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NCT00533702 · ClinicalTrials.gov registry record · Phase 2

A Study of IMC-1121B (Ramucirumab) With or Without Dacarbazine in Metastatic Malignant Melanoma

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

Completed
Registry status
Phase 2
Development phase
106
Enrollment target

NCT00533702: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT00533702 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 106 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00533702, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
106 participants
Enrollment target

Study Summary

The primary objective of this study is to determine the progression-free survival (PFS) of participants with previously untreated metastatic malignant melanoma when treated with IMC-1121B (ramucirumab) alone or in combination with dacarbazine.

Primary Outcome

PFS was defined as the time from the first day of therapy to the first evidence of disease progression as defined by Response Evaluation Criteria in Solid Tumors (RECIST v1.0) or death from any cause. Progressive disease (PD) was defined as at least a 20% increase in the sum of the longest diameter (LD) of the target lesions, taking as reference the smallest sum LD recorded since the treatment started in comparison with the measurement of the nadir or the appearance of 1 or more new lesions. In

Interventions

  • DRUG Dacarbazine
  • BIOLOGICAL IMC-1121B (ramucirumab)

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2007-11
Est. Completion 2011-05
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT00533702 record still lists

NCT00533702 is an interventional study that assigns participants to a tested intervention. The registered 106 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 (20% lower).

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

NCT00533702 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00533702 about?

NCT00533702 is a clinical study titled "A Study of IMC-1121B (Ramucirumab) With or Without Dacarbazine in Metastatic Malignant Melanoma". The primary objective of this study is to determine the progression-free survival (PFS) of participants with previously untreated metastatic malignant melanoma when treated with IMC-1121B (ramucirumab) alone or in combination with dacarbazine.

What is the current status of trial NCT00533702?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 106 participants. The study started on 2007-11. Estimated completion is 2011-05.

What interventions are being tested in trial NCT00533702?

The interventions under investigation include: Dacarbazine (DRUG), IMC-1121B (ramucirumab) (BIOLOGICAL).

Who is sponsoring clinical trial NCT00533702?

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 NCT00533702's enrollment target sits among peer trials

106 648th of 2000 higher than 1,351 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 NCT00533702, the US trial registry maintained by the National Library of Medicine. NCT00533702 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.