Pivotal trial dossier · BioIntel

Phase 3 Study to Assess Safety and Efficacy of 177Lu-TLX250 in Advanced Relapsed or Recurrent ccRCC

Telix Pharmaceuticals (Innovations) Pty Limited · Ph3 · NCT07197580   exact date enrolment is a target
Readout due
2027-08-31
Ph3
Patients
40
estimated
Sites
5
1 countries
Arms
2
randomized
Masking
None
blinding depth

Design

AllocationRandomized
MaskingNone
Primary purposeTreatment
Arms2
Planned duration17 months
Started2026-03-25

What is being measured

Endpoint classsafety
Primary outcomes2
Stated asDose Optimization -safety and tolerability | Efficacy- median mPFS
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

ConditionccRCC; Renal Cell Carcinoma (Kidney Cancer); Renal Cell Carcinoma (RCC); Renal Cell Cancer Metastatic; Renal Cell Cancer, Recurrent; Clear Cell Renal Cell Cancer (ccRCC)
Therapeutic areaoncology
Patient pre-selectionbiomarker / selected population
Modalitynon_drug
SexALL

Evidence trail

Linked references2 on the registry record
Results postednot yet
Stopped earlyno

Reference-class base rate

64%
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 oncology: 35.5% (Wong/Siah/Lo 2019) and 43.9% (BIO/Informa 2011–2020).
  2. Trial selects patients by biomarker. In oncology this is the one well-evidenced stratification: 63.6% for biomarker-selected versus 33.6% for all-comers, so the stratified rate replaces the band.

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.