A Study to Evaluate Safety and Tolerability of QLS-101 in NTG

  • STATUS
    Recruiting
  • End date
    Mar 12, 2022
  • participants needed
    30
  • sponsor
    Qlaris Bio, Inc.
Updated on 12 August 2021
ophthalmic solution
intraocular pressure
tension
timolol

Summary

A randomized active-controlled multi-site double-masked study to evaluate the safety and tolerability of 2 concentrations of QLS-101 versus timolol maleate Preservative Free (PF) 0.5% ophthalmic solution in subjects with normal tension glaucoma

Details
Condition Low Tension Glaucoma, Glaucoma, normal tension glaucoma
Treatment QLS-101
Clinical Study IdentifierNCT04857827
SponsorQlaris Bio, Inc.
Last Modified on12 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Visual acuity +1.0 logMAR or better
Willing to give informed consent
Ability to washout from current intraocular pressure lowering medications -

Exclusion Criteria

All secondary glaucomas
Previous glaucoma intraocular or laser surgery (selective laser trabeculoplasty permitted when done 18 months or longer from Screening)
Refractive surgery
Ocular infection or inflammation
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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