The SUNRISE trial is a first-in-human (FIH), open-label, Phase 1/2 clinical trial designed to assess the safety, tolerability and preliminary efficacy of a single intravenous infusion of hLB-001 in pediatric patients with MMA characterized by methylmalonyl-CoA mutase gene (MMUT) mutations. hLB-001 is a liver-targeted, recombinant engineered adeno-associated viral (rAAV) vector utilizing the LK03 capsid (rAAV-LK03), designed to non-disruptively integrate the human methylmalonyl-CoA mutase gene at the albumin locus. The trial is expected to enroll pediatric patients with ages ranging from 6 months to 12 years, initially starting with 3 to 12 year-old patients and then adding patients aged 6 months to 2 years.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
4
hLB-001 via IV infusion
Clinical Trial Site
Atlanta, Georgia, United States
Clinical Trial Site
Pittsburgh, Pennsylvania, United States
Clinical Trial Site
Nashville, Tennessee, United States
Clinical Trial Site
Seattle, Washington, United States
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
An adverse event (AE) was defined as any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related. TEAE was an AE that was not present prior to administration of hLB-001, or an event already present that worsened in either severity or frequency following hLB-001administration. A summary of serious adverse events (SAEs) and other non-serious AEs regardless of causality is located in the Reported Adverse Events module.
Time frame: From first dose of study drug up to Week 52
Number of Participants With Infusional Toxicities
An infusional toxicity was a hLB-001-related AE that limits, delays, or requires medical intervention during administration. A summary of SAEs and other non-serious AEs regardless of causality is located in the Reported Adverse Events module.
Time frame: Baseline up to Week 52
Change From Baseline in Serum Methylmalonic Acid Level at Week 52
Time frame: Baseline, Week 52
Change From Baseline in Serum Methylcitrate Level at Week 52
Time frame: Baseline, Week 52
Change From Baseline in Serum Fibroblast Growth Factor 21 (FGF21) Level at Week 52
Time frame: Baseline, Week 52
Percent Change From Baseline in Propionate Oxidation Rate at Week 52
Time frame: Baseline, Week 52
Change From Baseline in Serum Albumin-2A Level at Week 52
Below the limit of quantification (BLQ) value was 2.44 nanograms (ng)/milliliter (mL).
Time frame: Baseline, Week 52
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