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NCT ID: NCT05339685 Recruiting - Breast Cancer Clinical Trials

A Study of BL-M02D1 in Patients With Locally Advanced or Metastatic Triple Negative Breast Cancer or Other Solid Tumors

Start date: May 20, 2022
Phase: Phase 1
Study type: Interventional

In phase Ia study, the safety and tolerability of BL-M02D1 in patients with locally advanced or metastatic triple negative breast cancer or other solid tumors will be investigated to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) of BL-M02D1. In phase Ib study, the safety and tolerability of BL-M02D1 at the phase Ia recommended dose will be further investigated, and recommended phase II dose (RP2D) for phase II clinical studies will be determined. In addition, the preliminary efficacy, pharmacokinetic characteristics, and immunogenicity of BL-M02D1 in patients with locally advanced or metastatic triple negative breast cancer or other solid tumors will be evaluated.

NCT ID: NCT05339646 Recruiting - Clinical trials for Healthy Participants

A Phase I Clinical Study of SSD8432 in Healthy Adult Subjects

Start date: April 7, 2022
Phase: Phase 1
Study type: Interventional

This is a Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of SSD8432 in Healthy Adult Subjects

NCT ID: NCT05339568 Recruiting - Metastatic NSCLC Clinical Trials

Patient's Whole Process Follow-up Management(HOPE-1)

HOPE-1
Start date: May 22, 2022
Phase:
Study type: Observational

Our project is going to explore whether management and follow-up of locally advanced/metastatic patients using the patient process management platform can prolong patient survival and improve patient quality of life.

NCT ID: NCT05339529 Recruiting - Clinical trials for Acute Aortic Syndrome

Additive Anti-inflammatory Action for Aortopathy & Arteriopathy (Thymosin α1) V

Start date: July 1, 2022
Phase: N/A
Study type: Interventional

Systemic inflammatory response syndrome (SIRS) and multiple organ dysfunction syndrome (MODS) are the major causes of death in patients with acute aortic syndrome (AAS). Therefore, the prevention of SIRS and MODS is of great clinical value, and immunomodulatory therapy with thymosin alpha 1 may be beneficial. This study was designed to test the hypothesis that the administration of thymosin alpha 1 during the acute phase of AAS will result in a reduced incidence of SIRS and MODS.

NCT ID: NCT05339425 Recruiting - Osteoporosis Clinical Trials

Chinese Osteoporotic Fracture Registration Network Platform

CORN
Start date: December 1, 2021
Phase:
Study type: Observational [Patient Registry]

China has gradually entered an aging society, and the incidence of osteoporotic fractures is increasing rapidly. Although the harm of osteoporotic fracture is huge, its diagnostic rate in China is still low. China still lacks a national osteoporotic fracture registration system, which has been established in many countries. The purpose of this study is to establish a Chinese osteoporotic fracture registration network platform (CORN), which will be helpful for the long-term comprehensive management of osteoporotic fracture population in China. This platform will help to establish a large prospective clinical cohort database of osteoporotic fractures and high-risk population in China.

NCT ID: NCT05339321 Recruiting - Clinical trials for Hepatocellular Carcinoma

Autologous HBV-specific T Cell Receptor Engineered T Cells (TCR-T) in Patients With HBV-related Advanced HCC

Start date: April 14, 2021
Phase: Phase 1
Study type: Interventional

Adoptive cell therapy with TCR-T cells targeting HBV antigens represents an innovative opportunity for treatment of HBV-related HCC. SCG101 is a genetically modified autologous TCR-T cell therapy with a natural high-avidity TCR directed towards the HLA-A*02-restricted HBsAg peptide. This is a phase 1 clinical study of SCG101 alone and with PD-1/PD-L1 checkpoint inhibitors in HBV-related HCC.

NCT ID: NCT05339269 Recruiting - Cirrhosis, Liver Clinical Trials

The Effect of Laparoscopic Splenectomy on the Immune Function for Cirrhosis Patients

ELSI
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

In this study, the investigators compared the improvement of and azygoportal disconnection related indicators in patients with liver cirrhosis after laparoscopic splenectomy. To determine whether surgical treatment can help enhance postoperative immune function and improve patient prognosis.

NCT ID: NCT05339217 Recruiting - Clinical trials for Systemic Lupus Erythematosus

Efficacy and Immunological Evaluation of Telitacicept and Low Dose IL2 in the Treatment of Systemic Lupus Erythematosus

Start date: February 7, 2023
Phase: Phase 3
Study type: Interventional

The purpose of this study was to explore the clinical and immunological efficacy of Telitacicept and low dose IL-2 on systemic lupus erythematosus.

NCT ID: NCT05338957 Recruiting - Clinical trials for Advanced Malignant Solid Tumors

A Study of MRG002 in the Treatment of Patients With HER2-expressed Advanced Malignant Solid Tumors.

Start date: August 5, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to assess the safety and tolerability of MRG002 in combination with HX008 in patients with HER2-expressed advanced malignant solid tumors; and to , explore the maximum tolerated dose (MTD), and to determine the recommended phase II dose (RP2D) of combination therapy; , and to evaluate the preliminary efficacy, pharmacokinetics, and immunogenicity of combination therapy in the targeted study population.

NCT ID: NCT05338827 Recruiting - Clinical trials for Laparoscopic Surgery

Comparison of a Polyvinyl Chloride Tube With a Wire-reinforced Tube for Tracheal Intubation Through the SaCoVLM

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

To compare a polyvinyl chloride tube with a wire-reinforced tube for tracheal intubation through the SaCoVLM video laryngeal mask airway, to observe the success rate of intubation and the incidence of postoperative adverse reactions, and to explore the best type of endotracheal tube through the SaCoVLM video laryngeal mask airway, so as to provide reference for its clinical application.