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NCT02725268 · ClinicalTrials.gov registry record · Phase 2

A Study of Sapanisertib, Combination of Sapanisertib With MLN1117, Paclitaxel and Combination of Sapanisertib With Paclitaxel in Women With Endometrial Cancer

A Phase 2 study, sponsored by Millennium Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
241
Enrollment target

NCT02725268: Completed Phase 2 study, sponsored by Millennium Pharmaceuticals.

NCT02725268 is a Phase 2 study that has completed, run by Millennium Pharmaceuticals. The registered enrollment target is 241 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02725268, a Phase 2 study, has completed, sponsored by Millennium Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
241 participants
Enrollment target

Study Summary

The primary purpose of this study is to determine if sapanisertib in combination with weekly paclitaxel improves progression-free survival (PFS) compared to weekly paclitaxel alone.

Primary Outcome

PFS is defined as the time in months from the date of randomization to the date of first documentation of progressive disease (PD) or death due to any cause, whichever occurs first. Per RECIST v1.1, PD was defined as at least a 20% increase in the sum of the longest diameter (LD) of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.

Interventions

  • DRUG Paclitaxel
  • DRUG Sapanisertib
  • DRUG MLN1117

Trial Details

FieldValue
Enrollment Target 241 participants
Start Date 2016-04-01
Est. Completion 2020-10-30
Phase Phase 2
Millennium Pharmaceuticals

135 total trials

What the finished NCT02725268 record still lists

NCT02725268 is an interventional study that assigns participants to a tested intervention. The registered 241 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% higher).

The record links to 0 conditions, and to 3 interventions - of which Paclitaxel is the first listed.

NCT02725268 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02725268 about?

NCT02725268 is a clinical study titled "A Study of Sapanisertib, Combination of Sapanisertib With MLN1117, Paclitaxel and Combination of Sapanisertib With Paclitaxel in Women With Endometrial Cancer". The primary purpose of this study is to determine if sapanisertib in combination with weekly paclitaxel improves progression-free survival (PFS) compared to weekly paclitaxel alone.

What is the current status of trial NCT02725268?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 241 participants. The study started on 2016-04-01. Estimated completion is 2020-10-30.

What interventions are being tested in trial NCT02725268?

The interventions under investigation include: Paclitaxel (DRUG), Sapanisertib (DRUG), MLN1117 (DRUG).

Who is sponsoring clinical trial NCT02725268?

This trial is sponsored by Millennium Pharmaceuticals, which has 135 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02725268's enrollment target sits among peer trials

241 239th of 2000 higher than 1,762 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02725268, the US trial registry maintained by the National Library of Medicine. NCT02725268 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.