Solid Tumors Clinical Trials in Houston, Texas
21 studies are recruiting for 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.
Search these by distance from you
Studies now recruiting
-
Long-term Safety and Efficacy Extension Study for Participants With Advanced Tumors Who Are Currently on Treatment or in Follow-up in a Pembrolizumab (MK-3475) Study (MK-3475-587/KEYNOTE-587)
The purpose of this study is to evaluate the long-term safety and efficacy of pembrolizumab (MK-3475) in participants from previous Merck pembrolizumab-based parent studies who transition into this extension study. This study will consist of three phases: 1) First Course Phase, 2) Survival Follow-u…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- University of Texas MD Anderson Cancer Center ( Site 0007), Houston, Texas
- Locations
- 782 in total
- Run by
- Merck Sharp & Dohme LLC
-
A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Homozygous MTAP Deletion (MountainTAP-5)
This is an open-label, multicenter Phase 2 study evaluating BMS-986504 in participants with advanced and/or metastatic solid tumors that have MTAP deletion. The study includes a monotherapy component and a combination component in which BMS-986504 is given with other anti-cancer agents. The trial w…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Local Institution - 0085, Houston, Texas
- Locations
- 58 in total
- Run by
- Bristol-Myers Squibb
-
A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies
A study to evaluate the safety and tolerability of INCA036873 in participants with advanced solid tumors and hematological malignancies.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Md Anderson Cancer Center, Houston, Texas
- Locations
- 22 in total
- Run by
- Incyte Corporation
-
A Study to Evaluate Chemotherapy With or Without INCB161734 in Previously Untreated, KRAS G12D-Mutated Metastatic Pancreatic Ductal Adenocarcinoma
The purpose of this study is to evaluate the efficacy and safety of standard chemotherapy with or without INCB161734 in participants with metastatic pancreatic ductal adenocarcinoma (PDAC).
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Investigative Site US011, Houston, Texas
- Locations
- 229 in total
- Run by
- Incyte Corporation
-
A First-in-Human Study of BG-C0902 Alone and in Combination With Other Therapeutic Agents in Patients With Advanced Solid Tumors
This study is a first-in-human (FIH), Phase 1a/1b study of BG-C0902, a fully humanized anti-epidermal growth factor receptor (EGFR) and anti-mesenchymal-epithelial transition (MET) antibody, conjugated via an enzymatically cleavable linker to a topoisomerase 1 (TOPO1) inhibitor payload. The study a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas Md Anderson Cancer Center, Houston, Texas
- Locations
- 14 in total
- Run by
- BeOne Medicines
-
A Study to Evaluate the Safety and Pharmacokinetics of Eflapegrastim in Pediatric Participants With Solid Tumors or Lymphomas and Treated With Myelosuppressive Chemotherapy
The purpose of this study is to evaluate the safety and pharmacokinetics of eflapegrastim in pediatric participants with solid tumors or lymphoma and treated with myelosuppressive chemotherapy.
- Stage
- Phase 2
- Ages
- 0 to 17
- Site
- UT MD Anderson Cancer Center, Houston, Texas
- Locations
- 5 in total
- Run by
- Spectrum Pharmaceuticals, Inc
-
A Study of ZL-1310 in Participants With Selected Solid Tumors
A Phase 1b/2, Open-label, Multi-center Study of ZL-1310 in Participants With Selected Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas M. D. Anderson Cancer Center, Houston, Texas
- Locations
- 23 in total
- Run by
- Zai Lab (Shanghai) Co., Ltd.
-
A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations
The objective of this Master Protocol is to evaluate the efficacy and safety of plixorafenib in participants with BRAF altered (BRAF V600E or BRAF fusions) locally advanced or metastatic solid tumors, or recurrent or progressive primary central nervous system (CNS) tumors, including rare BRAF V600E…
- Stage
- Phase 2
- Ages
- 8 and older
- Site
- University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 70 in total
- Run by
- Fore Biotherapeutics
-
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
-
A Study to Evaluate INCB161734 in Participants With Advanced or Metastatic Solid Tumors With KRAS G12D Mutation
This study is conducted to determine the safety and tolerability of INCB161734 as a single agent or in combination with other anticancer therapies.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Md Anderson Cancer Center, Houston, Texas
- Locations
- 34 in total
- Run by
- Incyte Corporation
-
Study of AUBE00 in Patients With Solid Tumors
This is a first-in-human, Phase I, open-label, multicenter, multinational study, designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, and anti-tumor activity of AUBE00 in patients with locally advanced or metastatic solid tumors.The total numb…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 4 in total
- Run by
- Chugai Pharmaceutical
-
Phase II Biomarker Study of BND-22 in Combination With Cemiplimab in Solid Tumors
To study possible biomarkers that may be related to how SAR444881 works (either alone or when combined with cemiplimab) in participants with solid tumors.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Md Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
-
JAB-30355 in Patients With Advanced Solid Tumors Harboring TP53 Y220C Mutation
This study is to evaluate the efficacy and safety of JAB-30355 in adult participants with advanced solid tumors harboring TP53 Y220C mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research site, Houston, Texas
- Locations
- 15 in total
- Run by
- Jacobio Pharmaceuticals Co., Ltd.
-
DB-1311 in Combination With BNT327 or DB-1305 in Advanced/Metastatic Solid Tumors
A Phase II, Multicenter, Open-Label Trial of DB-1311 in combination with BNT327 or DB-1305 in Participants with Advanced/Metastatic Solid Tumors
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- USA12-0, Houston, Texas
- Locations
- 37 in total
- Run by
- DualityBio Inc.
-
Phase 1 Dose Escalation and Expansion Study of TROP2 CAR Engineered IL15-transduced Cord Blood-derived NK Cells in Patients With Advanced Solid Tumors (TROPIKANA)
To find the recommended dose of TROP2- CAR-NK cells that can be given to participants with advanced forms of solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- M D Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
-
QTX3034 in Patients With KRAS G12D Mutation
Phase 1 study to determine the safety and tolerability of QTX3034 as a single agent or in combination with cetuximab.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson, Houston, Texas
- Locations
- 14 in total
- Run by
- Quanta Therapeutics
-
A Study of HS-20110 in Participants With Advanced Solid Tumors
This is an open-label, multicenter study to evaluate the safety and tolerability of HS-20110 in participants with advanced solid malignant tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- Hansoh BioMedical R&D Company
-
S-531011 as Monotherapy and in Combination With an Immune Checkpoint Inhibitor in Advanced or Metastatic Solid Tumors
The primary objective of Part A is to evaluate the safety and tolerability of S-531011 and to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of S-531011 with or without pembrolizumab. The primary objective of Parts B and C is to evaluate the antitumor activity of …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- Shionogi
-
A Study of XB371 Administered in Participants With Locally Advanced or Metastatic Solid Tumors
The primary purpose of the study is to characterize the safety and tolerability of XB371. The dose-escalation cohorts and Part B of the expansion cohorts are non-randomized. Part A of the expansion cohorts is randomized.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Exelixis Clinical Site #8, Houston, Texas
- Locations
- 9 in total
- Run by
- Exelixis
-
Study of IBI3020 Treatment in Participants With Late-Stage Solid Tumors
The main purpose of this study is to evaluate the safety and tolerability of IBI3020 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RP2D) of IBI3020.
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- NEXT Houston, Houston, Texas
- Locations
- 9 in total
- Run by
- Innovent Biopharmaceutical Technology (Hangzhou) Co., LTD.
-
A Study of ADRX-0405 in Subjects With Select Advanced Solid Tumors
The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0405 in patients with select advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 8 in total
- Run by
- Adcentrx Therapeutics
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.