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Oxaliplatin

AbbVie Cancer, Parkinson

Suivi actif Phase 2

Résumé

Oxaliplatin est développé par AbbVie. Le traitement est actuellement en Phase 2. Il est associé à Cancer, Parkinson. Son objectif thérapeutique principal est À vérifier. Le statut actuel est : suivi actif.

À vérifier

À vérifier
Phase 2
AbbVie
United States, Australia, Austria, Brazil, Canada, Czechia, France, Greece, …
CRC is the third most common type of cancer diagnosed worldwide with developed countries at highest risk. The purpose of this study is to assess adverse events and change in disease activity when telisotuzumab adizutecan is given in combination with oxaliplatin, fluorouracil (5FU), leucovorin (LV) (FOLFOX), and bevacizumab or panitumumab. Telisotuzumab adizutecan is an investigational drug being developed for the treatment of mCRC. Fluorouracil and leucovorin are drugs approved for the treatment of mCRC. This study will be divided into two stages, with the first stage treating participants with increasing doses of telisotuzumab adizutecan with FOLFOX and bevacizumab or 5FU/LV and panitumumab until the dose reached is tolerable and expected to be efficacious. Participants will then be randomized into 3 groups called treatment arms where one group will receive one of two optimized doses of telisotuzumab adizutecan from the dose escalation phase with FOLFOX and bevacizumab or 5FU/LV and panitumumab, or a comparator of FOLFOX and bevacizumab or panitumumab. Approximately 390 adult participants with mCRC will be enrolled in the study in 100 sites worldwide. In the dose escalation stage participants will be treated with increasing intravenous (IV) doses of telisotuzumab adizutecan with FOLFOX and bevacizumab or 5FU/LV and panitumumab until the dose reached is tolerable and expected to be efficacious. In the dose optimization stage participants will be receive FOLFOX or receive 5FU/LV, but with one of two optimized doses of telisotuzumab adizutecan, or a comparator of FOLFOX and bevacizumab/pantitumumab. The study will run for a duration of approximately 6 years. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and side effects.
2026-09-10

Début phase actuelle
Non disponible dans les sources synchronisées
Timeline clinique

Phase 2
Préclinique
Phase 1
Phase 2
Phase 3
Approuvé

Objectif scientifique de l’étude

classification automatique vérifiable
À vérifier Confiance automatique : 0%

Description affichée depuis l’essai compatible NCT06820463, afin d’éviter le mélange entre plusieurs indications d’une même molécule.

Contrôle de cohérence : 85/100

L’objectif est absent ou classé « Autre » et doit être recalculé à partir du protocole.

Transparence et qualité de la fiche

données vérifiables
ClassificationÀ vérifier
Confiance de la fiche85 %
Source principaleSource officielle ou publication indexée
Dernière vérification2026-09-10
Anomalies détectées1
Validation humaineValidation humaine non effectuée
Donnée issue d’une source Donnée normalisée automatiquement Interprétation algorithmique

Classification scientifique multi-axes

ne pas confondre statut et résultat
État de l’étudeRecrutement en cours
Disponibilité des résultatsRésultats à vérifier
InterprétationImpossible à déterminer
Niveau de preuveNon évaluable

Un essai terminé n’est pas nécessairement positif. Un essai arrêté n’est classé comme échec scientifique que lorsqu’un résultat ou une raison explicite le confirme.

Indicateurs factuels

sans score subjectif
Phase enregistréePhase 2
Études associées5
Publications associées16
Statut consolidéSuivi actif

Aucune chance de succès, note d’innovation, potentiel thérapeutique ou probabilité de commercialisation n’est calculé tant qu’un modèle validé et des données suffisantes ne sont pas disponibles.

Historique factuel de la molécule

33 événement(s) daté(s)

Cette liste reprend uniquement les dates trouvées dans les registres et publications liés. Elle ne constitue pas une prévision.

DateÉvénementSource
2012-01-01Début de l’étudeNCT02867397Registre d’essai clinique
2015-08-01Fin de l’étude prévue / enregistréeNCT02867397Registre d’essai clinique
2025-03-05Début de l’étudeNCT06806033Registre d’essai clinique
2025-04-24Début de l’étudeNCT06820463Registre d’essai clinique
2026-03-01Début de l’étudeNCT07504198Registre d’essai clinique
2026-05-06Début de l’étudeNCT07549412Registre d’essai clinique
2026-07-08Création de l’enregistrementNCT02867397Registre d’essai clinique
2026-07-08PublicationClinical use of trastuzumab combined with different chemotherapy regimens in multi-line treatment of advanced human epidermal growth factor receptor 2-positive gastric cancer: A case report.Oncology letters
2026-07-08PublicationCase Report: Conversion therapy for initially unresectable intrahepatic cholangiocarcinoma.Frontiers in oncology
2026-07-08PublicationGastric Cancer Treated with 5-Fluorouracil following Discontinuation of Adjuvant S1 plus Docetaxel and Capecitabine plus Oxaliplatin due to Drug-Induced Acute Pancreatitis: A Case Report.Case reports in oncology
2026-07-08PublicationThe Landmark Series: Neoadjuvant Therapy for Patients with Resectable Gastroesophageal Junction Adenocarcinomas.Annals of surgical oncology
2026-07-10PublicationReal-world effectiveness of NALIRIFOX versus modified FOLFIRINOX or gemcitabine and nab-paclitaxel in first-line advanced pancreatic adenocarcinoma: a multicentre propensity-matched study.BMJ oncology
2026-07-13Dernière mise à jour du registreNCT02867397Registre d’essai clinique
2026-07-14PublicationSalvage ultra-low-dose radiotherapy for conjunctival mantle cell lymphoma - a case report and literature review.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology
2026-07-14PublicationBreakthrough reactions in pediatric chemotherapeutic desensitization: Outcomes and associated risk factors.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
2026-08-13PublicationResveratrol Modulates Phosphatidylcholine Metabolism-Related Enzymes and Enhances Chemosensitivity in Colorectal Cancer Models.International journal of molecular sciences
2026-08-13PublicationCost-effectiveness analysis of liposomal Irinotecan in combination with oxaliplatin, 5-fluorouracil and leucovorin (NALIRIFOX) for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas in Greece.Expert review of pharmacoeconomics & outcomes research
2026-08-16Création de l’enregistrementNCT06806033Registre d’essai clinique
2026-08-16Création de l’enregistrementNCT07549412Registre d’essai clinique
2026-08-16PublicationSingle-Institution Outcomes of Neoadjuvant Gemcitabine and Nab-Paclitaxel Combination in Borderline Resectable Pancreatic Adenocarcinoma: A Three-Year Retrospective Audit.Cureus
2026-08-16PublicationAddition of autologous stem-cell transplantation to an ibrutinib-containing first-line treatment in patients aged 18-65 years with mantle cell lymphoma (TRIANGLE): 4·5-year follow-up of a three-arm, randomised, open-label, phase 3 superiority trial of the European MCL Network.Lancet (London, England)
2026-08-16PublicationBacterial Ghosts as Innovative Transport Vehicles for Platinum-Based Anticancer Drugs.ChemMedChem
2026-08-16PublicationPooled analysis of 2 clinical trials of first-line chemoimmunotherapy for metastatic microsatellite stable colorectal cancer MEDITREME and METIMMOX studies.Oncoimmunology
2026-08-16PublicationInsights into neuropathic pain: From disease models to therapeutic interventions.Neuroscience and biobehavioral reviews
2026-08-16PublicationDomain-specific cognitive impairments following oxaliplatin and 5-fluorouracil treatment in rats: A preclinical study.Behavioural brain research
2026-08-16PublicationRandomized phase-II trial of surufatinib plus FOLFOX/FOLFIRI versus FOLFOXIRI as second-line therapy for metastatic colorectal cancer.Annals of medicine
2026-08-26Création de l’enregistrementNCT07504198Registre d’essai clinique
2026-09-10Dernière mise à jour des donnéesOxaliplatinBiomedical Watch
2026-09-14Création de l’enregistrementNCT06820463Registre d’essai clinique
2027-05-01Fin de l’étude prévue / enregistréeNCT07504198Registre d’essai clinique
2028-04-01Fin de l’étude prévue / enregistréeNCT06820463Registre d’essai clinique
2029-03-30Fin de l’étude prévue / enregistréeNCT06806033Registre d’essai clinique
2029-10-16Fin de l’étude prévue / enregistréeNCT07549412Registre d’essai clinique

Début phase actuelle
Non disponible dans les sources synchronisées
Essais cliniques liés

5 essai(s)
NCT Titre Phase Statut administratif Pays Sponsor
NCT06820463 AndroMETa-CRC — A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Telisotuzumab Adizutecan in Combination With IV Oxaliplatin, Fluorouracil, Folinic Acid/Leucovorin, Bevacizumab, Panitumumab in Adult Participants With Metastatic Colorectal Cancer Phase 2 RECRUITING United States, Australia, Austria, Brazil, Canada, Czechia, France, Greece, Israel, Japan, Puerto Rico, Spain, Taiwan, United Kingdom AbbVie
NCT07504198 Neuroprotection of Memantine and Rosuvastatin Phase 2/3 NOT_YET_RECRUITING Egypt Tanta University
NCT06806033 A Study to Evaluate the Optimization of the Cytokine Release Syndrome Profile for Glofitamab in Combination With Gemcitabine Plus Oxaliplatin in Participants With Relapsed/Refractory Aggressive B-Cell Non-Hodgkin's Lymphoma Phase 2 RECRUITING United States, Australia, Canada, France, Germany, Italy, South Korea Hoffmann-La Roche
NCT07549412 A Study of Precemtabart Tocentecan With or Without Bevacizumab Compared to Trifluridine/Tipiracil Plus Bevacizumab in Participants With Previously Treated Metastatic Colorectal Cancer (PROCEADE-CRC-03) Phase 3 RECRUITING United States, Australia, Canada, China, Japan, South Korea, Taiwan EMD Serono Research & Development Institute, Inc.
NCT02867397 Study of Teysuno (S-1) Combined With Epirubicin and Oxaliplatin in Patients With Advanced Solid Tumors Phase 1 COMPLETED Non communiqué Disphar International B.V.

Publications liées

16 publication(s)

Publications liées

16 publication(s)
Titre PMID DOI Journal Date
Single-Institution Outcomes of Neoadjuvant Gemcitabine and Nab-Paclitaxel Combination in Borderline Resectable Pancreatic Adenocarcinoma: A Three-Year Retrospective Audit. Voir source 42291898 10.7759/cureus.108823 Cureus
Addition of autologous stem-cell transplantation to an ibrutinib-containing first-line treatment in patients aged 18-65 years with mantle cell lymphoma (TRIANGLE): 4·5-year follow-up of a three-arm, randomised, open-label, phase 3 superiority trial of the European MCL Network. Voir source 42134356 10.1016/S0140-6736(26)00362-4 Lancet (London, England)
Bacterial Ghosts as Innovative Transport Vehicles for Platinum-Based Anticancer Drugs. Voir source 42350154 10.1002/cmdc.70351 ChemMedChem
Pooled analysis of 2 clinical trials of first-line chemoimmunotherapy for metastatic microsatellite stable colorectal cancer MEDITREME and METIMMOX studies. Voir source 42322272 10.1080/2162402X.2026.2671491 Oncoimmunology
Insights into neuropathic pain: From disease models to therapeutic interventions. Voir source 42498091 10.1016/j.neubiorev.2026.106878 Neuroscience and biobehavioral reviews
Domain-specific cognitive impairments following oxaliplatin and 5-fluorouracil treatment in rats: A preclinical study. Voir source 42336324 10.1016/j.bbr.2026.116331 Behavioural brain research
Randomized phase-II trial of surufatinib plus FOLFOX/FOLFIRI versus FOLFOXIRI as second-line therapy for metastatic colorectal cancer. Voir source 42421558 10.1080/07853890.2026.2698360 Annals of medicine
Resveratrol Modulates Phosphatidylcholine Metabolism-Related Enzymes and Enhances Chemosensitivity in Colorectal Cancer Models. Voir source 42589348 10.3390/ijms27156691 International journal of molecular sciences
Cost-effectiveness analysis of liposomal Irinotecan in combination with oxaliplatin, 5-fluorouracil and leucovorin (NALIRIFOX) for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas in Greece. Voir source 42583863 10.1080/14737167.2026.2718413 Expert review of pharmacoeconomics & outcomes research
Salvage ultra-low-dose radiotherapy for conjunctival mantle cell lymphoma - a case report and literature review. Voir source 42445702 10.5603/rpor.110467 Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology
Breakthrough reactions in pediatric chemotherapeutic desensitization: Outcomes and associated risk factors. Voir source 42444056 10.1111/pai.70425 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Real-world effectiveness of NALIRIFOX versus modified FOLFIRINOX or gemcitabine and nab-paclitaxel in first-line advanced pancreatic adenocarcinoma: a multicentre propensity-matched study. Voir source 42422059 10.1136/bmjonc-2026-001085 BMJ oncology
Clinical use of trastuzumab combined with different chemotherapy regimens in multi-line treatment of advanced human epidermal growth factor receptor 2-positive gastric cancer: A case report. Voir source 30214596 10.3892/ol.2018.9212 Oncology letters
Case Report: Conversion therapy for initially unresectable intrahepatic cholangiocarcinoma. Voir source 42415870 10.3389/fonc.2026.1722347 Frontiers in oncology
Gastric Cancer Treated with 5-Fluorouracil following Discontinuation of Adjuvant S1 plus Docetaxel and Capecitabine plus Oxaliplatin due to Drug-Induced Acute Pancreatitis: A Case Report. Voir source 42416521 10.1159/000552401 Case reports in oncology
The Landmark Series: Neoadjuvant Therapy for Patients with Resectable Gastroesophageal Junction Adenocarcinomas. Voir source 42414817 10.1245/s10434-026-20114-4 Annals of surgical oncology

Sources officielles

liens de recherche

Dernière mise à jour des données : 2026-09-10

Ces sources sont proposées pour vérification. Les informations de la fiche doivent être confirmées dans les registres officiels ou les publications originales.