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NCT01579994 · ClinicalTrials.gov registry record · Phase 1

Crizotinib and Ganetespib (STA-9090) in ALK Positive Lung Cancers

A Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
13
Enrollment target

NCT01579994: Completed Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01579994 is a Phase 1 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 13 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01579994, a Phase 1 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
13 participants
Enrollment target

Study Summary

About 18 patients will take part in the phase 1 portion of the trial. In the beginning of the study, 3 patients will be treated with a low dose of ganetespib (STA-9090) and the standard dose of crizotinib. If this dose does not cause significant side effects, it will be increased as new patients take part in the study. The study will only be open at Memorial Sloan Kettering Cancer Center.

Primary Outcome

A standard 3+3 design will be used to find the maximum tolerated dose (MTD). Patients who withdraw before completing a full cycle will be replaced. There will be three set dose levels, using the approved dose of crizotinib, with 50%, 75% and 100% of the ganetespib (STA-9090) maximum tolerated dose of 200 mg/m2.

Interventions

  • DRUG Ganetespib (STA-9090) and crizotinib

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2012-04-16
Est. Completion 2020-12-28
Phase Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT01579994 record still lists

NCT01579994 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower).

The record links to 0 conditions, and to 1 intervention - of which Ganetespib (STA-9090) and crizotinib is the first listed.

NCT01579994 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01579994 about?

NCT01579994 is a clinical study titled "Crizotinib and Ganetespib (STA-9090) in ALK Positive Lung Cancers". About 18 patients will take part in the phase 1 portion of the trial. In the beginning of the study, 3 patients will be treated with a low dose of ganetespib (STA-9090) and the standard dose of crizotinib. If this dose does not cause significant side effects, it will be increased as new patients tak...

What is the current status of trial NCT01579994?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2012-04-16. Estimated completion is 2020-12-28.

What interventions are being tested in trial NCT01579994?

The interventions under investigation include: Ganetespib (STA-9090) and crizotinib (DRUG).

Who is sponsoring clinical trial NCT01579994?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01579994's enrollment target sits among peer trials

13 1847th of 2000 higher than 149 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 NCT01579994, the US trial registry maintained by the National Library of Medicine. NCT01579994 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.