Personalized Tumor Neoantigen MRNA Therapy for Advanced Pancreatic Cancer.
Clinical Study to Evaluate the Safety and Efficacy of Personalized Tumor Neoantigen MRNA Therapy in Combination with PD-1 Antibody and Chemotherapy for Advanced Pancreatic Cancer.
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Tingbo Liang, MD., PhD.
- Phone Number: +8619941463683
- Email: liangtingbo@zju.edu.cn
Study Contact Backup
- Name: Yiwen Chen, MD.
- Phone Number: +8615088682641
- Email: yiwenchen0705@126.com
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China, 31000
- First Affiliated Hospital of Zhejiang University Schlool of Medicine
-
Contact:
- Yiwen Chen, MD.
- Phone Number: +8615088682641
- Email: yiwenchen0705@126.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
(1) Subjects who meet all the following entry criteria enter the pre-screening phase of the study:
- Voluntary signing of the informed consent form;
- Age: 18 and 75 years old, male or female;
- Evaluation as metastatic pancreatic cancer or postoperative recurrence according to the 2024 NCCN guidelines;
- No systemic treatment, or disease progression with gemcitabine-based first-line chemotherapy.
- An Eastern Cooperative Oncology Group (ECOG) physical fitness status score of 0 or 1;
- According to the efficacy evaluation criteria for solid tumors (RECIST 1.1);
- Can obtain sufficient fresh tumor tissue samples for exome and transcriptome sequencing analysis;
- Main organ function of heart, liver and kidney is normal:
- Ferproductive men and women of childbearing age agree to take effective contraception from the date to the last dose of test drug; women of childbearing age included premenopause and women within 2 years after menopause;
- Ability to follow the study protocol and follow-up procedures.
(2) Subjects who meet all the following enrollment criteria enter the formal screening stage of the study and enter the study medication process:
- Voluntary signing of the informed consent form;
- Age: 18 and 75 years old, male or female;
- Pancreatic ductal adenocarcinoma (PDAC) diagnosed by pathology (histology or cytology);
- No systemic treatment or gemcitabine-based first-line chemotherapy.
- An Eastern Cooperative Oncology Group (ECOG) physical fitness status score of 0 or 1;
- Main organ function of heart, liver and kidney is normal:
- Ferproductive men and women of childbearing age agree to take effective contraception from the date to the last dose of test drug; women of childbearing age include premenopause and women within 2 years after menopause;
- Ability to follow the study protocol and follow-up procedures.
Exclusion Criteria:
Subjects will be excluded from this study if they meet any of the following criteria:
- Pancreatic cancer has central nervous system metastasis or meningeal metastasis;
- At the same time with other malignant tumors, but cured basal cell cancer, thyroid cancer, cervical dysplasia, etc., have been in the disease for more than 5 years or do not considered to be easy to relapse except;
- History of bone marrow transplantation, allogeneic organ transplantation, or allogeneic hematopoietic stem cell transplantation;
- Patients with immunosuppressants, that is, those who require regular use of immunosuppressants 4 weeks before the screening period and the clinical study, including but not limited to the following conditions: severe asthma, autoimmune diseases or immune deficiency, treated with immunosuppressive drugs, and known history of primary immunodeficiency; except type 1 diabetes, autoimmune-related hypothyroidism requiring hormone therapy, vitiligo and psoriasis that do not require systemic therapy;
- Active bacterial or fungal infection identified by clinical diagnosis; a history of active TB or tuberculosis;
- Patients with positive human immunodeficiency virus (HIV) antibody, positive treponema pallidum for syphilis (TP) antibody, active hepatitis C (positive hepatitis C virus (HCV) antibody and positive HCV RNA result), active hepatitis B;
- Herpesvirus infection (except those who scab for more than 4 weeks); respiratory virus infection (except those who have recovered for more than 4 weeks);
- Uncontrolled complications include but are not limited to active infection, symptomatic congestive heart failure, unstable angina, arrhythmia; severe coronary artery disease or cerebrovascular disease, or other diseases considered unacceptable by the investigator;
- Previous history of drug abuse, clinical or psychological or social factors affecting informed consent or study implementation; a history of mental illness;
- Patients with a history of food, drug or vaccine allergy or other potential immunotherapy allergies as considered by the Investigator.
- Women born during pregnancy or lactation;
- The investigator is not fit for enrollment or may not complete the trial for other reasons.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Arm A
On D1 patients start the mFOLFIRINOX every 2 weeks, and the actual number of cycles of mFOLFIRINOX will be determined by the investigators according on the patients' physical condition, disease progression, adverse effects; on the same day, started Sintilimab, 200mg, intravenous infusion, every 3 weeks; On D43 ± 3, the first efficacy assessment will be conducted.
Patient with no disease progression, will continue the above treatment (mFOLFIRINOX Q2W + Sintilimab Q3W + individualized neoantigen mRNA injection Q3W); if disease progression, the patient will receive the second-line chemotherapy regimen (decided by investigators)+ Sintilimab Q3W + individualized neoantigen mRNA injection Q3W.
Patients will receive efficacy assessment every 6 weeks.
|
Sintilimab Injection, 200mg, intravenous infusion, every 3 weeks
The individualized anti-tumor new antigen iNeo-Vac-R01 injection was commissioned by Hangzhou Nuanjin Biotechnology Co., Ltd., and all patients were admitted into the therapeutic intervention group.
According to the results of previous non-clinical studies, the individualized mRNA injection of 100 μ g was a tolerable dose.
continuous intravenous infusion of fluorouracil 2400mg / m², for 46 hours, leucovorin 400mg / m², irinotecan 135mg / m², and oxaliplatin 68mg / m², every 2 weeks
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Occurence and frequence of AE and SAE
Time Frame: Up to 2 years
|
Occurence and frequence of Adverse Event (AE) and Serious Adverse Event (SAE) (NCI CTCAE 5.0)
|
Up to 2 years
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Objective reponse rate (ORR)
Time Frame: Up to 2 years
|
The proportion of patients who had tumor evaluated as PR according to RECIST1.1 criteria during the whole study
|
Up to 2 years
|
|
Disease control rate (DCR)
Time Frame: Up to 2 years
|
The proportion of patients who had tumor evaluated as PR or SD according to RECIST1.1 criteria during the whole study.
|
Up to 2 years
|
|
Progression-free survival (PFS)
Time Frame: Up to 2 years
|
The time from enrolled to disease pregression or death from any cause during the whole study.
|
Up to 2 years
|
|
Overall survival (OS)
Time Frame: Up to 2 years
|
The time from enrolled to death from any cause during the whole study
|
Up to 2 years
|
|
Progression-free survival Rate(1-Y-PFS%, 2-Y-PFS%,3-Y-PFS%)
Time Frame: Up to 3 years
|
The proportion of patients free from disease progression or death (whichever occurs first) at 12, 24, and 36 months.
|
Up to 3 years
|
|
Overall Survival Rate (1-Y-OS%,2-Y-OS%,3-Y-OS%)
Time Frame: Up to 3 years
|
The percentage of patients surviving at 12, 24, and 36 months.
|
Up to 3 years
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- CISPD-10
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.