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A Study to Assess Safety, Tolerability, and Pharmacokinetics of Ascending Concentrations of Topical Ocular BL1332 in Healthy Volunteers

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NCT06978244 · readout ≤ 102 d

Sponsored by Bausch & Lomb Incorporated (industry) · BLCO — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
24actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-07-29actualWhen the study began enrolling
Primary completionNov 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionNov 2026estimatedThe whole study's end, after follow-up
First posted2025-05-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-27actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Ocular Pain

Interventions

  • Drug: BL1332 ophthalmic solution
  • Drug: BL1332 ophthalmic vehicle

Primary outcomes

what the primary-completion date above is the date OF
Incidence of DLTs (dose-limiting toxicities)
measured Approximately 6 months
Incidence of treatment-emergent AEs (TEAEs)
measured Approximately 6 months
Treatment-emergent changes in systemic and ocular safety assessments
measured Approximately 6 months
PK profiles and following parameter, where data allow (Cmax)
measured Approximately 6 months
PK profiles and following parameter, where data allow ( Tmax)
measured Approximately 6 months
PK profiles and following parameter, where data allow (Ctau)
measured Approximately 6 months
PK profiles and following parameter, where data allow (Tlast)
measured Approximately 6 months
PK profiles and following parameter, where data allow ( AUClast)
measured Approximately 6 months
PK profiles and following parameter, where data allow (AUCtau)
measured Approximately 6 months
PK profiles and following parameter, where data allow (AUCinf)
measured Approximately 6 months
PK profiles and following parameter, where data allow (ke1)
measured Approximately 6 months
PK profiles and following parameter, where data allow (t1/2)
measured Approximately 6 months

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