Pivotal trial dossier · BioIntel

Safety and Tolerability of IRX-101 in Patients Receiving Intravitreal Injections

iRenix Medical, Inc. · Ph3 · NCT05750589   exact date enrolment is a target
Readout due
2027-01-31
Ph3
Patients
240
estimated
Sites
1
1 countries
Arms
2
randomized
Masking
Double
blinding depth

Design

AllocationRandomized
MaskingDouble
Primary purposeTreatment
Arms2
Planned duration4 months
Started2026-09-01

What is being measured

Endpoint classsymptom
Primary outcomes1
Stated asAssessment of post-intravitreal injection eye pain
Endpoint class is inferred from the sponsor's own wording of the primary outcome. Hard endpoints such as survival are generally harder to hit than scales or laboratory surrogates.

Population

ConditionRetinal Disease
Therapeutic areaophthalmology
Patient pre-selectionall-comers (no selection detected)
Modalitysmall_molecule_or_unspecified
SexALL

Evidence trail

Linked references0 on the registry record
Results postednot yet
Stopped earlyno

Reference-class base rate

47% – 75%
historical share of Phase 3 trials in this class that reached approval
This is a base rate, not a prediction about this trial. It is what happened to comparable trials historically. It is not a model fitted on outcomes — no outcome labels exist for trials that have not read out — and it uses none of this trial's own results.

How this number was reached

  1. Published Phase 3 → approval rate for ophthalmology: 74.9% (Wong/Siah/Lo 2019) and 46.7% (BIO/Informa 2011–2020).
  2. ⚠ These two sources disagree about whether this area runs above or below the all-area average. The band is wide for that reason and should not be narrowed.

Design flags

Flags are shown separately rather than folded into the number. Wood et al. (BMJ 2008) measured effect-size inflation, not approval probability, so multiplying it into an approval rate would misuse the finding.

Deliberately not adjusted for

Enrollment sizeno evidenced association with Phase 3 success
Number of sitesno evidenced association
Endpoint typeno evidenced association with success once area is held
Phase 2 designsingle-arm vs randomised Phase 2 does not predict Phase 3
Each of these is visible in the registry and each is evidenced to be null for Phase 3 success. Using them would add false precision.

Evidenced, but not in the registry

Sponsor approval track record51%→81% (Danzon 2005) — not a registry field
Orphan designationaOR 2.3 — zero CT.gov fields carry FDA designations
Phase 2 effect-size shrinkagerHR 0.73 — requires prior-trial results
The standing criticism, stated plainly. Hampson et al. (Pharmaceutical Statistics 2022;21(2):439–459, eight of nine authors at Novartis) argue that starting from industry rates and applying subjective adjustments "lacks transparency and fails to make full use of data from previous clinical trials". That criticism applies to this figure. The response here is to show every input and to refuse unsupported adjustments, not to claim the objection does not apply.
Rates: Wong, Siah & Lo, Biostatistics 2019 (CC BY 4.0; corrigendum values) and BIO/Informa/QLS Clinical Development Success Rates 2011–2020 (cited, not reproduced). MIT Project ALPHA is not used — its terms restrict use to governmental, charitable or social purposes and bar redistribution.