CompletedPhase 2NCT06176963
A Study to Evaluate the Usability of the SB11 PFS in Subjects With Wet AMD or Macular Oedema Secondary to RVO
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Samsung Bioepis Co., Ltd.
- Principal Investigator
- Piotr Oleksy, M.D., MDCentrum Medyczne Dietla 19 Krakow
- Intervention
- SB11 PFS(combination_product)
- Enrollment
- 34 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2023
Study locations (3)
- SB Investigational Site, Katowice, Poland
- SB Investigational Site, Krakow, Poland
- SB Investigational Site, Olsztyn, Poland
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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