MLE4901 vs. Placebo for the Treatment of PCOS
Status: | Terminated |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 18 - 45 |
Updated: | 10/4/2017 |
Start Date: | July 2016 |
End Date: | September 2017 |
A Double-blind, Randomized, Parallel-group, Placebo-controlled Study of MLE4901 for the Treatment of Polycystic Ovary Syndrome (PCOS)
This is a Phase 2b double-blind, randomized, parallel-group, placebo-controlled study of
MLE4901 versus placebo in women with PCOS.
MLE4901 versus placebo in women with PCOS.
Following a Screening/Wash-out Period of up to 12 weeks, an 8-week Lead-in Period (starting
with a progestin challenge) will be used to better characterize the study population. A
Treatment Period of 28 weeks' duration will follow the Lead-in Period. Then, an 8-week
Follow-up Period (i.e., no study drug) will be used to assess the durability of effects of
MLE4901. The study duration will be approximately 48 weeks (11 months) per subject
with a progestin challenge) will be used to better characterize the study population. A
Treatment Period of 28 weeks' duration will follow the Lead-in Period. Then, an 8-week
Follow-up Period (i.e., no study drug) will be used to assess the durability of effects of
MLE4901. The study duration will be approximately 48 weeks (11 months) per subject
Inclusion Criteria:
1. Oligo-/amenorrhea
2. At least one of the following during Screening:
- Clinical signs of hyperandrogenism, where clinical hyperandrogenism may include
hirsutism (defined as excessive terminal hair that appears in a male pattern),
acne, or androgenic alopecia
- Biochemical hyperandrogenism refers to an elevated serum androgen level (i.e.,
total, bioavailable or free testosterone level ≥ULN)
- Polycystic ovarian morphology, defined as the presence of 12 or more follicles
2-9 mm in diameter and/or an increased ovarian volume >10 mL (without a cyst or
dominant follicle) in either ovary
3. Body mass index (BMI) 22 to 45 kg/m2, inclusive
4. Must be willing to avoid use of all hair removal procedures and products during study
participation
5. Must be willing to avoid all prescription treatments for acne and not increase the
dose or frequency of their current non-prescription acne treatment regimen during
study participation
6. Must be willing to avoid the use of all hair growth procedures and products during
study participation
7. Permanently surgically sterilized (bilateral salpingectomy or tubal occlusion) >2
years or male partner(s) has had a vasectomy >2 years or must consent to use two
permitted medically-acceptable methods of contraception throughout the study during
any sexual intercourse with a male partner. Permitted medically-acceptable methods of
birth control for this study are defined as use of a male condom plus one of the
following: spermicide, diaphragm with spermicide, or an intrauterine device that does
not contain steroid hormones.
Exclusion Criteria:
1. Menopausal or peri-menopausal, defined for this study as FSH (follicle stimulating
hormone ) >10 IU/L
2. Irregular vaginal/menstrual bleeding caused by conditions other than PCOS (e.g.,
uterine polyps or submucosal uterine fibroids)
3. Abnormal Papanicolaou (Pap) test during Screening requiring follow-up sooner than 1
year after the test
4. Uncontrolled hypo- or hyperthyroidism
5. Post-hysterectomy or endometrial ablation
6. Post-oophorectomy (unilateral or bilateral) or other ovarian surgery
7. Medical history of type 1 or type 2 diabetes mellitus
We found this trial at
31
sites
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860 Peachwood Drive
DeLand, Florida 32720
DeLand, Florida 32720
(386) 740-0770
Phone: 386-740-0770
Site Overview Avail Clinical Research is a renowned and experienced clinical research site conducting Phase...
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100 West Gore St # 202
Orlando, Florida 32806
Orlando, Florida 32806
(407) 426-9299
Phone: 407-426-9299
Compass Research LLC Compass Research is a clinical research company dedicated to testing new medications...
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Hershey, Pennsylvania 17033
Phone: 717-531-4483
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3400 Civic Center Boulevard
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
Phone: 215-615-4202
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