Efficacy and Safety of Microtransplantation for Advanced and Relapsed Solid Tumors
1 other identifier
interventional
10
1 country
3
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started Jan 2026
Typical duration for phase_1
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 13, 2026
CompletedStudy Start
First participant enrolled
January 15, 2026
CompletedFirst Posted
Study publicly available on registry
January 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 16, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2028
January 21, 2026
January 1, 2026
2 years
January 13, 2026
January 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Treatment-Emergent Adverse Events
Treatment related mortality
1 month
time of hematopoietic recovery
Absolute neutrophil count \>500/μL; Platelets ≥20,000/μL
1 month
Secondary Outcomes (1)
Disease Control Rate, DCR
1 year
Study Arms (1)
microtransplantation; MST
EXPERIMENTALconventional chemotherapy with microtransplantation
Interventions
conventional chemotherapy with microtransplantation(MST). Microtransplantation, which is the infusion of granulocyte colony stimulating factor (G-CSF) mobilized HLA-mismatched peripheral blood mononuclear cells (GPBMC)
Eligibility Criteria
You may qualify if:
- Patients are 18 to 90 years old, regardless of gender or race;
- Advanced / relapsed solid tumors (small cell lung cancer, ovarian cancer, cervical cancer, gastric and colorectal cancer, sarcoma, head and neck tumor, etc.) are confirmed by clinical or histopathological diagnosis;
- More than two kinds of tumors are allowed;
- Karnofsky score ≥ 40, ECoG physical status ≤ 3;
- There are measurable lesions;
You may not qualify if:
- The researchers considered patients who were not suitable to participate in this experiment;
- Patients with mental disorders;
- Patients who refuse to cooperate with the treatment;
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
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
Study Officials
- PRINCIPAL INVESTIGATOR
Xiang Lu, Professor
The First People's Hospital of Nanning
- PRINCIPAL INVESTIGATOR
huiqin Wei, Professor
Minzu Hospital of Guangxi Zhuang Autonomous Region
- PRINCIPAL INVESTIGATOR
yajing Huang, Professor
Innovvy(Beijing) Biomedical Technology Co., Ltd
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director
Study Record Dates
First Submitted
January 13, 2026
First Posted
January 21, 2026
Study Start
January 15, 2026
Primary Completion (Estimated)
January 16, 2028
Study Completion (Estimated)
June 1, 2028
Last Updated
January 21, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share