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AGN-241622 for Presbyopia

Phase 1 & 2
Waitlist Available
Research Sponsored by Allergan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days

Summary

This trial is testing AGN-241622 eye drops to see if they are safe and effective. The study will check if the drops help with eye conditions without causing side effects.

Eligible Conditions
  • Presbyopia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 14 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Stage 1: Number of Participants Experiencing a Treatment Emergent Adverse Event After Single Administration of AGN-241622
Stage 2a: Number of Patients Experiencing a Treatment Emergent Adverse Event After Repeat Administration of AGN-241622
Secondary study objectives
Stage 1 Plasma Pharmacokinetics: Apparent Total Clearance of AGN-241622 From Plasma (CL/F)
Stage 1 Plasma Pharmacokinetics: Area Under the Concentration-time Curve From Time 0 to Infinity (AUC0-inf) of AGN-241622
Stage 1 Plasma Pharmacokinetics: Area Under the Concentration-time Curve From Time 0 to Time t (AUC0-t) of AGN-241622
+28 more

Trial Design

7Treatment groups
Experimental Treatment
Placebo Group
Group I: Cohort 6: AGN-241622 Dose 3 (High Dose)Experimental Treatment1 Intervention
Administered as single drop in each eye
Group II: Cohort 5: AGN-241622 Dose 2 (Medium Dose)Experimental Treatment1 Intervention
Administered as single drop in each eye
Group III: Cohort 4: AGN-241622 Dose 1 (Low Dose)Experimental Treatment1 Intervention
Administered as a single drop in each eye
Group IV: Cohort 3: AGN-241622 Dose 3 (High Dose)Experimental Treatment1 Intervention
Administered as single drop in one eye
Group V: Cohort 2: AGN-241622 Dose 2 (Medium Dose)Experimental Treatment1 Intervention
Administered as single drop in one eye
Group VI: Cohort 1: AGN-241622 Dose 1 (Low Dose)Experimental Treatment1 Intervention
Administered as single drop in one eye
Group VII: Placebo DosePlacebo Group1 Intervention
Administered as single drop in one or both eyes

Find a Location

Who is running the clinical trial?

AllerganLead Sponsor
781 Previous Clinical Trials
276,574 Total Patients Enrolled
8 Trials studying Presbyopia
1,402 Patients Enrolled for Presbyopia
AbbVieLead Sponsor
1,020 Previous Clinical Trials
520,011 Total Patients Enrolled
2 Trials studying Presbyopia
43 Patients Enrolled for Presbyopia
Wayne Chen, PharmDStudy DirectorAllergan
~15 spots leftby Nov 2025
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