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RecruitingNCT06910813CYStemUpdated Sep 22, 2026

DFT383 in Pediatric Participants With Nephropathic Cystinosis

A Phase 1/2 interventional study of DFT383 in Nephropathic Cystinosis, sponsored by Novartis Pharmaceuticals. Recruiting at 6 sites in United States. Open to participants aged 2 Years to 5 Years. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Novartis Pharmaceuticals · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
30
Allocation
Non-randomized
Ages
2 Years to 5 Years
Sex
All
01

Study summary

An open-label, multi-center, phase I/II study to assess the safety, tolerability and efficacy of DFT383 in pediatric participants with nephropathic cystinosis, followed by a long-term extension phase.

The purpose of this clinical study is to assess safety, tolerability, and efficacy of DFT383 in participants aged 2 to 5 years with nephropathic cystinosis. The study consists of a Core Phase and a long-term Extension Phase. DFT383 is a cellular gene therapy.

This study includes an active arm (Cohort 1) of participants treated with study treatment DFT383 and a concurrent reference arm (Cohort 0). Participants in Cohort 0 will not receive study treatment and will only participate in the Core Phase of the study. The study is not randomized and Cohort 0 aims to collect prospective and concurrent data in this rare disease.

Read the detailed description

This study is an open-label, multi-center, phase I/II study to assess the safety, tolerability, and efficacy of DFT383 in participants aged 2 to 5 years with nephropathic cystinosis, followed by a long-term extension phase.

The study includes two Treatment Groups (Cohort 1 and Cohort 0) and consists of a Core Phase and a long-term Extension Phase.

Participants in Cohort 1 will receive DFT383 and participate in both the Core and Extension Phase. Participants in Cohort 0 will not receive study treatment and will participate in the Core Phase only.

The two cohorts will be run in parallel. Investigational sites may participate in one or both cohorts.

Cohort 1 Approximately 15 participants will receive treatment with DFT383 in 3 (sub) cohorts (1A, 1B and 1C) dosed in a staggered approach. The total study duration for a participant in Cohort 1 will be up to 32 months in the core phase and up to 13 years for the long-term extension phase.

Cohort 0 Approximately 15 participants meeting similar inclusion/exclusion criteria and receiving SoC will be enrolled. The Schedule of Activities will be reduced for this Cohort. This cohort 0 is not a direct control but will provide essential context for interpreting the results observed in the participants receiving DFT383. The total study duration for a participant in Cohort 0 will be up to 24 months.

02

Conditions studied

  • Nephropathic Cystinosis

Keywords

  • Cystinosis
  • Nephropathic cystinosis
  • Lysosomal storage disorder
  • CTNS gene
  • DFT383
  • Cellular gene therapy
  • Cysteamine
  • Renal Fanconi syndrome
03

Who can participate

Ages eligible
2 Years to 5 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

Participants eligible for inclusion in this study must meet all the following criteria:

  1. Informed consent in writing from parent(s) or legal guardian(s) must be provided
  2. 2 to 5 years of age (including 5 years and 364 days old) at Screening
  3. Weight-for-stature is ≥ the third percentile, and is ≥ 10 kg
  4. Oral cysteamine therapy for at least 6 months
  5. Historic clinical diagnosis of nephropathic cystinosis
  6. Laboratory evidence of of renal fanconi syndrome (RFS)
  7. Relatively preserved kidney function (eGFR ≥ 60mL/min/1.73m2)
  8. Received all age-appropriate vaccinations

Key exclusion Criteria for Cohort 1 and 0

  1. A history of kidney transplantation
  2. A prior or planned bone marrow or stem cell transplantation or prior treatment with gene therapy
  3. History of malignancy
  4. A severe or uncontrolled medical disorder
  5. Major surgery within 90 days

Additional Key exclusion criteria for Cohort 1 - The following exclusion criterion applies to Cohort 1 only as it is related to DFT383 treatment:

1. Indomethacin within 2 weeks prior to Screening

Other protocol-defined inclusion/exclusion criteria may apply.

04

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Cohort 1 (DFT383)

    Treatment with DFT383

    Genetic: DFT383

  • No intervention
    Cohort 0 (SoC)

    No study treatment, will continue with standard of care (cysteamine).

Interventions

  • GeneticDFT383

    DFT383 is an autologous hematopoietic stem cell (HSC) gene therapy.

05

What researchers measure

Primary outcomes

  1. Core Phase - Incidence of adverse events (Cohort 1)

    Number and proportion of participants with adverse events (AEs) and serious adverse events (SAEs)

    Time frame: Up to 32 months

  2. Core Phase - Number of participants with hematological reconstitution (Cohort 1)

    Hematological reconstitution by Day 42 post-DFT383 infusion

    Time frame: 42 days post DFT infusion

  3. Core Phase - Proportion of participants with reversal of renal Fanconi syndrome (RFS)

    Proportion of participants with reversal of renal Fanconi syndrome (RFS)

    Time frame: Up to 32 months

Secondary outcomes

  1. Core Phase - Number of participants independent from cysteamine

    Independence from oral and ophthalmic cysteamine

    Time frame: up to 24 months

  2. Core Phase - Health-related quality of life (HRQOL)

    Health-related quality of life (HRQOL) as measured by QUALIFY (cystinosis-specific PRO)- Currently under development

    Time frame: Up to 32 months

  3. Core Phase - Time from infusion to reversal of RFS (Cohort 1)

    Time from infusion to reversal of renal Fanconi syndrome (RFS)

    Time frame: Up to 24 months

  4. Core Phase - Time from screening to reversal of RFS (Cohort 0)

    Time from screening to reversal of renal Fanconi syndrome (RFS)

    Time frame: Up to 24 months

  5. Core Phase - Duration of reversal of RFS

    Duration of reversal of renal Fanconi syndrome (RFS)

    Time frame: Up to 24 months

  6. Core Phase - Change from baseline on urine protein to creatinine ratio (UPr/CR)

    Change from baseline on urine protein to creatinine ratio (UPr/CR)

    Time frame: Up to 27 months

  7. Core Phase - Change from baseline on urine amino acids

    Change from baseline on urine amino acids

    Time frame: Up to 27 months

  8. Core Phase - Change from baseline on urinary glucose to creatinine ratio

    Change from baseline on urinary glucose to creatinine ratio

    Time frame: Up to 27 months

  9. Core Phase - Change from baseline on tubular maximum reabsorption of Phosphate/Glomerular Filtration Rate ratio (TmP/GFR)

    Change from baseline on tubular maximum reabsorption of Phosphate/Glomerular Filtration Rate ratio

    Time frame: Up to 27 months

  10. Core Phase - Change from baseline on urine retinol-binding protein/creatinine ratio (RBP/Cr)

    Change from baseline on urine retinol-binding protein/creatinine ratio

    Time frame: Up to 27 months

  11. Core Phase - Number of participants with improvement of proximal tubular function

    Improvement of proximal tubular function as defined by 2-fold change from Baseline of at least 4 out of 5 RFS parameters (urine protein to creatinine ratio, urine amino acids, urinary glucose to creatinine ratio, tubular maximum reabsorption of Phosphate/Glomerular Filtration Rate, urine retinol-binding protein/creatinine ratio). Improvement will also be considered if the change from Baseline is less than 2-fold but the value falls within the definition for normalization.

    Time frame: Up to 27 months

  12. Core Phase - Corneal cystine crystal content

    Corneal crystal content by anterior segment optical coherence tomography (AS-OCT)

    Time frame: Up to 27 months

  13. Core Phase - Number of participants with clinically significant changes in vital signs, physical examinations, laboratories, and ECG (Cohort 1)

    Vital signs, physical examinations, laboratories (eg., chemistry, hematology, liver function tests), and ECG

    Time frame: Up to 27 months

  14. Core Phase - Number of participants with presence/emergence of replication-competent lentivirus (Cohort 1)

    Number of participants with presence/emergence of replication-competent lentivirus

    Time frame: Up to 27 months

  15. Core Phase - Number of participants with malignancy (Cohort 1)

    Number of participants with malignancy

    Time frame: Up to 27 months

  16. Core Phase - Time to hematological reconstitution (Cohort 1)

    Time to hematological reconstitution

    Time frame: Up to 24 months

  17. Core Phase - Time to platelet engraftment (Cohort 1)

    Time to platelet engraftment

    Time frame: Up to 24 months

  18. Core Phase - Incidence of Adverse Events (Cohort 0)

    Number and proportion of participants with adverse events (AEs) and serious adverse events (SAEs)

    Time frame: up to 24 months

  19. Extension Phase Primary Objective - Incidence of Adverse events (Cohort 1)

    Number and proportion of participants with adverse events (AEs) and serious adverse events (SAEs)

    Time frame: Up to 15 years and 8 months

  20. Extension Phase - Number of participants with malignancy (Cohort 1)

    Number of participants with malignancy

    Time frame: Up to 15 years and 3 months

  21. Extension Phase - Number of participants with presence/emergence of replication-competent lentivirus (Cohort 1)

    Number of participants with presence/emergence of replication-competent lentivirus

    Time frame: Up to 15 years and 3 months

  22. Extension Phase - Number of participants with clinically significant changes in vital signs, physical examinations, laboratories, and ECG (Cohort 1)

    Vital signs, physical examinations, laboratories (eg., chemistry, hematology, liver function tests), and ECG

    Time frame: Up to 15 years and 3 months

  23. Extension Phase - Change from baseline on urine protein to creatinine ratio (UPr/CR) (Cohort 1)

    Change from baseline on urine protein to creatinine ratio (UPr/CR)

    Time frame: Up to 15 years and 3 months

  24. Extension Phase - Change from baseline on urine amino acids (Cohort 1)

    Change from baseline on urine amino acids

    Time frame: Up to 15 years and 3 months

  25. Extension Phase - Change from baseline on urinary glucose to creatinine ratio (Cohort 1)

    Change from baseline on urinary glucose to creatinine ratio

    Time frame: Up to 15 years and 3 months

  26. Extension Phase - Change from baseline on tubular maximum reabsorption of Phosphate/Glomerular Filtration Rate ratio (TmP/GFR) (Cohort 1)

    Change from baseline on tubular maximum reabsorption of Phosphate/Glomerular Filtration Rate ratio

    Time frame: Up to 15 years and 3 months

  27. Extension Phase - Change from baseline on urine retinol-binding protein/creatinine ratio (RBP/Cr) (Cohort 1)

    Change from baseline on urine retinol-binding protein/creatinine ratio

    Time frame: Up to 15 years and 3 months

  28. Extension Phase - Duration of reversal of RFS (Cohort 1)

    Duration of reversal of renal Fanconi syndrome (RFS)

    Time frame: Up to 15 years

  29. Extension Phase - Number of participants with kidney failure (Cohort 1)

    Number of participants with kidney failure

    Time frame: Up to 15 years

  30. Extension Phase - Number of participants independent from cysteamine (Cohort 1)

    Independence from oral and ophthalmic cysteamine

    Time frame: Up to 15 years

  31. Extension Phase - Corneal cystine crystal content (Cohort 1)

    Corneal crystal content by anterior segment optical coherence tomography (AS-OCT)

    Time frame: Up to 15 years and 3 months

  32. Extension Phase - Health-related quality of life (HRQOL) (Cohort 1)

    Health-related quality of life (HRQOL) as measured by QUALIFY (cystinosis-specific PRO)- Currently under development

    Time frame: Up to 15 years and 8 months

06

Study locations

4 of 6 sites recruiting
  • Phoenix Children's Hospital (Recruiting Cohort 0 and 1)
    Phoenix, Arizona 85016, United States
    Not yet recruiting
  • University of California at San Diego - Rady Children's Hospital (Recruiting Cohort 0 and 1)
    San Diego, California 92123, United States
    • Mieko Pretlow · Contact · mpretlow@rchsd.org · 858-966-1700
    • Nadine Benador nbenador@health.ucsd.edu · Principal investigator
    Recruiting
  • Stanford University - Stanford Children's Health (Recruiting Cohort 0 and 1)
    Stanford, California 94305, United States
    Recruiting
  • Emory University School of Medicine - Children's Healthcare of Atlanta (recuiting Cohort 0)
    Atlanta, Georgia 30322, United States
    • Laurence (Larry) Greenbaum · Contact · lgreen6@emory.edu · 404-712-6374
    • Laurence (Larry) Greenbaum · Principal investigator
    Recruiting
  • Children's Hospital of Philadelphia (Recruiting Cohort 0 and 1)
    Philadelphia, Pennsylvania 19104, United States
    • Melissa Cadnapaphornchai · Contact · 215-590-2449
    • Melissa Cadnapaphornchai · Principal investigator
    Not yet recruiting
  • Baylor College of Medicine - Texas Children's Hospital (recuiting Cohort 0)
    Houston, Texas 77030, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06910813
Lead sponsor
Novartis Pharmaceuticals
Responsible party
Sponsor
First posted
Apr 4, 2025
Start date
Jun 2, 2025
Primary completion
May 28, 2031 (estimated)
Completion
May 28, 2044 (estimated)
Last update
Sep 22, 2026

Study contacts

Novartis Pharmaceuticals
Contact
novartis.email@novartis.com
1-888-669-6682
Novartis Pharmaceuticals
Contact

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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