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Active Studies

Sumitomo Pharma Co., Ltd. Study

Study Details: This study is to evaluate bone mineral density with long-term use of the study drug in premenopausal women with heavy menstrual bleeding due to uterine fibroids or moderate-severe pain associated with endometriosis. 
Compensation: Up to $2,600.00
Length of Study: Approximately 5 years
You may qualify if you:

  • Are a premenopausal woman 18 to 50 years of age.   

  • Are willing to avoid pregnancy for 4 years using nonhormonal methods of contraception.

  • Have a diagnosis of either uterine fibroids with heavy menstrual bleeding or endometriosis with associated moderate to severe pain.

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Astellas Hot Flash Study

Study Details: An observational study among women 40-75 years of age with hot flashes associated with menopause.

Subjects will be required to wear a device on their wrist, like a watch, to record hot flashes.
Compensation: Up to $560.00
Length of Study: Approximately 12 months
You may qualify if you:

  • ​Are a woman of age between 40-75 years.

  • Have been diagnosed with bothersome hot flashes due to/associated with menopause for at least 3 months.

  • Have been newly prescribed a non-hormone medication for the treatment of hot flashes.

  • Willing to wear a device on your wrist, like a watch, in two-week intervals to record hot flashes.

Bacterial Vaginosis Study

Study Details: The purpose of this study is to assess the safety and tolerability of the study drug. 
Compensation: Up to $1302.00
Length of Study:  Approximately 130 days
You may qualify if you: 

  • Are a woman at least 18 years of age, diagnosed and suffer from recurrent Bacterial Vaginosis and currently have BV.

  • Able to participate in trial as an outpatient, to attend all required visits, and to comply with all trial requirements.

  • Apart from clinical diagnosis of BV, are healthy, in the clinical judgement of the investigator. 

  • Able to visit our office 6 times within a specified time frame. 

  • Agree to abstain from vaginal intercourse for 21 days.

Endometriosis Study

Study Details: The purpose of this study in to look at the safety and effectiveness of the study drug when taken together with a combination oral contraception.
Compensation: Up to $1600.00
Length of Study: Approximately 1 year
You may qualify if you:

  • Are a premenopausal female 18-49 years of age.​

  • Have a documented diagnosis of endometriosis.

  • Be willing to discontinue use of any prior medications for endometriosis.

  • Meet other testing criteria done in the office at your first visit.
     

Alternative Medicine
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Praetorian Pharmaceutical Research is a dedicated research facility experienced in Phase I-IV clinical study management. Since 2012, PPR has been dedicated to assisting pharmaceutical companies find new cures to help patients better manage their healthcare.

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