Overview

MENOPUR® Versus FOLLISTIM®

Status:
Completed
Trial end date:
2010-01-01
Target enrollment:
0
Participant gender:
Female
Summary
To compare the efficacy and safety of highly purified menotropin (Menopur®) with that of follitropin beta (FOLLISTIM®) in patients who are undergoing gonadotropin-releasing hormone (GnRH) antagonist in vitro fertilization (IVF) cycles
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Ferring Pharmaceuticals
Treatments:
Chorionic Gonadotropin
Follicle Stimulating Hormone
Ganirelix
Menotropins
Progesterone
Criteria
Inclusion Criteria:

1. Pre-menopausal females between the ages of 18 and 42 years

2. Body mass index (BMI) of 18-34

3. Early follicular phase (day 2-4) Follicle stimulating hormone (FSH) <15 IU/L and
Estradiol (E2) within normal limits

4. Documented history of infertility (e.g., unable to conceive for at least one year, or
for 6 months for women >38 years of age, or bilateral tubal occlusion or absence, or
male factor but excluding severe male factor requiring invasive or surgical sperm
retrieval. Donor sperm may be used.)

5. Transvaginal ultrasound at screening consistent with findings adequate for assisted
reproductive technology (ART) with respect to uterus and adnexa

6. Signed informed consent

Exclusion Criteria:

1. Gestational or surrogate carrier, donor oocyte

2. Presence of any clinically relevant systemic disease (e.g., insulin-dependent diabetes
mellitus, uterine cancer)

3. Surgical or medical condition which, in the judgment of the Investigator or Sponsor,
may interfere with absorption, distribution, metabolism, or excretion of the drugs to
be used

4. Previous In vitro fertilization (IVF) or Assisted reproductive technology (ART)
failure due to a poor response to gonadotropins. Poor response is defined as
development of 2 mature follicles or history of >2 previous failed in vitro
fertilization (IVF) cycles.

5. History of recurrent pregnancy loss (>2).

6. Presence of abnormal uterine bleeding of undetermined origin

7. Current or recent substance abuse, including alcohol or smoking >10 cigarettes per day

8. Refusal or inability to comply with the requirements of the Protocol for any reason,
including scheduled clinic visits and laboratory tests

9. Participation in any experimental drug study within 30 days prior to Screening

10. Severe male factor requiring invasive or surgical sperm retrieval (e.g., microsurgical
epididymal sperm aspiration [MESA], testicular sperm extraction [TESE])