Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Trial Evaluating Efficacy of AGA2118 in PostMenopausal Women wIth Low Bone MasS (ARTEMIS)
NCT06577935 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of this study is to determine the effect of treatment with AGA2118 versus placebo at Month 12 on lumbar spine bone mineral density (BMD) in postmenopausal women with low bone mass.
Conditions Studied
Interventions
- OTHER Placebo
- DRUG AGA2118
Study Locations (20)
Other
- CIDIIM — Córdoba
- Centro de Investigaciones Medicas Mar del Plata CIM — Mar del Plata
- Futuremeds Gdynia — Gdynia
- Krakowskie Centrum Medyczne — Krakow
- Futuremeds Lodz — Lodz
- Futuremeds Warszawa Centrum — Warsaw
- Futuremeds Targowek — Warsaw
- Futuremeds Wroclaw — Wroclaw
Argentina
- Centro Médico Dra Laura Maffei e Investigación Cliínica Aplicada — Buenos Aires
- Consultorio de Investigacion Clinica EMO SRL — Buenos Aires
- IDIM — Buenos Aires
- Investigaciones Reumatologicas y Osteologicas SRL — Buenos Aires
- Mautalen - Salud e Investigacion (Expertia S.A.) — Buenos Aires
- Stat Research — Buenos Aires
- Instituto Médico Strusberg — Córdoba
Alabama
- University of Alabama at Birmingham — Birmingham
Georgia
- Center for Advanced Research & Education — Gainesville
New Mexico
- NM Clinical Research & Osteoporosis Center, Inc. — Albuquerque
Pennsylvania
- Altoona Center for Clinical Research — Duncansville
Washington
- Puget Sound Osteoporosis Center — Burien
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 379 participants |
| Start Date | 2024-10-31 |
| Est. Completion | 2028-03 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06577935
The ClinicalTrials.gov registry entry for NCT06577935 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 379 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Angitia Biopharmaceuticals, which has 1 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 Postmenopausal Osteoporosis appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT06577935 reports 20 study locations spanning 7 distinct geographic areas — top geographies include Other, Argentina, Alabama. 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 NCT06577935 about?
NCT06577935 is a clinical study titled "A Trial Evaluating Efficacy of AGA2118 in PostMenopausal Women wIth Low Bone MasS (ARTEMIS)". The primary objective of this study is to determine the effect of treatment with AGA2118 versus placebo at Month 12 on lumbar spine bone mineral density (BMD) in postmenopausal women with low bone mass.
What is the current status of trial NCT06577935?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 379 participants. The study started on 2024-10-31. Estimated completion is 2028-03.
What conditions does trial NCT06577935 study?
This clinical trial studies the following conditions: Postmenopausal 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 NCT06577935?
The interventions under investigation include: Placebo (OTHER), AGA2118 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06577935?
This trial is sponsored by Angitia Biopharmaceuticals, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06577935 being conducted?
This trial has 20 study locations across Alabama, Georgia, New Mexico, Pennsylvania, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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