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NCT02737202 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy of Saracatinib In Subjects With Lymphangioleiomyomatosis

A Phase 2 study, sponsored by Baylor College of Medicine.

Terminated
Registry status
Phase 2
Development phase
28
Enrollment target

NCT02737202: Clinical Trial Phase 2 study, sponsored by Baylor College of Medicine.

NCT02737202 is a Phase 2 study that was terminated before completion, run by Baylor College of Medicine. The registered enrollment target is 28 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02737202, a Phase 2 study, was terminated before completion, sponsored by Baylor College of Medicine.

TERMINATED
Registry status
Phase 2
Development phase
28 participants
Enrollment target

Study Summary

This study is being done to determine if there is a potential benefit of saracatinib in LAM subjects. Based on the information of this trial, additional clinical development trials will be needed. The study will also test the tolerability of 125 mg of saracatinib given once daily over a 9 month period.

Interventions

  • DRUG saracatinib

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2016-04
Est. Completion 2019-07-30
Phase Phase 2
Baylor College of Medicine

616 total trials

Why NCT02737202 stopped before completion

NCT02737202 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower).

The record links to 0 conditions, and to 1 intervention - of which saracatinib is the first listed.

NCT02737202 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02737202 about?

NCT02737202 is a clinical study titled "Safety and Efficacy of Saracatinib In Subjects With Lymphangioleiomyomatosis". This study is being done to determine if there is a potential benefit of saracatinib in LAM subjects. Based on the information of this trial, additional clinical development trials will be needed. The study will also test the tolerability of 125 mg of saracatinib given once daily over a 9 month peri...

What is the current status of trial NCT02737202?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 28 participants. The study started on 2016-04. Estimated completion is 2019-07-30.

What interventions are being tested in trial NCT02737202?

The interventions under investigation include: saracatinib (DRUG).

Who is sponsoring clinical trial NCT02737202?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02737202's enrollment target sits among peer trials

28 1677th of 2000 higher than 304 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 NCT02737202, the US trial registry maintained by the National Library of Medicine. NCT02737202 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.