U.S., July 31 -- ClinicalTrials.gov registry received information related to the study (NCT07093255) titled 'Safety, PK and PD of FLQ-101 in Premature Neonates' on July 16.
Brief Summary: The purpose of this study is to evaluate safety and efficacy outcomes following exposure to FLQ-101.
Study Start Date: Oct. 01, 2025
Study Type: INTERVENTIONAL
Condition:
Retinopathy of Prematurity (ROP)
Intervention:
DRUG: FLQ-101
The invervention comprises 3 Groups:
* Group 1: Low Dose
* Group 2: Middle Dose
* Group 3: High Dose
Recruitment Status: NOT_YET_RECRUITING
Sponsor: FELIQS INC.
Published by HT Digital Content Services with permission from Health Daily Digest....