Healthy Females Needed for Investigational Drug

Healthy Females Needed for Investigational Drug

Study Reference: C1C02612
Cliantha Research - Saint Petersburg
Compensation
Minimum  
$2500

Recruiting

Study Details

The purpose of this study is to see if an investigational drug (new/not available on the market and not yet approved by the U.S Food and Drug Administration (FDA)) is bioequivalent. Bioequivalent means the active study drug is absorbed into the body at the same rate and amount as an already approved currently marketed drug.

Study Period

The duration of your participation will be up to 19 cliays not including the screening period. The study includes a medical screening and 2 periods with two overnight stays (in each period 1 and 2) which starts 36 hours prior to Day 1 (dosing) and lasts for up to 24 hours after dosing. There are a total of 4 return visits per period which are at 48, 72, 96 and 120 hours after dosing of study drug.

Compensation

$2,500

Eligibility Criteria

  • Healthy; females with non-childbearing potential
  • Post-menopausal or surgically sterile females (documentation from medical provider of surgical sterile status required); Non-smokers or smokers (smoking <10 cigarettes / day)
  • 18 to 65 years old

Research Location:

Cliantha Research - Saint Petersburg
Trialteer - Cliantha Paid Clinical Trials

Volunteer: Healthy

Gender: Woman

Age: 18-

63

Smokers Allowed: Not Specified

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Trialteer - Cliantha Paid Clinical Trials

Company Information

Cliantha Research
Cliantha Research, a full-service Clinical Research Organization (CRO), provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Tobacco Research, Dermatology, Consumer Research, Research Lab, IVRT, Biometrics, Pharmacovigilance & Medical Services, Environmental Exposure Chambers (EECs).

Contact Information

+17273626358
4711 34th Street North Saint Petersburg, FL 33714 United States

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