Clinical Trials Directory

Trials / Sponsors / Warner Chilcott

Warner Chilcott

Industry · 58 registered clinical trials.

StatusTrialPhaseStarted
CompletedA Safety and Efficacy Study of Estradiol Vaginal Capsule in Postmenopausal Women With Vulvovaginal Atrophy
Vulvovaginal Atrophy, Menopause, Dyspareunia
Phase 22016-02-15
CompletedAssess Safety & Efficacy of WC3055 in Men With Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hype
Benign Prostatic Hyperplasia
Phase 22013-08-01
CompletedStudy to Evaluate Safety and Efficacy of WC3011 (Estradiol Vaginal Cream) in Postmenopausal Women With Dyspare
Vulvovaginal Atrophy
Phase 32013-04-12
TerminatedEfficacy & Safety of Single Dose Alprostadil Cream (2 Concentrations Enhancer) to Vehicle in Men w/Erectile Dy
Erectile Dysfunction
Phase 22013-02-01
CompletedMulticenter Study to Evaluate Safety and Efficacy of WC3011 (Estradiol Vaginal Cream) in Postmenopausal Women
Vulvovaginal Atrophy
Phase 32013-01-31
CompletedEvaluate Long-Term Safety and Efficacy WC3011 (Estradiol Vaginal Cream)
Vulvovaginal Atrophy
Phase 32011-10-20
CompletedSafety & Efficacy WC3011 (Estradiol Vaginal Cream) in the Treatment of Vulvovaginal Atrophy in Postmenopausal
Postmenopausal Vulvovaginal Atrophy
Phase 32011-06-29
CompletedEffect of Udenafil on Spermatogenesis
Spermatogenesis, Erectile Dysfunction
Phase 12010-09-01
CompletedTreatment of Chlamydia Infection Comparing WC2031 Tablets With Vibramycin
Urogential Chlamydia Trachomatis Infection
Phase 32010-04-01
CompletedTreatment of Erectile Dysfunction - Long Term Safety and Efficacy
Erectile Dysfunction
Phase 32010-01-01
TerminatedAssessing the Safety/Efficacy of Asacol® Given Every 12 Hours to Children and Adolescents for the Maintenance
Ulcerative Colitis
Phase 32009-10-01
CompletedTreatment of Erectile Dysfunction II
Erectile Dysfunction
Phase 32009-09-01
CompletedTreatment of Erectile Dysfunction I
Erectile Dysfunction
Phase 32009-09-01
TerminatedAssessing the Safety/Efficacy of Transdermal Testosterone in Female Patients With Symptomatic Heart Failure
Heart Failure
Phase 22009-07-01
CompletedDelayed Release (DR) Risedronate Compared to Immediate Release (IR) in Postmenopausal Women
Postmenopausal Osteoporosis
Phase 22009-05-01
CompletedStudy Assessing Dosing Time and Calcium and Vitamin D on the Relative BA of 35 mg DR Risedronate Dosed With Fo
Healthy
Phase 12009-03-01
CompletedA Study to Assess the Bioequivalence of Different Formulations of Risedronate in Healthy Male and Female Subje
Osteoporosis
Phase 12009-01-01
CompletedAssessing the Safety/Efficacy of Asacol® Given Every 12 Hours to Children and Adolescents With Active Ulcerati
Ulcerative Colitis
Phase 32008-12-01
TerminatedA Two-week Open-label Pharmacodynamic and Pharmacokinetic Study of Multiple Doses of a Darifenacin Liquid Oral
Neurogenic Detrusor Overactivity
Phase 22008-10-07
CompletedFood Effects on the Relative Bioavailability of Different Dosages of Risedronate
Postmenopausal, Non-lactating, Surgically Sterile
Phase 12008-07-01
TerminatedBone Microarchitecture in Osteopenic Postmenopausal Women
Osteoporosis
Phase 42008-07-01
CompletedTreatment of Acne Vulgaris With Doryx Tablets Compared to Doxycyline Hyclate
Acne Vulgaris
Phase 42008-03-01
CompletedTreatment of Moderate to Severe Facial Acne Vulgaris
Acne Vulgaris
Phase 22008-02-01
CompletedAssess Bioequivalence of One 150 mg Risedronate Tablet Versus Two 75 mg Risedronate Tablets in Healthy Subject
Osteoporosis
Phase 12008-01-01
CompletedAsacol Acute Diverticulitis(DIVA)Study
Diverticulitis
Phase 22007-11-01
CompletedAssess the Influence of a High-fat Meal on the Relative Bioavailability Of Two Formulations of Risedronate
Bioavailability
Phase 12007-11-01
CompletedA Study of a 35 mg Delayed Release Formulation of Risedronate for Osteoporosis
Postmenopausal Osteoporosis
Phase 32007-10-01
CompletedFecal Biomarker Study for Patients With Ulcerative Colitis
Ulcerative Colitis
2007-08-01
CompletedA Comparison of Once a Day Dose Compared to 2 Doses/Day
Ulcerative Colitis
Phase 32007-07-01
CompletedBioequivalence of Testosterone Reduced-size Patch Relative to the Testosterone Reference Patch
Healthy
Phase 12007-07-01
CompletedStudy of Safety and Efficacy of an Oral Contraceptive
Contraception
Phase 32007-06-01
CompletedEndometrial Safety Study of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women
Hypoactive Sexual Desire Disorder
Phase 32007-04-01
CompletedPharmacokinetics of Asacol 2.4 g/Day and Lialda 2.4 g/Day in Healthy Volunteers
Healthy
Phase 12007-03-01
CompletedStudy of Safety and Efficacy of an Oral Contraceptive
Contraception
Phase 32006-11-01
CompletedTestosterone Therapy in Naturally Menopausal Women With Low Sexual Desire Receiving Transdermal Estrogen
Hypoactive Sexual Desire Disorder
Phase 32006-11-01
CompletedAssess the Safety, Efficacy, and Pharmacokinetics of Immediate and Delayed Release Weekly Risedronate
Postmenopausal Women
Phase 22006-07-01
CompletedA Double Blind Study for the Treatment of Acute Ulcerative Colitis
Ulcerative Colitis
Phase 32006-06-01
CompletedStudy of Bleeding With Extended Administration of an Oral Contraceptive
Contraception
Phase 22006-06-01
CompletedStudy of the Effect of Once a Week Risedronate on the Microstructure of Tibia and Radius Using a New Scanning
Osteopenia
Phase 32006-04-01
TerminatedA Study of Asacol Absorption, Metabolism and Excretion in Children and Adolescents With Ulcerative Colitis.
Ulcerative Colitis
Phase 12005-10-01
CompletedA Study of Monthly Risedronate for Osteoporosis
Postmenopausal Osteoporosis
Phase 32005-10-01
CompletedSafety and Efficacy of Risedronate in the Treatment of Osteogenesis Imperfecta in Children
Osteogenesis Imperfecta
Phase 32004-11-01
CompletedStudy of Transdermal Testosterone Patches in Menopausal Women With Low Libido
Hypoactive Sexual Desire Disorder
Phase 32004-07-01
CompletedSafety, Pharmacokinetics, and Efficacy of 100, 150, and 200 mg Risedronate Administered to Women With Low BMD
Postmenopausal
Phase 22004-04-01
CompletedStudy of Bone Histomorphometry, Microarchitecture, and Matrix Structure in Patients Receiving Alendronate or R
Postmenopausal Osteoporosis
2004-01-01
CompletedStudy of Safety and Efficacy of an Oral Contraceptive
Prevention of Pregnancy
Phase 32004-01-01
CompletedStudy to Assess BMD and Bone Turnover Response to 5 mg Daily Risedronate Treatment in Women With PMO
Postmenopausal Osteoporosis
Phase 32003-06-01
CompletedAnalysis of Iliac Crest Biopsies From Patients Receiving Risedronate
Osteoporosis
2003-04-01
CompletedHormone Replacement Therapy for Use in Postmenopausal Women for Relief of Hot Flushes and Urogenital Symptoms.
Hormone Replacement Therapy
Phase 32003-02-01
CompletedPharmacokinetics of a Single 14C-labeled Dose of Risedronate or Alendronate Followed by Once-a-week Unlabeled
Osteopenia, Osteoporosis
Phase 12002-11-01
CompletedEfficacy and Safety of Risedronate Therapy Administered 35 mg Once A Week in Men With Osteoporosis
Other Osteoporosis
Phase 32002-06-01
CompletedStudy of Transdermal Testosterone Patches in Surgically Menopausal Women With Low Libido
Hypoactive Sexual Desire Disorder
Phase 32002-06-01
CompletedStudy to Assess the Efficacy/Safety of Transdermal Testosterone Patches in Naturally Menopausal Women With Low
Hypoactive Sexual Desire Disorder (HSDD)
Phase 32002-06-01
CompletedStudy of Transdermal Testosterone Patches in Naturally Menopausal Women With Low Libido
Hypoactive Sexual Desire Disorder
Phase 32002-06-01
CompletedStudy of Transdermal Testosterone Patches in Surgically Menopausal Women With Low Libido
Hypoactive Sexual Desire Disorder
Phase 32002-05-01
CompletedEffect of Stopping Risedronate After Long Term Treatment on Bone Turnover
Postmenopausal Women With Osteoporosis
Phase 32001-10-01
CompletedSafety and Efficacy of Asacol 4.8 g/Day Versus Asacol 2.4 g/Day (ASCEND I)
Ulcerative Colitis
Phase 32001-02-01
CompletedSafety and Efficacy of Two Different Doses of Asacol in the Treatment of Moderately Active Ulcerative Colitis
Ulcerative Colitis
Phase 32000-09-01