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RecruitingPhase 1

Safety, PK and PD of FLQ-101 in Premature Neonates

FELIQS INC. · NCT07093255

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 0 mo–0 mo · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 1
Target enrollment
18
US sites recruiting
1
Study start
April 3, 2026
Record last updated
October 13, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The purpose of this study is to evaluate safety and efficacy outcomes following exposure to FLQ-101.

Being studied: FLQ-101

Conditions: Retinopathy of Prematurity (ROP)

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Written consent is obtained from parent(s) or legal guardian.
  • Neonates born at 25 weeks +0 days and 27 weeks +6 days of gestation.

Exclusion Criteria

  • Neonates with congenital malformation of the eye or any other ocular condition that may prevent or relevantly affect any of the assessments or procedures.
  • Neonates with serious congenital anomalies, severe congenital infection, and chromosomal abnormalities.
  • Neonates who are seriously ill and not expected to survive.
  • Neonates with heart disease, including cardiomyopathy, serious arrhythmias, and congenital heart disease. (Neonates with patent foramen ovale may be included in the study if clinically stable).
  • Neonates that are small for gestational age defined as having a weight \<10th percentile at birth based on the Fenton growth charts for gestational age and sex.
  • Neonates with history of or ongoing intraventricular hemorrhage (IVH) grades 2, 3 or 4. Neonates with IVH grade 1 may be included in the study at the discretion of the PI.
  • Neonates with any other medical conditions or clinically significant comorbidities or circumstances that in the opinion of the investigator may have a relevant impact on study participation or any of the study assessments or procedures.
  • Infants scheduled to participate in other interventional clinical trials while participating in the study and until reaching end of study.

Recruiting US locations

  • St. David's Medical Center

    Austin, TX 78705

    Site contact: Clininical Research Cordinator · 512-544-8070

Study contacts (from the official record)

  • Clinical Trial Office · +81-942-707-330 · clinicaltrial@feliqs.com
All phase 1 studies in Texas →
Safety, PK and PD of FLQ-101 in Premature Neonates (NCT07093255) | Bored Studies