3