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Phase II trial of rucaparib maintenance in metastatic endometrial cancer completes follow-up

Phase II trial of rucaparib maintenance in metastatic endometrial cancer completes follow-up
Photo by National Cancer Institute / Unsplash
Key Takeaway
Await full results from phase II rucaparib maintenance trial in endometrial cancer.

A phase II randomized controlled trial assessed rucaparib maintenance therapy versus placebo in 79 patients with metastatic or recurrent endometrial cancer who had received 1-2 prior lines of therapy. The primary outcome was progression-free survival (PFS), with follow-up reported at 55.8 months. The study sponsor was the University of Colorado, Denver.

No specific efficacy results for the primary PFS outcome are reported in the provided data. Effect size, absolute numbers, p-values, and direction of effect are all listed as not reported. Secondary outcomes were not specified in the input.

Safety and tolerability data, including adverse events, serious adverse events, and discontinuation rates, are also not reported in the provided information. No specific study limitations were listed in the input.

As a completed phase II trial, this research represents an early-stage investigation. The absence of reported efficacy and safety outcomes prevents any assessment of rucaparib's potential benefit-risk profile in this setting. Clinicians should await peer-reviewed publication of the full trial results before considering any practice implications.

Study Details

Study typePhase2
Sample sizen = 79
EvidenceLevel 3
Follow-up55.8 mo
PublishedMar 2026
View Original Abstract ↓
Status: COMPLETED | Phase: PHASE2 Condition(s): Metastatic Endometrial Cancer Intervention(s): Rucaparib (DRUG), Placebo Oral Tablet (DRUG) This study seeks to determine the effectiveness of Rucaparib as maintenance therapy for metastatic and recurrent endometrial cancer, after 1-2 prior lines of therapy. Detailed: This is a phase II clinical trial, that administers a maintenance treatment after first line chemotherapy is complete. It is designed to have a 1:1 randomization technique. Half the participants who enter the study will receive the active ingredient, Rucaparib, while the other half will receive a placebo. Treatment will be until progression with follow up until death. Primary Outcome(s): Progression Free Survival (PFS) Enrollment: 79 (ACTUAL) Lead Sponsor: University of Colorado, Denver Start: 2019-03-06 | Primary Completion: 2023-10-31 Results posted: 2024-07-01
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