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Efficacy, Safety of T2769 in Dry Eye Disease

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Thea Pharma

Status

Completed

Conditions

Dry Eye Syndrome

Treatments

Other: T2769

Study type

Interventional

Funder types

Industry

Identifiers

NCT03830359
LT2769-001

Details and patient eligibility

About

Efficacy of T2769 in Dry Eye Desease

Full description

Multicenter and open study

Enrollment

62 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed and dated informed consent
  • Male or female aged from ≥ 18 years old
  • Known Dry Eye Syndrome requiring artificial tears within the last 3 months prior to study screening

Exclusion criteria

  • Best far corrected visual acuity ≤ 2/10
  • Severe blepharitis Severe dry eye

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

62 participants in 1 patient group

T2769
Experimental group
Description:
T2769 Ophthalmic solution patients treated with 1 drop in each eye 3 to 6 times daily
Treatment:
Other: T2769

Trial documents
2

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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