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Anti-VEGF Antibody
RBM-007 Injectable Solution for Age-Related Macular Degeneration (TEMPURA Trial)
Phase 1 & 2
Waitlist Available
Research Sponsored by Maturi, Raj K., M.D., P.C.
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 3 months
Awards & highlights
TEMPURA Trial Summary
This study is evaluating whether a new drug may help reduce swelling in the eye for individuals with macular degeneration.
Eligible Conditions
- Age-Related Macular Degeneration
TEMPURA Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Macular Edema
Secondary outcome measures
Visual Acuity
Side effects data
From 2021 Phase 2 trial • 94 Patients • NCT0420024846%
Eye disorders
18%
Conjunctival haemorrhage
14%
Dry eye
7%
Eye irritation
7%
Eye pain
7%
Iritis
7%
Vitritis
100%
80%
60%
40%
20%
0%
Study treatment Arm
Sham + RBM-007
RBM-007 + Aflibercept
Sham + Aflibercept
TEMPURA Trial Design
1Treatment groups
Experimental Treatment
Group I: RBM-007 Injectable Solution - 2.0 mgExperimental Treatment1 Intervention
Single intravitreal injection in study eye
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RBM-007 Injectable Solution
2019
Completed Phase 2
~110
Find a Location
Who is running the clinical trial?
Maturi, Raj K., M.D., P.C.Lead Sponsor
6 Previous Clinical Trials
180 Total Patients Enrolled
Raj K. Maturi, M.D.Study ChairMidwest Eye Institute
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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