Research Study of ATG and Rituximab in Renal Transplantation

Part of paid clinical trials in San Francisco, California.

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Study ID
NCT01318915
Phase
EARLY_PHASE1
Status
Terminated

Conditions

  • Renal Transplant Recipients

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • ATG — DRUG
    1.5 mg/kg IV infusion on day of transplant, and 3 additional on days 2 through 7 after transplant.
  • Rituximab — DRUG
    375 mg/m\^2 IV infusion on day -6 before transplant and on day 1 after transplant.
  • Tacrolimus — DRUG
    Taken orally. Tacrolimus dose adjusted to maintain target blood levels of 6-10 ng/mL.
  • Sirolimus — DRUG
    Taken orally. Initial dose, 2 mg daily on day 10 post-transplant, subsequently adjusted to achieve trough levels of 8-12 ng/mL through week 56. Sirolimus withdrawal will be initiated between week 56 and week 88 in eligible participants.
  • MMF — DRUG
    1 g twice daily on days 0 through 12

Study Details

The purpose of this study is see if a combination of two drugs, (ATG and rituximab), given at the time of the transplant surgery, will help reduce or eliminate the need for long term immunosuppressive medication.

Key Dates

Start date
Jul 25, 2011
Status verified
Nov 2018
Primary completion
Jun 17, 2016
Completion
Aug 25, 2017

Study Design

Enrollment
10 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Induction (Rituximab and ATG)
    Study participants will undergo induction with rituximab and ATG and an initial maintenance therapy with tacrolimus, mycophenolate mofetil (MMF) and sirolimus. MMF will be discontinued on day 12. Participants will be evaluated for eligibility for tacrolimus withdrawal which must be initiated between weeks 26 and 38. Tacrolimus withdrawal must be completed in no fewer than 4 weeks and no more than 8 weeks. Then after at least 26 weeks on sirolimus monotherapy, participants will be evaluated for eligibility for sirolimus withdrawal which must be initiated between weeks 56 and 88. Sirolimus withdrawal must be completed in no fewer than 12 weeks and no more than 26 weeks.

Primary Outcome Measure

Percent of Participants Successfully Withdrawn From Immunosuppression and Remained Off Immunosuppression for at Least 52 Weeks [ Time Frame: Transplantation through 52 weeks after discontinuation of all immunosuppression ]

Locations (6)

FacilityCityStateZIPSite coordinators
University of California San Francisco Medical CenterSan FranciscoCalifornia94143-
University of Maryland Medical CenterBaltimoreMaryland21201-
Massachusetts General HospitalBostonMassachusetts02114-
Rogosin Institute/New York Presbyterian-CornellNew YorkNew York10021-
Hospital at the University of PennsylvaniaPhiladelphiaPennsylvania19104-
University of WisconsinMadisonWisconsin53792-

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