Ovarian Cancer Clinical Trials in Houston, Texas
52 studies are recruiting for ovarian cancer 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
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Study of RGT-490 in Patients With PIK3CA-Mutated Advanced Solid Tumors
This is a phase 1/1b, open-label, multicenter study consisting of sequential parts designed to evaluate the safety, tolerability, and effects pharmacokinetic (PK) profile, and antitumor activity of RGT-490, an investigational oral therapy, in adults with locally advanced or metastatic solid tumors …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 6 in total
- Run by
- Regor Pharmaceuticals Inc.
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A Phase 1 Study of LNCB74 in Advanced Solid Tumors
This is an open-label, phase 1, dose escalation and dose expansion study to determine safety and tolerability, and to determine the maximum tolerated dose and / or recommended phase 2 dose of LNCB74 in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson, Houston, Texas
- Locations
- 17 in total
- Run by
- LigaChem Biosciences, Inc.
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A Study of MGC026 in Participants With Advanced Solid Tumors
The study is designed to understand the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of vobramitamab tavatecan (MGC026) in participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors The study has a dose escalatio…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 12 in total
- Run by
- MacroGenics
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Lead-212 PSV359 Therapy for Patients With Solid Tumors
Phase I/IIa image-guided, alpha-particle therapy study of [203Pb]Pb-PSV359 and [212Pb]Pb-PSV359 in patients with solid tumors that are known to be Fibroblast Activation Protein (FAP)-positive.
- Stage
- Phase 1
- Ages
- 18 to 90
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 16 in total
- Run by
- Perspective Therapeutics
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A Phase 1/2 Trial of TER-2013 in Patients With Solid Tumors Harboring AKT/PI3K/PTEN Pathway Alterations
This is a Phase 1/2, open-label, multicenter study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics and anti-tumor activity of TER-2013 in patients with advanced solid tumors harboring AKT/PI3K/PTEN pathway alterations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 25 in total
- Run by
- Terremoto Biosciences Inc.
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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
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 16 in total
- Run by
- A2 Biotherapeutics Inc.
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A Phase 1 Study to Evaluate OPB-201 in Recurrent Endometrial and Platinum-resistant Ovarian Cancer.
The goal of this clinical trial is to learn if OPB-201 is safe in recurrent endometrial and platinum resistant ovarian cancer participants and also to find the optimal dose of OPB-201. Participants will have their own T cells modified in a laboratory and given back to them as OPB-201 in this one-ti…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 5 in total
- Run by
- Outpace Bio, Inc.
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A Study of ART0380 for the Treatment of Advanced or Metastatic Solid Tumors
This clinical trial is evaluating a drug called ART0380 in participants with advanced or metastatic solid tumors. The main goals of this study are to: * Find the recommended dose of ART0380 that can be given safely to participants alone and in combination with gemcitabine or irinotecan * Learn more…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Oncology Consultants, Houston, Texas
- Locations
- 88 in total
- Run by
- Artios Pharma Ltd
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A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 39 in total
- Run by
- Eli Lilly and Company
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A Phase I/II, First-in-Human Study to Evaluate TJ102 in Participants With Advanced or Metastatic Ovarian Cancer and Other Solid Tumors.
The goal of this clinical trial is to evaluate whether TJ102, an investigational antibody-drug conjugate (ADC), can safely and effectively treat patients with advanced ovarian or other solid tumors. The main objectives of this study are : • To Determine the maximum tolerated dose (MTD) and recommen…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Houston, Houston, Texas
- Locations
- 9 in total
- Run by
- Phrontline Biopharma
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Risk Reducing Salpingectomy With Delayed Oophorectomy as an Alternative to Risk- Reducing Salpingo-oophorectomy in High Risk-Women to Assess the Safety of Prevention - US Cohort Study
This is a prospective preference study that will evaluate non-inferiority of the innovative treatment (RRS with delayed RRO) as compared to the standard treatment (RRSO) with respect to high grade serous (ovarian) cancer incidence
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Lyndon Baines Johnson General, Houston, Texas
- Locations
- 11 in total
- Run by
- M.D. Anderson Cancer Center
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Dose Escalation and Dose Expansion Study of MDX2001 in Patients With Advanced Solid Tumors
This study is designed to characterize the safety, tolerability, and anti-tumor activity of MDX2001 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 6 in total
- Run by
- ModeX Therapeutics, An OPKO Health Company
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Study to Evaluate INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
The purpose of this study is to evaluate INCB123667 versus investigator's choice of chemotherapy in participants with platinum-resistant ovarian cancer with cyclin E1 overexpression.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- The University of Texas Health Science Center Houston, Houston, Texas
- Locations
- 198 in total
- Run by
- Incyte Corporation
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A Phase I/IIa Study of AZD8205 Given Alone or Combined, in Participants With Advanced/Metastatic Solid Malignancies
This research study is studying a new compound, AZD8205, as a possible treatment for advanced or metastatic solid tumours alone or in combination with anti-cancer agents
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Houston, Texas
- Locations
- 67 in total
- Run by
- AstraZeneca
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Open Label Study to Evaluate BL-M07D1 in HER2 Expressing Malignant Solid Tumors
The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-M07D1 in patients with HER2 expressing advanced tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Oncology Consultants, Houston, Texas
- Locations
- 26 in total
- Run by
- SystImmune Inc.
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First-in-Human Study of ATX-295, an Oral Inhibitor of KIF18A, as Monotherapy and in Combination With Anticancer Therapy in Patients With Advanced or Metastatic Solid Tumors, Including Ovarian Cancer
The goal of this study is to identify a safe and tolerated dose of the orally administered KIF18A inhibitor ATX-295. In addition, this study will evaluate the pharmacokinetics, pharmacodynamics and preliminary antitumor activity of ATX-295 as a monotherapy and in combination with bevacizumab (or a …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 11 in total
- Run by
- Accent Therapeutics
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Use of CA125 and Complementary Biomarkers for the Early Detection of Ovarian Cancer in Low Risk Women
The goal of this clinical research study is to find out if combining a standard blood test (CA-125) that checks for ovarian cancer with other blood tests that check for related tumor markers may be helpful in the early detection of ovarian cancer in women who are at low risk. Tumor markers are subs…
- Stage
- Not phased
- Ages
- 50 to 74
- Site
- University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 12 in total
- Run by
- M.D. Anderson Cancer Center
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Secondary Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) for Recurrent Mucinous Ovarian Cancer (HI-MOC Study)
The primary objective is to estimate overall survival after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
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Spanish Decision Tool for Ovarian Cancer Maintenance Therapy
To develop a shared decision-making (SDM) tool to help Spanish-speaking patients make decisions about their maintenance therapy
- Stage
- Not phased
- Ages
- 18 and older
- Site
- M D Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
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Phase II IMNN-001 (Also Known as GEN-1) on SLL With BEV and NACT, Newly Diagnosed Advanced Ovarian, Fallopian Tube or Primary Peritoneal Cancer
This is a 1:1 randomized, open label, multi-center phase I/II trial to evaluate the safety, dosing, efficacy, and biological activity of adding IMNN-001 to chemotherapy + BEV compared to chemotherapy + BEV alone.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 4 in total
- Run by
- Imunon
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Phase I/IIa Study of AZD5335 as Monotherapy and Combination Therapy in Participants With Solid Tumors
This research is designed to determine if experimental treatment with Antibody-drug conjugate, AZD5335, alone, or in combination with anti-cancer agents is safe, tolerable, and has anti-cancer activity in patients with advanced tumors
- Stage
- Phase 1
- Ages
- 18 to 130
- Site
- Research Site, Houston, Texas
- Locations
- 60 in total
- Run by
- AstraZeneca
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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 anticancer therapies (Phase 1b) in adult participants with advan…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 20 in total
- Run by
- Pheast Therapeutics
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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
- The University of Texas MD Anderson Cancer Center, Houston, Texas
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
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177Lu-BetaBart in Patients With Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors
This is a Phase 1/2a dose escalation and expansion study to determine the safety, tolerability, and preliminary clinical activity of 177LuBetaBart, a lutetium-labeled anti-B7-H3 monoclonal antibody, in patients with relapsed/refractory, locally advanced inoperable, or metastatic solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 5 in total
- Run by
- Radiopharm Theranostics, Ltd
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Leveraging Methylated DNA Markers (MDMs) in the Detection of Endometrial Cancer, Ovarian Cancer, and Cervical Cancer
The overarching objective of this project is to develop a pan-gynecologic cancer detection test using gynecologic (unique endometrial, cervical, and ovarian cancer) cancer-specific methylated DNA markers and high-risk human papilloma virus (HR-HPV) detected in vaginal fluid and/or plasma. This prop…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Total Women's Care of the Heights, Houston, Texas
- Locations
- 25 in total
- Run by
- Mayo Clinic
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.