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NCT03443128CompletedPhase 2

Vinorelbine for Recurrent ALCL-2017

Phase II Study of Vinorelbine for Children with Recurrent Anaplastic Large Cell Lymphoma

Source: ClinicalTrials.gov · Last updated 13 Feb 2025

Brief summary (registry, in English)

The purpose of this study is to assess the efficiency and safety of vinorelbine in the treatment of relapsed / advanced ALCL in children and adolescents.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
17 Feb 2018
Start date
1 Nov 2016
Primary completion date
31 Dec 2024
Lead sponsor
Children's Cancer Group, China
NCT number
NCT03443128

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 20
  • From 1 Nov 2016 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • 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.

Other illness

  • Patients with other systemic diseases, severe infections or critically illness.

Who the study is looking for

  • Children and adolescents with a clear diagnosis of recurrent / progressive ALCL at Shanghai Children's Medical Center or other centers since September 2017 include:
  • Diagnosed as ALCL, already received first-line treatment, but get disease progression; After receiving ALCL treatment has got CR then diagnosed relapse, need for pathological diagnosis.

Age in the registry: - to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Shanghai Children's Medical Center
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

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