Trials / Recruiting
RecruitingNCT02693535
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
Targeted Agent and Profiling Utilization Registry (TAPUR) Study
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 4,200 (estimated)
- Sponsor
- American Society of Clinical Oncology · Academic / Other
- Sex
- All
- Age
- 12 Years
- Healthy volunteers
- Not accepted
Summary
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. NOTE: Due to character limits, the arms section does NOT include all TAPUR Study relevant biomarkers. For additional information, contact TAPUR@asco.org, or if a patient, your nearest participating TAPUR site (see participating centers). \*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\* Results in publication or poster presentation format are posted as they become available for individual cohorts at www.tapur.org/news. The results may be accessed at any time. All results will be made available on clinicaltrials.gov at the end of the study. Indexing of available results on PubMed is in progress. \*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*\*
Detailed description
The Targeted Agent and Profiling Utilization Registry (TAPUR) Study is a non-randomized clinical trial that aims to describe the safety and efficacy of commercially available, targeted anticancer drugs prescribed for treatment of patients with advanced cancer that has a potentially actionable genomic variant. TAPUR will study Food and Drug Administration (FDA)-approved targeted therapies that are contributed by collaborating pharmaceutical companies, catalogue the choice of molecular profiling test by clinical oncologists and develop hypotheses for additional clinical trials.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Palbociclib | drug |
| DRUG | Sunitinib | drug |
| DRUG | Temsirolimus | drug |
| DRUG | Trastuzumab and Pertuzumab | drug |
| DRUG | Vemurafenib and Cobimetinib | drug |
| DRUG | Regorafenib | drug |
| DRUG | Olaparib | drug |
| DRUG | Nivolumab and Ipilimumab | drug |
| DRUG | Abemaciclib | drug |
| DRUG | Talazoparib | drug |
| DRUG | Atezolizumab and Talazoparib | drug |
| DRUG | Tucatinib plus Trastuzumab Subcutaneous (SC) | drug |
| DRUG | Futibatinib | drug |
| DRUG | Dabrafenib plus Trametinib | Drug |
| DRUG | Fam-Trastuzumab Deruxtecan-Nxki (TDxD) | Drug |
Timeline
- Start date
- 2016-03-14
- Primary completion
- 2027-12-31
- Completion
- 2028-12-31
- First posted
- 2016-02-26
- Last updated
- 2026-04-02
Locations
174 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02693535. Inclusion in this directory is not an endorsement.