Phase I/IIa Trial of scAAV1.tMCK.NTF3 for Treatment of CMT1A

A vizsgálat adatai

Ki végzi

Nationwide Children's Hospital

Azonosító

NCT03520751

A regiszteradat frissítve

2026. július 29.

Eredeti leírás

This clinical trial is an open-label one-time injection dose study in which scAAV1.tMCK.NTF3 will be administered by intramuscular injections into muscles in both legs in CMT1A subjects with PMP22 gene duplication. Three subjects ages 18 to 35 years receiving (8.87e11 vg/kg) will be enrolled.A teljes eredeti leírásKevesebb

Phase I/IIa Trial Evaluating scAAV1.tMCK.NTF3 for Treatment of Charcot-Marie-Tooth Neuropathy Type 1A (CMT1A)

This clinical trial is an open-label one-time injection dose study in which scAAV1.tMCK.NTF3 will be administered by intramuscular injections into muscles in both legs in CMT1A subjects with PMP22 gene duplication. Three subjects ages 18 to 35 years receiving (8.87e11 vg/kg) will be enrolled.

Bevonási feltételek: Subjects 18- 35 years old inclusive with CMT1A will be enrolled; Must exhibit a 1.5 Mb duplication at 17p11.2 inclusive of the peripheral myelin protein 22 (PMP22) gene; Males and females of any ethnic or racial group; Must exhibit weakness of the ankle dorsiflexion muscle (but has full ROM against gravity and is able to stand on heels 3 seconds or greater); Abnormal nerve conduction velocities; Ability to cooperate for clinical evaluation and repeat nerve conduction studies; Willingness of sexually active subjects to practice a reliable method of contraception during the study.

Kizáró feltételek: Ongoing immunosuppressive therapy or immunosuppressive therapy within 6 months of starting the trial (e.g., corticosteroids, cyclosporine, tacrolimus, methotrexate, cyclophosphamide, intravenous immunoglobulin); Subjects with AAV1 binding antibody titers ≥ 1:50 as determined by ELISA immunoassay; Treat with any investigational medication within 30 days before the infusion of study drug; Limb surgery in the past six months; Severe infection (e.g. pneumonia, pyelonephritis, or meningitis) within 4 weeks before gene transfer visit (enrollment may be postponed); Concomitant illness or requirement for chronic drug treatment that in the opinion of the PI creates unnecessary risks for gene transfer; Active viral infection based on clinical observations or serological evidence of HIV, or Hepatitis B or C infection, herpesvirus or adenovirus; Any medical condition or extenuating circumstance that, in the opinion of the investigator, might compromise the subject's ability to comply with the protocol required testing or procedures or compromise the subject's wellbeing, safety, or clinical interpretability; Persistent leukopenia or leukocytosis (WBC ≤ 3.5 K/µL or ≥ 20.0 K/µL) or an absolute neutrophil count < 1.5K/µL; Abnormal laboratory values considered clinically significant (GGT > 3XULN, bilirubin ≥ 3.0 mg/dL, creatinine ≥ 1.8 mg/dL, Hgb < 8 or > 18 g/Dl; WBC > 15,000 per cmm); Subjects with circulating anti-NT-3 titers ≥ 1:50 as determined by ELISA immunoassay; Ankle contractures or surgeries preventing proper muscle strength testing; Pregnancy or lactation (females subjects will be tested for pregnancy); Anyone unwilling to disclose study participation with primary care physician and other medical providers.

ClinicalTrials.gov NCT03520751