Study to Assess the Use of JSP191 in Matched Unrelated Donor Transplantation for Chronic Granulomatous Disease (CGD)
- Conditions
- Chronic Granulomatous DiseaseCGD
- Interventions
- Biological: JSP191
- Registration Number
- NCT05600907
- Brief Summary
Background:
Chronic granulomatous disease (CGD) is a rare immune disorder that can cause serious infections throughout the body. The only cure for CGD is a stem cell transplant. Transplants from a sibling are best, but many people must get transplants from unrelated donors. However, these transplants can cause serious complications in people with CGD.
Objective:
To see if a study drug (JSP191) can help improve the success rates of stem cell transplants for people with CGD from an unrelated donor.
Eligibility:
People aged 4 to 65 years with CGD who require a transplant.
Design:
Participants will be screened. Part of the screening will help to identify the best match to a transplant donor. Participants will have a physical exam, including dental and eye exams. They will have blood and urine tests. They will have tests of their breathing and heart function. A bone marrow sample will be taken. They will have their stem cells collected.
Participants will have a catheter inserted into a vein in their chest. It will remain in place for the entire period of transplant and recovery.
Participants will be in the hospital 40 to 50 days for the transplant. This will include a conditioning phase, to prepare their body for the procedure, as well as the transplant and recovery phases. As part of the conditioning phase, participants will receive JSP191 through a vein for 1 hour.
After discharge, participants will have follow-up visits 2 times a week for 100 days. Additional follow-up visits will continue for 5 years....
- Detailed Description
Study Description:
This is a pilot study for individuals with chronic granulomatous disease (CGD) using an unmanipulated matched unrelated donor (MUD) graft. The conditioning regimen will use alemtuzumab (Campath-1H, Genzyme Corporation) and total body irradiation (T BI) combined with the investigational new drug JSP191.
Participants will receive a high-dose donor graft infusion followed by post-transplant cyclophosphamide (Cytoxan, Baxter International, Inc). This study will determine whether replacing busulfan with the new investigational drug, JSP191, within the alemtuzumab/T BI- based conditioning regimen yields engraftment in patients with CGD.
Objectives:
Primary Objective:
- To measure the engraftment rates using JSP191 in conjunction with a high cell-dose graft.
Secondary Objectives:
* To assess overall survival.
* To evaluate the safety and efficacy of JSP191 in a TBI- and alemtuzumab-based regimen for transplantation of unmanipulated unrelated donor grafts in patients with CGD.
* Assessment of graft versus host disease (GvHD).
* Evaluate the long-term engraftment of those receiving JSP191.
* To assess the level and kinetics of immune reconstitution.
* To evaluate the pharmacokinetic (PK) properties of JSP191 in patients with CGD.
Exploratory Objectives:
* To assess the impact of inflammatory cytokines on engraftment, inflammatory reactions, and graft rejection.
* To further elucidate the factors involved in the development of GvHD and graft rejection/failure.
Endpoints:
Primary Endpoint:
- Reduced incidence of graft failure or rejection (as defined by \>= 20% engraftment by oxidase-positive neutrophils in \>= 85% of participants by Day 100, 1 year, and 2 years after transplant). Myeloid chimerism and/or oxidase positivity of \>= 20% will be considered engrafted.
Secondary Endpoints:
* Overall survival.
* Safety will be evaluated by recording of adverse events (AEs) related to JSP191 rather than to GvHD or engraftment. An increase in incidence of AEs or development of AEs not typically seen in patients receiving a busulfan-based regimen will be attributed to the use of JSP191.
* Assessment of rates of GvHD.
* Rates of grade 3 and 4 acute GvHD (aGvHD) of \< 20% (see Appendix B on grading).
* Development and incidence of aGvHD and chronic GvHD
(cGvHD) with a comparison to historical controls and incidence on parallel protocols using busulfan.
* Engraftment at \>2 years and up to 5 years post-transplant.
* Reconstitution kinetics using absolute neutrophil and absolute
lymphocyte recovery kinetics will be compared as well as impact on immunoglobulin (Ig) levels.
- PK will be measured and compared to historical data supplied by Jasper Therapeutics, Inc. and from other patient populations on other studies at the NIH.
Exploratory Endpoints:
* Evaluation of inflammatory markers as risk factors for engraftment syndrome and/or graft failure.
* Obtain samples for cytokine profiles at various timepoints post-transplant to assess the impact on inflammation profiles by JSP191 in the setting of the conditioning regimen.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 30
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Single arm study JSP191 Eligible CGD patients will receive one time infusion of study product along with Alemtuzumab and TBI as part of HSCT conditioning regimen
- Primary Outcome Measures
Name Time Method Early and long term engraftment Day 100 and 2 years post transplant To determine the engraftment rates, both early and long term, when using JSP191 in conjunction with TBI, Alemtuzumab and post transplant cyclophosphamide and sirolimus for unrelated donor transplantation of patients with Chronic Granulomatous Disease.
- Secondary Outcome Measures
Name Time Method Incidence of graft-vs-host disease (GvHD) Through study completion about 104 weeks To determine and compare the rates and severity of GvHD.
Incidence of viral reactivation Through study completion about 104 weeks To compare the incidence of peri and post transplant complications including viral reactivation with this new regimen compared to historical data.
Safety Through study completion about 104 Weeks To determine and assess the toxicity of JSP191 in combination with Campath, TBI and post transplant cyclophosphamide.
Trial Locations
- Locations (1)
National Institutes of Health Clinical Center
🇺🇸Bethesda, Maryland, United States