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NCT06599463Completed

Efficacy Assessment of Lenvatinib Associated with Pembrolizumab in Metastatic Endometrial Cancer: a French Multicentric Retrospective Early Access Program-based Study

Source: ClinicalTrials.gov · Last updated 20 Mar 2025

Brief summary (registry, in English)

LARENA is a multicentric retrospective study (secondary use of data) of consecutive patients prospectively registered in the lenvatinib plus pembrolizumab French early access program (Temporary Authorisation for Use). The source of data will be the patient's medical file. We will manually review all files of the participating centers.

Status (registry)
Completed
Study type
Observational
Enrollment
351 (actual)
First submitted
11 Sept 2024
Start date
Aug 2024
Primary completion date
Feb 2025
Lead sponsor
ARCAGY/ GINECO GROUP
NCT number
NCT06599463

What you commit to

  • Study type: Observational
  • Participants enrolled: 351
  • From Aug 2024 to the primary completion date, Feb 2025
  • 24 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients who refuse the collection and use of their personal data in the course of this research.

Who the study is looking for

  • Patients having received at least one dose of lenvatinib plus pembrolizumab in the context of the French early access program (Temporary Authorisation for Use) approved by the French Health Autority.
  • Patients with advanced or recurrent endometrial cancer whose disease is progressing during or following prior platinum-based chemotherapy at any stage and who are not eligible for curative surgery or radiotherapy, according to the French early access program (Temporary Authorisation for Use) approved by the French Health Autority criteria.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (24)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
ICO Paul Papin
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AngersFranceUnknown status
Sainte Catherine - Institut du Cancer Avignon
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AvignonFranceUnknown status
Chu Jean Minjoz
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BesançonFranceUnknown status
ICONE
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BezannesFranceUnknown status
Clinique Tivoli
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BordeauxFranceUnknown status
Centre François Baclesse
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CaenFranceUnknown status
Centre Hospitalier William Morey
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Chalon-sur-SaôneFranceUnknown status
Centre Jean Perrin
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Clermont-FerrandFranceUnknown status
Centre Georges François Leclerc
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DijonFranceUnknown status
CHU de DIJON
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DijonFranceUnknown status
Centre Leon Berard
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LyonFranceUnknown status
Institut Paoli-Calmettes
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MarseilleFranceUnknown status
ICM Val d'Aurelle
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MontpellierFranceUnknown status
Hopital Européen George Pompidou
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ParisFranceUnknown status
Centre Cario HPCA
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PlérinFranceUnknown status
CHU de Poitiers - Hôpital de la Milétrie
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PoitiersFranceUnknown status
CHI de Cornouaille
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QuimperFranceUnknown status
Centre Eugène Marquis
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RennesFranceUnknown status
Institut Curie
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Saint-CloudFranceUnknown status
CHU Saint-Etienne - Hôpital Bellevue
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Saint-EtienneFranceUnknown status
ICANS
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StrasbourgFranceUnknown status
Oncopole Claudius Regaud IUCT ONCOPOLE
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ToulouseFranceUnknown status
CHU Tours Hôpital Bretonneau
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ToursFranceUnknown status
Centre Hospitalier de Valence
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ValenceFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.