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NCT02904226 · ClinicalTrials.gov registry record · Phase 1

JTX-2011 Alone and in Combination With Anti-PD-1 or Anti-CTLA-4 in Subjects With Advanced and/or Refractory Solid Tumors

A Phase 1 study, sponsored by Jounce Therapeutics.

Completed
Registry status
Phase 1
Development phase
242
Enrollment target

NCT02904226: Completed Phase 1 study, sponsored by Jounce Therapeutics.

NCT02904226 is a Phase 1 study that has completed, run by Jounce Therapeutics. The registered enrollment target is 242 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (303% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02904226, a Phase 1 study, has completed, sponsored by Jounce Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
242 participants
Enrollment target

Study Summary

JTX-2011-101 is a Phase 1/2, open label, dose escalation and expansion clinical study of JTX-2011 alone and in combination with nivolumab, ipilimumab, or pembrolizumab in adult subjects with advanced and/or refractory solid tumors, to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D), as well as to evaluate preliminary efficacy.

Primary Outcome

Number of participants with an adverse event occurring from the time of informed consent until resolution or new therapy initiated or for 28 days post final dose if no new therapy is initiated

Interventions

  • DRUG Pembrolizumab
  • DRUG Nivolumab
  • DRUG Ipilimumab
  • DRUG JTX-2011

Trial Details

FieldValue
Enrollment Target 242 participants
Start Date 2016-08
Est. Completion 2020-07-01
Phase Phase 1
Jounce Therapeutics

5 total trials

What the finished NCT02904226 record still lists

NCT02904226 is an interventional study that assigns participants to a tested intervention. The registered 242 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (303% higher).

The record links to 0 conditions, and to 4 interventions - of which Pembrolizumab is the first listed.

NCT02904226 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02904226 about?

NCT02904226 is a clinical study titled "JTX-2011 Alone and in Combination With Anti-PD-1 or Anti-CTLA-4 in Subjects With Advanced and/or Refractory Solid Tumors". JTX-2011-101 is a Phase 1/2, open label, dose escalation and expansion clinical study of JTX-2011 alone and in combination with nivolumab, ipilimumab, or pembrolizumab in adult subjects with advanced and/or refractory solid tumors, to determine the maximum tolerated dose (MTD) and recommended Phase ...

What is the current status of trial NCT02904226?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 242 participants. The study started on 2016-08. Estimated completion is 2020-07-01.

What interventions are being tested in trial NCT02904226?

The interventions under investigation include: Pembrolizumab (DRUG), Nivolumab (DRUG), Ipilimumab (DRUG), JTX-2011 (DRUG).

Who is sponsoring clinical trial NCT02904226?

This trial is sponsored by Jounce Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02904226's enrollment target sits among peer trials

242 194th of 2000 higher than 1,805 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 NCT02904226, the US trial registry maintained by the National Library of Medicine. NCT02904226 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.