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NCT02834247 · ClinicalTrials.gov registry record · Phase 1

A Study of TAK-659 in Combination With Nivolumab in Participants With Advanced Solid Tumors

A Phase 1 study, sponsored by Calithera Biosciences.

Terminated
Registry status
Phase 1
Development phase
41
Enrollment target

NCT02834247: Clinical Trial Phase 1 study, sponsored by Calithera Biosciences.

NCT02834247 is a Phase 1 study that was terminated before completion, run by Calithera Biosciences. The registered enrollment target is 41 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02834247, a Phase 1 study, was terminated before completion, sponsored by Calithera Biosciences.

TERMINATED
Registry status
Phase 1
Development phase
41 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D), safety and efficacy of TAK-659 in combination with nivolumab in participants with advanced solid tumors.

Primary Outcome

The MTD was defined as the dose range at which less than or equal to (\<=) 1 of 6 evaluable participants experience dose limiting toxicities (DLT) within the first 28 days of treatment (end of Cycle 1). Toxicities were evaluated according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4.03.

Interventions

  • DRUG Nivolumab
  • DRUG TAK-659

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2016-08-12
Est. Completion 2018-11-30
Phase Phase 1
Calithera Biosciences

22 total trials

Why NCT02834247 stopped before completion

NCT02834247 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower).

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

NCT02834247 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02834247 about?

NCT02834247 is a clinical study titled "A Study of TAK-659 in Combination With Nivolumab in Participants With Advanced Solid Tumors". The purpose of this study is to evaluate the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D), safety and efficacy of TAK-659 in combination with nivolumab in participants with advanced solid tumors.

What is the current status of trial NCT02834247?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 41 participants. The study started on 2016-08-12. Estimated completion is 2018-11-30.

What interventions are being tested in trial NCT02834247?

The interventions under investigation include: Nivolumab (DRUG), TAK-659 (DRUG).

Who is sponsoring clinical trial NCT02834247?

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

How this trial's enrollment target compares

Where NCT02834247's enrollment target sits among peer trials

41 1125th of 2000 higher than 871 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 NCT02834247, the US trial registry maintained by the National Library of Medicine. NCT02834247 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.