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Safety and Efficacy of ALLO-316 in Subjects With Advanced or Metastatic Clear Cell Renal Cell Carcinoma

← catalyst calendar

NCT04696731 · readout ≤ 1,261 d

Sponsored by Allogene Therapeutics (industry) · ALLO — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
120estimated
Sites
10
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-02-24actualWhen the study began enrolling
Primary completionJan 2030estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2030estimatedThe whole study's end, after follow-up
First posted2021-01-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced/Metastatic Clear Cell Renal Cell Carcinoma

Interventions

  • Genetic: ALLO-316
  • Biological: ALLO-647
  • Drug: Fludarabine
  • Drug: Cyclophosphamide

Primary outcomes

what the primary-completion date above is the date OF
Proportion of subjects experiencing Dose Limiting Toxicities at increasing doses of ALLO-316
measured 28 days
Proportion of patients experiencing Dose Limiting Toxicity with ALLO-647 in combination with fludarabine/cyclophosphamide administered prior to ALLO-316
measured 33 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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