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NCT05495269 · ClinicalTrials.gov registry record · Phase 2

Safety and Tolerability Study of QLS-101 in Adolescents With Sturge-Weber Syndrome (SWS)-Related Glaucoma Due to Elevated Episcleral Venous Pressure (EVP)

A Phase 2 study, sponsored by Qlaris Bio.

Completed
Registry status
Phase 2
Development phase
2
Enrollment target

NCT05495269: Completed Phase 2 study, sponsored by Qlaris Bio.

NCT05495269 is a Phase 2 study that has completed, run by Qlaris Bio. The registered enrollment target is 2 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05495269, a Phase 2 study, has completed, sponsored by Qlaris Bio.

COMPLETED
Registry status
Phase 2
Development phase
2 participants
Enrollment target

Study Summary

Open-label study of an investigational product (IP), QLS-101, with 28-day every morning (QAM) dosing to both eyes (OU) in adolescents with SWS who have clinical evidence of glaucoma and/or ocular hypertension (OHT) related to SWS elevated EVP in at least one eye.

Primary Outcome

Incidence of ocular treatment emergent adverse events (TEAEs)

Interventions

  • DRUG QLS-101 ophthalmic solution, 2.0 %

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2022-11-23
Est. Completion 2023-03-20
Phase Phase 2
Qlaris Bio

8 total trials

What the finished NCT05495269 record still lists

NCT05495269 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which QLS-101 ophthalmic solution, 2.0 % is the first listed.

NCT05495269 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05495269 about?

NCT05495269 is a clinical study titled "Safety and Tolerability Study of QLS-101 in Adolescents With Sturge-Weber Syndrome (SWS)-Related Glaucoma Due to Elevated Episcleral Venous Pressure (EVP)". Open-label study of an investigational product (IP), QLS-101, with 28-day every morning (QAM) dosing to both eyes (OU) in adolescents with SWS who have clinical evidence of glaucoma and/or ocular hypertension (OHT) related to SWS elevated EVP in at least one eye.

What is the current status of trial NCT05495269?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2022-11-23. Estimated completion is 2023-03-20.

What interventions are being tested in trial NCT05495269?

The interventions under investigation include: QLS-101 ophthalmic solution, 2.0 % (DRUG).

Who is sponsoring clinical trial NCT05495269?

This trial is sponsored by Qlaris Bio, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05495269's enrollment target sits among peer trials

2 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05495269, the US trial registry maintained by the National Library of Medicine. NCT05495269 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.