A Phase 1b Study to Assess the Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy of Intravitreal OLN324
NCT07484074
Phase
Phase 1
Recruitment status
Completed
Participants
Lead sponsor
Ollin Biosciences, Inc.
Start date
2025-02-12
Number of sites
- Summary
- A Phase 1b Study to Assess the Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy of Intravitreal OLN324
- Acronym
- Short title
- A Phase 1b Study to Assess the Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy of Intravitreal OLN324
- Official title
- A Phase 1b Study to Assess the Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy of Two Different Formulations of Intravitreal OLN324 in Adult Participants With Either Neovascular (Wet) Age-related Macular Degeneration (nAMD) or Diabetic Macular Edema (DME)
- Control arm
- Active comparator
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Completion date
- 2025-12-09
- First posted
- 2026-03-19
- Registry last updated
- 2026-03-19
- Primary completion date
- 2025-10-10
- Start date
- 2025-02-12
- Actual participants
- Participants
- Participant count basis
- Actual
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- Ollin Biosciences, Inc.
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT07484074
- ClinicalTrials.gov ID
- NCT07484074
- Registry record
- Open registry record
- Allocation
- Randomised
- Model
- Parallel groups
- Purpose
- Treatment
- Masking
- Quadruple masking
- Masked roles
- Participants, Care providers, Investigators, Outcome assessors
Sources for study design
Adverse Events
Timeframe: Week 12 and Week 20
Sources for outcomes
- Sex
- All
- Age groups
- Adults, Older adults
- Minimum age
- 18 Years
- Healthy volunteers
- No
- Be willing and able to understand the study procedures and the risks involved and provide written informed consent before the first study-related activity
- DME patients must be ≥ 18 years of age, nAMD patients must be ≥ 50 years of age
- Diagnosis of either DME or nAMD. nAMD patients must be treatment naïve. DME patients can be either treatment naïve or treatment experienced
- DME patients must have best corrected visual acuity of 78 to 25 letters
- nAMD patients must have best corrected visual acuity of 80 to 25 letters
- If pregnant or breastfeeding
- History of cataract surgery and/or Yttrium-Aluminum Garnet (YAG) for removal of posterior capsular opacification (PCO) within 90 days
Sources for eligibility
- Phoenix, AZPhoenix, United States
- Glendale, CAGlendale, United States
- Pasadena, CAPasadena, United States
- Sacramento, CASacramento, United States
- Walnut Creek, CAWalnut Creek, United States
- Waterford, CTWaterford, United States
- Fort Myers, FLFort Myers, United States
- Saint Petersburg, FLSt. Petersburg, United States
- Winter Haven, FLWinter Haven, United States
- Oak Forest, ILOak Forest, United States
- Hagerstown, MDHagerstown, United States
- Grand Rapids, MIGrand Rapids, United States
- Reno, NVReno, United States
- Wake Forest, NCWake Forest, United States
- Tulsa, OKTulsa, United States
- Springfield, ORSpringfield, United States
- Germantown, TNGermantown, United States
- Abilene, TXAbilene, United States
- Arlington, TXArlington, United States
- Austin, TXAustin, United States
- Bellaire, TXBellaire, United States
- Dallas, TXDallas, United States
- Katy, TXKaty, United States
- Plano, TXPlano, United States
- Round Rock, TXRound Rock, United States
And 5 more, listed on the interactive page.
Sources for sites
Related records
Drugs (1)
Lead sponsors (1)
Conditions (2)
- Diabetic macular edema Primary condition
- Macular degeneration