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Spots Global Cancer Trial Database for Phase II Study of NGR-hTNF Versus Placebo as Maintenance Treatment in Patients With Advanced MPM

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Trial Identification

Brief Title: Phase II Study of NGR-hTNF Versus Placebo as Maintenance Treatment in Patients With Advanced MPM

Official Title: NGR019: Randomized Double-blind Phase II Study of NGR-hTNF Versus Placebo as Maintenance Treatment in Patients With Advanced Malignant Pleural Mesothelioma (MPM)

Study ID: NCT01358084

Study Description

Brief Summary: The main objective of the trial is to document the efficacy of NGR-hTNF administered as maintenance treatment at 0.8 µg/m2 weekly in advanced malignant pleural mesothelioma

Detailed Description: First-line treatment of advanced malignant pleural mesothelioma (MPM) is based on six cycles of a pemetrexed-based chemotherapy, with a median progression-free survival (PFS) of approximately 6 months.However, the median time from completion of first-line treatment to initiation of second-line therapy is approximately 3 months. Recent experiences in non-small cell lung cancer patients have shown that a maintenance treatment given immediately after first-line treatment regimens can improve PFS and survival. Considering the toxicity profile of NGR-hTNF characterized by mild-to-moderate constitutional symptoms registered in a phase II trial in previously treated MPM patients, as well as the disease control observed in about half of the patients and maintained for more than four months and more than nine months in the triweekly and weekly cohorts, respectively, seems justified to compare in a randomized phase II trial the time-related efficacy of NGR-hTNF against placebo in advanced MPM patients who did not progress after six cycles of a standard pemetrexed-based treatment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Zentralklinik Bad Berka GmbH, Bad Berka, Thuringia, Germany

Asklepios Fachkliniken München-Gauting, München-Gauting, , Germany

Ospedale Santo Spirito, Casale Monferrato, Alessandria, Italy

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori-IRST, Meldola, Forlì-Cesena, Italy

Istituto Clinico Humanitas, Rozzano, Milan, Italy

Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria, Alessandria, , Italy

IRCCS Azienda Ospedaliera Universitaria San Martino IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, , Italy

Asl 3 genovese, Ospedale Villa Scassi, Genova, , Italy

IRCCS Ospedale San Raffaele, Milano, , Italy

Istituto Oncologico Veneto, Padova, , Italy

Azienda Ospedaliero-Universitaria di Parma, Parma, , Italy

IRCCS Policlinico S. Matteo, Pavia, , Italy

Azienda Unità Sanitaria locale di Ravenna, Ravenna, , Italy

Ospedale Ca' Foncello, Treviso, , Italy

Saint Petersburg State Medical University n.a. I. P. Pavlov, Saint-Petersburg, , Russian Federation

Contact Details

Name: Antonio Lambiase, MD

Affiliation: AGC Biologics S.p.A.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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