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Study identifier: NCT06572735 Synced from ClinicalTrials.gov · July 29, 2026
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Study on the Relative Dose Intensity of PARP Inhibitors in Real-life on a Population of Patients Over 70 Years With Advanced Ovarian Cancer

Condition: Ovarian Cancer  ·  Sponsor: Hospices Civils de Lyon

PhaseN/A
Planned participants50
Who can joinFemale, 70 Years to no upper limit
Healthy volunteersNo

About this study

Poly(ADP-ribose) polymerase (PARP) inhibitors are anti-cancer treatments that induce preferential tumor cell death. Their efficacy has been demonstrated in many tumor models, primarily in advanced ovarian cancer. PARP inhibitors also exhibit a particular toxicity, damaging the hematopoietic tissue. With age, pharmacokinetic changes or a reduction in medullary cavity may increase these toxicities and may lead to dose reductions/postponements or premature discontinuation of PARP inhibitors, which may impact the efficacy of treatment. Close biological monitoring must be carried out to limit these toxicities, in most cases anemia, thrombocytopenia and neutropenia. Until now, the geriatric factors impacting the tolerance and uptake of PARP inhibitors in the elderly patient population with advanced ovarian cancer are not clearly established. It is therefore necessary to have prospective real-life data in order to support patients in a decision-making process on whether or not to continue such treatments. PARIB-OLD-PRO² will evaluate the association between various clinical, biological, and geriatric factors and the relative dose intensity (RDI) of therapy by PARP inhibitors. This is a prospective, multicenter longitudinal and non-interventional study and will involve a population of 50 patients, aged 70 years and elder, with advanced ovarian cancer who are scheduled to start a therapy with PARP inhibitors for the first time. The aim of the study is to better understand the effects…

This description comes directly from the study's public registry record.

Talk to the study team

Claire FALANDRY, Professor  ·  04.72.07.18.15  ·  claire.falandry@chu-lyon.fr

Gabriel ANTHERIEU, MD, PhD  ·  04.78.86.15.20  ·  gabriel.antherieu@chu-lyon.fr

Always discuss trial participation with your own doctor first.

Locations (16)

Centre Hospitalier Universitaire d'Amiens Picardie Site SudAmiens, FranceRecruiting
Clinique de l'EuropeAmiens, FranceRecruiting
Hôpital Femme-Mère-EnfantBron, FranceRecruiting
Centre de lutte contre le cancer Jean PerrinClermont-Ferrand, FranceRecruiting
Groupe Hospitalier Public Sud de l'OiseCreil, FranceRecruiting
Centre Georges François LeclercDijon, FranceRecruiting
Service Hôpital de jour / Oncologie Médicale, Hôpital de la Croix RousseLyon, FranceRecruiting
Hôpital Privé Jean MermozLyon, FranceRecruiting
Service de Gériatrie, Hôpital Dr Frédéric DugoujonLyon, FranceRecruiting
Groupe Hospitalier Diaconesses Croix Saint SimonParis, FranceRecruiting
Service Oncologie Médicale, Hôpital Lyon SudPierre-Bénite, FranceRecruiting
Clinique MathildeRouen, FranceRecruiting

+ 4 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06572735