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In this study, microtransplantation (MST) will be administrated to patients diagnosed with advanced / relapsed solid tumors to assess the therapeutic efficacy and safety of conventional chemotherapy in combination with MST for the treatment of advanced/relapsed solid tumors.
In this study, the eligible patients will receive MST treatment following conventional chemotherapy, MST is the infusion of G-PBMCs after chemotherapy. G-PBMCs are peripheral blood mononuclear cells from HLA mismatched unrelated donors mobilized by granulocyte colony-stimulating factor (G-CSF). Based on the patient's medical history, current tumor assessment results, and the latest cancer treatment guidelines, an individualized chemotherapy plan for the patient is formulated through discussions among more than three oncologists. After each course of treatment, all relevant indicators, including efficacy and safety measures are evaluated. Patients will receive all treatment for four courses, with an interval of 21 to 28 days. After completing all the treatment courses, the patient will enter the evaluation stage. Patients who have entered the evaluation stage are permitted to receive any treatments, including symptomatic support treatment, after the completion of treatment or withdrawal from the study.
Age
18 - 90 years
Sex
ALL
Healthy Volunteers
No
Innovvy(Beijing) Biomedical Technology Co., Ltd
Haidian, Beijing Municipality, China
Minzu Hospital of Guangxi Zhuang Autonomous Region
Nanning, Guangxi, China
The First People's Hospital of Nanning
Nanning, Guangxi, China
Start Date
January 15, 2026
Primary Completion Date
January 16, 2028
Completion Date
June 1, 2028
Last Updated
January 21, 2026
10
ESTIMATED participants
MST
BIOLOGICAL
Lead Sponsor
The Affiliated Hospital of the Chinese Academy of Military Medical Sciences
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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