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NCT04947124 · ClinicalTrials.gov registry record · Phase 2

A Study to Determine the Safety and Tolerability of 2 Concentrations of QLS-101

A Phase 2 study, sponsored by Qlaris Bio.

Completed
Registry status
Phase 2
Development phase
3
Enrollment target

NCT04947124: Completed Phase 2 study, sponsored by Qlaris Bio.

NCT04947124 is a Phase 2 study that has completed, run by Qlaris Bio. The registered enrollment target is 3 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

NCT04947124, a Phase 2 study, has completed, sponsored by Qlaris Bio.

COMPLETED
Registry status
Phase 2
Development phase
3 participants
Enrollment target

Study Summary

Safety and tolerability study of 2 concentrations of QLS-101 for adult subjects with Sturge Weber Syndrome (SWS)-related glaucoma due to elevated episcleral venous pressure (EVP).

Primary Outcome

Standard safety endpoint, ocular AEs, (including elevated IOP)

Interventions

  • DRUG QLS-101ophthalmic solution 1%
  • DRUG QLS-101ophthalmic solution 2%

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2021-10-19
Est. Completion 2022-08-01
Phase Phase 2
Qlaris Bio

8 total trials

What the finished NCT04947124 record still lists

NCT04947124 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 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 2 interventions - of which QLS-101ophthalmic solution 1% is the first listed.

NCT04947124 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04947124 about?

NCT04947124 is a clinical study titled "A Study to Determine the Safety and Tolerability of 2 Concentrations of QLS-101". Safety and tolerability study of 2 concentrations of QLS-101 for adult subjects with Sturge Weber Syndrome (SWS)-related glaucoma due to elevated episcleral venous pressure (EVP).

What is the current status of trial NCT04947124?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 3 participants. The study started on 2021-10-19. Estimated completion is 2022-08-01.

What interventions are being tested in trial NCT04947124?

The interventions under investigation include: QLS-101ophthalmic solution 1% (DRUG), QLS-101ophthalmic solution 2% (DRUG).

Who is sponsoring clinical trial NCT04947124?

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 NCT04947124's enrollment target sits among peer trials

3 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 NCT04947124, the US trial registry maintained by the National Library of Medicine. NCT04947124 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.