Search clinical trials for: Extended Release

Total 5397 results

Johnson & Johnson Pharmaceutical Research & Development...
Grünenthal GmbH

Completed

A Study to Compare the Frequency of Constipation Symptoms With Tapentadol Immediate Release (IR) Treatment Versus Oxycodone IR Treatment in Patients With End-stage Joint Disease

Arthritis | Joint Diseases | Osteoarthritis
Takeda

Completed

Efficacy and Safety of Azilsartan Medoxomil Combined With Chlorthalidone in Participants With Moderate to Severe Hypertension

Hypertension

United States, Chile, Russian Federation, Mexico, Peru
Merz Pharmaceuticals GmbH

Terminated

Blepharospasm Short Interval

Blepharospasm

Germany
Washington University School of Medicine
Eunice Kennedy Shriver National Institute of Child Health and Human Development...

Completed

Botulinum Toxin Effects on Plantar Ulcer Recurrence

Diabetes Mellitus | Peripheral Neuropathy | Plantar Ulcers

United States
Biolex Therapeutics, Inc.

Completed

Study of Safety, Tolerability, and Anti-Viral Effect of Locteron Compared to PEG-Intron in Patients With Chronic Hepatitis C (PLUS)

Hepatitis C

United States
Bulent Haydardedeoglu

Terminated

In Vitro Fertilization Outcomes of Two Treatment Protocols in Women With Polycystic Ovary Syndrome (PCOS and ivf)

PCOS GnRH Antagonist and GnRH Agonist IVF/ICSI Cycles

Turkey
Alcon Research
Optometric Technology Group Ltd

Completed

Evaluation of Extended Tear Film Break Up Time (TFBUT) With an Ocular Emulsion

Dry Eye

United States, United Kingdom
Yonsei University

Completed

Diagnostic Usefulness of Interferon Gamma Release Assay for Active Tuberculosis in Immunocompromised Patients

Tuberculosis

Korea, Republic of
Biolex Therapeutics, Inc.

Completed

Phase 2B Dose Ranging Study of Locteron Plus Ribavirin to Treat HCV (SELECT-2)

Hepatitis C, Chronic

United States, Bulgaria, Puerto Rico, Romania
Pfizer

Completed

Phase 1 Study To Test the Bioequivalence Between Two 25 mg Tablets vs. One 50 mg Tablet Under Fast/Fed Condition and Evaluate Food Effect of Desvenlafaxine Succinate Sustained Release (DVS SR)

Depression - Major Depressive Disorder

Belgium
Bayer

Completed

Controlled Release Nifedipine and Valsartan Combination Therapy in Patients With Essential Hypertension

Hypertension

Japan
Pfizer

Completed

A Study Of PF-04620110 As A Modified-Release Formulation In Healthy Overweight Or Obese Subjects

Healthy

Belgium
Warner Chilcott

Completed

Assess the Safety, Efficacy, and Pharmacokinetics of Immediate and Delayed Release Weekly Risedronate

Postmenopausal Women

United States
Pfizer

Completed

A Phase 1 Study To Evaluate The Pharmacokinetics And Safety Of Three Modified Release And One Immediate Release Formulations Of Tofacitinib (CP-690,550) In Healthy Volunteers

Healthy

Singapore
Samsung Medical Center

Completed

Diagnosis of Tuberculosis Infection in Health Care Workers Using Ex-vivo Interferon-gamma Assay

Latent Tuberculosis Infection

Korea, Republic of
University of Parma

Terminated

Controlled-Release Oxycodone For Postoperative Analgesia After Video-Assisted Thoracic Surgery

Pain, Postoperative | Anesthesia Recovery Period

Italy
Pfizer

Completed

Pharmacokinetics and Safety of Desvenlafaxine in Korean Healthy Subjects Following Single and Multiple Oral Doses of Desvenlafaxine Succinate Sustained Release Tablet

Major Depressive Disorder

Korea, Republic of
Uppsala University
Landstinget i Värmland

Completed

Antibiotic Therapy of Acute Uncomplicated Colonic Diverticulitis

Colonic Diverticulitis

Sweden
Cliniques universitaires Saint-Luc- Université...
Fonds National de la Recherche Scientifique

Completed

Efficacy Study of Selective Tibial Neurotomy in the Treatment of the Spastic Equinovarus Foot Among Adult Hemiplegic Patients (Neurotomy)

Stroke | Spastic Equinovarus Foot

Belgium
Children's Hospital of Philadelphia
Ortho-McNeil Janssen Scientific Affairs, LLC

Completed

Study of the Effects of Osmotic-Release Oral System (OROS) Methylphenidate (Concerta) on Attention and Memory (CHOP)

Attention Deficit Hyperactivity Disorder

United States
Allergan

Terminated

Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Moderate to Severe Cervical Dystonia

Spasmodic Torticollis

Argentina, India, Australia
Allergan

Completed

Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Type A in Moderate to Severe Cervical Dystonia

Spasmodic Torticollis

Poland, Turkey, Italy, Croatia, Australia
Federal University of Bahia

Unknown

Botulinum Toxin Type A and Kinesitherapy of Post-stroke Patients

Stroke

Brazil
Università degli Studi dell'Insubria

Completed

Double Balloon Catheter Versus Dinoprostone Vaginal Insert for Cervical Ripening.

Cervical Ripening | Labor Induction

Italy
Valley Retina Institute
Pfizer

Unknown

Macugen for Proliferative Diabetic Retinopathy Study With Extended Dosing (M-PDRS ED)

Proliferative Diabetic Retinopathy

United States
University of British Columbia
Pfizer

Completed

Smoke-Free Living Study

Additional, Effective Methods to Stop Smoking

Canada
Ivo Pitanguy Institute
Allergan

Completed

Radial Diffusion of the Botulinum Toxin Type A (Botox®): Electromyographic Evaluation of the Frontal Muscle

Wrinkles

Brazil
University of British Columbia

Completed

The Big Squeeze (Lessening the Big Squeeze: The Effect of the Trunk Release on Interface Pressures of Individuals Seated in a High Fowler's Positions)

Elderly

Canada
Centre Hospitalier Universitaire Vaudois
University of Zurich

Unknown

Right Hepatectomy in Patients Beyond 70 Years Old

Liver Failure, Acute | Complications

Switzerland
Centro de Reabilitação e Readaptação Dr. Henrique...

Completed

A Comparison Study of Oxybutynin and Botulinum Toxin for Neurogenic Detrusor Overactivity

Spinal Cord Injury

Brazil
The Foundation Institute San Raffaele G. Giglio...
Azienda Ospedaliero, Universitaria Pisana; Università degli Studi di Ferrara; IRCCS San Camillo, Venezia, Italy and other collaborators

Unknown

Botulinum Toxin Type A (BT-A) in Hemiplegic Shoulder Pain Versus Steroid

Stroke | Shoulder Pain | Hemiparesis

Italy
Novartis

Completed

Safety/Efficacy of Letrozole Monotherapy or in Combination With Zoledronic Acid as Extended Adjuvant Treatment of Postmenopausal Patients With Primary Breast Cancer

Osteoporosis | Postmenopausal

Germany
Meda Pharmaceuticals

Completed

A Study to Evaluate Two Formulations of Carisoprodol in Subjects With Musculoskeletal Spasm of the Lower Back

Lower Back Pain

United States
Synerx Pharma, LLC

Completed

Comparative Bioavailability Study of Synerx and Verelan PM 300 mg Verapamil HCl ER Capsules Under Fed Conditions

Healthy
Gynuity Health Projects
University of Puerto Rico

Terminated

Mifepristone and Misoprostol Versus Misoprostol Alone for Mid-trimester Termination of Pregnancy (14-21 Weeks LMP)

Abortion, Induced

Puerto Rico
Pfizer

Completed

Open Label Drug Interaction Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) 100mg On The Pharmacokinetics Of Aripiprazole When Coadministered To Healthy Subjects

Pharmacokinetics | Cytochrome P-450 CYP2D6 | CYP3A4 Protein, Human

United States
Pfizer

Completed

Open-Label Drug Interaction Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) 100mg On The Pharmacokinetics Of Tamoxifen When Coadministered To Healthy Post-Menopausal Female Subjects

Pharmacokinetics

United States
Sun Yat-sen University

Completed

Efficacy and Safety of Tacrolimus Sustained-release Capsules in Induction Treatment in Refractory Lupus Nephritis

Nephritis, Lupus

China
Sun Yat-sen University

Completed

The Efficacy and Tolerance of Tacrolimus Sustained-release Capsules on Refractory Nephrotic Syndrome (RNS)

Nephrotic Syndrome

China
Napp Pharmaceuticals Limited

Completed

A Study to Compare Oxycodone/Naloxone Prolonged Release Against Codeine/Paracetamol in the Treatment of Moderate to Severe Chronic Low Back Pain or Pain Due to Osteoarthritis

Osteoarthritis | Back Pain

United Kingdom
University of Palermo

Completed

Troponin I Release After High Diuretic Doses (Tra-HSS-Fur)

ADHF

Italy
Merz Pharmaceuticals GmbH

Completed

IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Glabellar Frown Lines

Glabellar Frown Lines

Germany
Pfizer

Completed

The Effect Of Dose Titration And Dose Tapering On The Tolerability Of DVS SR In Women With Vasomotor Symptoms

Vasomotor Symptoms

Canada, United States
University of Campinas, Brazil

Completed

Comparison of Two Treatments for Strabismus Correction: Botulinum Toxin A Associated to Surgery and Surgery Alone

Exotropia | Esotropia

Brazil
Wyeth is now a wholly owned subsidiary of Pfizer

Terminated

Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy

Pain | Diabetic Neuropathies

United States
Merz Pharmaceuticals GmbH

Completed

IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Glabellar Frown Lines

Moderate to Severe Glabellar Frown Lines

United States
Astellas Pharma Inc

Completed

A Study to Evaluate Efficacy and Safety of Zolpidem Modified Release Formulation in Insomnia Patients

Sleep Initiation and Maintenance Disorders | Primary Insomnia

Taiwan
Allergan

Completed

Safety Study of Botulinum Toxin Type A in Post-Upper Limb Stroke Patients With Reduced Lung Function

Stroke | Motor Neuron Disease | Muscle Spasticity

Poland, United States, Czech Republic, Hungary
University Health Network, Toronto
Schering-Plough

Terminated

EXtended Therapy in Hepatitis C Genotype 3 Infected Patients (EXACT-R(3))

Chronic Hepatitis C

Canada
Watson Pharmaceuticals

Completed

Cognitive Effects of Oral Oxybutynin and Oxybutynin Chloride Topical Gel in Older Volunteers

Healthy Volunteers

United States

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