Advanced Solid Tumor Clinical Trials in Los Angeles, California
20 studies are recruiting for advanced solid tumor in Los Angeles, California right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Phase 1a/1b First-in-Human Study of BG-C9074 Alone and in Combination With Other Anticancer Therapies in Patients With Advanced Solid Tumors
This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with other anticancer therapies in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Usc Norris Comprehensive Cancer Center (Nccc), Los Angeles, California
- Locations
- 37 in total
- Run by
- BeOne Medicines
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The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- UCLA Jonsson Comprehensive Cancer Center, Los Angeles, California
- Locations
- 77 in total
- Run by
- PMV Pharmaceuticals, Inc
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A Study Investigating BGB-26808 Alone or in Combination With Tislelizumab in Participants With Advanced Solid Tumors
This is an open-label, multicenter, and nonrandomized dose escalation and dose expansion study to evaluate BGB-26808 as monotherapy or in combination with tislelizumab in participants with advanced solid tumors. The main purpose of this study is to explore the recommended dosing for BGB-26808.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Southern California Norris Comprehensive, Los Angeles, California
- Locations
- 28 in total
- Run by
- BeOne Medicines
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An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
This is an open-label, multicenter, first-in-human dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of BGB-58067 alone, in combination with BG-89894 (discontinued), and in combination with standard …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Usc Norris Comprehensive Cancer Center (Nccc), Los Angeles, California
- Locations
- 101 in total
- Run by
- BeOne Medicines
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A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA Department of Medicine-Hematology/Oncology, Los Angeles, California
- Locations
- 39 in total
- Run by
- Eli Lilly and Company
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A Study of IDP-001 in Advanced or Metastatic Solid Tumors
This clinical study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of IDP-001 in participants with advanced or metastatic squamous and non-squamous NSCLC and other squamous cell solid tumors (for example, head and neck, esophageal, cervical, cutan…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Los Angeles, Los Angeles, California
- Locations
- 6 in total
- Run by
- InduPro, Inc.
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SW-682 in Advanced Solid Tumors
This is a first-in-human (FIH), Phase 1a/1b open-label, multicenter, dose escalation and dose expansion study of SW-682 in adult participants with metastatic or unresectable advanced solid tumors with or without Hippo pathway alterations that are refractory to, or have progressed, during or after a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC Norris Comprehensive Cancer Center and Hospital, Los Angeles, California
- Locations
- 8 in total
- Run by
- SpringWorks Therapeutics, Inc., a healthcare company of Merck KGaA, Darmstadt, Germany
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Study of Lunresertib Alone or in Combination With RP-3500 or Debio 0123 in Patients With Advanced Solid Tumors
The primary purpose of this study is to assess the safety and tolerability of lunresertib alone and in combination with RP-3500 or in combination with Debio 0123 in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- # 1019, UCLA, Westwood Cancer Center, Los Angeles, California
- Locations
- 26 in total
- Run by
- Debiopharm International SA
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A Study of MGC026 in Participants With Advanced Solid Tumors
The study is designed to understand the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of MGC026 in participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors The study has a dose escalation portion and a cohort ex…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Angeles Clinic and Research Institute, Los Angeles, California
- Locations
- 12 in total
- Run by
- MacroGenics
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Study of STK-012 Alone and With Other Treatments in Patients With Advanced Lung Cancer and Other Cancers
This is a phase 1/2, multicenter, open-label study. The phase 1 portion is a dose escalation and expansion study of STK-012 as monotherapy and in combination therapy in patients with selected advanced solid tumors. The phase 2 portion is a randomized study of STK-012 in combination with standard of…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars Sinai, Los Angeles, California
- Locations
- 47 in total
- Run by
- Synthekine
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A First-in-Human (FIH) Study of BG-C137, an Anti-Fibroblast Growth Factor Receptor 2b (FGFR2b) Antibody Drug Conjugate, in Participants With Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C137 alone and in combination with anticancer agents in participants with advanced solid tumors. The study will be conducted in two phases: Phase 1a (…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Usc Norris Comprehensive Cancer Center (Nccc), Los Angeles, California
- Locations
- 52 in total
- Run by
- BeOne Medicines
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A Study of PYX-201 in Advanced Solid Tumors
The primary objectives of this study are to determine the recommended dose(s) of PYX-201 for participants with recurrent/metastatic (R/M) solid tumors, and to determine the objective response rate (ORR) in participants treated with PYX-201 as a single agent.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Ronald Reagan UCLA Medical Center, Los Angeles, California
- Locations
- 29 in total
- Run by
- Pyxis Oncology, Inc
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Study of Ifinatamab Deruxtecan (DS-7300a, I-DXd) in Participants With Advanced Solid Malignant Tumors
This is a single group study of participants with advanced solid tumors who have not been cured by other treatments. It is the first time the drug will be used in humans, and will be in two parts. The primary purpose of the parts are: * Dose Escalation Part: To evaluate the safety and tolerability …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars-Sinai Medical Center- Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California
- Locations
- 28 in total
- Run by
- Daiichi Sankyo
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A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
The goal of the Dose Escalation phase of the study is to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary anti-tumor activity to determine the preliminary recommended dose for expansion (RDE) of NKT3964 in adults with advanced or metastatic solid tumors. The goal of the Expa…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California - Los Angeles, Los Angeles, California
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, Inc.
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First in Human Study of TORL-1-23 in Participants With Advanced Cancer
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-1-23 in patients with advanced cancer
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA - JCCC Clinical Research Unit, Los Angeles, California
- Locations
- 14 in total
- Run by
- TORL Biotherapeutics, LLC
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A Study of CLSP-1025 in Adult Patients With Solid Tumors That Harbor the p53 R175H Mutation
Phase 1 dose escalation and expansion study of CLSP-1025, a first-in-class HLA-A*02:01 specific T cell engager (TCE) targeting solid tumors that harbor the p53 R175H mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC - Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 21 in total
- Run by
- Clasp Therapeutics, Inc.
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A Phase I/II Study of VLS-1488 in Subjects With Advanced Cancer
This is a first-in-human phase I/II study to examine the safety, tolerability and preliminary efficacy of VLS-1488 in subjects with advanced cancers.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Southern California, Los Angeles, California
- Locations
- 14 in total
- Run by
- Volastra Therapeutics, Inc.
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A Study of LM-24C5 For Advanced Solid Tumors
To assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-24C5 in subjects with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Southern California (USC) - Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 6 in total
- Run by
- LaNova Medicines Limited
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A Phase 1, First in Human Study of TORL-4-500 in Patients With Advanced Cancer
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-4-500 in patients with advanced cancer. For Part 1, any advanced or metastatic solid tumor malignancy will be evaluated including, for example, adrenocortical carcinoma (ACC).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA - JCCC Clinical Research Unit, Los Angeles, California
- Locations
- 10 in total
- Run by
- TORL Biotherapeutics, LLC
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This is a Study to Evaluate the Safety and Tolerability of ABL503, and to Determine the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D) of ABL503 in Subjects with Any Progressive Locally Advanced or Metastatic Solid Tumors
This is a first-in-human Phase 1, single-arm, open-label, multicenter, multiple-dose, dose-escalation and dose-expansion study of ABL503 to evaluate the safety, tolerability, MTD and/or RP2D, PK, immunogenicity, preliminary antitumor activity, and the PD effect of ABL503 in subjects with any progre…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC, Los Angeles, California
- Locations
- 8 in total
- Run by
- ABL Bio, Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
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