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Spots Global Cancer Trial Database for TALazoparib and Avelumab as Maintenance Therapy in Platinum-Sensitive Metastatic or Locally Advanced URothelial Carcinoma

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Trial Identification

Brief Title: TALazoparib and Avelumab as Maintenance Therapy in Platinum-Sensitive Metastatic or Locally Advanced URothelial Carcinoma

Official Title: TALazoparib and Avelumab as Maintenance Therapy in Platinum-Sensitive Metastatic or Locally Advanced URothelial Carcinoma: A Single-arm Phase 2 Trial

Study ID: NCT04678362

Study Description

Brief Summary: The main objectif is to determine the efficacy of a maintenance treatment combining Talazoparib and Avelumab after platinum-based chemotherapy in patients with locally advanced/metastatic urothelial carcinoma.

Detailed Description: The first line treatment of urothelial carcinoma is a platinum-based chemotherapy. This treatment is efficient with a response rate \> 50 % but the progression-free survival is short (7.7 months) and the chemotherapy is too toxic to be used in a prolonged time. Traditionally, maintenance chemotherapy refers to the utilization of regimens with less toxicity after the initial upfront treatment. This concept has already been efficient with PARP inhibitors in ovarian carcinoma and more recently with durvalumab in lung carcinoma. The prevalence of somatic mutations in homologous recombination genes in UC as well as their association with platinum sensitivity suggests Talazoparib to be a target for a maintenance treatment of urothelial carcinoma. Moreover, there is a strong rational with both pre-clinical and clinical data to associate Avelumab and Talazoparib. This appears all the more relevant that Avelumab has already demonstrated its efficacy in urothelial carcinoma (after platinum-based chemotherapy failure). In this context, the sponsorpropose a phase 2 study to assess the antitumor activity of the combination of Avelumab plus Talazoparib in metastatic urothelial carcinoma in maintenance therapy after platinum-based chemotherapy. Considering the doubts about the best molecular predictive factors of Talazoparib and Avelumab, the sponsor willingly propose a non-selective study, without molecular screening. Tumors will be selected according to the platinum sensitivity which has the advantage to exclude poor prognosis tumors and will allow increasing the HRD tumor population.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Institut de Cancérologie de l'Ouest, Angers, , France

CHU Jean Minjoz, Besançon, , France

Centre François baclesse, Caen, , France

Centre Jean Perrin, Clermont-Ferrand, , France

Centre George-François Leclerc, Dijon, , France

Centre Léon Bérard, Lyon, , France

Hospices civils de Lyon, Lyon, , France

Institut Paoli Calmettes, Marseille, , France

Institut de Cancérologie de l'Ouest, Nantes, , France

Centre Antoine Lacassagne, Nice, , France

Croix Saint-Simon Diaconesses, Paris, , France

Hopital Tenon, Paris, , France

Centre Eugène Marquis, Rennes, , France

IUCT, Toulouse, , France

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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