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NCT02343718

Vinblastine and Temsirolimus in Pediatrics With Recurrent or Refractory Lymphoma or Solid Tumours Including CNS Tumours

Completed Phase 1 Last updated 4 August 2023
What this trial tests

Phase 1 trial testing Vinblastine in Recurrent Lymphoma in 7 participants. Completed in 16 January 2019.

Timeline
24 June 2015
Primary endpoint
28 September 2017
16 January 2019

Quick facts

Lead sponsorCanadian Cancer Trials Group
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment7
Start date24 June 2015
Primary completion28 September 2017
Estimated completion16 January 2019
Sites6 locations across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Canadian Cancer Trials Group — full company profile →

Who can join

Adults 1 to 18, any sex, with Recurrent Lymphoma or Refractory Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the best dose of vinblastine that can be given with a new drug, temsirolimus.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Novel Therapies for Relapsed and Refractory Neuroblastoma.
    Zage PE. · · 2018 · cited 39× · PMID 30384486 · DOI 10.3390/children5110148
  2. Targeting mTOR for the treatment of B cell malignancies.
    Lee JS, Vo TT, Fruman DA. · · 2016 · cited 30× · PMID 26805380 · DOI 10.1111/bcp.12888

Verify or expand the search:

Other trials of Vinblastine

Trials testing the same drug.

Other recruiting trials for Recurrent Lymphoma

Currently open trials in the same condition.

Other Canadian Cancer Trials Group trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02343718.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing