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NCT05069935 · ClinicalTrials.gov registry record · Phase 1

FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors

A Phase 1 study, sponsored by Fate Therapeutics.

Terminated
Registry status
Phase 1
Development phase
16
Enrollment target

NCT05069935: Clinical Trial Phase 1 study, sponsored by Fate Therapeutics.

NCT05069935 is a Phase 1 study that was terminated before completion, run by Fate Therapeutics. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05069935, a Phase 1 study, was terminated before completion, sponsored by Fate Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

This is a Phase 1 dose-finding study of FT538 in combination with monoclonal antibodies.

Primary Outcome

To define the RP2D of FT538 in combination with the following mAbs in subjects with advanced solid tumors: avelumab, trastuzumab, cetuximab, atezolizumab, nivolumab, and pembrolizumab

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG FT538
  • COMBINATION_PRODUCT Monoclonal antibody - Dose Escalation
  • COMBINATION_PRODUCT Monoclonal antibody - Dose Expansion

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2021-10-15
Est. Completion 2023-08-11
Phase Phase 1
Fate Therapeutics

22 total trials

Why NCT05069935 stopped before completion

NCT05069935 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT05069935 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05069935 about?

NCT05069935 is a clinical study titled "FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors". This is a Phase 1 dose-finding study of FT538 in combination with monoclonal antibodies.

What is the current status of trial NCT05069935?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2021-10-15. Estimated completion is 2023-08-11.

What interventions are being tested in trial NCT05069935?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), FT538 (DRUG), Monoclonal antibody - Dose Escalation (COMBINATION_PRODUCT), Monoclonal antibody - Dose Expansion (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT05069935?

This trial is sponsored by Fate Therapeutics, which has 22 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05069935's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05069935, the US trial registry maintained by the National Library of Medicine. NCT05069935 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.