Advanced Solid Tumors Clinical Trials in Houston, Texas
34 studies are recruiting for advanced solid tumors in Houston, Texas 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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A Study to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of VVD-133214 as Monotherapy and in Combination in Participants With Advanced Solid Tumors
This is a first-in-human, Phase I, open-label, multicenter, dose-escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of VVD-133214 monotherapy, and in combination with bevacizumab or pembrolizumab, in part…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 47 in total
- Run by
- Vividion Therapeutics, Inc.
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First-in-Human Study of ATX-295, an Oral Inhibitor of KIF18A, in Patients With Advanced or Metastatic Solid Tumors, Including Ovarian Cancer
The goal of this study is to identify a safe and tolerated dose of the orally administered KIF18A inhibitor ATX-295. In addition, this study will evaluate the pharmacokinetics, pharmacodynamics and preliminary antitumor activity of ATX-295 in patients with advanced solid tumors and ovarian cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 9 in total
- Run by
- Accent Therapeutics
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A Study of BG-C477 in Participants With Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of BG-C477 alone and in combination with anticancer agents in participants with selected advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas Md Anderson Cancer Center, Houston, Texas
- Locations
- 59 in total
- Run by
- BeOne Medicines
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A Study to Evaluate the Safety and Efficacy of MK-3120 in Participants With Advanced Solid Tumors (MK-3120-002)
Researchers are looking for new ways to treat people with certain advanced solid tumors. Advanced means the cancer has spread to other parts of the body and cannot be removed with surgery. Solid tumors are cancers mostly in body organs and tissues, not in the blood or other body liquids. The main g…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology ( Site 1011), Houston, Texas
- Locations
- 49 in total
- Run by
- Merck Sharp & Dohme LLC
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A Study of PARG Inhibitor FORX-428 in Patients With Advanced Solid Tumors.
The goal of this interventional study is to evaluate the safety and tolerability of escalating doses of FORX-428 as monotherapy in patients with select advanced solid tumors with BRCA1/2 mutations or other DDR deficiencies or high replication stress, and to determine the maximum tolerated dose (MTD…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas - MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- FoRx Therapeutics AG
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A Study to Learn More About How Well Treatment With Sevabertinib (BAY 2927088) Tablets Works and How Safe it is in Participants Who Have a Solid Tumor With Mutations of the Human Epidermal Growth Factor Receptor 2 (HER2)
Researchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works. In this trial, the researchers want to learn how wel…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center - Texas Medical Center, Houston, Texas
- Locations
- 54 in total
- Run by
- Bayer
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Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors
The primary objective of this study is to determine the recommended Phase 2 doses (RP2D(s)) and maximum tolerated dose (MTD) of PYX-201 in combination with pembrolizumab for participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas - M.D. Anderson Cancer Center, Houston, Texas
- Locations
- 22 in total
- Run by
- Pyxis Oncology, Inc
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TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer
The purpose of the study is to learn from the real world practice of prescribing targeted therapies to patients with advanced cancer whose tumor harbors a genomic variant known to be a drug target or to predict sensitivity to a drug. NOTE: Due to character limits, the arms section does NOT include …
- Stage
- Phase 2
- Ages
- 12 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 181 in total
- Run by
- American Society of Clinical Oncology
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Study of GS-0201 Alone and in Combination in Participants With Advanced Solid Tumors
The main goal of this first in human (FIH) study is to learn about the safety and dosing of GS-0201 when given alone or in combination with sacituzumab govitecan (SG) in participants with advanced solid tumors. The primary objectives of this study are to: * To assess the safety and tolerability of …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- Gilead Sciences
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Safety,Tolerability, Pharmacokinetics, and Efficacy of YL211 in Patients With Advanced Solid Tumors
This is a multicenter, open-label, Phase 1 study. The study will enroll subjects with advanced solid tumors. It consists of six parts. Objectives for Dose-Escalation Parts (Part 1 and Part 4) To evaluate the safety and tolerability of YL211 as monotherapy in patients with selected advanced solid tu…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas - MD Anderson Cancer Center, Houston, Texas
- Locations
- 21 in total
- Run by
- MediLink Therapeutics (Suzhou) Co., Ltd.
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A Study of PHST001 in Advanced Solid Tumors
This is a multi-center, first-in-human (FIH), open-label, Phase 1a/1b dose escalation and dose expansion study to assess the safety, PK, pharmacodynamics, and antitumor activity of PHST001 monotherapy (Phase 1a) or in combination with chemotherapy (Phase 1b) in adult participants with advanced rela…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 20 in total
- Run by
- Pheast Therapeutics
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A Study of a Selective T Cell Receptor (TCR) Targeting, Bifunctional Antibody-fusion Molecule STAR0602 in Participants With Advanced Solid Tumors
This is an open label, multicenter, phase 1/2 study to assess the safety/tolerability and preliminary clinical activity of STAR0602 as a single agent and in combination with chemotherapy administered intravenously in participants with advanced solid tumors that are antigen-rich.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas, MD Anderson Cancer Center, Houston, Texas
- Locations
- 19 in total
- Run by
- Marengo Therapeutics, Inc.
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A Study of PHN-012 in Patients With Advanced Solid Tumors
This first-in-human study will evaluate safety, tolerability, anti-tumor activity, immunogenicity, pharmacokinetics and pharmacodynamics of PHN-012, a novel antibody-drug conjugate (ADC), in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- PHN-012-001 Site, Houston, Texas
- Locations
- 26 in total
- Run by
- Pheon Therapeutics
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Study of RAS(ON) Inhibitors in Combination With Ivonescimab in Patients With Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of RAS(ON) inhibitors in combination with ivonescimab in adults with advanced or metastatic solid tumors with a RAS mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 9 in total
- Run by
- Revolution Medicines, Inc.
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A Study to Test the Safety and Tolerability of SBO-154 in Patients With Advanced Solid Tumors.
This is a Phase 1 study of SBO-154 in patients with advanced cancers who are unable to tolerate or have not previously responded to standard therapy available in the country. The study involves multiple doses and takes place at several centers.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 16 in total
- Run by
- Sun Pharma Advanced Research Company Limited
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A Study to Evaluate Claudin 18.2-Directed ADC LCB02A in Advanced Solid Tumors
This is a Phase 1/2 open label study consisting of dose escalation cohorts (Phase 1) followed by expansion cohorts (Phase 2). The Phase 1 dose escalation population includes subjects with advanced solid tumors that are refractory to standard of care therapy or for whom no standard of care options a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- LigaChem Biosciences, Inc.
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A Study to Evaluate the Safety of INCA33890 in Participants With Advanced or Metastatic Solid Tumors
To evaluate the safety, tolerability, and DLTs and determine the MTD and/or RDE(s) of INCA33890 in participants with select advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas Md Anderson Cancer Center, Houston, Texas
- Locations
- 39 in total
- Run by
- Incyte Corporation
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A Rollover Study Evaluating Sotorasib With or Without Panitumumab in Participants With KRAS p.G12C Mutation
The primary objective of the study is to evaluate the safety and tolerability of the continuation of sotorasib with or without panitumumab and/or other anti-cancer therapies in participants continuing to derive benefit in Amgen-sponsored protocols.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 11 in total
- Run by
- Amgen
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Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors
Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 15 in total
- Run by
- Ensem Therapeutics
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A Study to Learn About Study Medicine ALTA3263 in Adults With Advanced Solid Tumors With KRAS Mutations
The purpose of this study is to characterize the safety and tolerability of ALTA3263 in adults with advanced solid tumors with KRAS mutations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Houston, Texas
- Locations
- 12 in total
- Run by
- Alterome Therapeutics, Inc.
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Study of RMC-9805 in Participants With KRAS G12D-Mutant Solid Tumors
This study is to evaluate the safety and tolerability of RMC-9805 as monotherapy and in combination with RMC-6236 in adults with KRAS G12D-mutant solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas, MD Anderson Cancer Center, Houston, Texas
- Locations
- 17 in total
- Run by
- Revolution Medicines, Inc.
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A Phase 1/1B Study of ST-01156, a Small Molecule RBM39 Degrader, in Patients With Advanced Solid Malignancies
A Phase 1/1B Study of ST-01156 in Patients with Advanced Solid Malignancies
- Stage
- Phase 1
- Ages
- 16 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 6 in total
- Run by
- SEED Therapeutics, Inc.
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A TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND EFFICACY OF SHR-A1904 IN SUBJECTS WITH ADVANCED SOLID TUMORS
The study (dose escalation/expansion) is being conducted to assess the safety and tolerability of SHR-A1904 in subjects with advanced solid tumors, and to determine maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D), to assess preliminary efficacy of SHR-A1904, pharmacokinetic (PK…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 28 in total
- Run by
- Jiangsu HengRui Medicine Co., Ltd.
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Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS
Evaluate the safety and tolerability of RMC-6236 in adults with specific RAS mutant advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 21 in total
- Run by
- Revolution Medicines, Inc.
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A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors
A FIH dose escalation and dose expansion study to evaluate VVD-130037 in participants with advanced solid tumors as a single agent, and in combination with docetaxel, paclitaxel, or pembrolizumab.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MDACC, Houston, Texas
- Locations
- 26 in total
- Run by
- Vividion Therapeutics, 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.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.