Status:
TERMINATED
Safety, Tolerability, Efficacy and Pharmacokinetics of Copanlisib in Pediatric Patients
Lead Sponsor:
Bayer
Conditions:
Relapsed or Refractory Solid Tumors or Lymphoma in Children
Neuroblastoma
Eligibility:
All Genders
6-21 years
Phase:
PHASE1
PHASE2
Brief Summary
This study is designed to investigate whether the use of copanlisib is safe, feasible and beneficial to pediatric patients with solid solid tumors or lymphoma that are recurrent or refractory to stand...
Eligibility Criteria
Inclusion
- Signed informed consent form by patients and/or patients' parents/legal guardians and age appropriate assent form by the patients obtained before any study specific procedure
- Male or female patients from 6 months to ≤ 21 years old at the time of study enrollment
- Confirmation of diagnosis:
- Phase I: Patients must have histologic verification of a solid tumor or lymphoma malignancy at diagnosis, with measurable or evaluable disease, for which there is no standard curative anti-cancer treatment or treatment is no longer effective and must have received ≥ 1 prior line of therapy.
- Phase II: patients must have histologically verified tumor at initial diagnosis and radiologically or histologically confirmed status at inclusion as indicated in the following: neuroblastoma, osteosarcoma, rhabdomyosarcoma or Ewing sarcoma.
- Patients with solid tumors must have measurable disease (evaluable disease is acceptable for neuroblastoma and Ewing sarcoma). Tumor assessment will be done via computed tomography (CT), magnetic resonance imaging (MRI) or positron emission tomography-computed tomography (PET-CT). Tumor lesions situated in a previously irradiated area, or in an area subjected to other loco-regional therapy, may be considered measurable if there has been demonstrated progression in the lesion. Bone scans (if clinically indicated) should be obtained within ≤ 4 weeks prior to the start of treatment.
- Performance level: Lansky ≥ 50% for patients ≤ 16 years of age and Karnofsky ≥ 50% for patients \> 16 years of age.
- Adequate bone marrow, renal and liver function.
Exclusion
- Active or uncontrolled infection (National Cancer Institute (NCI)-CTCAE Grade ≥ 2).
- History or concurrent condition of interstitial lung disease of any severity and/or severely impaired lung function (as judged by the investigator).
- Diabetes mellitus.
- Uncontrolled arterial hypertension despite optimal medical management (per institutional guidelines).
- Patients with central nervous system (CNS) malignancies.
Key Trial Info
Start Date :
April 30 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2023
Estimated Enrollment :
31 Patients enrolled
Trial Details
Trial ID
NCT03458728
Start Date
April 30 2018
End Date
February 1 2023
Last Update
December 4 2023
Active Locations (14)
Enter a location and click search to find clinical trials sorted by distance.
1
Children's Hospital of Alabama
Birmingham, Alabama, United States, 35233
2
Children's Hospital of Orange County
Orange, California, United States, 92868-3974
3
The Children's Hospital
Aurora, Colorado, United States, 80045
4
Children's National Medical Center
Washington D.C., District of Columbia, United States, 20010-2970