A Phase I/II Clinical Study to Evaluate SKG0201 Injection in Subjects With Spinal Muscular Atrophy Type I

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
AgeUp to 180
SponsorLanyue Biotech (Hangzhou) Co., Ltd.

About this trial

This is a phase I/II clinical study to evaluate the safety, preliminary efficacy and immunogenicity of SKG0201 injection in subjects with Spinal Muscular Atrophy Type I.

Eligibility criteria

Qualifiers

Type I SMA, defined by bi-allelic mutations in the SMN1 gene.

Clinical history and signs are consistent with type I SMA, such as hypotonia, delayed motor function development, and poor head control.

On the day of administration, the age of the subjects do not exceed 180 days after birth.

Disqualifiers

Pulse oximetry < 96% saturation at screening while the patient is awake or asleep without any supplemental oxygen or respiratory support.

Weight-for-age below the 3rd percentile for the same sex and age based on WHO Child Growth Standards.

Active viral infection.

In the presence of other severe infections or diseases that require systemic anti-infection treatment.

Trial design

Treatments tested in this trial

  • SKG0201 Injection

Treatment groups

11 Participants
are divided into 1 treatment group