NCT02693535: Phase 2: TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs
Updated: May 19, 2022
NCT02693535: Phase 2: TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer (TAPUR)
TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer (TAPUR)
The purpose of the study is to learn from the real world practice of prescribing targeted therapies to patients with advanced cancer whose tumor harbors a genomic variant known to be a drug target or to predict sensitivity to a drug
Sponsor:
American Society of Clinical Oncology
Collaborators:
AstraZeneca
Bayer
Bristol-Myers Squibb
Eli Lilly and Company
Genentech, Inc.
Merck Sharp & Dohme Corp.
Pfizer
Boehringer Ingelheim
Seagen Inc.
Multiple Locations
ClinicalTrials.gov Identifier: NCT02693535
Official Title: Targeted Agent and Profiling Utilization Registry (TAPUR) Study
First Posted : February 26, 2016
Drug: Crizotinib
Drug: Palbociclib
Drug: Sunitinib
Drug: Temsirolimus
Drug: Trastuzumab and Pertuzumab
Drug: Vemurafenib and Cobimetinib
Drug: RegorafenibDrug: Olaparib
Drug: Pembrolizumab
Drug: Nivolumab and Ipilimumab
Drug: Abemaciclib
Drug: Afatinib
Drug: Talazoparib
Drug: Atezolizumab and PHESGO
Drug: Atezolizumab and Talazoparib
Drug: Entrectinib
Drug: Larotrectinib
Drug: Tucatinib plus Trastuzumab Subcutaneous (SC)