Advanced Solid Tumor Clinical Trials in Jacksonville, Florida
8 studies are recruiting for advanced solid tumor in Jacksonville, Florida 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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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
- Mayo Clinic Jacksonville, Jacksonville, Florida
- Locations
- 32 in total
- Run by
- Kyowa Kirin Co., Ltd.
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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
- Mayo Clinic, Jacksonville, Florida
- Locations
- 25 in total
- Run by
- Bristol-Myers Squibb
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Study of Lunresertib Alone or in Combination With RP-3500 or Debio 0123 in Patients With Advanced Solid Tumors
The primary purpose of this study is to assess the safety and tolerability of lunresertib alone and in combination with RP-3500 or in combination with Debio 0123 in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- #1017, Mayo Clinic, Jacksonville, Florida
- Locations
- 26 in total
- Run by
- Debiopharm International SA
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A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers
This is a multi-center, first-in-human, open label, dose escalation (Part A) and expansion (Part B) Phase 1 study in subjects with advanced solid tumors and in subjects with solid tumors with selected genetic alterations that are either direct (YES1 amplification) or dependent (Hippo Pathway altera…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic, Jacksonville, Florida
- Locations
- 15 in total
- Run by
- Nuvectis Pharma, Inc.
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Evaluate the Safety and Clinical Activity of HH2853
This is an open-label, multicenter, first-in-human phase I/II study which is composed of 3 parts: phase I dose escalation, phase I dose extension and phase II. HH2853 will be administered orally on a continuous BID schedule on a continuous 28-day treatment cycle.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic, Jacksonville, Florida
- Locations
- 25 in total
- Run by
- Haihe Biopharma Co., Ltd.
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A Phase 1 Study of XL309 (ISM3091) Alone and in Combination in Participants With Advanced Solid Tumors
This is a first-in-human (FIH), multicenter, open-label Phase I study to investigate the safety, tolerability, preliminary antitumor activity, as well as pharmacokinetics (PK) and pharmacodynamics of XL309 (previously ISM3091) administered alone or in combination with olaparib in participants with …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Exelixis Clinical Site #15, Jacksonville, Florida
- Locations
- 16 in total
- Run by
- Exelixis
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A Phase 1, First in Human Study of TORL-4-500 in Patients With Advanced Cancer
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-4-500 in patients with advanced cancer. For Part 1, any advanced or metastatic solid tumor malignancy will be evaluated including, for example, adrenocortical carcinoma (ACC).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic Jacksonville, Jacksonville, Florida
- Locations
- 10 in total
- Run by
- TORL Biotherapeutics, LLC
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A Study to Evaluate the Safety and Therapeutic Activity of GI-102 As a Single Agent and in Combination with Conventional Anti-cancer Drugs, Pembrolizumab or Trastuzumab Deruxtecan(T-DXd) in Patients with Advanced Solid Tumors (KEYNOTE-G08)
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and therapeutic activity of GI-102 as a single agent and in combination with conventional anti-cancer drugs, pembrolizumab or trastuzumab deruxtecan(T-DXd) over a range of advanced and/or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic in Florida, Jacksonville, Florida
- Locations
- 11 in total
- Run by
- GI Innovation, 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.