A Study of MF101 in Postmenopausal Women



Status:Recruiting
Conditions:Hot Flash, Other Indications
Therapuetic Areas:Other, Reproductive
Healthy:No
Age Range:40 - 65
Updated:4/2/2016
Start Date:October 2011
Contact:Jesse Langon, MPH
Phone:510-4204182

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A Phase 3, Double-blind, Placebo-Controlled, Randomized Clinical Trial, Assessing Safety and Efficacy of MF101 for Hot Flushes and Menopausal Symptoms in Postmenopausal Women

This phase 3a study is designed to assess the safety and efficacy of MF101 on the frequency
of moderate to severe hot flushes in postmenopausal women.

Menopausal women often experience debilitating menopausal vasomotor symptoms and associated
insomnia. Until recently, vasomotor symptoms were often treated with estrogens, which are
very effective; however, randomized clinical trials have shown that postmenopausal
combination hormone therapy increases the risks for stroke, cardiovascular events, and
breast cancer. New, more effective, and safer treatments for menopausal vasomotor symptoms
are therefore needed.

MF101, a botanical extract, is a non-hormonal investigational treatment being tested in a
randomized, double-blind, placebo-controlled phase 3a clinical trial to assess the safety
and efficacy of MF101 on the frequency of moderate to severe hot flushes in postmenopausal
women. Approximately 1200 healthy post-menopausal women, aged 40-65, with moderate to severe
hot flushes will be enrolled to determine the safety and efficacy of two doses of MF101 (5
g/day and 10 g/day) compared to placebo after 12 weeks of treatment.

Inclusion Criteria (limited):

- Confirmed postmenopausal women aged 40-65

- Provide written informed consent

Exclusion Criteria (limited):

- History of malignancy, with the exception of certain types of skin cancer or cervical
cancer

- Known carrier of BRCA1 or BRCA2

- Abnormal mammogram or breast examination suggestive of cancer within 9 months of
screening

- Endometrial hyperplasia, polyps or abnormal uterine masses (with the exception of
fibroids)

- Clinical evidence of active ischemic heart disease, history of cardiovascular
disease, uncontrolled hypertension, or a history of transient ischemic attacks or
cerebrovascular accidents

- History of deep vein thrombosis, pulmonary embolism, severe chronic diarrhea, chronic
constipation, uncontrolled inflammatory bowel syndrome or disease (IBS or IBD), or
unexplained weight loss

- Active liver disease or gall bladder disease

- History of chronic hepatitis B, hepatitis C, hepatitis within 3 months, or HIV
infection

- Use of prescription medications or herbal/dietary supplements for the treatment of
hot flushes or those with known estrogenic/progestogenic activity within required
wash-out timeframes

- Use of selective receptor modulators (SERMs), aromatase inhibitors,
gonadotropin-releasing hormone agonists, selective serotonin reuptake inhibitors
(SSRIs), selective norepinephrine reuptake inhibitors (SNRIs), gabapentin or
clonidine within required wash-out timeframes

- Chronic use of morphine or other opiates
We found this trial at
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New Bern, North Carolina 28562
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3400 N Charles St
Baltimore, Maryland 21205
410-516-8000
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100 West Gore St # 202
Orlando, Florida 32806
(407) 426-9299
Compass Research LLC Compass Research is a clinical research company dedicated to testing new medications...
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3890 Tampa Rd # 302
Palm Harbor, Florida 34684
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4200 Fifth Ave
Pittsburgh, Pennsylvania 15260
(412) 624-4141
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Albuquerque, New Mexico
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Berkeley, California
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Boynton Beach, Florida 33472
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Bradenton, Florida
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Brooksville, Florida
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Charlottesville, Virginia 22903
(434) 924-0311
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Cleveland, Ohio 44122
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Denver, Colorado 80218
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Eugene, Oregon 97401
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Jackson, Tennessee 37805
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Jenkintown, Pennsylvania 19046
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Lake Jackson, Texas 77566
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Memphis, Tennessee 38163
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Mt. Pleasant, South Carolina
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New Brunswick, New Jersey 08903
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New Port Richey, Florida 34652
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Norfolk, Virginia
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3451 Walnut St
Philadelphia, Pennsylvania 19104
1 (215) 898-5000
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Phoenix, Arizona 85023
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