{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?sponsor=FHI+360", "query": { "sponsor": "FHI 360" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 14, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?sponsor=FHI+360&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-30T11:01:58.385Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT01722552", "title": "China Adherence Through Technology Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Medication Adherence" ], "interventions": [ { "name": "adherence feedback", "type": "BEHAVIORAL" }, { "name": "standard of care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Boston University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2012-11", "completion_date": "2014-04", "has_results": true, "last_update_posted_date": "2017-04-21", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01722552" }, { "nct_id": "NCT01143207", "title": "PK of Depo SubQ Injected in the Upper Arm", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Contraception" ], "interventions": [ { "name": "Medroxyprogesterone acetate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "FHI 360", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 26, "start_date": "2010-05", "completion_date": "2012-10", "has_results": true, "last_update_posted_date": "2013-08-19", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Norfolk, Virginia", "locations": [ { "city": "Norfolk", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01143207" }, { "nct_id": "NCT02817464", "title": "Study to Evaluate Suppression of Ovulation and Pharmacokinetics of Medroxyprogesterone Acetate Following Administration of TV-46046 in Women With Ovulatory Cycle", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Pregnancy", "Contraception" ], "interventions": [ { "name": "TV-46046 - 400 mg/mL", "type": "DRUG" }, { "name": "TV-46046 - 200 mg/mL", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Teva Branded Pharmaceutical Products R&D, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 12, "start_date": "2016-10-26", "completion_date": "2018-12-03", "has_results": true, "last_update_posted_date": "2024-02-12", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 2, "location_summary": "Philadelphia, Pennsylvania • Norfolk, Virginia", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Norfolk", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02817464" }, { "nct_id": "NCT04125368", "title": "A Feasibility Study of Integrating Maternal Nutrition Interventions Into Antenatal Care Services in Ethiopia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Maternal Dietary Diversity", "Iron-Folic Acid Supplementation", "Early Initiation of Breastfeeding" ], "interventions": [ { "name": "Health Facility Interventions", "type": "BEHAVIORAL" }, { "name": "Community Interventions", "type": "BEHAVIORAL" }, { "name": "Health System Interventions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "International Food Policy Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": "49 Years", "sex": "FEMALE", "summary": "15 Years to 49 Years · Female only" }, "enrollment_count": 4256, "start_date": "2019-10-08", "completion_date": "2021-09-04", "has_results": false, "last_update_posted_date": "2022-03-10", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04125368" }, { "nct_id": "NCT04121559", "title": "A Feasibility Study of Delivering Adolescent Nutrition Interventions Through School-Based Platforms in Ethiopia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dietary Diversity" ], "interventions": [ { "name": "School Interventions", "type": "BEHAVIORAL" }, { "name": "Community Interventions", "type": "BEHAVIORAL" }, { "name": "School System Interventions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "International Food Policy Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "10 Years", "maximum_age": "14 Years", "sex": "FEMALE", "summary": "10 Years to 14 Years · Female only" }, "enrollment_count": 1712, "start_date": "2019-10-08", "completion_date": "2021-04-29", "has_results": false, "last_update_posted_date": "2022-03-10", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04121559" }, { "nct_id": "NCT01299116", "title": "Long-Acting Reversible Contraception", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Contraception" ], "interventions": [ { "name": "DMPA", "type": "DRUG" }, { "name": "oral contraceptives", "type": "DRUG" }, { "name": "Implanon®", "type": "DRUG" }, { "name": "ParaGard®", "type": "DRUG" }, { "name": "Mirena®", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "FHI 360", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "29 Years", "sex": "FEMALE", "summary": "18 Years to 29 Years · Female only" }, "enrollment_count": 916, "start_date": "2011-12", "completion_date": "2016-12", "has_results": true, "last_update_posted_date": "2018-02-28", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01299116" }, { "nct_id": "NCT01047540", "title": "Safety and Efficacy Study for a New Antiviral Drug to Treat Genital Herpes Type 2", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "HSV-2" ], "interventions": [ { "name": "AIC316", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "AiCuris Anti-infective Cures AG", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 156, "start_date": "2010-03", "completion_date": "2011-03", "has_results": true, "last_update_posted_date": "2023-04-21", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 6, "location_summary": "Miami, Florida • Indianapolis, Indiana • Portland, Oregon + 3 more", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Portland", "state": "Oregon" }, { "city": "Houston", "state": "Texas" }, { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT01047540" }, { "nct_id": "NCT02456584", "title": "Pharmacodynamics and Pharmacokinetics Study of Existing DMPA Contraceptive Methods", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Contraception" ], "interventions": [ { "name": "DMPA 150", "type": "DRUG" }, { "name": "DMPA 300", "type": "DRUG" }, { "name": "DMPA 104", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "FHI 360", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 42, "start_date": "2015-09", "completion_date": "2018-08-30", "has_results": false, "last_update_posted_date": "2018-10-18", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT02456584" }, { "nct_id": "NCT04155437", "title": "Assessing the Feasibility of Integrating a Package of Maternal Nutrition Interventions Into Antenatal Care Services in Burkina Faso", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Maternal Dietary Diversity", "Iron-Folic Acid Supplementation", "Early Initiation of Breastfeeding" ], "interventions": [ { "name": "Health Facility Level Interventions", "type": "BEHAVIORAL" }, { "name": "Community Level Interventions", "type": "BEHAVIORAL" }, { "name": "Health System Level Interventions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "International Food Policy Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": "49 Years", "sex": "FEMALE", "summary": "15 Years to 49 Years · Female only" }, "enrollment_count": 8110, "start_date": "2019-11-06", "completion_date": "2021-03-05", "has_results": false, "last_update_posted_date": "2022-03-10", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04155437" }, { "nct_id": "NCT04682353", "title": "A Study to Evaluate the Pharmacokinetics (PK) of Medroxyprogesterone Acetate Following an Injection of TV-46046 in Healthy Women of Reproductive Age", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Contraception" ], "interventions": [ { "name": "TV-46046", "type": "DRUG" }, { "name": "Depo-subQ Provera", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Teva Branded Pharmaceutical Products R&D, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 60, "start_date": "2020-12-14", "completion_date": "2023-01-12", "has_results": true, "last_update_posted_date": "2024-02-26", "last_synced_at": "2026-09-30T11:01:58.385Z", "location_count": 2, "location_summary": "Cypress, California • San Antonio, Texas", "locations": [ { "city": "Cypress", "state": "California" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04682353" } ] }