Clinical Study of a Personalized Neoantigen Cancer Vaccine in Treating Patients With Advanced Pancreatic Cancer

NCT ID: NCT03645148

Last Updated: 2021-11-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-24

Study Completion Date

2021-04-01

Brief Summary

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This research study is evaluating a new type of pancreatic cancer vaccine called "Personalized Neoantigen Cancer Vaccine" as a possible treatment for advanced pancreatic cancer. The purpose of the clinical study is evaluating the safety, tolerability and partial efficacy of the personalized neoantigen cancer vaccine in the treatment of Chinese patients with advanced pancreatic cancer, so as to provide a new personalized therapeutic strategy for advanced pancreatic cancer patients.

It is known that cancer patients have mutations (changes in genetic material) that are specific to an individual patient and tumor. These mutations can cause the tumor cells to produce proteins that appear very different from the body's own cells. It is possible that these proteins used in a vaccine may induce strong immune responses, which may help the participant's body fight any tumor cells that could cause the cancer to come back in the future. The study will examine the safety of the vaccine when given at several different time points and will examine the participant's blood cells for signs that the vaccine induced an immune response.

Detailed Description

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Conditions

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Pancreatic Cancer Pancreatic Carcinoma

Keywords

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Neoantigen, Pancreatic Cancer, iNeo-Vac-P01,Peptide Vaccine

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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iNeo-Vac-P01

Personal Cancer Vaccine: iNeo-Vac-P01 (peptides)+ GM-CSF;

Peptides: 4 x 100 mcg per peptide given on days 1, 4, 8, 15, 22, 78, and 162 for a total of 7 doses;

GM-CSF: 4 x 40 mcg (total dose 160 mcg) given on days 1, 4, 8, 15, 22, 78, and 162 for a total of 7 doses

Group Type EXPERIMENTAL

iNeo-Vac-P01

Intervention Type BIOLOGICAL

Neoantigen peptides

GM-CSF

Intervention Type OTHER

immune adjuvant

Interventions

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iNeo-Vac-P01

Neoantigen peptides

Intervention Type BIOLOGICAL

GM-CSF

immune adjuvant

Intervention Type OTHER

Other Intervention Names

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granulocyte-macrophage colony stimulating factor

Eligibility Criteria

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Inclusion Criteria

* Must freely sign informed consent;
* Aged 18 to 70 years old;
* The expected survival period is more than 6 months;
* ECOG score is 0 or 1;
* Advanced pancreatic cancer diagnosed by Pathology and imageology;
* Tumor cannot be excised by surgery, and multiline chemotherapy, radiation, targeted therapy fails, or other treatments cannot be tolerated;
* At least one measurable lesions;
* To be able to obtain sufficient tumor tissue samples and blood samples for analysis, or to have genomic/exon/transcriptional data of tumor tissues and normal tissues, and the data meet the analysis requirements;
* The main organs function is normal, such as the heart, liver and kidney;
* Haematological index:

neutrophil count≥1.5×10e9/L hemoglobin≥10g/dL platelet count≥100×10e9/L

* Biochemical index:

Total bilirubin is less than or equal to 1.5 times the upper limit of normal value (ULN) AST and ALT is less than or equal to 2.5 times the upper limit of normal value Serum creatinine and urea nitrogen (BUN) is less than or equal to 1.5 times the upper limit of normal value

* Pregnant, lactating women and women of child-bearing age must have a negative pregnancy test within 7 days before entering the group, and short-term have no fertility plan, and are willing to take protective measures (contraception or other birth control methods) before and during the clinical trial;
* Good compliance, able to follow research protocols and follow-up procedures.

Exclusion Criteria

* Diagnosed as other malignant tumor;
* There have been bone marrow or stem cell transplants;
* No neoantigen was found in the sequencing data;
* Systemic cancer treatment or other drugs under study were treated within 4 weeks prior to Individualized tumor targeted polypeptides treatment;
* Received other polypeptide inoculation 4 weeks before treatment; Patients may not be vaccinated with other polypeptides 8 weeks after the last individualized tumor targeted polypeptides trentment;
* Active bacterial or fungal infections identified clinically (\>= level 2 of NCI-CTC edition 3);
* Patients with HIV, HCV, HBV infection, severe asthma, autoimmune disease, immunodeficiency or treated with immunosuppressive drugs;
* Severe coronary or cerebrovascular disease, or other diseases that the investigators considered should to be exclusion;
* Drug abuse. Clinical, psychological or social factor result in affecting informed consent or research implementation;
* Have a history of drug or polypeptide allergies, or people who are allergic to other potential immunotherapies.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hangzhou Neoantigen Therapeutics Co., Ltd.

INDUSTRY

Sponsor Role collaborator

Zhejiang Provincial People's Hospital

OTHER

Sponsor Role lead

Responsible Party

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Liu Yang

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Zhejiang Provincial People's Hospital

Hangzhou, Zhejiang, China

Site Status

Countries

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China

References

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Ott PA, Hu Z, Keskin DB, Shukla SA, Sun J, Bozym DJ, Zhang W, Luoma A, Giobbie-Hurder A, Peter L, Chen C, Olive O, Carter TA, Li S, Lieb DJ, Eisenhaure T, Gjini E, Stevens J, Lane WJ, Javeri I, Nellaiappan K, Salazar AM, Daley H, Seaman M, Buchbinder EI, Yoon CH, Harden M, Lennon N, Gabriel S, Rodig SJ, Barouch DH, Aster JC, Getz G, Wucherpfennig K, Neuberg D, Ritz J, Lander ES, Fritsch EF, Hacohen N, Wu CJ. An immunogenic personal neoantigen vaccine for patients with melanoma. Nature. 2017 Jul 13;547(7662):217-221. doi: 10.1038/nature22991. Epub 2017 Jul 5.

Reference Type BACKGROUND
PMID: 28678778 (View on PubMed)

Weden S, Klemp M, Gladhaug IP, Moller M, Eriksen JA, Gaudernack G, Buanes T. Long-term follow-up of patients with resected pancreatic cancer following vaccination against mutant K-ras. Int J Cancer. 2011 Mar 1;128(5):1120-8. doi: 10.1002/ijc.25449.

Reference Type BACKGROUND
PMID: 20473937 (View on PubMed)

Chen Z, Zhang S, Han N, Jiang J, Xu Y, Ma D, Lu L, Guo X, Qiu M, Huang Q, Wang H, Mo F, Chen S, Yang L. A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment. Front Immunol. 2021 Aug 13;12:691605. doi: 10.3389/fimmu.2021.691605. eCollection 2021.

Reference Type DERIVED
PMID: 34484187 (View on PubMed)

Other Identifiers

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INEO-P-001

Identifier Type: -

Identifier Source: org_study_id