{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Component+C&page=7", "query": { "intervention": "Component C", "page": 7 }, "page_size": 10 }, "pagination": { "page": 7, "page_size": 10, "total_count": 286, "total_pages": 29, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Component+C&page=8&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Component+C&page=6&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T11:26:39.947Z", "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": "NCT05214144", "title": "The In4M Study: Integrating 4 Methods to Assess Physical Function in Cancer Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Physical Function", "Cancer, Breast", "Lymphoma", "Patient Empowerment", "Patient Education", "Quality of Life" ], "interventions": [ { "name": "PRO Instruments assessment questionnaire", "type": "OTHER" }, { "name": "Baseline Survey Clinician- reported (ClinRO) ECOG", "type": "OTHER" }, { "name": "Fitbit", "type": "DEVICE" }, { "name": "Hugo Health (\"Hugo\")", "type": "OTHER" }, { "name": "6 Minute Walk Test (6MWT)", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 208, "start_date": "2022-01-27", "completion_date": "2024-10-24", "has_results": false, "last_update_posted_date": "2024-11-07", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 2, "location_summary": "New Haven, Connecticut • Rochester, Minnesota", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05214144" }, { "nct_id": "NCT06121843", "title": "A Study to Evaluate the Safety, Effectiveness and Tolerable Dose of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Multiple Myeloma" ], "interventions": [ { "name": "BMS-986393", "type": "DRUG" }, { "name": "Alnuctamab", "type": "DRUG" }, { "name": "Mezigdomide", "type": "DRUG" }, { "name": "Iberdomide", "type": "DRUG" }, { "name": "Elranatamab", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Juno Therapeutics, Inc., a Bristol-Myers Squibb Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 187, "start_date": "2024-02-22", "completion_date": "2028-08-01", "has_results": false, "last_update_posted_date": "2026-07-16", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 17, "location_summary": "Birmingham, Alabama • Phoenix, Arizona • Duarte, California + 11 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Duarte", "state": "California" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06121843" }, { "nct_id": "NCT06474715", "title": "Free Time For Wellness Pilot Effectiveness Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Inactivity" ], "interventions": [ { "name": "Arms", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 89, "start_date": "2024-05-30", "completion_date": "2025-04-01", "has_results": true, "last_update_posted_date": "2026-04-24", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 3, "location_summary": "Astoria, New York • Bayside, New York • Richmond Hill, New York", "locations": [ { "city": "Astoria", "state": "New York" }, { "city": "Bayside", "state": "New York" }, { "city": "Richmond Hill", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06474715" }, { "nct_id": "NCT07690657", "title": "Evaluating Intervention Allocation Policies for Reducing Hospital Readmissions at Michigan Medicine", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Transition of Care" ], "interventions": [ { "name": "C-HARP TOC assignment", "type": "DEVICE" }, { "name": "The LACE Index TOC assignment", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5000, "start_date": "2026-07", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-07-08", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07690657" }, { "nct_id": "NCT03283254", "title": "PREPP: Preventing Postpartum Depression", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postpartum Depression (PPD)" ], "interventions": [ { "name": "Practical Resources for Effective Postpartum Parenting (PREPP)", "type": "BEHAVIORAL" }, { "name": "Enhanced Treatment As Usual (ETAU)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 216, "start_date": "2018-02-12", "completion_date": "2024-02-28", "has_results": true, "last_update_posted_date": "2025-09-26", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03283254" }, { "nct_id": "NCT03015805", "title": "Teen Success Project", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Substance Abuse" ], "interventions": [ { "name": "Contingency Management", "type": "BEHAVIORAL" }, { "name": "Probation as Usual", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Chestnut Health Systems", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "12 Years to 18 Years" }, "enrollment_count": 310, "start_date": "2017-10-01", "completion_date": "2023-06-05", "has_results": false, "last_update_posted_date": "2025-10-21", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 14, "location_summary": "Burley, Idaho • Caldwell, Idaho • Gooding, Idaho + 11 more", "locations": [ { "city": "Burley", "state": "Idaho" }, { "city": "Caldwell", "state": "Idaho" }, { "city": "Gooding", "state": "Idaho" }, { "city": "Hailey", "state": "Idaho" }, { "city": "Jerome", "state": "Idaho" } ], "official_url": "https://clinicaltrials.gov/study/NCT03015805" }, { "nct_id": "NCT01649141", "title": "Trauma-Focused Cognitive Behavior Therapy for Youth: Effectiveness in a Community Setting", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Posttraumatic Stress Disorder" ], "interventions": [ { "name": "Trauma-Focused Cognitive Behavioral Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Delaware Division of Prevention and Behavioral Health Services", "sponsor_class": "OTHER_GOV", "healthy_volunteers": false, "eligibility": { "minimum_age": "7 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "7 Years to 17 Years" }, "enrollment_count": 110, "start_date": "2006-08", "completion_date": "2012-12", "has_results": false, "last_update_posted_date": "2012-07-25", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 1, "location_summary": "Wilmington, Delaware", "locations": [ { "city": "Wilmington", "state": "Delaware" } ], "official_url": "https://clinicaltrials.gov/study/NCT01649141" }, { "nct_id": "NCT02260661", "title": "Phase I, Dose Study to Look at the Safety and Pharmacokinetics of AZD8835 in Patients With Advanced Solid Tumours", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Advanced Solid Malignancies", "Breast Cancer - ER+, HER2 -", "Breast Cancer - ER+, HER2-, PIK3CA Gene Mutation" ], "interventions": [ { "name": "AZD8835", "type": "DRUG" }, { "name": "AZD8835 in combination with fulvestrant", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "AstraZeneca", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "130 Years", "sex": "ALL", "summary": "18 Years to 130 Years" }, "enrollment_count": 20, "start_date": "2014-11", "completion_date": "2016-07", "has_results": false, "last_update_posted_date": "2016-10-10", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 5, "location_summary": "Denver, Colorado • Greenville, South Carolina • Nashville, Tennessee + 2 more", "locations": [ { "city": "Denver", "state": "Colorado" }, { "city": "Greenville", "state": "South Carolina" }, { "city": "Nashville", "state": "Tennessee" }, { "city": "Houston", "state": "Texas" }, { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT02260661" }, { "nct_id": "NCT04891224", "title": "Use of a Digitally Enabled App With Clinical Team Interface in the Management of Depression", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Major Depressive Disorder" ], "interventions": [ { "name": "Pathway Platform mobile app", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 89, "start_date": "2021-02-19", "completion_date": "2023-01-30", "has_results": true, "last_update_posted_date": "2025-03-24", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 1, "location_summary": "Oak Lawn, Illinois", "locations": [ { "city": "Oak Lawn", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04891224" }, { "nct_id": "NCT07873944", "title": "Recovery Management Checkup Scalability and Sustainability Hybrid Experiment", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Substance Use Disorder (SUD)", "Opioid Use Disorders", "Stimulant Overdose", "Overdose Risk", "Alcohol Use Disorder" ], "interventions": [ { "name": "Recovery Management Checkups (RMC) delivered by community-based agencies (RMC adopters)", "type": "BEHAVIORAL" }, { "name": "Recovery Management Checkups (RMC) delivered by staff under the research team (RMC by research staff)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Chestnut Health Systems", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 600, "start_date": "2026-11-02", "completion_date": "2029-04-30", "has_results": false, "last_update_posted_date": "2026-10-14", "last_synced_at": "2026-10-23T11:26:39.947Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07873944" } ] }