Bioequivalence Study of Patches With Different Release Profiles
NCT00697307 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 43
Last updated 2011-06-08
Summary
The purpose of this study was to determine the bioequivalence of a norelgestromin/ethinyl estradiol (NGMN/EE) transdermal contraceptive system.
Conditions
- Female Contraception
Sponsors & Collaborators
-
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
lead INDUSTRY
Principal Investigators
-
Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial · Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2003-03-31
- Completion
- 2003-07-31
More Related Trials
-
A Study of Efficacy and Safety With the Transdermal Contraceptive System Versus Mercilon.
NCT00236782 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Hormone Exposure From Multiple Commercial Lots of ORTHO EVRA (a Transdermal Contraceptive Patch)
NCT00258076 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of the Oral Contraceptive Tablet Containing Norgestimate (NGM)/Ethinyl Estradiol (EE) With or Without Folic Acid in Healthy Women.
NCT00709189 ·Status: COMPLETED ·Phase: PHASE1
-
Study Investigating the Efficacy and Safety of a Contraceptive Patch for 13 Cycles
NCT00910637 ·Status: COMPLETED ·Phase: PHASE3
-
Birth Control Patch Study
NCT00984789 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Exposure of Norelgestromin and Ethinyl Estradiol From Commercial Lots of EVRA (a Transdermal Contraceptive Patch Manufactured by LOHMANN Therapie-Systeme) and CILEST (an Oral Contraceptive)
NCT00258063 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Efficacy and Safety With the Transdermal Contraceptive System Versus Triphasil.
NCT00236795 ·Status: COMPLETED ·Phase: PHASE3
-
Bioequivalence Study of the Oral Contraceptive (OC) Tablet Containing Norgestimate (NGM)/Ethinyl Estradiol (EE) With or Without Folic Acid in Healthy Women.
NCT00709644 ·Status: COMPLETED ·Phase: PHASE1
-
An Open-label Study to Evaluate Contraceptive Efficacy and Safety of the Transdermal Contraceptive System of Norelgestromine and Ethinyl Estradiol
NCT00307632 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of Efficacy and Safety With the Transdermal Contraceptive System.
NCT00236769 ·Status: COMPLETED ·Phase: PHASE3
-
An Open-label, Multicentre Study on Preference and Satisfaction of Canadian Women for the Transdermal Contraceptive Patch vs. Previous Primary Contraceptive Method
NCT00653016 ·Status: COMPLETED ·Phase: PHASE4
-
An Open-Label Study to Compare the Bleeding Profile of Norelgestromin/Ethinyl Estradiol in an Extended Regimen to Norelgestromin/Ethinyl Estradiol Given in a Traditional Regimen
NCT00320580 ·Status: COMPLETED ·Phase: PHASE2
-
Study Comparing Two Manufacturing Processes for Levonorgestrel 90 mg/Ethinyl Estradiol 20 mg (LNG/EE) in Healthy, Cycling Women
NCT00319163 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of Women's Experience With EVRA (Norelgestromin + Ethinyl Estradiol) Transdermal Contraceptive Patch Compared With Previous Methods of Contraception.
NCT00261482 ·Status: COMPLETED ·Phase: PHASE4
-
A Comparative Pharmacokinetic Study of ORTHO EVRA (a Transdermal Contraceptive Patch) and CILEST (an Oral Contraceptive) in Healthy Female Volunteers
NCT00254865 ·Status: COMPLETED ·Phase: PHASE1
-
Transdermal Contraceptive Patch - Endometrial Effects Study
NCT00896571 ·Status: COMPLETED ·Phase: PHASE2
-
Study Evaluating Levonorgestrel and Ethinyl Estradiol for Oral Contraception
NCT02021097 ·Status: UNKNOWN ·Phase: PHASE3
-
Study of Safety and Efficacy of an Oral Contraceptive
NCT00391807 ·Status: COMPLETED ·Phase: PHASE3
-
A Trial in Healthy Female Subjects to Compare the Pharmacokinetics of Ethinyl Estradiol of NuvaRing®, a Contraceptive Patch (EVRA(TM)) and an Oral Contraceptive (Microgynon® 30) (Study 34237 (P06650)) (COMPLETED)
NCT01044056 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate Contraceptive Efficacy and Safety of a Progestin Only Patch in Women of Childbearing Potential
NCT06672016 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Postmarketing Study of the Risk of Venous Thromboembolism (Blood Clots), Myocardial Infarction (Heart Attacks), and Stroke Among Women Using ORTHO EVRA (Norelgestromin and Ethinyl Estradiol Contraceptive Patch) Compared With Women Who Take Oral Contraceptives for Birth Control
NCT00377988 ·Status: COMPLETED
-
Study Evaluating the Bioequivalence of Levonorgestrel/Ethinyl Estradiol Combinations in Cycling Women
NCT00447863 ·Status: WITHDRAWN ·Phase: PHASE1
-
Investigation of Three Contraceptive Hormone Patches in Regard to Inhibition of Ovulation Following Application Over 3 Treatment Cycles in Healthy, Young Women.
NCT01204190 ·Status: COMPLETED ·Phase: PHASE2
-
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
NCT01166412 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Bioavailability of Levonorgestrel and Ethinyl Estradiol Tablets 15.0 mg/0.03 mg With Regards to Reference Product
NCT04230070 ·Status: COMPLETED ·Phase: PHASE1