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Clinical Trials/NCT06061614
NCT06061614
Recruiting
Early Phase 1

A Clinical Study for the Safety and Efficacy of IV Infusion of NGGT002 in the Treatment of Phenylketonuria

The First Affiliated Hospital of Bengbu Medical University1 site in 1 country15 target enrollmentMarch 30, 2023
InterventionsNGGT002 Injection

Overview

Phase
Early Phase 1
Intervention
NGGT002 Injection
Conditions
Phenylketonurias
Sponsor
The First Affiliated Hospital of Bengbu Medical University
Enrollment
15
Locations
1
Primary Endpoint
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
Status
Recruiting
Last Updated
last month

Overview

Brief Summary

This is a single-center, open-label, non-randomized, dose escalation study to evaluate the safety, tolerability and efficacy of NGGT002 in adult Phenylketonuria (PKU) subjects. All subjects will receive a single administration of NGGT002 and will be followed for safety and efficacy for 5 years.

Detailed Description

This study is designed to evaluate the safety and efficacy of NGGT002 gene therapy in adult subjects diagnosis with PKU due to confirmed PAH gene mutations indicative of PAH deficiency. NGGT002 will be administered via intravenous infusion. The study will begin with Dose Level 1, followed by a stepwise dose escalation. After evaluating the safety and efficacy data, a decision will be made to either expand the current cohort or proceed to the next dose level. The same process will be followed for subsequent dose cohorts.

Registry
clinicaltrials.gov
Start Date
March 30, 2023
End Date
December 30, 2028
Last Updated
last month
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
The First Affiliated Hospital of Bengbu Medical University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Voluntarily sign informed consent form;
  • Male and female subjects with diagnosis of PKU caused by confirmed phenylalanine hydroxylase(PAH) mutation according to the "Clinical Practice Guidelines for Phenylketonuria, 2020 Edition";
  • Age ≥ 18 years;
  • Blood phenylalanine (Phe) concentration ≥ 600 μmol/L at least once within 2 years prior to screening, with one measurement confirmed within six months of enrollment;
  • Subjects are able to maintain their baseline diet throughout the study (regardless of dietary phenylalanine restriction), and willingness to follow the instruction of investigators to manage the diet for the duration of the trial;
  • Subjects are required to obtain approval from the investigator prior to the use of any concomitant medications during the study period;
  • Willingness and capable per Investigator opinion to comply with study procedures and requirements;
  • Female participants of childbearing potential must have abstained from unprotected sexual intercourse for at least 14 days prior to dosing, and must have a documented negative serum hCG test between Day -7 and Day
  • All participants must be willing to use a highly effective method of contraception for at least 12 months following NGGT002.

Exclusion Criteria

  • Anti-AAV8 neutralizing antibody\>1:10
  • Prior gene therapy
  • Positive hepatitis B virus surface antigen, hepatitis C virus antibody, anti-human immunodeficiency virus antibody or treponema pallidum-specific antibody
  • Hepatic function abnormal: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \> 1.5 × ULN; alkaline phosphatase (ALP) \> 1.5 × ULN; total bilirubin (TBil) \> 1.5 × ULN; international normalized ratio (INR) \> 1.3
  • Hematology values outside of the normal range (Hemoglobin \< 110 g/L (male), \< 100 g/L (female), white blood cells \< 3.0 × 10\^9/L, neutrophils \< 1.5 × 10\^9/L, platelet counts \< 100 × 10\^9/L;
  • Hemoglobin A1c \> 6%, or fasting glucose \> 6.1 mmol/L;
  • Clinically significant abnormalities in vital signs, physical examination findings, laboratory tests, or other assessments that, in the Investigator's judgment, are deemed unsuitable for study enrollment;
  • Any contraindications to corticosteroid use or conditions potentially worsened by corticosteroids, as assessed by the Investigator, including but not limited to hypersensitivity to glucocorticoids, epilepsy, recent or unresolved bone fractures, ongoing wound healing, uncontrolled infections, or clinically significant osteoporosis;
  • Subjects with a history of allergy to human serum albumin;
  • All types of past and current malignancy;

Arms & Interventions

Dose level 1

Dose level 1 will be administered

Intervention: NGGT002 Injection

Dose level 2

Dose level 2 will be administered

Intervention: NGGT002 Injection

Dose level 3

Dose level 3 will be administered

Intervention: NGGT002 Injection

Dose level 4

Dose level 4 will be administered

Intervention: NGGT002 Injection

Dose level 5

Dose level 5 will be administered

Intervention: NGGT002 Injection

Outcomes

Primary Outcomes

Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)

Time Frame: Week 52

Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) from baseline to week 52 (W52)

Secondary Outcomes

  • Plasma Phe levels(Baseline Week 12, Week 28, Week 52)
  • Nature protein intake(Baseline, Week 12, Week 28, and Week 52)
  • Food Phe intake(Baseline, Week 12, Week 28, and Week 52)

Study Sites (1)

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