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NCT01900652 · ClinicalTrials.gov registry record · Phase 2

A Study of Emibetuzumab in Non Small Cell Lung Cancer (NSCLC) Participants

A Phase 2 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
111
Enrollment target

NCT01900652: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT01900652 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 111 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01900652, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
111 participants
Enrollment target

Study Summary

The primary purpose of this study is to evaluate the efficacy of the study drug known as LY2875358, administered alone or in combination with a second drug named Erlotinib, in participants affected by a defined type of lung cancer (MET biomarker diagnostic positive Non-Small-Cell Lung Cancer) that experienced a disease progression during the most recent treatment with Erlotinib.

Primary Outcome

ORR is confirmed best overall tumor response of CR or PR. According to RECIST v1.1, CR was defined as the disappearance of all target and non-target lesions; PR defined as a \>30% decrease in the sum of the longest diameters (LD) of the target lesions, taking as reference the baseline sum of the LD. Percentage of participants was calculated as: (total number of participants with CR or PR from start of the treatment until disease progression or recurrence)/total number of participants treated) \*

Interventions

  • DRUG Erlotinib
  • DRUG Emibetuzumab

Trial Details

FieldValue
Enrollment Target 111 participants
Start Date 2013-08
Est. Completion 2016-03
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT01900652 record still lists

NCT01900652 is an interventional study that assigns participants to a tested intervention. The registered 111 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower).

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

NCT01900652 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01900652 about?

NCT01900652 is a clinical study titled "A Study of Emibetuzumab in Non Small Cell Lung Cancer (NSCLC) Participants". The primary purpose of this study is to evaluate the efficacy of the study drug known as LY2875358, administered alone or in combination with a second drug named Erlotinib, in participants affected by a defined type of lung cancer (MET biomarker diagnostic positive Non-Small-Cell Lung Cancer) that e...

What is the current status of trial NCT01900652?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 111 participants. The study started on 2013-08. Estimated completion is 2016-03.

What interventions are being tested in trial NCT01900652?

The interventions under investigation include: Erlotinib (DRUG), Emibetuzumab (DRUG).

Who is sponsoring clinical trial NCT01900652?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01900652's enrollment target sits among peer trials

111 632nd of 2000 higher than 1,369 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 NCT01900652, the US trial registry maintained by the National Library of Medicine. NCT01900652 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.