Phase 1 Study of Autologous CD4LVFOXP3 in Participants with IPEX Syndrome [revised IND and clinical protocol to be submitted to FDA by 10/11/2021]

NIH RePORTER · FDA · R01 · $668,482 · view on reporter.nih.gov ↗

Abstract

Project Summary We propose a novel regulatory T (Treg) cell therapy to treat IPEX syndrome, a rare autoimmune monogenic disease. IPEX is a life-threatening disease caused by loss-of-function FOXP3 mutations leading to dysfunctional Treg cells. The only current curative treatment for IPEX is allogeneic hematopoietic stem cell transplantation (allo-HSCT), which is only available to a minority of patients. The proposed product, CD4LVFOXP3 consists of autologous CD4+ T cells that have undergone lentiviral vector (LV)-mediated gene transfer of wild-type human FOXP3 leading to persistent high FOXP3 expression and acquisition of Treg cell phenotype and function. CD4LVFOXP3 were granted Orphan Drug designation in October, 2020. Based on the etiology of IPEX, our hypothesis is that the administration of autologous CD4+ T cells converted into CD4LVFOXP3 Treg-like cells by LV-mediated FOXP3 gene transfer, will reduce the immune dysregulation and the autoimmune manifestations. CD4LVFOXP3 is functionally equivalent to Treg cells and therefore, offer a novel cell therapy approach that circumvents the requirement for generalized immune suppression (IS) and could improve the clinical status of participants. This First-Time-in-Human (FTiH) Phase 1 clinical trial will test the feasibility of the manufacturing and the safety of the administration of CD4LVFOXP3 (Aim 1) in minimum of 20 up to 36 evaluable human participants with IPEX, who meet eligibility criteria. The secondary objective is to evaluate the impact of the CD4LVFOXP3 infusion on clinical manifestations. The dosing rationale has been developed with a conservative approach based on initial cell doses used in previous clinical trials with Treg cells of different origins. CD4LVFOXP3 also express membrane NGFR (CD271) encoded within the same LV construct that contains the FOXP3 gene. allowing ex vivo purification and traceability enabling further studies of CD4LVFOXP3survival, phenotypic stability and functional characteristics. Thus, during this clinical trial, we will perform exploratory studies to build knowledge on the CD4LVFOXP3 pharmacokinetics (PK) (Aim2) and pharmacodynamics (PD) (Aim 3) by monitoring the immune phenotype and function of patient immune cells. The possibility to provide functional autologous Treg-like cells is expected to be of benefit to all eligible IPEX patients. CD4LVFOXP3 could: 1. improve control of clinical manifestations resulting in the reduction of IS and related side effects, and 2. diminish the need for allo- HSCT, or allow patients to be transplanted in a more stable clinical condition, resulting in improved allo-HSCT outcomes. Successful completion of this clinical trial in patients with IPEX using CD4LVFOXP3 Treg-like cells as a functional replacement for FOXP3 mutated Treg cells, addresses a significant unmet medical need while also providing proof of safety and preliminary indications of benefit in controlling autoimmune disease manifestations. As such, data from thi...

Key facts

NIH application ID
10503570
Project number
1R01FD007540-01
Recipient
STANFORD UNIVERSITY
Principal Investigator
Rosa Bacchetta
Activity code
R01
Funding institute
FDA
Fiscal year
2022
Award amount
$668,482
Award type
1
Project period
2022-08-15 → 2026-07-31