Colorectal Cancer Clinical Trials in Nashville, Tennessee
32 studies are recruiting for colorectal cancer in Nashville, Tennessee 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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A Study of Bispecific Antibody MCLA-158 in Patients With Advanced Solid Tumors
This is a Phase 1/2 open-label, multi-center, multi-national study with an initial dose escalation part to determine the recommended Phase II dose (RP2D) of MCLA-158 single agent in patients with mCRC. The dose escalation part has been completed and the RP2D will be further evaluated in an expansio…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute, Nashville, Tennessee
- Locations
- 54 in total
- Run by
- Genmab
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LYL273 for Patients With Relapsed or Refractory mCRC
This is a Phase 1/2 open-label, multicenter study evaluating the safety and efficacy of LYL273 in participants with relapsed or refractory metastatic colorectal cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI Oncology Partners and Tristar Centennial Hospital, Nashville, Tennessee
- Locations
- 5 in total
- Run by
- Lyell Immunopharma, Inc.
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Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors
This is a Phase 1/2A, open label, multicenter, nonrandomized, multiple dose, safety, tolerability, pharmacokinetic and pharmacodynamic study of PF-07220060 administered as a single agent and in combination with endocrine therapy. Part 1 includes dose escalation cohorts evaluating PF-07220060 as sin…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute - Pharmacy, Nashville, Tennessee
- Locations
- 39 in total
- Run by
- Pfizer
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Beamion BCGC-1: A Study to Find a Suitable Dose of Zongertinib Used Alone and in Combination With Other Treatments to Test Whether it Helps People With Different Types of HER2+ Cancer That Has Spread
This study is open to adults aged 18 years and older with different types of HER2+ cancer that has spread and cannot be removed by surgery. People can take part in this study if their tumours show HER2 aberrations and previous treatment was not successful. The purpose of this study is to find a sui…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 104 in total
- Run by
- Boehringer Ingelheim
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Solid Tumor Analysis for HLA Loss of Heterozygosity (LOH) and Apheresis for CAR T- Cell Manufacturing
Objective: To collect information on how often a solid tumor cancer might lose the Human Leukocyte Antigen (HLA) by next generation sequencing and perform apheresis to collect and store an eligible participant's own T cells for future use to make CAR T-Cell therapy for their disease treatment. Desi…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Vanderbilt University Medical Center, Nashville, Tennessee
- Locations
- 16 in total
- Run by
- A2 Biotherapeutics Inc.
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A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Colorectal Cancer
This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute Oncology Partners, Nashville, Tennessee
- Locations
- 30 in total
- Run by
- Verastem, Inc.
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A Phase 1/2 Study of VS-7375 in Patients With KRAS G12D-Mutated Solid Tumors
This study will assess the safety and efficacy of VS-7375 alone and in combination in patients with advanced solid tumors harboring a KRAS G12D-mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 20 in total
- Run by
- Verastem, Inc.
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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
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 55 in total
- Run by
- Vividion Therapeutics, Inc.
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A Randomized Phase 2 Trial of Fruquintinib and TAS-102 as Compared to Fruquintinib in Patients With Refractory Advanced/Metastatic Colorectal Cancer
A Randomized Phase 2 Trial of Fruquintinib and TAS-102 as Compared to Fruquintinib in Patients with Refractory Advanced/Metastatic Microsatellite Stable Colorectal Cancer
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Vanderbilt University Medical Center, Nashville, Tennessee
- Locations
- 13 in total
- Run by
- Criterium, Inc.
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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
- Sarah Canon Research Institute (SCRI) Oncology Partners, Nashville, Tennessee
- Locations
- 49 in total
- Run by
- Institut de Recherches Internationales Servier
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A Study to Assess Adverse Events and Change in Disease Activity in Adult Participants Receiving Intravenously Infused Telisotuzumab Adizutecan Alone or With Standard of Care in Participants With Post Adjuvant Circulating Tumor DNA Positive Colorectal Cancer and No Radiographic Evidence of Disease
Colorectal cancer (CRC) is the third most common type of cancer diagnosed worldwide. The purpose of this study is to assess change in disease activity when telisotuzumab adizutecan is given alone compared to standard of care (SOC) given alone. Telisotuzumab adizutecan is an investigational drug bei…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- SCRI Oncology Partners /ID# 274522, Nashville, Tennessee
- Locations
- 48 in total
- Run by
- AbbVie
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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
- Sarah Cannon Research Institute, Nashville, Tennessee
- Locations
- 33 in total
- Run by
- Parabilis Medicines, Inc.
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Study of Safety and Tolerability of BCA101 Monotherapy and in Combination Therapy in Patients With EGFR-driven Advanced Solid Tumors
The investigational drug to be studied in this protocol, BCA101, is a first-in-class compound that targets both EGFR with TGFβ. Based on preclinical data, this bifunctional antibody may exert synergistic activity in patients with EGFR-driven tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Vanderbilt University Medical Center, Nashville, Tennessee
- Locations
- 21 in total
- Run by
- Bicara Therapeutics
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A Phase 1 Study Evaluating DISP-10 in Participants With Advanced Gastrointestinal Cancers
This is a Phase 1, multicenter, open-label study of DISP-10, a combination therapy consisting of DV-10 (adenovirus) and idecabtagene vicleucel (ide-cel, BCMA-directed chimeric antigen receptor [CAR] T), in adult participants with advanced gastrointestinal (GI) cancers. The study will consist of 2 p…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Tennessee Oncology, Nashville, Tennessee
- Locations
- 7 in total
- Run by
- Dispatch Biotherapeutics
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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
- Sarah Cannon Research Institute, Nashville, Tennessee
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
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Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain Metastasis
This multi-site, Phase 1/2 clinical trial is an open-label study to identify the safety, pharmacokinetics, and efficacy of a repeated dose regimen of NEO212 alone for the treatment of patients with radiographically-confirmed progression of Astrocytoma IDH- mutant, Glioblastoma IDH-wildtype, and the…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Vanderbilt University Medical Center, Nashville, Tennessee
- Locations
- 8 in total
- Run by
- Neonc Technologies, Inc.
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Study of Dato-DXd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03)
TROPION-PanTumor03 will investigate the safety, tolerability, and anti-tumour activity of Datopotamab Deruxtecan (Dato-DXd) as Monotherapy and in Combination with Anticancer Agents in Patients with Advanced/Metastatic Solid Tumours.
- Stage
- Phase 2
- Ages
- 18 to 130
- Site
- Research Site, Nashville, Tennessee
- Locations
- 96 in total
- Run by
- AstraZeneca
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Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Participants With Advanced KRAS G12C Mutant Solid Tumors
This study is to evaluate the safety, tolerability, and PK profiles of Elironrasib and Daraxonrasib as monotherapies and combination therapy in patients with KRAS G12C-mutated solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institue, Nashville, Tennessee
- Locations
- 56 in total
- Run by
- Revolution Medicines, Inc.
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Study of RAS(ON) Inhibitors in Patients With Gastrointestinal Solid Tumors
The purpose of this platform study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of novel RAS(ON) inhibitors combined with Standard(s) of Care (SOC) or with novel agents. The current subprotocols include the following: Subprotocol A: RMC-6236 + 5…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 32 in total
- Run by
- Revolution Medicines, Inc.
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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
- Sarah Cannon Research Center, Nashville, Tennessee
- Locations
- 7 in total
- Run by
- Angiex, Inc.
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A Study of MRG007 (ARR-217) in Patients With Advanced Solid Tumors
This is an open-label, multi-center, phase I study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of MRG007 (ARR-217) in patients with unresectable locally advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute, Nashville, Tennessee
- Locations
- 21 in total
- Run by
- ArriVent BioPharma, Inc.
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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
- Sarah Cannon Research Institute Oncology Partners (SCRI-Nashville), Nashville, Tennessee
- Locations
- 19 in total
- Run by
- Marengo Therapeutics, Inc.
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A Phase 2 Study of Zanidatamab in Patients With HER2-expressing Tumors
The purpose of this study is to evaluate the efficacy and safety of zanidatamab for the treatment of participants with previously treated solid tumors that have Human Epidermal Growth Factor Receptor 2 (HER2) Immunohistochemistry (IHC) 3+ overexpression.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 28 in total
- Run by
- Jazz Pharmaceuticals
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A Trial to Evaluate the Safety and Activity of Fruquintinib in Minority Populations With Advanced, Previously Treated Colorectal Cancer
High blood pressure (hypertension) is a known side effect of the treatment with fruquintinib. Current research does not provide a clear answer whether minority groups such as Black/African American and/or Hispanic/Latino with refractory metastatic colorectal cancer (mCRC) have a bigger risk of high…
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- Vanderbilt University Medical Center, Nashville, Tennessee
- Locations
- 45 in total
- Run by
- Takeda
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A Study of IDE034 in Adult Participants With Locally Advanced/Metastatic Solid Tumors Types
This is a Phase 1a/1b, open-label, multicenter dose escalation and dose expansion clinical study to evaluate the safety, PK, immunogenicity and preliminary efficacy of IDE034 in participants with locally advanced/metastatic solid tumor types that express B7-H3 and PTK7.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI Oncology Partners, Nashville, Tennessee
- Locations
- 15 in total
- Run by
- IDEAYA Biosciences
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.