New study aims to tailor ovarian cancer treatment for women over 70
NCT ID NCT06572735
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 50 women aged 70 and older with advanced ovarian cancer who are starting PARP inhibitors for the first time. Researchers will track how much of the planned dose patients actually receive, and look at factors like age, genetics, and overall health that might affect tolerance. The goal is to better understand how to manage side effects and keep patients on effective treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PARP inhibitors
- What this could lead to
- If successful, this could help doctors better manage side effects and dosing of PARP inhibitors in elderly patients, potentially improving treatment outcomes.
- What could go wrong
- This is a small observational study (50 patients) that does not test a new treatment. It only gathers data, so it will not directly change care immediately.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2024
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients of 70 years and elder with an advanced ovarian cancer who are scheduled to start a maintenance therapy with PARP inhibitors for the first time. The necessary number of patients in the study is 50.
- Ages
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70 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 70 years * Histologically or cytologically confirmed diagnosis of advanced ovarian cancer (FIGO stage III or IV) * PARP inhibitors -naive patient who need to initiate maintenance treatment with PARP inhibitors for the first time (according the the marketing authorization) * Patient with a life expectancy of more then 3 months * Informed patient which does not oppose to participate to the study Exclusion Criteria: * Prior treatment with PARP inhibitors * Patient incapable to take oral tablets/capsules * Participation in a drug trial that does not authorize concurrent participation in another trials * Person unable to attend scheduled examinations/appointments as part of routine care for geographical, social or psychological reasons * Concomitant cancer or f cancer history (other than those included in the inclusion criteria) treated and considered cured for less than 2 years. However, patients with the following pathologies are eligible: * Basal cell carcinoma or non-invasive cutaneous squamous cell carcinoma * Stage 1B or less cervical carcinoma * Non-invasive superficial bladder cancer
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
16 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centre Georges François Leclerc
RECRUITINGDijon, 21079, France
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Centre Hospitalier Privé Saint-Grégoire - Les Hôpitaux Privés Rennais
RECRUITINGSaint-Grégoire, 35760, France
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Centre Hospitalier Universitaire d'Amiens Picardie Site Sud
RECRUITINGAmiens, 80054, France
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Centre Hospitalier Valence
RECRUITINGValence, 26953, France
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Centre de lutte contre le cancer Jean Perrin
RECRUITINGClermont-Ferrand, 63011, France
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Clinique Mathilde
RECRUITINGRouen, 76100, France
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Clinique de l'Europe
RECRUITINGAmiens, 80090, France
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Groupe Hospitalier Diaconesses Croix Saint Simon
RECRUITINGParis, 75020, France
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Groupe Hospitalier Public Sud de l'Oise
RECRUITINGCreil, 60100, France
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Hôpital Femme-Mère-Enfant
RECRUITINGBron, 69500, France
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Hôpital Privé Jean Mermoz
RECRUITINGLyon, 69008, France
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Institut de Cancérologie et d'Hématologie Universitaire de Saint Etienne
RECRUITINGSaint-Priest-en-Jarez, 42271, France
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Médipôle Hôpital Mutualiste
RECRUITINGVilleurbanne, 69100, France
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Service Hôpital de jour / Oncologie Médicale, Hôpital de la Croix Rousse
RECRUITINGLyon, 69004, France
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Service Oncologie Médicale, Hôpital Lyon Sud
RECRUITINGPierre-Bénite, 69495, France
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Service de Gériatrie, Hôpital Dr Frédéric Dugoujon
RECRUITINGLyon, 69317, France
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Other studies related to the condition(s) this trial covers.
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- Can inhaled manganese make ovarian cancer immunotherapy hit harder?
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- New antibody aims to preserve immune checkpoint while fighting cancer