drugset / Trial / NCT02987543

Study of Olaparib (Lynparza™) Versus Enzalutamide or Abiraterone Acetate in Men With Metastatic Castration-Resistant Prostate Cancer (PROfound Study)

NCT02987543 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of olaparib versus enzalutamide or abiraterone acetate in subjects with metastatic castration-resistant prostate cancer who have failed prior treatment with a new hormonal agent and have homologous recombination repair gene mutations.

Timeline

Start
2017-02-06
Primary completion
2019-06-04
Completion
2023-02-15

Outcome

Met primary endpoint

registry p <0.0001; Hazard Ratio (HR) 0.34 (95% CI 0.25 to 0.47) NCT02987543 ↗

release “the PROfound trial met its primary endpoint, showing a statistically significant and clinically meaningful improvement in radiographic progression-free survival compared to enzalutamide or abiraterone” merck.com ↗

release “PROfound trial are a testament to MSD and AstraZeneca’s lasting commitment to patients with cancer. The trial met the primary endpoint” astrazeneca.com ↗

release “Results of the PROfound trial showed Lynparza met its primary endpoint” merck.com ↗

release “In the PROfound trial, LYNPARZA more than doubled the median radiographic progression-free survival” merck.com ↗

release “The PROfound Phase III trial met its primary endpoint in August 2019, showing Lynparza significantly improved radiographic progression-free survival (rPFS)” astrazeneca.com ↗

release “The subgroup analysis from the PROfound Phase III trial showed Lynparza reduced the risk of disease progression or death by 78%” astrazeneca.com ↗

release “The subgroup analysis from the PROfound Phase III trial showed Lynparza reduced the risk of disease progression or death by 78%” astrazeneca.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Abiraterone acetate Small molecule 1000 mg Oral
Comparator Enzalutamide Other / unclassified 160 mg Oral
Subject Olaparib Small molecule 300 mg Oral

Indications