Solid Tumor Clinical Trials in Dallas, Texas
17 studies are recruiting for solid tumor in Dallas, 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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Dabrafenib and/or Trametinib Rollover Study
This study is to provide access for patients who are receiving treatment with dabrafenib and/or trametinib in a Novartis-sponsored Oncology Global Development, Global Medical Affairs or a former GSK-sponsored study who have fulfilled the requirements for the primary objective, and who are judged by…
- Stage
- Phase 4
- Ages
- 18 to 100
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 34 in total
- Run by
- Novartis Pharmaceuticals
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Phase 1 Study of MRTX1719 in Solid Tumors With MTAP Deletion
This is a Phase 1, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Ut Southwestern, Dallas, Texas
- Locations
- 25 in total
- Run by
- Bristol-Myers Squibb
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Study of Zanzalintinib in Combination With Immuno-Oncology or Other Agents in Participants With Solid Tumors
This is a multicenter Phase 1b, open label, dose-escalation and cohort-expansion study, evaluating the safety, tolerability, pharmacokinetics (PK), preliminary antitumor activity, and effect of biomarkers of zanzalintinib administered alone, and in combination with nivolumab (doublet), nivolumab + …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Exelixis Clinical Site #111, Dallas, Texas
- Locations
- 122 in total
- Run by
- Exelixis
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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
- Sarah Cannon Research Institute at Mary Crowley, Dallas, Texas
- Locations
- 42 in total
- Run by
- Inhibrx Biosciences, Inc
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Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmocodynamics and Preliminary Antitumor Activity of AT-1965 in Patients With Advanced, Refractory or Recurrent Solid Tumors
This is a first-in-human, multicenter, open-label, dose escalation and dose expansion Phase 1/2 study to determine the MTD and/or the recommended Phase 2 dose (RP2D) and to characterize DLTs of AT-1965 as well as to investigate the safety, pharmacokinetics (PK), pharmacodynamics, and preliminary an…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- CBCC Global Research Site 006, Dallas, Texas
- Locations
- 9 in total
- Run by
- Alyssum Therapeutics
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A Study of Pembrolizumab (MK-3475) in Pediatric Participants With an Advanced Solid Tumor or Lymphoma (MK-3475-051/KEYNOTE-051)
Researchers are looking for new ways to treat children with different types of melanoma (skin cancer), solid tumors, and lymphomas (blood cancers) that are any of these: * Advanced, which means cancer spread in the body or cannot be removed with surgery * Relapsed, which means cancer has come back …
- Stage
- Phase 1
- Ages
- 0 to 17
- Site
- Call for Information (Investigational Site 0054), Dallas, Texas
- Locations
- 16 in total
- Run by
- Merck Sharp & Dohme LLC
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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
- NEXT Dallas, Dallas, Texas
- Locations
- 29 in total
- Run by
- Pyxis Oncology, Inc
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Study of STP938 (Dencatistat) in Advanced Solid Tumours
The Phase 1a part of the study is a dose escalation of STP938 as a monotherapy. The Phase 1b part of the study is a safety expansion cohort of STP938 as a monotherapy.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Center, Dallas, Texas
- Locations
- 7 in total
- Run by
- Step Pharma, SAS
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VITAS: Atezolizumab in Combination With Chemotherapy for Pediatric Relapsed/Refractory Solid Tumors
This trial is a multi-center, non-randomized, open-label Phase I/II study evaluating the feasibility and efficacy of vincristine, irinotecan, temozolomide, and atezolizumab in children with relapsed/refractory solid tumors.
- Stage
- Phase 1
- Ages
- 0 to 30
- Site
- The University of Texas Southwestern Medical Center, Dallas, Texas
- Locations
- 7 in total
- Run by
- University of Texas Southwestern Medical Center
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A Study to Evaluate the Efficacy and Safety of TL118 in Solid Tumors Patients
The main objective of the study will be to evaluate the efficacy of TL118 in participants with solid tumors harboring NTRK gene fusions
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Texas Oncology, Dallas, Texas
- Locations
- 19 in total
- Run by
- Teligene US
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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
- UT Southwestern, Dallas, Texas
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, Inc.
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Open-Label Study to Evaluate the Safety, Tolerability, PK, and Efficacy of INX-315 in Patients With Advanced Cancer
Incyclix Bio (Incyclix) is developing INX-315 as an oral, small molecule inhibitor of cyclin dependent kinase 2 (CDK2) for the treatment of human cancers. This first-in-human study is designed to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary antitumor activity of INX-315 …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology, Dallas, Texas
- Locations
- 18 in total
- Run by
- Incyclix Bio
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A Phase 1/2 Study of BHV-1510 (Previously PBI-410) in Advanced Solid Tumors
This is a Phase 1/2, first in human (FIH), open-label, multicenter study of BHV-1510 monotherapy and in Combination with Cemiplimab in participants with previously treated, advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Site-104, Dallas, Texas
- Locations
- 17 in total
- Run by
- Biohaven Therapeutics Ltd.
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Study of TJ033721 (Givastomig) in Subjects With Advanced or Metastatic Solid Tumors
This is an open label, multi-center, multiple dose Phase 1 study to evaluate the safety, tolerability, MTD PK, and PD of TJ033721 (givastomig) in subjects with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 21 in total
- Run by
- I-Mab Biopharma US Limited
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A Clinical Study of Intratumoral MVR-T3011 (T3011) Given as a Single Agent and in Combination With Intravenous Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors
This is a Phase 1/2a, open-label, study to evaluate the safety and preliminary efficacy of intratumoral T3011 given alone and in combination with intravenous pembrolizumab in partients with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 9 in total
- Run by
- ImmVira Pharma Co. Ltd
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Study to Evaluate IMP9064 as a Monotherapy or in Combination in Patients With Advanced Solid Tumors
This is a Phase 1/2, multicenter, open-label study to evaluate the safety and efficacy of IMP9064 as monotherapy or in combination with PARP inhibitor Senaparib in patients with advanced solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Centers, Dallas, Texas
- Locations
- 8 in total
- Run by
- Impact Therapeutics, Inc.
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BP1001-A in Patients With Advanced or Recurrent Solid Tumors
This is a phase I, open-label, study of BP1001-A in participants with advanced or recurrent solid tumors. The dose escalation phase will determine the safety and the maximum tolerated dose (MTD) or maximum administered dose (MAD) of BP1001-A as a single agent. After the MTD or MAD of BP1001-A is es…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 4 in total
- Run by
- Bio-Path Holdings, 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.
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