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Spots Global Cancer Trial Database for Anti-PD-1 Antibody Alone or in Combination With Decitabine/Chemotherapy in Relapsed or Refractory Malignancies

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Trial Identification

Brief Title: Anti-PD-1 Antibody Alone or in Combination With Decitabine/Chemotherapy in Relapsed or Refractory Malignancies

Official Title: Anti-PD-1 Antibody Alone or in Combination With Low-dose Decitabine and/or Chemotherapy in Relapsed or Refractory Malignancies: an Open-label Phase I/II Trial

Study ID: NCT02961101

Study Description

Brief Summary: The purpose of this study is to assess the feasibility, safety, and efficacy of anti-PD-1 antibody alone or in combination with low-dose decitabine in patients with relapsed or refractory malignancies, including Non-Hodgkin'lymphoma, Hodgkin'lymphoma, gastrointestinal cancers, hepatocellular carcinoma, breast cancer, ovarian cancer or lung cancer or renal-cell cancer or pancreatic cancer or bile duct cancer.

Detailed Description: Primary objective: To assess the feasibility and safety for Anti-PD-1 antibody alone or in combination with decitabine and/or chemotherapy administered every 3 weeks to subjects with relapsed or refractory malignancies. Secondary objectives: 1) To assess the antitumor activity of Anti-PD-1 antibody alone or in combination with decitabine and/or chemotherapy in subjects with relapsed or refractory malignancies. 2) To characterize the immunological effects of Anti-PD-1 antibody alone or in combination with decitabine and/or chemotherapy. 3) To characterize the immunological effects of Anti-PD-1 antibody alone or in combination with decitabine and/or chemotherapy. Exploratory objectives: 1) To analysis of potential biological parameters correlated to clinical response and toxicities. 2) To search predictive biomarkers to guide the choose of patients undergoing the treatment of Anti-PD-1 antibody alone or in combination with decitabine and/or chemotherapy. Safety Evaluation: Adverse events will be assessed continuously during the study and for 100 days post last treatment, and will be evaluated according to the NCI CTCAE Version 4.0. Efficacy Evaluation: 1) Treatment response to lymphoma was defined using the International Workshop to Standardize Response Criteria for Lymphomas; 2) Treatment response to solid tumors was defined using Response Evaluation Criteria in Solid Tumors (RECIST1.1). evaluation index: BOR; ORR; PFS and OS.

Eligibility

Minimum Age: 12 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Biotherapeutic Department of Chinese PLA General Hospital, Beijing, Beijing, China

Contact Details

Name: Chunmeng Wang, Master

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: STUDY_DIRECTOR

Name: Wenying Zhang, Master

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: STUDY_DIRECTOR

Name: Yang Liu, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: STUDY_DIRECTOR

Name: Meixia Chen, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: STUDY_DIRECTOR

Name: Yan Zhang, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: PRINCIPAL_INVESTIGATOR

Name: Qian Mei, Doctor

Affiliation: Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, 100853, China.

Role: STUDY_DIRECTOR

Name: Jing Nie, Doctor

Affiliation: Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, 100853, China.

Role: STUDY_DIRECTOR

Name: Xiang Li, Master

Affiliation: Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, 100853, China.

Role: PRINCIPAL_INVESTIGATOR

Name: Liang Dong, Master

Affiliation: Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, 100853, China.

Role: PRINCIPAL_INVESTIGATOR

Name: Lu Shi, Master

Affiliation: Department of Molecular Biology, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, 100853, China.

Role: PRINCIPAL_INVESTIGATOR

Name: Kaichao Feng, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: PRINCIPAL_INVESTIGATOR

Name: Jingdan Qiu, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: PRINCIPAL_INVESTIGATOR

Name: Hejin Jia, Doctor

Affiliation: Biotherapeutic Department of Chinese PLA General Hospital, Beijing, China, 100853

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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