Advanced Solid Tumor Clinical Trials in Dallas, Texas
21 studies are recruiting for advanced 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.
Search these by distance from you
Studies now recruiting
-
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
- UT Southwest Simmons Cancer Center, Dallas, Texas
- Locations
- 77 in total
- Run by
- PMV Pharmaceuticals, Inc
-
Study of ART6043 in Advanced/Metastatic Solid Tumors Patients (POLKA)
This interventional study will evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of ART6043 as monotherapy or in combination with olaparib.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Center - Clinic, Dallas, Texas
- Locations
- 18 in total
- Run by
- Artios Pharma Ltd
-
A Study of KK2269 in Adult Participants With Solid Tumors
This is a first-in-human study of KK2269. Part 1 and Part 2 will be conducted as a multicenter, open-label, non-randomized, dose-escalation study. Participants with advanced or metastatic solid tumors for which no standard therapy is available will be enrolled in Part 1. In Part 1, the primary obje…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas Southwestern Medical Center, Dallas, Texas
- Locations
- 32 in total
- Run by
- Kyowa Kirin Co., Ltd.
-
Safety and Preliminary Effectiveness of BNT317, an Investigational Therapy for Advanced Solid Tumors
This is a first-in-human (FIH), open-label, multi-site study which will evaluate the safety, efficacy, tolerability, pharmacokinetics (PK), and immunogenicity of increasing doses of BNT317 in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 11 in total
- Run by
- BioNTech SE
-
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
-
SW-682 in Advanced Solid Tumors
This is a first-in-human (FIH), Phase 1a/1b open-label, multicenter, dose escalation and dose expansion study of SW-682 in adult participants with metastatic or unresectable advanced solid tumors with or without Hippo pathway alterations that are refractory to, or have progressed, during or after a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Research Center US Oncology, Dallas, Texas
- Locations
- 8 in total
- Run by
- SpringWorks Therapeutics, Inc., a healthcare company of Merck KGaA, Darmstadt, Germany
-
A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours
The purpose of this study is to determine the appropriate dosage, safety and effectiveness of a new study drug IPN01195 in adults with advanced solid tumours. The participants in this study will have advanced solid tumours. 'Advanced solid tumours' refers to cancers that can occur in several places…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Centers - Medical City Hospital - Dallas, Dallas, Texas
- Locations
- 13 in total
- Run by
- Ipsen
-
Study of Orally Administered MOMA-341 in Participants With Advanced or Metastatic Solid Tumors
This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-341 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #127, Dallas, Texas
- Locations
- 15 in total
- Run by
- MOMA Therapeutics
-
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
-
BAL0891 in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Baylor University Medical Center, Dallas, Texas
- Locations
- 17 in total
- Run by
- SillaJen, Inc.
-
A Study to Evaluate PEEL-224 in Patients With Advanced Solid Tumors
This is a first-in-human, dose escalation, repeat-dose, multi-center, open-label study evaluating safety, tolerability, PK, and preliminary antitumor activity of PEEL-224 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 8 in total
- Run by
- Peel Therapeutics Inc
-
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.
-
A Study of CLSP-1025 in Adult Patients With Solid Tumors That Harbor the p53 R175H Mutation
Phase 1 dose escalation and expansion study of CLSP-1025, a first-in-class HLA-A*02:01 specific T cell engager (TCE) targeting solid tumors that harbor the p53 R175H mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 21 in total
- Run by
- Clasp Therapeutics, Inc.
-
A Safety and Efficacy Study of HCB101, Fc-fusion Protein Targeting SIRPα-CD47 Pathway, in Solid or Hematological Tumors
The purpose of this study is to find out whether IV injection of HCB101 is an effective treatment for different types of advanced solid tumors or relapsed and refractory non-Hodgkin lymphoma and what side effects (unwanted effects) may occur in subjects aged 18 years old and above.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UT Southwestern Medical Center, Dallas, Texas
- Locations
- 8 in total
- Run by
- FBD Biologics Limited
-
JZP898 Intravenous Infusion as Monotherapy and Combination With Pembrolizumab in Adults With Advanced/Metastatic Solid Tumors
This Phase 1 first-in-human study will investigate the safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary antitumor activity of JZP898 monotherapy as well as JZP898 in combination with pembrolizumab in adult participants with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Texas Oncology - Baylor Charles A Sammons Cancer Center, Dallas, Texas
- Locations
- 10 in total
- Run by
- Jazz Pharmaceuticals
-
Study of AVZO-021 in Patients With Advanced Solid Tumors
This study, the first clinical trial of AVZO-021, aims to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, maximum tolerated dose, and anti-tumor effects of AVZO-021 in patients with advanced solid tumors. AVZO-021 is an oral medication that inhibits cyclin-dependent kinase 2…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Texas Oncology - DFW, Dallas, Texas
- Locations
- 13 in total
- Run by
- Avenzo Therapeutics, Inc.
-
A Study of LM-24C5 For Advanced Solid Tumors
To assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-24C5 in subjects with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Center, Dallas, Texas
- Locations
- 6 in total
- Run by
- LaNova Medicines Limited
-
AMT-116 in Patients With Advanced Solid Tumors
This first-in-human study will evaluate the Maximum Tolerated Dose (MTD) / the Recommended Phase 2 Dose (RP2D), safety, tolerability, anti-tumor activity, pharmacokinetics, pharmacodynamics and immunogenicity of AMT-116, in Patients with Advanced Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Centers, Dallas, Texas
- Locations
- 10 in total
- Run by
- Multitude Therapeutics Inc.
-
A Phase I/II, Open-label Study to Investigate the Safety, Tolerability, PK, and Preliminary Efficacy of FB849
This is the first-in-human, multicenter, open-label Phase I/II study to investigate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary efficacy of FB849 alone and in combination with pembrolizumab in subjects with advanced solid tumors for whom no standard therapy is…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research Center, Dallas, Texas
- Locations
- 5 in total
- Run by
- 1ST Biotherapeutics, Inc.
-
Study of SGR-3515 In Participants With Advanced Solid Tumors.
The purpose of this study is to learn about the effects of a new study drug, called SGR-3515 that may be a treatment for advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas Southwestern, Dallas, Texas
- Locations
- 14 in total
- Run by
- Schrödinger, Inc.
-
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.
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.