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PHOENIX DDR/Anti-PD-L1 Trial: A Pre-surgical Window of Opportunity and Post-surgical Adjuvant Biomarker Study of DNA Damage Response Inhibition With or Without Anti-PD-L1 Immunotherapy in Patients With Neoadjuvant Treatment Resistant Residual Triple Negative Breast Cancer

Study acronym: PHOENIX
StatusRecruiting
PhasePhase 2
Started
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Record History

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  1. Notable Primary completion date: Mar 2023 to Dec 2026v3 Show 9 more changesShow less
    • Primary endpoints: 4 to 7
    • Enrollment target: 81 to 119
    • Study sites: 9 to 6
    • Study completion date: Dec 2025 to Jun 2029
    • Eligibility criteria shortened, about 369 words
    • Secondary endpoints: 10 to 3
    • Study description expanded, about 12 words
    • Study arms: 4 to 7
    • Study title expanded, about 2 words
  2. Notable Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Primary completion date: May 2021 to Mar 2023
    • Start date changed from estimate of Feb 2019 to Oct 15, 2019
    • Study completion date: Aug 2023 to Dec 2025
    • Eligibility criteria expanded, about 37 words
    • Site details revised at 9 of 9 sites
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
PHOENIX is a window of opportunity (WOP), open-label, multi-centre, phase IIa trial comprising multiple non-comparative treatment cohorts with patient allocation via minimisation (cohorts A-D) or allocation according to HRD and germline BRCA1/2 mutation status (cohorts E-G). The trial consists of two parts: a post-neoadjuvant treatment preoperative WOP component (PART 1); and a post-operative component (PART 2). Cohorts A-D: To assess whether short exposure to a DDR inhibitor or anti-PD-L1 immunotherapy in a preoperative WOP in patients with post-NACT high risk residual disease, generates a signal of anti-tumour biological activity within residual disease tissue. Cohort E: To assess whether short exposure to a DDR inhibitor with or without anti-PD-1 immunotherapy in a preoperative WOP in patients with non-HRD associated TNBC and post-neoadjuvant treatment high risk residual disease, generates a signal of anti-tumour biological activity within residual disease tissue. Cohorts F \& G: To assess whether short exposure to the DDR inhibitor olaparib with or without anti-PD-1 immunotherapy in a preoperative WOP in patients with HRD associated TNBC and post-neoadjuvant treatment high risk residual disease, generates a signal of anti-tumour biological activity within residual disease tissue.
Trial Details
NCT Number NCT03740893
Lead Sponsor Institute of Cancer Research, United Kingdom
Collaborators: AstraZeneca
Conditions
(from sponsor)
Breast Neoplasm, Triple Negative Breast Cancer (TNBC), HRD
Related terms Breast Neoplasms, Triple Negative Breast Neoplasms
Enrollment 119 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov