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A Study of Thymoglobuline? Induction Therapy in Adult Recipients of Donated After Cardiac Death Kidney Transplant

A Study of Thymoglobuline? Induction Therapy in Adult Recipients of Donated After Cardiac Death Kidney Transplant

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIN-17011174
Enrollment
Unknown
Registered
2017-04-18
Start date
2017-06-16
Completion date
Unknown
Last updated
2018-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diseases of the kidney and urinary system

Interventions

None listed

Sponsors

The First Affiliated Hospital of Xi'an JiaoTong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Male or female; 2) Patient is a Chinese recipient of kidney transplant for the first time; 3) Patient is a recipient of kidney allograft from Chinese donors donated after cardiac death (including kidney donated after brain death followed by circulatory death); 4) Recipients age is between 18 to 65 years old (including 18 years); 5) Donors age is more than 5 years old; 6) Recipients weight is greater than or equal to 50 kg but less than or equal to 80 kg; 7) Patient fully understands the study and signs the informed consent form (ICF) prior to any study procedure.

Exclusion criteria

Exclusion criteria: 1. Patient is a multiple organ transplant recipient; 2. Recipient with previous kidney or other organ transplant history; 3. Recipient and donor have incompatible blood types; 4. Recipient and donor have 5 or 6 mismatched human leucocyte antigen (HLA); 5. Recipient is known to have an active infection or active chronic infection, or is seropositive for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV Ab), or human immunodeficiency virus (HIV). (Serological test results within 12 months before transplantation are acceptable.); 6. Recipient with cytomegalovirus (CMV) IgG negative who receives an allograft from CMV IgG positive donor (CMV IgG (D+/R-)); 7. Recipient with any systemic infection requiring continuous treatment at enrolment, but prophylactic treatment of CMV and/or Pneumocystis carinii pneumonia (PCP) is allowed; 8. Recipient has severe thrombocytopenia or leucopenia before operation (platelet count <75,000/ul, or the number of white blood cells <3,000 cells/mm3); 9. Serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST) or gamma glutamine transferase (GGT) =3ULN (upper limit of normal) within 1 week before transplantation, and not normalized at time of transplantation; 10. Recipient has a history of malignancy within 5 years; 11. Recipient with history of allergy and anaphylaxes to rabbit proteins or to any excipients; 12. Recipient has known contraindications to the administration of Thymoglobuline; 13. Recipient has taken other investigational drugs or prohibited therapy for this study within 1 month or 5 of half-lives from screening, whichever is longer; 14. Recipient has previously used Thymoglobuline or has participated in any clinical trial of any other medicine or device within 30 days before signing ICF; 15. Pregnant or lactating women; 16. Male and female patients do not agree to practice medically acceptable contraception (i.e., barrier or pharmacologic: male patient must use condoms or his female partner must take oral contraceptives; the male partner of a female patient must use condoms) for at least 6 months following the study treatment; 17. Conditions/situations such as: (1) Recipient not suitable for participation, whatever the reason, as judged by the Investigator, including medical, clinical, or psychosocial conditions, or patient potentially at risk of noncompliance to study procedures. (2) Donor known or suspected to have active infection before donation (such as blood cultures positive, seropositive for hepatitis B surface antigen (HBsAg), or antibody against hepatitis C virus (HCVAb), or human immunodeficiency virus (HIV) ) or hypersensitive recipients(eg. PRA positive)before transplantation, judged by the Investigator.

Design outcomes

Primary

MeasureTime frame
The incidence of biopsy-proven acute rejection (BPAR) at Month 6 after DCD kidney transplant among recipients receiving standard dose of Thymoglobuline;

Secondary

MeasureTime frame
The incidence of DGF and duration of DGF;Graft survival and patient survival at 6 months post-transplantation;The incidence of infection, leucopenia, thrombocytopenia, malignancies at 6 months post-transplantation 6;Possible risk factors of AR/DGF in recipients of DCD kidney transplant;The incidence of AR and DGF under differential risk stratification;

Countries

China

Contacts

Public ContactXinxin Song

SANOFI (CHINA) INVESTMENT CO., LTD. SHANGHAI BRANCH

Xinxin.song@sanofi.com+86 010-65634709

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026