Sintilimab and Lenalidomide as a Treatment for CAEBV

CAEBV Clinical Trial

Official title:

Sintilimab and Lenalidomide as a Treatment for CAEBV：a Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04518982
• Other study ID #: Sintilimab,Lenalidomide,CAEBV
• Status: Recruiting
• Phase: Phase 2
• Start date: August 1, 2020
• Est. completion date: August 1, 2021

Study information

• Verified date: August 2020
• Source: Beijing Friendship Hospital
• Contact: jingshi wang
• Phone: 86-010-63139862
• Email: wangjingshi987[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a multi-center, prospective, randomized, controlled clinical study to evaluate the effectiveness of a combination regimen of Sintilimab and lenalidomide in patients with chronic active EBV infection.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 51
• Est. completion date: August 1, 2021
• Est. primary completion date: August 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Patients with CAEBV confirmed by WHO criteria.

2. The Eastern United States Oncology Cooperative group (ECOG) Physical Status score is 0 or 1.

3. Before the study, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =3× normal upper limit (ULN); Total bilirubin =2 times the normal upper limit; Serum creatinine =1.5 times the normal value.

4. Absolute neutrophil count =1×109/L; Platelet =50×109/L; Hemoglobin =60 g/L.

5. International standardized ratio =2.0, prothrombin time =1.5×ULN.

6. A woman of childbearing age must be determined not to be pregnant by a pregnancy test and is willing to take effective measures to prevent pregnancy during the trial period and =12 months after the last administration of the drug; All male subjects used contraceptive methods during the study period and =6 months after the last administration;

7. Sign the informed consent.

Exclusion Criteria:

1. There is evidence that EBV is associated with hematologic disease or malignancy, such as hemophagocytic syndrome, lymphoma-like granulomatosis, post-transplant lymphoproliferative disease, non-Hodgkin's lymphoma, Burkitt lymphoma, nasopharyngeal cancer, and gastric cancer.

2. Symptomatic EBV-associated diseases of the major organs, including the central nervous system and lungs.

3. Abnormal thyroid function.

4. Patients with grade II or above heart disease (including grade II) were identified according to the New York Heart Association (NYHA) score.

5. Have received any of the following treatments: PD-1 antibody, PD-L1 antibody or lenalidomide; Received any research drug within 12 weeks prior to the first use of the study drug; Another clinical study was also included.

6. Other primary malignancies occur within 5 years before the first administration of the drug, except those that are locally curable after radical treatment (such as basal or squamous cell skin cancer, superficial bladder cancer or carcinoma of the prostate, cervix or breast in situ, etc.).

7. A history of organ transplantation (such as liver transplantation, kidney transplantation, etc.).

8. Hematopoietic stem cell transplantation is expected during the study period.

9. Active hepatitis B (defined as hepatitis B surface antigen [HBsAg] positive during screening, or hepatitis B virus DNA titer test in peripheral blood greater than 1×103 copies/ml), and active hepatitis C (defined as hepatitis C antibody [HCV-AB] and HCV-RNA positive during screening). Serum HIV antigen or antibody positive. A history of syphilis.

10. Had major surgery within 4 weeks prior to the first medication or was expected to require major surgery during the study period.

11. Pregnant and lactating women;

12. A history of serious mental illness or drug abuse;

13. Uncontrollable infections (including lung infections, intestinal infections, etc.); Internal organ active massive hemorrhage (including gastrointestinal hemorrhage, alveolar hemorrhage, intracranial hemorrhage, etc.);

14. Allergic to the test drug ingredients or to a more severe allergic constitution;

15. Patients who cannot comply during the trial and/or follow-up phase.

Related Conditions & MeSH terms

• CAEBV

Intervention

Drug:
• Sintilimab and lenalidomide
Drug: Sintilimab 200mg ivgtt on day 1. Drug: lenalidomide 10mg orally once a day, day 1-14.
• Sintilimab placebo and lenalidomide placebo
Drug: Sintilimab placebo ivgtt on day 1. Drug: lenalidomide placebo orally once a day, day 1-14.

Locations

Country	Name	City	State
China	Beijing Friendship Hospital, Capital Medical University	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Zhao Wang

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Response rate	The rate of decline in ebV-DNA copy (defined as a 2log decrease in EBV-DNA copy) or negative rate in peripheral blood mononuclear cells and plasma	Twelve weeks after treatment
Secondary	Spleen size		Twelve weeks after treatment
Secondary	T and B lymphocyte subsets		Twelve weeks after treatment
Secondary	Pathological tissue or bone marrow		Twelve weeks after treatment
Secondary	treatment-related adverse events as assessed by CTCAE v4.0	Adverse events including thyroid function, liver function damage, myelosuppression, infection, bleeding and so on.	through study completion, an average of 1 years
Secondary	survival	From enrollment until death or the end of the experiment	1 year