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DURAMED RESEARCH

🇺🇸United States
Ownership
-
Employees
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Market Cap
-
Website

A Multicenter Study to Evaluate the Effects of a 91-day Oral Contraceptive on Bone Mineral Density in Adolescent Females

First Posted Date
2009-06-19
Last Posted Date
2014-10-22
Lead Sponsor
Duramed Research
Target Recruit Count
1361
Registration Number
NCT00924560
Locations
🇺🇸

Teva Investigational Site 025, Torrance, California, United States

🇺🇸

Teva Investigational Site 033, Cleveland, Ohio, United States

🇺🇸

Teva Investigational Site 013, San Diego, California, United States

and more 43 locations

A Safety Extension Study of DR-OXY-301

Phase 3
Completed
Conditions
Overactive Bladder
Interventions
Drug: Oxybutinyn Vaginal Ring 4mg
Drug: Oxybutinyn Vaginal Ring 6mg
First Posted Date
2008-10-31
Last Posted Date
2023-03-16
Lead Sponsor
Duramed Research
Target Recruit Count
240
Registration Number
NCT00782769
Locations
🇺🇸

Duramed Investigational Site, Tacoma, Washington, United States

A Multicenter Study to Evaluate the Efficacy of a 91-Day Extended Cycle Oral Contraceptive for Menstrually-Related Migraine Headaches

Phase 2
Completed
Conditions
Migraine
Interventions
First Posted Date
2008-10-29
Last Posted Date
2017-02-06
Lead Sponsor
Duramed Research
Target Recruit Count
109
Registration Number
NCT00781456
Locations
🇺🇸

Teva Investigational Site, Houston, Texas, United States

🇺🇸

Duramed Investigational Site, Seattle, Washington, United States

Emergency Contraception Actual Use Study

Phase 3
Completed
Conditions
Emergency Contraception
Interventions
Drug: DR-104
First Posted Date
2008-10-22
Last Posted Date
2012-10-18
Lead Sponsor
Duramed Research
Target Recruit Count
343
Registration Number
NCT00777556
Locations
🇺🇸

Duramed Research Investigational Site, Philadelphia, Pennsylvania, United States

🇺🇸

Teva Investigational Site, Pittsburgh, Pennsylvania, United States

A Clinical Trial to Evaluate the Efficacy and Safety of DR-3001 in Women With Overactive Bladder

Phase 3
Completed
Conditions
Overactive Bladder
Interventions
Drug: DR-3001
Drug: Placebo
First Posted Date
2008-05-28
Last Posted Date
2016-07-20
Lead Sponsor
Duramed Research
Target Recruit Count
1104
Registration Number
NCT00685113
Locations
🇨🇦

Duramed Investigational Site, Thunder Bay, Ontario, Canada

🇺🇸

Duramed Investigation Site, Decatur, Georgia, United States

🇨🇦

Duramed Investigatinal Site, Vancouver, British Columbia, Canada

A Clinical Trial to Evaluate the Efficacy and Safety of DR-2011 for In Vitro Fertilization

Phase 3
Completed
Conditions
Infertility
Interventions
First Posted Date
2008-02-14
Last Posted Date
2013-09-13
Lead Sponsor
Duramed Research
Target Recruit Count
1297
Registration Number
NCT00615251
Locations
🇺🇸

Duramed Investigational Site, Norfolk, Virginia, United States

Study to Evaluate the Effects of Synthetic Conjugated Estrogens, B (SCE-B) on Nocturnal Vasomotor Symptoms in Postmenopausal Women

Phase 4
Completed
Conditions
Nocturnal Vasomotor Symptoms
Interventions
Drug: Placebo
First Posted Date
2008-01-14
Last Posted Date
2013-07-19
Lead Sponsor
Duramed Research
Target Recruit Count
157
Registration Number
NCT00592839
Locations
🇺🇸

Duramed Investigational Site, San Antonio, Texas, United States

A Study to Evaluate Bleeding Patterns With Three Different Doses of DR-1031 Compared to Seasonale

Phase 2
Completed
Conditions
Breakthrough Bleeding
Interventions
First Posted Date
2006-11-01
Last Posted Date
2013-07-26
Lead Sponsor
Duramed Research
Target Recruit Count
567
Registration Number
NCT00394771
Locations
🇺🇸

Duramed Investigational Site, Williston, Vermont, United States

A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001

Phase 3
Completed
Conditions
Respiratory Tract Diseases
Interventions
Biological: DR-5001
Other: Placebo
First Posted Date
2006-09-29
Last Posted Date
2017-04-10
Lead Sponsor
Duramed Research
Target Recruit Count
4040
Registration Number
NCT00382408
Locations
🇺🇸

Duramed Investigational Site, Fort Jackson, South Carolina, United States

Open-Label Study to Evaluate the Safety and Efficacy of a Low-Dose 28-Day Oral Contraceptive

Phase 3
Completed
Conditions
Contraception
Interventions
Drug: DR-1021
First Posted Date
2006-08-10
Last Posted Date
2013-08-21
Lead Sponsor
Duramed Research
Target Recruit Count
1347
Registration Number
NCT00362479
Locations
🇺🇸

Duramed Investigational Site, Tacoma, Washington, United States

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