Advanced Solid Tumors Clinical Trials in Irving, Texas
11 studies are recruiting for advanced solid tumors in Irving, 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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First in Human Study of TUB-030 in Patients With Advanced Solid Tumors
The goal of this clinical trial is to learn if the drug TUB-030 works to treat solid cancer in adults. The study will also explore the safety of TUB-030. The main questions it aims to answer are: To determine the safety and tolerability of TUB-030 To determine the maximum tolerated dose of TUB-030 …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology - Dallas, Irving, Texas
- Locations
- 20 in total
- Run by
- Tubulis GmbH
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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 1012), Irving, Texas
- Locations
- 49 in total
- Run by
- Merck Sharp & Dohme LLC
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A Phase I/II Study of CS2009 in Participants With Advanced Solid Tumors
This is a first-in-human (FIH), open-label, and multi-center Phase I/II study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of CS2009 as Monotherapy and Combination Therapy in Participants with Advanced Solid Tumors. The study is comprised of a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Dallas, Irving, Texas
- Locations
- 33 in total
- Run by
- CStone Pharmaceuticals
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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
- NEXT Dallas, Irving, 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
- NEXT Oncology - Dallas, Irving, 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
- NEXT Oncology - Dallas, Irving, Texas
- Locations
- 20 in total
- Run by
- Pheast 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
- NEXT Dallas, Irving, Texas
- Locations
- 9 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
- NEXT Dallas, Irving, Texas
- Locations
- 26 in total
- Run by
- Vividion Therapeutics, Inc.
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Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TGW101 in Participants With Advanced Solid Tumors
The primary objectives of this study are to evaluate the safety and tolerability of TGW101 and determine the recommended dosing regimen(s) for further study. The secondary objectives are to assess pharmacokinetics and preliminary antitumor activity.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Dallas, Irving, Texas
- Locations
- 7 in total
- Run by
- Tagworks Pharmaceuticals BV
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A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-159642 in Participants With Advanced Solid Tumors
A FIH study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary anti-tumor activity of VVD-159642, a rat sarcoma viral oncogene-phosphatidylinositol 3-kinase alpha (RAS-PI3Kα) inhibitor, as a single agent and in combination with either sotorasib or tr…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Dallas, Irving, Texas
- Locations
- 9 in total
- Run by
- Vividion Therapeutics, Inc.
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PAS-004 in Patients With Advanced Solid Tumors
The main purpose of this clinical trial is to test PAS-004 in people with advanced solid tumors with rat sarcoma virus (RAS), neurofibromatosis type I (NF1), or rapidly accelerated fibrosarcoma (RAF) mutations. The main questions it aims to answer are: * How well participants are able tolerate diff…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology, Irving, Texas
- Locations
- 7 in total
- Run by
- Pasithea Therapeutics Corp.
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.