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NCT03158636: PROSPER

Profiling of Oncology Patients as Part of Clinical Care and Research

Completed Last updated 16 May 2024
What this trial tests

trial in Gynecologic Cancer in 37 participants. Completed in 7 May 2024.

Timeline
1 September 2016
Primary endpoint
7 May 2024
7 May 2024

Quick facts

Lead sponsorUniversity of Auckland, New Zealand
StatusCompleted
Study typeOBSERVATIONAL
Enrollment37
Start date1 September 2016
Primary completion7 May 2024
Estimated completion7 May 2024
Sites1 location across New Zealand

Conditions studied

Sponsor

University of Auckland, New Zealand

Who can join

18 and older, any sex, with Gynecologic Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The era of precision medicine is an exciting time for clinicians, scientists and patients alike. The increasing appreciation and identification of specific mutations that drive cancers, leaves us on the threshold of a new era in which biomarkers will be used to direct targeted agents to only those patients most likely to respond. The potential medical and scientific benefits of such a personalised approach to cancer therapy are immense. However, a number of barriers challenge successful implementation of this approach of which spatial and temporal heterogeneity are a major concern. Gynaecological cancers are a major cause of mortality and morbidity internationally. In Auckland 150 new patients with ovarian, endometrial or cervical cancer are seen by a medical oncologist each year. In general, when these diseases recur, there are few effective therapeutic options and prognosis is poor. Better therapeutic targets and treatments are an unmet need across these tumour types with treatment paradigms still based upon platinum based therapy. PROSPER (Profiling of Oncology Patients as part of Clinical care and Research) will investigate the evolution of gynaecological cancers over time and in response to treatment to develop better biomarkers to guide treatment decisions and ultimately improve patient outcomes. Biopsies at relapse will be collected and profiled with a 580 cancer gene panel. Circulating tumour DNA will be collected and analysed alongside biopsies as a potential non-invasive alternative. Linking genomic and clinical data will allow us to learn more to begin to change our paradigm of care.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Gynecologic Cancer

Currently open trials in the same condition.

Other University of Auckland, New Zealand trials

Trials by the same sponsor.

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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/NCT03158636.

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