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Comparison of MENOPUR Liquid and Powder in Women Undergoing Assisted Reproductive Technology (ART)
NCT04163458 · View on ClinicalTrials.gov ↗
Study Summary
Development of multiple follicles and pregnancy in ovulatory women undergoing controlled ovarian stimulation as part of an assisted reproductive technology (ART) cycle.
Conditions Studied
Interventions
- DRUG MENOPUR solution for injection in pre-filled pen, 1200 IU/1.92 mL
- DRUG MENOPUR powder and solvent for solution for injection, 75 IU
- OTHER Placebo (for MENOPUR solution for injection in pre-filled pen)
- OTHER Placebo (for MENOPUR powder and solvent for solution for injection)
Study Locations (20)
Texas
- Center for Assisted Reproduction — Bedford
- Houston Fertility Institute — Houston
- Center of Reproductive Medicine — Webster
Connecticut
- Center for Advanced Reproductive Services PC — Farmington
- Yale Fertility Center — New Haven
Florida
- Fertility and IVF Center of Miami — Miami
- Center for Reproductive Medicine — Winter Park
Illinois
- Fertility Centers of Illinois — Chicago
- InVia Fertility Specialists, SC — Hoffman Estates
North Carolina
- Reproductive Endocrinology Associates of Charlotte — Charlotte
- Carolina Conceptions — Raleigh
Arizona
- Fertility Treatment Center — Tempe
California
- Fertility Specialists Medical Group - San Diego Center for Reproductive Surgery — San Diego
Idaho
- Idaho Center for Reproductive Medicine — Boise
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 405 participants |
| Start Date | 2019-10-25 |
| Est. Completion | 2021-07-16 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04163458
The ClinicalTrials.gov registry entry for NCT04163458 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 405 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ferring Pharmaceuticals, which has 27 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Infertility appearing as the primary indexed condition, and to 4 interventions — of which MENOPUR solution for injection in pre-filled pen, 1200 IU/1.92 mL is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04163458 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Texas, Connecticut, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04163458 about?
NCT04163458 is a clinical study titled "Comparison of MENOPUR Liquid and Powder in Women Undergoing Assisted Reproductive Technology (ART)". Development of multiple follicles and pregnancy in ovulatory women undergoing controlled ovarian stimulation as part of an assisted reproductive technology (ART) cycle.
What is the current status of trial NCT04163458?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 405 participants. The study started on 2019-10-25. Estimated completion is 2021-07-16.
What conditions does trial NCT04163458 study?
This clinical trial studies the following conditions: Infertility. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04163458?
The interventions under investigation include: MENOPUR solution for injection in pre-filled pen, 1200 IU/1.92 mL (DRUG), MENOPUR powder and solvent for solution for injection, 75 IU (DRUG), Placebo (for MENOPUR solution for injection in pre-filled pen) (OTHER), Placebo (for MENOPUR powder and solvent for solution for injection) (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04163458?
This trial is sponsored by Ferring Pharmaceuticals, which has 27 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04163458 being conducted?
This trial has 20 study locations across Arizona, California, Connecticut, Florida, Idaho. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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