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NCT04106219Active, not recruitingPhase 1

A Study of LY3295668 Erbumine in Participants With Relapsed/Refractory Neuroblastoma

A Phase 1 Study of Aurora Kinase A Inhibitor LY3295668 Erbumine as a Single Agent and in Combination in Patients With Relapsed/Refractory Neuroblastoma

Source: ClinicalTrials.gov · Last updated 21 Aug 2026

Brief summary (registry, in English)

The reason for this study is to see if the study drug LY3295668 erbumine is safe in participants with relapsed/refractory neuroblastoma.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
71 (estimated)
First submitted
25 Sept 2019
Start date
11 Jun 2020
Primary completion date
13 Apr 2022
Lead sponsor
Eli Lilly and Company
NCT number
NCT04106219
EU CT number
2024-512102-25-00
EudraCT number
2019-001042-18

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 71
  • From 11 Jun 2020 to the primary completion date, 13 Apr 2022
  • 16 sites in 9 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants must not have had an allogeneic hematopoietic stem cell, bone marrow, or solid organ transplant.
  • Participants must not have had prior aurora kinase inhibitor exposure.

Other illness

  • Participants must not have a serious active disease other than neuroblastoma.
  • Participants must not have a condition affecting absorption.
  • Participants must not have a known allergy to the study treatment.
  • Participants must not have symptomatic human immunodeficiency virus (HIV) infection or symptomatic activated/reactivated hepatitis A, B, or C.

Other

  • Participants must not have untreated tumor that has spread to the brain or spinal cord.

Who the study is looking for

  • Participants must have relapsed/refractory neuroblastoma and have active disease in at least one site: bone, bone marrow or soft tissue. Participants must be able to submit an archival sample of tissue.
  • Participants must be able to swallow capsules.

Age in the registry: 2 years to 21 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Perth Children's Hospital
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PerthAustraliaUnknown status
UZ Gent
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GhentBelgiumUnknown status
Universitätsklinikum Köln
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CologneGermanyUnknown status
Hospital Universitari Vall d'Hebron
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BarcelonaSpainActive, not recruiting
Centre Leon Berard
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LyonFranceUnknown status
Institut Curie
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ParisFranceUnknown status
Alder Hey Children's Hospital
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LiverpoolUnited KingdomUnknown status
Istituto Nazionale dei Tumori
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MilanItalyUnknown status
National Cancer Center Hospital
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Chuo KuJapanUnknown status
Children's Hospital Colorado
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AuroraUnited StatesUnknown status
Dana-Farber Cancer Institute
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BostonUnited StatesUnknown status
University of Chicago Comer Children's Hospital
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ChicagoUnited StatesUnknown status
Cincinnati Childrens Hospital Medical Center
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CincinnatiUnited StatesUnknown status
Texas Childrens Hospital
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HoustonUnited StatesUnknown status
Children's Hospital of Philadelphia
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PhiladelphiaUnited StatesUnknown status
UCSF Medical Center at Mission Bay
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San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.