Multiple Myeloma Trial of Orally Administered Salmonella Based Survivin Vaccine
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 1
- 试验地点
- 1
- 主要终点
- Number of patients with dose limiting toxicity (DLT) by CTCAE, v5.0
研究概览
简要总结
Multiple myeloma patients will receive a cancer vaccine, called TXSVN that has been derived from the bacteria Salmonella. TXSVN is a weakened form of a live vaccine strain of the Salmonella bacteria (also known as the CVD908ssb strain) that has been genetically modified in the laboratory to produce a protein known as Survivin that stimulates an immune response in the body to the Survivin tumor antigen. CVD908ssb has been administered to over 80 healthy donors as a Salmonella vaccine in reported clinical trials. This trial intends to explore administration of this vaccine at a lower dose than what was tested in healthy individuals.
Survivin belongs to the group of proteins known as tumor-associated antigens (TAAs). These are cell proteins that are specific to the cancer cell. They either are not found or are found in low levels normal cells in the human body. More than 90% of myeloma cancer cells have been shown to possess large quantities of Survivin.
TXSVN may activate the immune system which is your body's ability to fight disease, and help develop a response against cancer cells that express Survivin. Survivin has been safely targeted using immune cells, drugs or direct inhibitors in over 50 patients with cancers in published reports.
TXSVN, the modified strain of CVD908ssb has not been tested in humans to this date. TXSVN is an investigational product not approved by the U.S. Food and Drug Administration.
The purpose of this study is to find the largest safe dose of TXSVN, to learn what the side effects are, and to see whether this therapy might help participants with multiple myeloma.
详细描述
The vaccine will be administered orally (by mouth) as a solution mixed with sodium bicarbonate. Approximately 10 minutes prior to receiving the vaccine, participants will take sodium bicarbonate pills to assist with the absorption of the vaccine. Participants may be pre-treated with acetaminophen (Tylenol) and diphenhydramine (Benadryl). Acetaminophen (Tylenol) and diphenhydramine (Benadryl) are given to prevent a possible allergic reaction to the vaccine. Participants will remain in the clinic for three hours after receiving the vaccine for monitoring.Two doses of TXSVN will be given two weeks apart. Participants disease will be assessed pre-treatment and then 6 weeks after the second treatment. All of the treatments will be given by the Center for Cell and Gene Therapy at Houston Methodist Hospital.
In between the first and second treatments, and for 6 weeks after the last treatment, the investigators ask that participants not receive any other anti-cancer treatments such as radiation therapy or chemotherapy. If participants do receive any other therapies in-between the first and second treatment, then they will be taken off treatment and will not be able to receive the second treatment of cells.
This is a dose escalation study. This means that at the beginning, patients will be started on the lowest dose (1 of 3 different levels) of TXSVN. Once that dose schedule proves safe, the next group of patients will be started at a higher dose. This process will continue until all 3 dose levels are studied. If the side-effects are too severe, the dose will be lowered or the TXSVN administrations will be stopped.
Before being treated, participants will receive a series of standard medical tests:
- Physical exam.
- Blood tests to measure blood cells, kidney and liver function.
- Measurement of participants multiple myeloma by blood tests and bone marrow biopsy (when available).
- Measurements of participants tumor by routine imaging studies. The investigators will use the imaging study that was used before to follow the participants tumor: Computerized Tomography (CT), Magnetic Resonance Imaging (MRI), or Positron Emission Tomography (PET/CT), skeletal bone survey. These studies will be done on a case-by-case basis at the discretion of the participants treating physician.
- Pregnancy test (using a blood sample) if the participants is a female who can have children.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any patient, greater than or equal to 18 yrs old regardless of sex, with a diagnosis of Myeloma after receiving at least two lines of conventional therapy which can include an autologous HSCT. If a patient has received an autologous or syngeneic SCT they must be greater than 90 days post-transplant
- •Patients with life expectancy greater than or equal to 6 weeks.
- •Pulse oximetry of greater than 90% on room air in patients who previously received radiation therapy to the chest. This is not required in patients who have not received radiation therapy to the chest in the past.
- •Patients with a Karnofsky score of greater than or equal to 50
- •Patients with bilirubin less than or equal to 2x upper limit of normal and Hgb greater than or equal to 7.0 (transfusion allowed).
- •AST less than or equal to 3x upper limit of normal.
- •ANC greater than 1000 at the time of vaccination and an ALC greater than
- •Patients with a creatinine less than or equal to 2x upper limit of normal for age.
- •Patients should have been off other investigational therapy for one month prior to entry in this study.
- •Patients should be off anti-bacterial therapy for 14 days prior to vaccination
- •Patients should have been off conventional therapy for at least 1 week prior to entry in this study except immunomodulator drugs
- •Informed consent explained to, understood by and signed by patient. Patient given copy of informed consent.
- •Due to unknown effects of this therapy on a fetus, pregnant women are excluded from this research. The male partner should use a condom. Females of child-bearing potential must be willing to utilize one of the more effective birth control methods during the study unless female has had a hysterectomy or tubal ligation.
- •Ability to swallow medications
- •Exclusion Criteria
- •Severe intercurrent infection.
- •Patients receiving greater than 0.5 mg/kg/day (prednisone equivalent) of systemic corticosteroids
- •Pregnant or breast feeding.
- •Grade II or higher nausea, vomiting or diarrhea.
- •History of allergy to prior vaccination with a Salmonella vaccine
- •HIV infection
- •Unable to tolerate Salmonella directed antibiotics
- •Household contacts who are immunocompromised, pregnant or under 2 years of age.
排除标准
- 未提供
研究组 & 干预措施
CVD908ssb-TXSVN
3 different dosing schedules will be studied (3+3 design). At the beginning, patients will start on the lowest dose (1 of 3 different levels) of TXSVN. Once that dose schedule proves safe, the next group of patients will be started at a higher dose. This process will continue until all 3 dose levels are studied. If the side-effects are too severe, the dose will be lowered or the TXSVN administrations will be stopped. Each patient will receive 2 vaccinations at the same dose, 2 weeks apart, according to the following dosing schedules: The administration will be oral.
Dose Level 1
Day 0: 2 x 10^5 cfu
Day 14: 2 x 10^5 cfu
Dose Level 2
Day 0: 2 x 10^6 cfu
Day 14: 2 x 10^6 cfu
Dose Level 3
Day 0: 2 x 10^7 cfu
Day 14: 2 x 10^7 cfu
干预措施: CVD908ssb-TXSVN (Biological)
结局指标
主要结局
Number of patients with dose limiting toxicity (DLT) by CTCAE, v5.0
时间窗: 8 weeks
Incidence of dose limiting toxicities (DLT) of CVD908ssb-TXSVN vaccine in patients with multiple myeloma.
次要结局
- Overall response rate according to the modified International Myeloma Working Group (IMWG) Uniform Response criteria.(8 weeks)
研究者
Premal Lulla
Assistant Professsor, Center for Cell and Gene Therapy
Baylor College of Medicine