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NCT04730349 · ClinicalTrials.gov registry record · Phase 1

A Study of Bempegaldesleukin (BEMPEG: NKTR-214) in Combination With Nivolumab in Children, Adolescents and Young Adults With Recurrent or Treatment-resistant Cancer

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Terminated
Registry status
Phase 1
Development phase
15
Enrollment target

NCT04730349: Clinical Trial Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT04730349 is a Phase 1 study that was terminated before completion, run by Bristol-Myers Squibb. The registered enrollment target is 15 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04730349, a Phase 1 study, was terminated before completion, sponsored by Bristol-Myers Squibb.

TERMINATED
Registry status
Phase 1
Development phase
15 participants
Enrollment target

Study Summary

The purpose of this study is to first, in Part A, assess the safety, tolerability and drug levels of Bempegaldesleukin (BEMPEG) in combination with nivolumab and then, in Part B, to estimate the preliminary efficacy in children, adolescents and young adults with recurrent or treatment-resistant cancer.

Primary Outcome

Number of participants with dose-limiting toxicities (DLTs). DLTs were collected and evaluated for Part A within the DLT evaluation period, which started on Cycle 1 Day 1 (first dose) and ended at Day 42 (42 days after first dose of the study therapy).

Interventions

  • BIOLOGICAL Nivolumab
  • BIOLOGICAL NKTR-214

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2021-06-03
Est. Completion 2022-06-22
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

Why NCT04730349 stopped before completion

NCT04730349 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% lower).

The record links to 0 conditions, and to 2 interventions - of which Nivolumab is the first listed.

NCT04730349 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04730349 about?

NCT04730349 is a clinical study titled "A Study of Bempegaldesleukin (BEMPEG: NKTR-214) in Combination With Nivolumab in Children, Adolescents and Young Adults With Recurrent or Treatment-resistant Cancer". The purpose of this study is to first, in Part A, assess the safety, tolerability and drug levels of Bempegaldesleukin (BEMPEG) in combination with nivolumab and then, in Part B, to estimate the preliminary efficacy in children, adolescents and young adults with recurrent or treatment-resistant canc...

What is the current status of trial NCT04730349?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2021-06-03. Estimated completion is 2022-06-22.

What interventions are being tested in trial NCT04730349?

The interventions under investigation include: Nivolumab (BIOLOGICAL), NKTR-214 (BIOLOGICAL).

Who is sponsoring clinical trial NCT04730349?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04730349's enrollment target sits among peer trials

15 1798th of 2000 higher than 157 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 NCT04730349, the US trial registry maintained by the National Library of Medicine. NCT04730349 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.