跳至主要内容
临床试验/CTRI/2010/091/001348
CTRI/2010/091/001348进行中(未招募)2 期

PHASE II CLINICAL TRIAL OF IMMUNOTHERAPY WITH AN ALLOGENEIC B7.1/HLA-A1 TRANSFECTED TUMOR CELL VACCINE (PT 107) IN PATIENTS WITH STAGES IIIB/IV NON-SMALL CELL LUNG CANCER THAT HAVE COMPLETED FIRST LINE CHEMOTHERAPY

PIQUE THERAPEUTICS INC0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Patients with documented stage IIIB or IV advanced or metastatic NSCLC who have completed 4-6 cycles of platinum based chemotherapy, with or without radiation, and have either stable disease or have experienced disease progression (additional prior adjuvant chemotherapy is permitted).
  • 2. ECOG performance status 0-2.
  • 3. Presence of at least one measurable lesion according to RECIST criteria.
  • 4. Renal Requirements: The calculated creatinine clearance must be at least 50 ml/min.
  • 5. Pulmonary Function Requirements
  • All patients will undergo evaluation of pulmonary function prior to enrollment. Patients should have a FeV1 more than 30% of the predicted value and/or DLCO more than 30% of the predicted value with a PCO2 < 45mm. Any patient enrolled in the protocol whose respiratory symptoms have experienced marked deterioration not related to a known cause (e.g. pneumonia, CHF or PE) will have request PFT evaluation and if the above parameters are not fulfilled will be excluded from the protocol.
  • 6. Age > or = 18 years.
  • 7. Signed informed consent.
  • 8. ANC > or =1000/mm3; PLT> or = 80,000/mm3.
  • 9. Hemoglobin > or = 10 g/dL.

排除标准

  • 1. Small cell carcinoma of the lung.
  • 2. Existing autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus, Sjogren's disease etc; colitis, inflammatory bowel disease or pancreatitis within 10 years of study.
  • 3. Other active malignancies present within the past three years, except for basal and / or squamous cell carcinoma(s) or in situ cervical cancer.
  • 4. Concomitant steroid or other immunosuppressive therapy.
  • 5. Active infection, or less than 7 days since therapy for acute infections.
  • 6. Pericardial effusion.
  • 7. Currently receiving chemotherapy for another condition (such as arthritis).
  • 8. Active or symptomatic cardiac disease such as congestive heart failure, angina pectoris or recent myocardial infarction.
  • 9. Pregnant or lactating women (negative test for pregnancy required of women of child bearing potential).
  • 10. Refusal in fertile men or women to use effective birth control measures during and for six months after the completion of treatment on study.
  • 11. Known HIV infection.
  • 12. Untreated or uncontrolled brain metastasis.
  • 13. ASL or ALT > or = 2.5 times the upper limit of normal (ULN).
  • 14. Alkaline Phosphatase > or = 5 times ULN.

研究者

相似试验

已完成
不适用
Phase II Study of Adoptive Immunotherapy Comprising 2-Methyl-3-Butenyl-1-Pyrophosphate-Stimulated Gamma Delta T Cells, Teceleukin, and Zoledronic acid in Patients With Stage IV Renal Cell CarcinomaCytokine refractory Renal cell carcinoma
JPRN-UMIN000004482Tokyo Women&#39;s Medical University35
进行中(未招募)
不适用
A Phase II trial evaluating the immunological and clinical efficay and safety of HER-2 Protein Autovac(TM) monotherapy in patients with metastatic breast cancer - NAFemale patients with histologically proven metastatic or locally advanced breast cancer who have HER-2 overexpression in the primary tumour and/or a metastatic lesion.
EUCTR2004-000838-36-HUPharmexa A/S60
进行中(未招募)
不适用
A Phase II trial evaluating the immunological and clinical efficacy and safety of HER-2 Protein AutoVac(TM) and Stimulon® Adjuvant QS-21 monotherapy in patients with metastatic breast cancer
EUCTR2005-000558-60-HUPharmexa A/S60
未知
1 期
Phase I/II study of adoptive immunotherapy using cytotoxic T cells specific for minor histocompatibility antigen restricted to hematopoietic cells for patients with high-risk leukemia that relapsed following allogeneic hematopoietic stem cell transplantatio1) RAEB, CMML 2) AML or ALL in induction failure or beyond first remission 3) Ph/p190-positive ALL at any stage 4) imatinib-resistant CM
JPRN-C000000162Aichi Cancer Center30
已完成
1 期
A phase I clinical study of immune cell therapy with MAGE-A4- or Survivin-specific Th1 cells for patients with refractory virulent tumorsRefractory cancer patients (MAGE-A4- or Survivin-expressing, non origin-limited) or the patients who refuse standard cancer therapy
JPRN-UMIN000004828Department of General Surgery, Hokkaido University Graduated School of Medicine18
A CLINICAL TRIAL TO STUDY THE EFFICACY AND SAFETY OF... | 临床试验