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ACTAVIS INC

🇺🇸United States
Ownership
-
Employees
-
Market Cap
-
Website

Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design Study in Patients With Moderate to Severe Facial Erythema Associated With Rosacea

Phase 3
Completed
Conditions
Rosacea
Interventions
Drug: placebo
First Posted Date
2014-11-13
Last Posted Date
2020-01-14
Lead Sponsor
Actavis Inc.
Target Recruit Count
462
Registration Number
NCT02289352
Locations
🇺🇸

Investigator site 2, Hot Springs, Arkansas, United States

🇺🇸

Investigator site 16, Long Beach, California, United States

🇺🇸

Investigator site 5, Miami, Florida, United States

and more 13 locations

A Study To Evaluate The Safety And Therapeutic Equivalence of Tazarotene Foam 0.1% in Subjects With Acne Vulgaris

Phase 3
Completed
Conditions
Acne Vulgaris
Interventions
First Posted Date
2014-10-17
Last Posted Date
2020-06-12
Lead Sponsor
Actavis Inc.
Target Recruit Count
893
Registration Number
NCT02267746
Locations
🇺🇸

Center for Dermatology Clinical Research, Fremont, California, United States

🇺🇸

Moore Clinical Research, Tampa, Florida, United States

🇺🇸

LCC Medical Research Institute, Miami, Florida, United States

and more 8 locations

A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate Vaginal Cream 2% (Watson Laboratories, Inc.) to Clindesse® (Ther-Rx™, Clindamyin Phosphate Vaginal Cream 2%) and Both Active Treatments to a Placebo Control in the Treatment of Bacterial Vaginosis in Non-pregnant Women

Phase 3
Completed
Conditions
BACTERIAL VAGINOSIS
Vaginal Discharge Color, Odor, and Consistency
Vulvovaginal Itching and Irritation (Subjective) Absent, Mild, Moderate, or Severe
Vulvovaginal Inflammation (Objective) Absent, Mild, Moderate, or Severe
Signs and Symptoms to be Evaluated and Recorded Include
Interventions
First Posted Date
2014-08-07
Last Posted Date
2020-01-28
Lead Sponsor
Actavis Inc.
Target Recruit Count
604
Registration Number
NCT02210689
Locations
🇺🇸

Akesis Investigator site 5, Birmingham, Alabama, United States

🇺🇸

Akesis Investigator site 12, La Mesa, California, United States

🇺🇸

Akesis investigator site 6, San Diego, California, United States

and more 15 locations

A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Patients With Moderate Facial Rosacea

Phase 3
Completed
Conditions
Rosacea
Interventions
First Posted Date
2014-04-23
Last Posted Date
2020-06-02
Lead Sponsor
Actavis Inc.
Target Recruit Count
1009
Registration Number
NCT02120924
Locations
🇺🇸

Site 24, Fremont, California, United States

🇺🇸

Site 22, Santa Monica, California, United States

🇺🇸

Site 1, Brandon, Florida, United States

and more 27 locations

A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participants With Actinic Keratoses

Phase 3
Completed
Conditions
Actinic Keratosis
Interventions
First Posted Date
2014-04-23
Last Posted Date
2019-12-13
Lead Sponsor
Actavis Inc.
Target Recruit Count
467
Registration Number
NCT02120898
Locations
🇺🇸

Site 1, Birmingham, Alabama, United States

🇺🇸

Site 10, Fremont, California, United States

🇺🇸

Site 8, Los Angeles, California, United States

and more 24 locations

A Study Comparing Diclofenac Sodium Gel 3% to Solaraze® (Diclofenac Sodium) Gel 3% in the Treatment of Actinic Keratosis

Phase 3
Completed
Conditions
Actinic Keratosis
Interventions
First Posted Date
2013-10-16
Last Posted Date
2020-07-20
Lead Sponsor
Actavis Inc.
Target Recruit Count
476
Registration Number
NCT01962987
Locations
🇺🇸

Investigator Site 23, Fremont, California, United States

🇺🇸

Investigator Site 9, Long Beach, California, United States

🇺🇸

Investigator Site 12, Newport Beach, California, United States

and more 28 locations

Clinical Equivalence Study of Mometasone Nasal Spray

Phase 3
Completed
Conditions
Seasonal Allergic Rhinitis
Interventions
First Posted Date
2013-05-10
Last Posted Date
2020-08-19
Lead Sponsor
Actavis Inc.
Target Recruit Count
880
Registration Number
NCT01850823
Locations
🇺🇸

Investigator site 18, Stockbridge, Georgia, United States

🇺🇸

Investigator site 1, Louisville, Kentucky, United States

🇺🇸

Investigator site 3, Bethesda, Maryland, United States

and more 22 locations

Pivotal Bioequivalence Study of Exemestane 25 mg Tablets Under Fasting Conditions in Healthy Subjects

Phase 1
Withdrawn
Conditions
Healthy
Interventions
Drug: Test product (B) Exemestane
Drug: Reference product (A) Aromasin (Exemestane)
First Posted Date
2013-01-04
Last Posted Date
2019-07-05
Lead Sponsor
Actavis Inc.
Registration Number
NCT01760980
Locations
🇿🇦

Bloemfontein Early Phase Clinical Unit, PAREXEL International (South Africa), Bloemfontein, South Africa

Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Dose in Healthy Subjects Under Fed Conditions

First Posted Date
2010-08-30
Last Posted Date
2010-08-30
Lead Sponsor
Actavis Inc.
Target Recruit Count
24
Registration Number
NCT01190761
Locations
🇨🇦

SFBC Anapharm, Sainte-Foy, Quebec, Canada

Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Dose in Healthy Subjects Under Fasting Conditions

First Posted Date
2010-08-30
Last Posted Date
2024-02-22
Lead Sponsor
Actavis Inc.
Target Recruit Count
24
Registration Number
NCT01190748
Locations
🇨🇦

SFBC Anapharm, Sainte-Foy, Quebec, Canada

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