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NCT02564198 · ClinicalTrials.gov registry record · Phase 1

A Study of Ramucirumab (LY3009806) in Children With Refractory Solid Tumors

A Phase 1 study of Pediatric Solid Tumor and Recurrent Tumor, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
29
Enrollment target
20
Study locations

NCT02564198: Completed Phase 1 study of Pediatric Solid Tumor and Recurrent Tumor, sponsored by Eli Lilly and Company.

NCT02564198 is a Phase 1 study of Pediatric Solid Tumor and Recurrent Tumor that has completed, run by Eli Lilly and Company. The registered enrollment target is 29 participants, below the 1,130-participant average among 10 other Pediatric Solid Tumor trials with a reported enrollment target (97% lower). The trial reports 20 study locations across 17 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02564198, a Phase 1 study of Pediatric Solid Tumor and Recurrent Tumor, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
29 participants
Enrollment target
20
Study locations

Study Summary

The main purpose of this study is to evaluate the safety of the study drug known as ramucirumab in children with recurrent or refractory solid tumors including central nervous system (CNS) tumors.

Primary Outcome

A DLT is defined as an Adverse Event (AE) that is likely related to the study medication or combination, and fulfills any one of the following criteria, graded according to the National Cancer Institute's (NCI) Common Terminology Criteria for Adverse Events (NCI-CTCAE) Version 5.0: 1\. Any death not clearly due to the underlying disease or extraneous causes 2. Neutropenic fever 2. Any Grade ≥3 non-hematologic toxicity 3. Grade ≥4 neutropenia or thrombocytopenia \>7 days 4. Grade ≥3 thrombocytop

Interventions

  • DRUG Ramucirumab

Study Locations (20)

California

  • Children's Oncology Group - Monrovia
  • Childrens Hospital of Orange County - Orange
  • University of California, San Francisco - San Francisco

Pennsylvania

  • Children's Hospital of Philadelphia - Philadelphia
  • Childrens Hospital of Pittsburgh - Pittsburgh

Alabama

  • Childrens Hospital of Alabama - Birmingham

District of Columbia

  • Children's National Medical Center - Washington D.C.

Georgia

  • Children's Healthcare of Atlanta at Scottish Rite - Atlanta

Illinois

  • Ann & Robert H Lurie Children's Hospital of Chicago - Chicago

Indiana

  • Riley Hospital for Children - Indianapolis

Maryland

  • Mark O Harfield-Warren Grant Magnuson Clinical Center - Bethesda

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2015-12-11
Est. Completion 2019-07-16
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT02564198 record still lists

NCT02564198 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 1,130-participant average among 10 other Pediatric Solid Tumor trials with a reported enrollment target (97% lower).

The record links to 4 conditions, with Pediatric Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which Ramucirumab is the first listed.

NCT02564198 names 20 study sites across 17 states, led by California, Pennsylvania, Alabama.

Frequently Asked Questions

What is clinical trial NCT02564198 about?

NCT02564198 is a clinical study titled "A Study of Ramucirumab (LY3009806) in Children With Refractory Solid Tumors". The main purpose of this study is to evaluate the safety of the study drug known as ramucirumab in children with recurrent or refractory solid tumors including central nervous system (CNS) tumors.

What is the current status of trial NCT02564198?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2015-12-11. Estimated completion is 2019-07-16.

What conditions does trial NCT02564198 study?

This clinical trial studies the following conditions: Pediatric Solid Tumor, Recurrent Tumor, Refractory Tumor, CNS Malignancies.

What interventions are being tested in trial NCT02564198?

The interventions under investigation include: Ramucirumab (DRUG).

Who is sponsoring clinical trial NCT02564198?

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

Where is trial NCT02564198 being conducted?

This trial has 20 study locations across Alabama, California, District of Columbia, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pediatric Solid Tumor

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02564198's enrollment target sits among peer trials

29 10th of 10 higher than 1 of 10 other Pediatric Solid Tumor trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pediatric Solid Tumor 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 NCT02564198, the US trial registry maintained by the National Library of Medicine. NCT02564198 (small enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.