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Clinical Trial Summary

This is a prospective randomized, double blind, placebo controlled phase II study planned in patients with advanced ACC. The study will be conducted at ASST Spedali Civili Hospital and University of Brescia in Brescia.


Clinical Trial Description

As no effective second-line therapies are available for patients with disease progression to EDPM, including modern molecular target therapies and immunotherapy, it is reasonable to expect that no newer drugs or combination regimens will be able to replace EDPM in the next 5 years. Since EDP-M is destined to remain the standard first line therapy, research strategies aimed to improve the efficacy of this regimen are of relevance. In this study, investigators will address the hypotheses that progesterone has a synergistic and/or additive effect to EDP-M in inducing cytotoxicity in ACC cells in vitro and the antineoplastic activity of EDP-M in locally advanced/metastatic ACC patients could be improved by the addition of megestrol acetate. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05913427
Study type Interventional
Source Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
Contact Aldo Roccaro
Phone +390303996851
Email coordinamento.ricerca@asst-spedalicivili.it
Status Recruiting
Phase Phase 2
Start date June 8, 2022
Completion date June 8, 2027

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