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NCT ID: NCT04606446 Recruiting - Clinical trials for Locally Advanced or Metastatic Non-small Cell Lung Cancer

Study of PF-07248144 in Advanced or Metastatic Solid Tumors

KAT6
Start date: November 16, 2020
Phase: Phase 1
Study type: Interventional

This is an open-label, multi center study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-07248144 and early signs of clinical efficacy of PF-07248144 as a single agent and in combination with either fulvestrant or letrozole + palbociclib or with PF-07220060 + fulvestrant

NCT ID: NCT04606433 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Phase I Clinical Study of GNC-038 in Patients With Non-Hodgkin's Lymphoma or Acute Lymphoblastic Leukemia

Start date: November 4, 2020
Phase: Phase 1
Study type: Interventional

An open, multicenter, Phase I clinical study to evaluate the safety, tolerability, pharmacokinetics/pharmacokinetics, and antitumor activity of GNC-038 quad-specific antibody injection in relapsed or refractory non-Hodgkin's lymphoma, relapsed or refractory acute lymphoblastic leukemia, and refractory or metastatic solid tumors.

NCT ID: NCT04606225 Recruiting - Healthy Clinical Trials

Losartan Effects on Emotion-memory Interaction

Start date: October 10, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether a single dose of losartan (50 mg) can affect emotion-memory interaction in healthy humans and its underlying neural mechanisms.

NCT ID: NCT04606212 Recruiting - Healthy Clinical Trials

The Effects of Losartan on Emotion Processing

Start date: October 10, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the effect of losartan (50mg, single dose) on salience processing

NCT ID: NCT04606108 Recruiting - Soft Tissue Sarcoma Clinical Trials

Study of Camrelizumab in Combination With Neoadjuvant Chemotherapy in the Treatment of High-risk Soft Tissue Sarcoma

Start date: October 19, 2020
Phase: Phase 2
Study type: Interventional

This study is a open-lable , single arm,single center, phase II clinical study. Target population is patients with high-risk Soft tissue sarcoma. Study objective is to compare the efficacy and safety of camrelizumab in combination with Liposome doxorubicin and Ifosfamide in study population in China. Camrelizumab is a humanized anti-PD1 IgG4 monoclonal antibody.

NCT ID: NCT04605939 Recruiting - Clinical trials for Magnetic Resonance Imaging

Clinical Application of Fibroblast Activation Protein PET/MRI in Liver Fibrosis

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Positron Emission Tomography (PET) provides a valuable tool for the diagnosis and staging of liver fibrosis. Activation of hepatic stellate cell (HSC) is a key link in the pathophysiological development of liver fibrosis. In human liver tissue, fibroblast activation protein (FAP) was only expressed in active HSCs and fibroblasts, but not in static HSCs. Therefore, FAP has become an excellent target for diagnosis and treatment of liver fibrosis. Recently, radionuclide-labeled fibroblast activation protein inhibitors (FAPI) as a new novel positron tracer has shown to be effective to detect various cancers. In this prospective study, the investigators will use the most advanced imaging equipments, integrated PET/MR, and PET/CT with gallium-68 (68Ga) -FAPI to image patients with or suspected of liver fibrosis, the aim is to explore the value of 68Ga-FAPI hybrid PET/MR and PET/CT in liver fibrosis.

NCT ID: NCT04605666 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia, in Relapse

CD19-CAR-T2 Cells for CD19 Positive Acute Lymphoblastic Leukemia

Start date: May 1, 2020
Phase: Phase 2
Study type: Interventional

Relapsed and refractory B cell acute lymphoblastic leukemia (B-ALL) shows unfavorable prognosis, especially for adult patients. Besides, minimal residual disease (MRD) positive at transplant has been considered risk factor for relapse after transplantation. Worse yet, there is no standard management for these patients. Chimeric antigen receptor T cells (CAR-T cells) has been recognized a promising treatment option for treating B cell derived malignancy. The purpose of this study is to evaluate the efficacy and safety of chimeric antigen receptor 19 (CD19-CAR-T2 Cells) infusions in patients with CD19+ ALL.

NCT ID: NCT04605575 Recruiting - Breast Cancer Clinical Trials

Pyrotinib Plus Vinorelbine in Participants With HER2-positive Previously Treated Locally Advanced or Metastatic Breast Cancer

Start date: May 22, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to identify the highest tolerable dose of pyrotinib in combination with vinorelbine and to assess the safety and efficacy of the combination in Patients With HER2-Positive Locally Advanced or Metastatic Breast Cancer. The study will be conducted in two parts. In the first part, testing will be done on up to 12 subjects to determine the highest tolerable dose of pyrotinib and vinorelbine in patients with advanced solid tumors. In the second part of the study, we will explore the safety and efficacy of Pyrotinib + vinorelbine in Patients With HER2-Positive Locally Advanced or Metastatic Breast Cancer Who Have Received Prior Trastuzumab-Based Therapy. Participants will be treated until disease progression (PD), unmanageable toxicity, or study termination.

NCT ID: NCT04604938 Recruiting - Healthy Clinical Trials

The Effects of Losartan on Reward Reinforcement Learning

Start date: October 10, 2020
Phase: N/A
Study type: Interventional

This study aims to investigate whether a single dose of losartan (50 mg) can affect learning from positive and negative outcomes and its related neural mechanisms.

NCT ID: NCT04604886 Recruiting - Cardiac Surgery Clinical Trials

The Consistency of Cardiac Output Measured by Pulmonary Artery Catheter and LiDCO in Cardiac Surgical Patients

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

1. To evaluate the consistency of cardiac output measured by pulmonary artery catheter and LiDCO in cardiac surgical patients 2. To evaluate whether different hemodynamic monitoring methods can accurately detect the trend of cardiac output changes