- Conditions
- Adamantinomatous Craniopharyngioma, Cancer, Colorectal Cancer, Desmoid, Endometrial Carcinoma, Familial Adenomatous Polyposis (FAP), HCC, Locally Advanced Solid Tumor, Metastatic Cancer, Metastatic Castration-resistant Prostate Cancer, Microsatellite Instability-High Colorectal Cancer, Microsatellite Stable Colorectal Cancer, Prostate Cancer, Solid Tumor, WNT Pathway
- Interventions
- Bevacizumab, FOG-001, Nivolumab, Trifluridine/tipiracil, mFOLFOX-6
- Drug
- Lead sponsor
- Parabilis Medicines, Inc.
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 619 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2023 – 2027
- U.S. locations
- 31
- States / cities
- Phoenix, Arizona • Scottsdale, Arizona • Tucson, Arizona + 25 more
Institution Directory
Clinical trials at UCLA Health
Sites in Los Angeles, CA
Institution pages show live ClinicalTrials.gov records that list this campus as a study site, whoever sponsors them. They do not rate, rank, or describe the institution.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official matching trials
1095
Shown on this page
12
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Recently updated
Campus scope
UCLA Health, Los Angeles, CA
Additional filters apply within this campus.
The live registry is temporarily unavailable. These stored records may be incomplete or out of date. Check the official record for current status and contact information.
Showing 133–144 of 1,095 matching trials with a site at UCLA Health, Los Angeles, CA.
Indexed local directory records.
Stored official records
A Trial to Learn How Well Linvoseltamab Works Compared to the Combination of Elotuzumab, Pomalidomide and Dexamethasone for Adult Participants With Relapsed/Refractory Multiple Myeloma
NCT05730036
Status at this site: Active, not recruiting
- Conditions
- Relapsed Refractory Multiple Myeloma (RRMM)
- Interventions
- Dexamethasone, Elotuzumab, Linvoseltamab, Pomalidomide
- Drug
- Lead sponsor
- Regeneron Pharmaceuticals
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 410 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2023 – 2033
- U.S. locations
- 10
- States / cities
- Los Angeles, California • Gainesville, Florida • Lexington, Kentucky + 7 more
Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001)
NCT05579366
Status at this site: Recruiting
- Conditions
- Breast Adenocarcinoma, Cervical Cancer, Endometrial Cancer, Epidermal Growth Factor Receptor (EGFR)-Mutated Non-Small Cell Lung Cancer (NSCLC), Fallopian Tube Cancer, High Grade Epithelial Ovarian Cancer, High Grade Serous Ovarian Cancer, Hormone Receptor-positive/Her2 Negative Breast Cancer, Mesothelioma, Non-small Cell Lung Cancer, Platinum Sensitive Ovarian Cancer (PSOC), Platinum-resistant Ovarian Cancer (PROC), Primary Peritoneal Carcinoma, Primary Refractory Ovarian Cancer, Triple Negative Breast Cancer, Uterine Cancer
- Interventions
- Bevacizumab, Carboplatin, Erythromycin, Itraconazole, Pembrolizumab, Rina-S
- Drug
- Lead sponsor
- Genmab
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 952 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2022 – 2027
- U.S. locations
- 37
- States / cities
- Phoenix, Arizona • Tucson, Arizona • Los Angeles, California + 32 more
Metabolic Mechanisms Induced by Enteral DHA and ARA Supplementation in Preterm Infants
NCT05380401
Status at this site: Recruiting
- Conditions
- Premature
- Interventions
- Enfamil® DHA & ARA Supplement for Special Dietary Use
- Dietary Supplement
- Lead sponsor
- The University of Texas Health Science Center at San Antonio
- Other
- Eligibility
- Up to 36 Weeks
- Enrollment
- 328 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2023 – 2028
- U.S. locations
- 7
- States / cities
- Los Angeles, California • New Haven, Connecticut • Chicago, Illinois + 2 more
- Conditions
- Esophageal Squamous Cell Carcinoma
- Interventions
- Acetaminophen (or equivalent), Antihistamine, Dexamethasone (or equivalent), H2 Receptor Antagonist, Irinotecan, Lenvatinib, MK-4830, Paclitaxel, Pembrolizumab, Sacituzumab tirumotecan, Steroid Mouthwash (dexamethasone or equivalent), Supportive care measures
- Drug · Biological
- Lead sponsor
- Merck Sharp & Dohme LLC
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 230 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2023 – 2029
- U.S. locations
- 5
- States / cities
- Tucson, Arizona • Los Angeles, California • East Syracuse, New York + 2 more
- Conditions
- Multiple Myeloma
- Interventions
- Lenalidomide, Teclistamab
- Drug
- Lead sponsor
- European Myeloma Network B.V.
- Network
- Eligibility
- 18 Years and older
- Enrollment
- 1,594 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2022 – 2032
- U.S. locations
- 42
- States / cities
- Phoenix, Arizona • Los Angeles, California • Sacramento, California + 34 more
(HARBOR) Study to Evaluate Efficacy and Safety of BLU-263 Versus Placebo in Patients With Indolent Systemic Mastocytosis
NCT04910685
Status at this site: Recruiting
- Conditions
- Indolent Systemic Mastocytosis, Smoldering Systemic Mastocytosis
- Interventions
- Elenestinib, Placebo
- Drug
- Lead sponsor
- Blueprint Medicines Corporation
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 534 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2021 – 2032
- U.S. locations
- 15
- States / cities
- Birmingham, Alabama • La Jolla, California • Los Angeles, California + 12 more
ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration (ALLFTD)
NCT04363684
Status at this site: Recruiting
- Conditions
- Amyotrophic Lateral Sclerosis, Behavioral Variant Frontotemporal Dementia (bvFTD), C9orf72, Corticobasal Degeneration (CBD), FTD With Amyotrophic Lateral Sclerosis (FTD/ALS), Frontotemporal Lobar Degeneration (FTLD), GRN Related Frontotemporal Dementia, MAPT Gene Mutation, Nonfluent Variant Primary Progressive Aphasia (nfvPPA), Oligosymptomatic PSP (oPSP), Oligosymptomatic Progressive Supranuclear Palsy, Progressive Supranuclear Palsy (PSP), Semantic Variant Primary Progressive Aphasia (svPPA), TBK1 Gene Mutation
- Interventions
- Not listed
- Lead sponsor
- Mayo Clinic
- Other
- Eligibility
- 18 Years and older
- Enrollment
- 2,100 participants
- Healthy volunteers
- Accepts healthy volunteers
- Timeline
- 2020 – 2030
- U.S. locations
- 24
- States / cities
- Birmingham, Alabama • Los Angeles, California • San Diego, California + 20 more
A Study of LY4584180 in Adult Participants With Previously Treated Blood Cancers
NCT07226843
Status at this site: Recruiting
- Conditions
- Follicular Lymphoma, Lymphoma, Diffuse Large B-Cell, Lymphoma, Non-Hodgkin's
- Interventions
- LY4584180, Rituximab
- Drug
- Lead sponsor
- Eli Lilly and Company
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 460 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2026 – 2030
- U.S. locations
- 21
- States / cities
- Scottsdale, Arizona • Duarte, California • Los Angeles, California + 16 more
A Long Term Extension Study to Evaluate the Safety and Efficacy of Afimkibart (RO7790121) in Participants With Atopic Dermatitis
NCT07223697
Status at this site: Active, not recruiting
- Conditions
- Atopic Dermatitis
- Interventions
- Afimkibart
- Drug
- Lead sponsor
- Hoffmann-La Roche
- Industry
- Eligibility
- 18 Years and older
- Enrollment
- 120 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2026 – 2033
- U.S. locations
- 7
- States / cities
- Los Angeles, California • Tampa, Florida • Alpharetta, Georgia + 3 more
A Study to Evaluate the Efficacy and Safety of Intravenous (IV) Prasinezumab in Participants With Early-Stage Parkinson's Disease
NCT07174310
Status at this site: Recruiting
- Conditions
- Parkinson's Disease
- Interventions
- Placebo, Prasinezumab
- Drug
- Lead sponsor
- Hoffmann-La Roche
- Industry
- Eligibility
- 50 Years to 85 Years
- Enrollment
- 900 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2025 – 2031
- U.S. locations
- 53
- States / cities
- Birmingham, Alabama • Phoenix, Arizona • Fullerton, California + 47 more
A Study to Assess Sulbactam-durlobactam in Pediatric Patients With Acinetobacter Baumannii-calcoaceticus Complex Infection
NCT06801223
Status at this site: Recruiting
- Conditions
- Acinetobacter Baumannii-calcoaceticus Complex Infection (ABC)
- Interventions
- Sulbactam 20mg/kg-Durlobactam 20mg/kg (Every 12 hours), Sulbactam 20mg/kg-Durlobactam 20mg/kg (Every 8 hours), Sulbactam 25mg/kg -Durlobactam 25mg/kg (Every 6 hours), Sulbactam 25mg/kg -Durlobactam 25mg/kg (Every 8 hours)
- Drug
- Lead sponsor
- Innoviva Specialty Therapeutics
- Industry
- Eligibility
- 1 Day to 18 Years
- Enrollment
- 48 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2026 – 2028
- U.S. locations
- 4
- States / cities
- Los Angeles, California • San Diego, California • Greenville, North Carolina + 1 more
About this UCLA Health institution page
- What this page lists
- ClinicalTrials.gov records that list UCLA Health in Los Angeles, CA as a study site, whoever sponsors them, among recruiting, not yet recruiting, and active not recruiting trials.
- Site status
- A study's overall status can differ from this site's status. Sites marked withdrawn, terminated, or completed are not counted here. Each record shows the status listed for this site when the official record provides one.
- Where the data comes from
- Records are sourced from the official ClinicalTrials.gov public API. Each result links back to the official study page, which is the source of truth for eligibility, enrollment, and contact information.
- What this page does not do
- No medical advice, eligibility judgments, ranking of trials, or AI-generated medical summaries. This page does not rank or rate institutions.
Related: all institution pages, browse by condition, or browse by U.S. city.