- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03034304
A Phase I Clinical Study for Evaluating the Safety and Efficacy of MASCT-I in Patients With Advanced Solid Tumors
Multi-center, Phase I Clinical Study to Evaluate the Safety and Tolerability of Multi-antigen Autologous Immune Cell Injection (MASCT-I) in Patients With Advanced Solid Tumor, and to Preliminarily Evaluate the Anti-tumor Efficacy of MASCT-I Alone, in Combination With Chemical Drugs, and in Combination With PD1 Antibody
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The multiple-antigen specific cell therapy which was developed by Hengrui Yuanzheng is optimized continuously and has been upgraded from the first-generation MASCT technology to MASCT-I. MASCT-I is a technology which add PD1 antibody in vitro cell culture process of MASCT cell culture to block PD1 receptor on immunocytes, release the brake on immunocytes' reinfusion and interaction with tumor cells for enhancing the efficacy of immunocytes' killing tumor cells. At present, the development and validation of manufacturing process has been completed, and it is urgently needed to conduct the validation of clinical effect.
This is a Multi-center, phase I clinical study to evaluate the safety and tolerability of multi-antigen autologous immune cell injection (MASCT-I) in patients with advanced solid tumor, and to preliminarily evaluate the anti-tumor efficacy of MASCT-I alone, in combination with chemical drugs, and in combination with PD1 antibody. About 193 cases of adult patients with advanced solid tumors will be recruited.
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Contacts and Locations
Study Contact
- Name: Xuemin Rao
- Phone Number: 021-61049928
- Email: raoxuemin@shhryz.com
Study Contact Backup
- Name: Fendi Yang
- Email: yangfendi@shhryz.com
Study Locations
-
-
Beijing
-
Beijing, Beijing, China
- Completed
- Cancer Hospital Chinese Academy of Medical Sciences
-
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Guangdong
-
Guangzhou, Guangdong, China, 510000
- Recruiting
- Sun Yat-Sen University Cancer Center
-
Principal Investigator:
- Ruihua Xu, doctor
-
Contact:
- Fendi Yang
- Email: yangfendi@shhryz.com
-
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Shanghai
-
Shanghai, Shanghai, China
- Not yet recruiting
- Ruijin Hospital, Shanghai Jiaotong University School of Medicine
-
Contact:
- Fendi Yang, master
- Email: yangfendi@shhryz.com
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Principal Investigator:
- Weibin Zhang, doctor
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Shanghai, Shanghai, China
- Not yet recruiting
- Shanghai Tenth People's Hospital
-
Contact:
- Fendi Yang, master
- Email: yangfendi@shhryz.com
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Principal Investigator:
- Qing Xu, doctor
-
Shanghai, Shanghai, China, 200032
- Completed
- Zhongshan Hospital affiliated to Fudan University
-
Shanghai, Shanghai, China
- Completed
- Shanghai Sixth People's Hospital
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Tianjin
-
Tianjin, Tianjin, China
- Completed
- Tianjin cancer hospital
-
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Zhejiang
-
Hangzhou, Zhejiang, China
- Not yet recruiting
- The Second Affiliated Hospital of Zhejiang University School of Medicine
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Contact:
- Fendi Yang, master
- Email: yangfendi@shhryz.com
-
Principal Investigator:
- Zhaoming Ye, doctor
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Hangzhou, Zhejiang, China
- Completed
- Zhejiang Tumor Hospita
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Major Inclusion Criteria:
- Age 18-70 at screening;
- Obtain written informed consent of the subject/legal representative prior to conducting any program related procedures, including evaluation during the screening period;
- Scored 0 -1 on ECOG;
- Life expectancy ≥6 months;
- Cardiopulmonary function is basically normal;
- Results of blood test and biochemistry at baseline meeting the following criteria:Hemoglobin≥85g/L,Leucocyte≥3.0×109/L,Absolute neutrophil count(ANC)≥1.5×109/L,Trombocyte≥70×109/L,ALT/AST ≤ 2.5×ULN or ≤ 5×ULN for patients with hepatic metastases, ALP≤2.5 times of upper limit of normal, Serum total bilirubin < 1.5×ULN,Serum urea nitrogen and creatinine ≤ 1.5×ULN,patients with urothelial carcinoma,Serum urea nitrogen and creatinine ≤ 2.5×ULN, Serum albumin ≥30g/L
For the first group of subjects, the following criteria should be met:
- Patients who suffer from advanced (unresectable) or recurrent solid tumors (only limited to bladder cancer and soft tissue sarcoma) confirmed by histology and cytology and are treated unsuccessfully with various standard therapies;
- According to RECIST1.1 criteria, there must be one measurable focus;
- Time interval between end of other anti-tumor measures and this study treatment is at least 1 month;
For the second group of subjects, the following criteria should be met:
- Urothelial carcinoma: histologically or cytologically confirmed that gemcitabine + platinum-based first-line chemotherapy achieved clinical benefit after 4-6 cycles of advanced recurrence or metastasis;
- Soft tissue sarcoma or osteosarcoma: Subjects who histologically or cytologically demonstrated clinical benefit after at least 4 cycles of doxorubicin-based first-line chemotherapy following advanced recurrence or metastasis. For some subjects who are intolerant or insensitive to chemotherapy, screening can also be conducted after other first-line treatment regiments achieve clinical benefit.
- Cholangiocarcinoma: Histologically or cytologically confirmed, first-line treatment after advanced recurrence or metastasis is beneficial.
Note: Clinical benefit is defined as complete response (CR), partial response (PR), or disease stabilization (SD). The disease stabilizes for more than 2 months.
For subjects in the third group, the following criteria should be met:
- Urothelial carcinoma: histologically or cytologically confirmed disease progression after advanced recurrence or metastasis following gemcitabine + platinum regimen first-line chemotherapy;
- Soft tissue sarcoma or osteosarcoma: histologically or cytologically confirmed disease progression after advanced recurrence or metastasis followed by first-line chemotherapy dominated by adriamycin; For some subjects who are intolerant or insensitive to chemotherapy, they can also be screened after other first-line treatment regiments fail.
- Cholangiocarcinoma: histologically or cytologically confirmed, progression after first-line treatment after advanced recurrence or metastasis;
- According to RECIST1.1, at least one measurable lesion must be present;
- An interval of at least 4 weeks between the end of other anticancer treatments and the treatment in this study;
For the fourth group of subjects, the following criteria should be met:
- Solid tumor with advanced recurrence or metastasis;
- PD1 antibody therapy has been used before, and the disease is progressing. The interval between the end of PD1 antibody therapy and this study is at least 4 weeks;
- According to RECIST1.1, at least one measurable lesion must be present;
- The interval between the end of other anticancer treatments and the treatment in this study should be at least 4 weeks;
For the fifth group of subjects, the following criteria should be met:
- Subjects with pathologically confirmed soft tissue sarcoma, locally advanced or metastatic, and inoperable, have not undergone systemic treatment;
- According to RECIST1.1, at least one measurable lesion must be present
For the sixth group of subjects, the following criteria should be met:
- Histologically or cytologically confirmed inoperable locally advanced or metastatic urothelial carcinoma (T4b, any N; Or any T, N 2-3) or metastatic urothelial carcinoma (M1, stage IV) including renal pelvis, ureter, bladder, and urethra);
- Had not previously received systemic chemotherapy for locally advanced or metastatic urothelial carcinoma (UC);
- At least one measurable lesion was evaluated (based on RECIST1.1 criteria); If the measurable lesion has previously undergone radiotherapy, it needs to be clearly documented that it is now a lesion after disease progression.
- For subjects who had previously received local intravesical infusion chemotherapy or immunotherapy, this local therapy needed to be completed at least 4 weeks prior to the initiation of the first chemotherapy in this trial
- Glomerular filtration rate ≥30ml/ min (creatinine clearance was calculated using the standard Cockcroft-Gault formula);
Major Exclusion Criteria:
- Subjects have clinically manifested central nervous system metastases (such as brain edema, need for hormonal intervention, or progression of brain metastases). Subjects who have received previous treatment for brain or meningeal metastasis, such as clinical stability (MRI) for at least 2 months, and have ceased systemic sex hormone therapy (>10mg/ day prednisone or other therapeutic hormones) for more than 2 weeks may be included;
- Subjects are receiving immunosuppressive, or systemic, or absorbable local hormone therapy for immunosuppression purposes (>10mg/ day prednisone or other therapeutic hormones) and continue to receive such therapy within 2 weeks prior to enrollment;
- Subjects are taking immunomodulator drugs and continue to use them within 2 weeks prior to enrollment;
- Subjects have received MASCT or other cellular immunotherapy or PD1 antibody therapy in the previous year (subjects in the fourth group are not limited to PD1 antibody therapy);
- Subject has any active autoimmune disease or a history of autoimmune disease;
- The subject has active tuberculosis;
- Subject has hepatitis C or HIV infection, or syphilis infection;
- Patients with gastrointestinal stromal tumor, Ewing sarcoma and rhabdomyosarcoma
- Patients with recurrence or metastasis during the adjuvant treatment after radical surgery or within 6 months after the end of the treatment (only for patients in Group 5 and Group 6):
- Those who have used targeted therapy, radiotherapy, immunotherapy or other treatment schemes with clear anti-tumor effect within 4 weeks before enrollment, such as arrotinib, gemcitabine and traditional Chinese medicine; However, if the focus of radiotherapy is not a target focus or there is clear progress after radiotherapy, it can be considered to be included in the group (only for the fifth and sixth groups of subjects);
- Those who are not suitable for treatment with A1 scheme (only for the fifth group of subjects)
- Hearing impairment with CTCAE grade>2 (for the sixth group)
- Peripheral neuropathy with CTCAE grade >2 (such as sensory degeneration, sensory abnormality, including tingling sensation) (for the sixth group);
- The investigators believed that the subjects were not suitable for chemotherapy containing platinum or gemcitabine (for the sixth group);
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MASCT-I alone or in combination with chemical drugs or in combination with PD-1 antibody
Group 1: MASCT-I alone; Group 2: Advanced urothelial carcinoma and cholangiocarcinoma treatment with MASCT-I alone,Advanced soft tissue sarcoma and osteosarcoma treatment with MASCT-I alone or combination with ifosfamide. In the event of disease progression, treatment with MASCT-I +PD1 antibody; Group 3: Advanced metastatic or recurrent urothelial carcinoma, soft tissue sarcoma/osteosarcoma, and cholangiocarcinoma that progressed after first line chemotherapy were treated with MASCT-I combined with PD1 antibody; Group 4: Recurrent metastatic solid tumors that had failed previous treatment with PD1 antibody were treated with MASCT-I + PD1 antibody; Group 5: Untreated advanced soft tissue sarcom treatment with MASCT-I+AI (Adriamycin+ifosfamide); Group 6: Untreated advanced urothelial carcinoma treatment with MASCT-I+GP/GC(Gemcitabine+cisplatin/ Gemcitabine+carboplatin); |
The final products of MASCT-I technology are dendritic cells (DC) and effector T cells
2g/m2/d, intravenous drip for 30min.
Administration is conducted for continuous 5 days.
After 4 weeks, the above cycle is repeated for 6 continuous cycles
200 mg/every two weeks ,four weeks is a cycle.
Subjects were treated with MASCT-I combined with PD1 antibody until disease progression, MASCT-I intolerance or study completion.
If PD1 antibody intolerance occurs, MASCT-I therapy alone will continue.
MASCT-I and PD1 antibody are adminnistered according to their respective drug cycle without interfering with each other.
60mg/m2, from the first day of each cycle, it is used for 1-2 days, intravenous drip.
Repeat the above cycle after 4 weeks, no more than 8 cycles
1000 mg/m2, Intravenous drip for about 30 min, used on the first and eighth days of each cycle, and every 3-4 weeks as a cycle
70mg/m2, Use on the first day of each chemotherapy cycle, intravenous drip for 30-120 min, and every 3-4 weeks as a cycle;
5mg/ml/min, Use it on the first day of each chemotherapy cycle, intravenous drip for 30 minutes, and every 3-4 weeks as a cycle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence of Treatment-Emergent Adverse Events(Safety)
Time Frame: up to 96 weeks
|
All the local reactions, systemic reactions, adverse events and serious adverse events of all the patients will be collected from the informed consent to the end of the study.
|
up to 96 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Overall Survival (OS)
Time Frame: up to 96 weeks
|
From enrollment to death of patients
|
up to 96 weeks
|
Time to recurrence (TTR)
Time Frame: up to 96 weeks
|
the period of time from signing of the ICF by the patient to progression of tumor
|
up to 96 weeks
|
Objective response rate
Time Frame: up to 96 weeks
|
The percentage of subjects with PR or CR.
|
up to 96 weeks
|
Incidence of Treatment-Emergent Adverse Events(Safety)
Time Frame: up to 96 weeks
|
All the local reactions, systemic reactions, adverse events and serious adverse events of all the patients will be collected from the the informed consent to the end of the study.
|
up to 96 weeks
|
Disease Control Rate (DCR)
Time Frame: up to 96 weeks
|
Disease control rate is defined as the number of patients with a best overall response of complete response (CR), partial response (PR), or stable disease (SD) based on RESIST v1.1 criteria
|
up to 96 weeks
|
Progression-Free Survival (PFS)
Time Frame: up to 96 weeks
|
The length of time from enrollment until the time of progression of disease
|
up to 96 weeks
|
time to progression(TTP)
Time Frame: up to 96 weeks
|
Time from the first successful apheresis to the first progression of the tumor.
|
up to 96 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ruihua Xu, Doctor, Sun Yat-sen University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neoplasms
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Anti-Infective Agents
- Antiviral Agents
- Enzyme Inhibitors
- Antimetabolites, Antineoplastic
- Antimetabolites
- Antineoplastic Agents
- Immunosuppressive Agents
- Immunologic Factors
- Antineoplastic Agents, Alkylating
- Alkylating Agents
- Topoisomerase II Inhibitors
- Topoisomerase Inhibitors
- Antibiotics, Antineoplastic
- Gemcitabine
- Carboplatin
- Antibodies
- Ifosfamide
- Doxorubicin
- Liposomal doxorubicin
Other Study ID Numbers
- HRYZ MASCT-I-1001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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