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A Comparison of PF708 and Forteo in Osteoporosis Patients
NCT03002428 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to compare the effects of two teriparatide products, PF708 and Forteo, in patients with osteoporosis.
Conditions Studied
Interventions
- DRUG Teriparatide (PF708)
- DRUG Teriparatide (Forteo)
Study Locations (20)
Arizona
- Radiant Research — Chandler
- Radiant Research — Mesa
- SunValley Arthritis Center — Peoria
- Radiant Research — Phoenix
Alabama
- Radiant Research — Birmingham
- The Orthopaedic Group — Mobile
Nevada
- Radiant Research — Henderson
- Radiant Research — Las Vegas
Ohio
- Radiant Research — Akron
- Radiant Research — Cincinnati
Pennsylvania
- Altoona Center for Clinical Research — Duncansville
- Pennsylvania Regional Center for Arthritis & Osteoporosis Research — Wyomissing
Colorado
- Radiant Research — Colorado Springs
Florida
- OB-GYN Associates of Mid-Florida — Leesburg
Georgia
- Atlanta Research Center — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 181 participants |
| Start Date | 2016-12 |
| Est. Completion | 2018-05 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03002428
The ClinicalTrials.gov registry entry for NCT03002428 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 181 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfenex, which has 2 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 Osteoporosis appearing as the primary indexed condition, and to 2 interventions — of which Teriparatide (PF708) 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: NCT03002428 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Arizona, Alabama, Nevada. 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 NCT03002428 about?
NCT03002428 is a clinical study titled "A Comparison of PF708 and Forteo in Osteoporosis Patients". The purpose of this study is to compare the effects of two teriparatide products, PF708 and Forteo, in patients with osteoporosis.
What is the current status of trial NCT03002428?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 181 participants. The study started on 2016-12. Estimated completion is 2018-05.
What conditions does trial NCT03002428 study?
This clinical trial studies the following conditions: Osteoporosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03002428?
The interventions under investigation include: Teriparatide (PF708) (DRUG), Teriparatide (Forteo) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03002428?
This trial is sponsored by Pfenex, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03002428 being conducted?
This trial has 20 study locations across Alabama, Arizona, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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