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Spots Global Cancer Trial Database for Maintenance With OSE2101 Plus FOLFIRI, or FOLFIRI After FOLFIRINOX-based Induction Therapy in Locally Advanced or Metastatic Pancreatic Ductal Adenocarcinoma

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Trial Identification

Brief Title: Maintenance With OSE2101 Plus FOLFIRI, or FOLFIRI After FOLFIRINOX-based Induction Therapy in Locally Advanced or Metastatic Pancreatic Ductal Adenocarcinoma

Official Title: A Randomized Non-comparative Phase II Study of Maintenance Therapy With OSE2101 Plus FOLFIRI, or FOLFIRI After Induction Therapy With FOLFIRINOX in Patients With Locally Advanced or Metastatic Pancreatic Ductal Adenocarcinoma (TEDOPaM-D17-01 PRODIGE 63 Study)

Study ID: NCT03806309

Interventions

FOLFIRI
OSE2101

Study Description

Brief Summary: TEDOPAM is a randomized (1.1.1) non-comparative phase II study. This study will assess the efficacy and safety of OSE2101 alone or in combination with nivolumab followed by FOLFIRI reintroduction, versus FOLFIRI as maintenance therapy in patients with advanced PDAC after induction therapy with FOLFIRINOX.

Detailed Description: Current standard of care for patients with advanced pancreatic ductal adenocarcinoma (PDAC) is chemotherapy, preferential regimen being FOLFIRINOX (5FU, leucovorin, irinotecan, and oxaliplatin) in fit patients (PS 0-1, bilirubin \< 1.5 ULN). The question of how and when the FOLFIRINOX regimen and doses can be deescalated after a period of disease control (i.e. maintenance therapy) remains unanswered. In routine practice, oxaliplatin is usually stopped after 6-8 cycles due to limiting neuropathy, and the fluoropyrimidine is continued, either alone or, more frequently, in combination with irinotecan (FOLFIRI regimen), until disease progression. Immune therapies have opened new opportunities in cancer therapy. However, results of immunotherapy in PDAC have been disappointing so far, with failure of checkpoint inhibitor monotherapies (anti-CTLA4 and anti-PD-L1 monoclonal antibodies \[mAb\]) in progressive advanced PDAC, while monovalent vaccines were demonstrated to be safe but with limited activity.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Clinique de l'Europe, Amiens, , France

Hôpital Sud CHU Amiens, Amiens, , France

CH Beauvais, Beauvais, , France

CHRU Jean Minjoz, Besançon, , France

Clinique Tivoli Ducos, Bordeaux, , France

CHU Morvan, Brest, , France

GHPSO Site de Creil, Creil, , France

Hôpital Henri Mondor, Créteil, , France

Centre Georges François Leclerc, Dijon, , France

CHU Dijon, Dijon, , France

CHRU Lille, Lille, , France

centre Léon Bérard, Lyon, , France

Hôpital Edouard Herriot, Lyon, , France

Hôpital la Croix Rousse, Lyon, , France

Hôpital Lyon Sud Hospices Civils de Lyon, Lyon, , France

Hôpital Privé Jean Mermoz, Lyon, , France

Hôpital Européen, Marseille, , France

Institut Paoli Calmette, Marseille, , France

Hôpital Pitié Salpêtrière, Paris, , France

Hôpital Saint Antoine, Paris, , France

Institut Mutualiste Montsouris, Paris, , France

CHU Poitiers, Poitiers, , France

CHU Robert Debré, Reims, , France

Institut Curie, Saint-Cloud, , France

Centre Paul Strauss, Strasbourg, , France

Clinique Pasteur, Toulouse, , France

Hôpital TROUSSEAU, Tours, , France

Insitut de Cancérologie de Lorraine, Vandœuvre-lès-Nancy, , France

Contact Details

Name: Cindy NEUZILLET, MD

Affiliation: Institut Curie site de Saint Cloud

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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