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NCT ID: NCT05863260 Recruiting - Cervical Cancer Clinical Trials

Tislelizumab Combing Chemoradiotherapy in Recurrent Cervical Cancer

Start date: November 9, 2020
Phase:
Study type: Observational

Tislelizumab combined with chemoradiotherapy in the treatment of recurrent/ metastasis cervical cancer: a single arm,single center, phase ii and observational clinical study

NCT ID: NCT05862974 Completed - Healthy Clinical Trials

A Dose-escalation Study of LPM3480392 in Chinese Healthy Subjects

Start date: February 25, 2021
Phase: Phase 1
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, dose-increasing Phase I clinical trial to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of a single intravenous infusion of LPM3480392 injection in healthy subject

NCT ID: NCT05862831 Recruiting - Clinical trials for Advanced Solid Tumors

Clinical Study of PM1003 in Phase I/IIa Treatment of Advanced Malignant Solid Tumors

Start date: September 7, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

This is a single-arm, open-lable, multicenter phase I/IIa clinical trial evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of PM1003 in the treatment of advanced solid tumors.

NCT ID: NCT05862389 Recruiting - Anorexia Nervosa Clinical Trials

Study on the Mechanism of Eating Disorder

Start date: September 1, 2022
Phase:
Study type: Observational

Eating disorders (EDs) are severe chronic psychiatric disorders with a not fully understood etiopathogenesis. Previous studies have revealed some biological mechanisms of EDs. However, the etiology and maintenance mechanism of EDs, especially the neuro-mechanisms is still unknown. To explore the pathogenic mechanism and treatment biomarkers of EDs, we design this study. the multidimensional data including the clinicopathological features, neuroimaging data (functional and structural magnetic resonance imaging), electroencephalogram and inflammatory cytokines will be used to investigate the biomarkers for diagnosis and treatment effectiveness.

NCT ID: NCT05862337 Recruiting - Clinical trials for Hepatocellular Carcinoma

Anlotinib Hydrochloride Capsules Combined With Penpulimab Injection for the Treatment of Hepatocellular Carcinoma at High Risk of Recurrence.

Start date: May 10, 2023
Phase: Phase 3
Study type: Interventional

The primary objective of this study was to evaluate the efficacy of anlotinib hydrochloride capsules combined with penpulimab injection (test group) versus placebo (control group) for adjuvant therapy after radical surgery or ablation in HCC patients with high risk of recurrence by assessing recurrence-free survival (RFS).

NCT ID: NCT05862259 Recruiting - Immunotherapy Clinical Trials

A Real-world Study of the Efficacy and Safety of ICIs as First-line Therapy for Advanced Malignancies

Start date: August 10, 2023
Phase:
Study type: Observational

In this study, we collected the data of immunohistochemistry, gene detection, image, OS, PFS, Orr, and so on. Secondly, the database of immunotherapy for malignant tumor was established, and the predictive model was constructed to verify and establish the rationality and validity of the biomarkers and predictive system of immunotherapy

NCT ID: NCT05862233 Recruiting - Clinical trials for Primary Membranous Nephropathy

A Clinical Study of MIL62 in Primary Membranous Nephropathy

Start date: June 2, 2023
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy, safety, pharmacokinetics(PK) ,pharmacodynamics and anti-drug antibodies(ADA) of MIL62 compared with cyclosporine in participants with primary membranous nephropathy (pMN).

NCT ID: NCT05862181 Recruiting - Clinical trials for Advanced Hepatocellular Carcinoma (HCC)

The Comparison Between HepaSphere Drug-eluting Bead Transarterial Chemoembolization Combined With Hepatic Arterial Infusion Chemotherapy in Advanced Hepatocellular Carcinoma

Start date: January 1, 2023
Phase:
Study type: Observational

Transarterial chemoembolization (TACE) is widely applied and shows good efficacy in advanced hepatocellular carcinoma (HCC). Recently, hepatic arterial infusion chemotherapy (HAIC) has also gained popularity in the treatment of HCC. Several studies have described the comparison between HAIC and TACE or TACE combined with HAIC. However, the evaluation between TACE plus HAIC and HAIC is rarely reported. Here, we will evaluate the performance of HepaSphere DEB-TACE combined with HAIC (HEPA-HAIC) comparing to HAIC in patients with advanced HCC

NCT ID: NCT05862168 Recruiting - Clinical trials for Oral Squamous Cell Carcinoma

Neoadjuvant Treatment of Tislelizumab Combined Chemotherapy for Locally Advanced Oral Squamous Cell Carcinoma :A Single-arm, Prospective, Phase II Trial

Start date: May 8, 2023
Phase: Phase 2
Study type: Interventional

TPF is still recommended as the preferred induction chemotherapy regimen for nonsurgical treatment of patients with LA HNSCC. Based on the KEYNOTE-048 study, all major guidelines recommend PD-1 monotherapy or PD-1 combined with chemotherapy as the new first-line standard treatment for patients with advanced HNSCC. The immunotherapy in operable LA HNSCC was also explored as neoadjuvant therapy due to the excellent data in advanced HNSCC. These explorations have also achieved good results. Therefore, this study aims to explore the pathological remission rate, the long-term benefit and safety of Tislelizumab combined with albumin paclitaxel, cisplatin and fluorouracil for locally advanced oral squamous cell carcinoma.

NCT ID: NCT05862103 Recruiting - Clinical trials for Acute Myocardial Infarction

Long-Term Follow-Up in Patients With Acute Myocardial Infarction Cohort

Start date: December 20, 2022
Phase:
Study type: Observational

AMI Survivors who participated in the project "Construction and key technology research of the whole myocardial protection system for acute myocardial infarction" (project number 2016YFC1301100) and completed the 1-year visit were followed up by telephone at 3 years (within the corresponding follow-up time window) and 5 years after discharge to acquire the patients' medication, health status, and major adverse cardiovascular and cerebrovascular events, including death, heart failure, rehospitalization, re-myocardial infarction, revascularization, stroke, malignant arrhythmia, and bleeding events.