Solid Tumor Clinical Trials in Los Angeles, California
18 studies are recruiting for 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.
Search these by distance from you
Studies now recruiting
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Phase 1/2 Trial of S241656 in Selected RAS/MAPK Mutation- Positive Malignancies
BDTX-4933-101 is a first-in-human, open-label, Phase 1/2 dose escalation, dose optimization and expansion study designed to evaluate the safety and tolerability of S241656 as monotherapy and in combination with other anti-cancer therapies in participants with selected advanced malignancies. The stu…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Angeles clinic - A cedars SINAI AFFILIATE, Los Angeles, California
- Locations
- 49 in total
- Run by
- Institut de Recherches Internationales Servier
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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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A Study to Evaluate Safety, Tolerability and Preliminary Activity of AGX101 in Participants With Advanced Solid Tumors
AGX101 is an antibody-drug conjugate (ADC) therapy for tumor-forming cancers. The purpose of this study is to learn about AGX101 effects and safety at various dose levels in an all-comers advanced solid cancer patient population. AGX101will be administered intravenously. Dosing of AGX101 will be re…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC/Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 7 in total
- Run by
- Angiex, Inc.
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FOG-001 in Locally Advanced or Metastatic Solid Tumors
The goal of this clinical trial is to determine if FOG-001 is safe and effective in participants with locally advanced or metastatic solid tumors or in participants with familial adenomatous polyposis (FAP).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, Los Angeles (UCLA), Los Angeles, California
- Locations
- 33 in total
- Run by
- Parabilis Medicines, Inc.
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Safety and Tolerability Study of GIM-531 in Advanced Solid Tumors
GIM-531 is a first-in-class, orally bioavailable small molecule that is being developed for the treatment of advanced solid tumors as a single agent and rescue therapy. GIM-531 exhibits its primary effect through selective inhibition of regulatory T-cells (Tregs).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate, Los Angeles, California
- Locations
- 11 in total
- Run by
- Georgiamune Inc
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SMP-3124LP in Adults With Advanced Solid Tumors
An Open-label, Phase I Dose Escalation and Phase 2 Dose Expansion Study to Assess Safety, Tolerability, Preliminary Antitumor Activity of SMP 3124LP in Adults with Advanced Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars Sinai Medical Center, Los Angeles, California
- Locations
- 12 in total
- Run by
- Sumitomo Pharma America, Inc.
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A Study of PT0253 in Participants With KRAS G12D Mutated Advanced Solid Tumors
The primary purpose of this study is to evaluate the safety and tolerability, determine the maximally tolerated dose (MTD) and/or recommended Phase 2 dose(s) (RP2D) of PT0253 in adult participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) G12D mutated advanced solid tumors as monothera…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Los Angeles, Los Angeles, California
- Locations
- 15 in total
- Run by
- PAQ Therapeutics, Inc.
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Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)
This is a Phase 1/2, open-label, non-randomized, 4-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX 106 administered as a single agent or in combination with the anti-PD-1 checkpoint inhibitor (CPI) pembrolizuma…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- California Research Institute, Los Angeles, California
- Locations
- 42 in total
- Run by
- Inhibrx Biosciences, Inc
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A Study of 177Lu-FAP-2286 in Advanced Solid Tumors
Fibroblast activation protein (FAP) is a cell surface protein that is highly expressed on the surface of cancer-associated fibroblasts (CAFs) present in the tumor microenvironment of most epithelial cancers, whereas limited expression of FAP is observed in normal tissues. In some cancers of mesench…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California Los Angeles (UCLA), Los Angeles, California
- Locations
- 41 in total
- Run by
- Novartis Pharmaceuticals
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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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An Extension Study for Patients Previously Enrolled in Studies With Pelabresib
The purpose of this study is to evaluate the long-term safety and the clinical benefit of pelabresib in patients with hematological and/or solid tumor indications or advanced malignancies. Additionally, participants previously enrolled in studies with pelabresib who received placebo or participants…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- University of California LA, Los Angeles, California
- Locations
- 15 in total
- Run by
- Novartis Pharmaceuticals
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Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors
The primary purpose of this study is to determine the safety, tolerability, and maximum tolerated dose (MTD) of EXS74539 (REC-4539) in participants with select solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Start Lacn, Los Angeles, California
- Locations
- 3 in total
- Run by
- Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
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A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors
The purpose of this study is to find out whether selinexor is an effective treatment for people who have a relapsed/refractory Wilms tumor, rhabdoid tumor, MPNST, BCOR-driven sarcoma, or another solid tumor that makes a higher than normal amount of XPO1 or has genetic changes that increase the acti…
- Stage
- Phase 2
- Ages
- 1 and older
- Site
- Children's Hospital of Los Angeles (Data Collection Only), Los Angeles, California
- Locations
- 16 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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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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Safety and Tolerability of TNG456 Alone and in Combination With Abemaciclib in Patients With Solid Tumors With MTAP Loss
This is a first in human study of TNG456 alone and in combination with abemaciclib in patients with advanced or metastatic solid tumors known to have an MTAP loss. The first part of the study is an open-label, dose escalation and the second part is an open label dose expansion in specific solid tum…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California Los Angeles, Los Angeles, California
- Locations
- 15 in total
- Run by
- Tango Therapeutics, Inc.
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Safety and Preliminary Efficacy of OBT076 in Recurrent/Metastatic CD205+ Solid Tumors
The purpose of this study is to evaluate OBT076, which is a drug that combines an antibody with an anti-cancer drug. This class of drugs are called Antibody-Drug Conjugates (ADC). Antibodies are normally produced in the human body by the immune system to fight infections but can be designed to targ…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars-Sinai, Los Angeles, California
- Locations
- 27 in total
- Run by
- Oxford BioTherapeutics Ltd
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First-in-human Study of CRB-601-01 to Treat Patients With Advanced Solid Tumor.
The purpose of this study is to determine the safety, blood concentrations and treatment effect of CRB-601 in combination with immunotherapy in patients who have advanced solid tumors (cancer) and have exhausted other therapeutic options.CRB-601 targets a protein called avb8 integrin which is expre…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars-Sinai Medical Center, Los Angeles, California
- Locations
- 26 in total
- Run by
- Corbus Pharmaceuticals Inc.
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Trial of DFP-14927 in Advanced Solid Tumors
This is a Phase I, open-label, single-arm, dose escalation study of DFP-14927 intravenous infusion administered to patients with refractory or relapsed solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA Department of Medicine- Hematology/Oncology, Los Angeles, California
- Locations
- 2 in total
- Run by
- Delta-Fly Pharma, 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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