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  • Stereotactic Body Radiation and Tumor Treating Fields for Locally Advanced Pancreas Cancer

    Phase

    N/A

    Span

    197 weeks

    Sponsor

    Baptist Health South Florida

    Miami, Florida

    Recruiting

  • Zanubrutinib With Pemetrexed to Treat Relapsed/Refractory Primary and Secondary Central Nervous System (CNS) Lymphomas

    Pemetrexed, when used by itself, is beneficial and is a standard of care therapy for RR PCNSL and can be used to treat SCNSL. Zanubrutinib is an oral drug that is approved by the Food and Drug Administration (FDA) as safe and effective to treat certain lymphoma types.

    Phase

    2

    Span

    358 weeks

    Sponsor

    Baptist Health South Florida

    Miami, Florida

    Recruiting

  • Testing the Addition of Total Ablative Therapy to Usual Systemic Therapy Treatment for Limited Metastatic Colorectal Cancer, the ERASur Study

    PRIMARY OBJECTIVE: I. To evaluate and compare overall survival (OS) (measured from time of randomization) in patients with newly diagnosed oligometastatic colorectal cancer (oCRC) treated with total ablative therapy (TAT) in addition to standard of care (SOC) systemic therapy versus SOC systemic therapy. SECONDARY OBJECTIVES: I. To evaluate and compare event-free survival (EFS) (measured from time of randomization) between the two treatment arms. II. To assess the adverse events (AE) profile within each of the two treatment arms. III. To evaluate the time to local recurrence (TLR) (measured from completion of TAT) in patients with newly diagnosed oCRC treated with TAT + SOC systemic therapy. OUTLINE: Patients are randomized to 1 of 2 arms. ARM 1: Patients undergo TAT on study, consisting of SABR with or without surgical resection and/or microwave ablation. Patients also receive SOC chemotherapy on study. Patients also undergo computed tomography (CT) or magnetic resonance imaging (MRI) or positron emission tomography (PET)/CT scans throughout the trial. ARM 2: Patients receive SOC chemotherapy on study. Patients also undergo Patients also undergo CT or MRI or PET/CT scans throughout the trial.

    Phase

    3

    Span

    462 weeks

    Sponsor

    Alliance for Clinical Trials in Oncology

    Miami, Florida

    Recruiting

  • Silicone Gel Vs. Estrogen Vaginal Cream for the Management of Genitourinary Syndrome of Menopause

    Phase

    N/A

    Span

    139 weeks

    Sponsor

    Stratpharma AG

    Miami, Florida

    Recruiting

  • Heated Intraperitoneal Chemotherapy Followed by Niraparib for Ovarian, Primary Peritoneal and Fallopian Tube Cancer

    Phase

    3

    Span

    543 weeks

    Sponsor

    GOG Foundation

    Miami, Florida

    Recruiting

  • Safety and Effectiveness of the Genio® bilAteral Stimulation for Treatment of Complete Concentric CollapsE and OSA.

    Nyxoah has developed the Genio® 2.1 System with the intention of treating patients with moderate to severe obstructive sleep apnea. In overview, the System includes an Implantable Stimulator (IS) designed to stimulate the hypoglossal nerve branches (i.e., both the left and the right). The IS does not include a battery but receives energy pulses transmitted by an Activation Chip (AC) which is attached to an adhesive Disposable Patch (DP) and placed on the patient's skin under the chin. Stimulation of the hypoglossal nerve causes the tongue muscles to contract with the intention to maintain an open airway.

    Phase

    N/A

    Span

    253 weeks

    Sponsor

    Nyxoah S.A.

    Miami, Florida

    Recruiting

  • Tucatinib, Trastuzumab, and Capecitabine With SRS for Brain Metastases From HER-2 Positive Breast Cancer

    Phase

    1

    Span

    266 weeks

    Sponsor

    Baptist Health South Florida

    Miami, Florida

    Recruiting

  • Characterization of 18F-Fluciclovine PET Amino Acid Radiotracer in Resected Brain Metastasis

    Phase

    2

    Span

    369 weeks

    Sponsor

    Baptist Health South Florida

    Miami, Florida

    Recruiting

  • Study of Iadademstat and Gilteritinib in Patients With R/R AML With FMS-like Tyrosine Kinase Mutation (FLT3 Mut+)

    This is an escalation/expansion, open label, single arm, study to investigate the safety and the RP2D of the combination of iadademstat with gilteritinib in FLT3-mutated R/R AML. This study consists of 2 parts. A dose finding part to evaluate the safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD) and emerging activity of iadademstat and gilteritinib combination, and to determine the pharmacologically-active dose (i.e., the minimum safe and biologically active dose) of iadademstat in combination with gilteritinib, and an expansion part at the specific dose/s selected to evaluate the activity of iadademstat in combination with gilteritinib in patients with FLT3-mutated R/R AML.

    Phase

    1

    Span

    159 weeks

    Sponsor

    Oryzon Genomics S.A.

    Miami, Florida

    Recruiting

  • Radioembolization Trial Utilizing Eye90 Microspheres™ for the Treatment of Hepatocellular Carcinoma (HCC)

    Phase

    N/A

    Span

    111 weeks

    Sponsor

    ABK Biomedical

    Miami, Florida

    Recruiting

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