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Spots Global Cancer Trial Database for Treatment of Relapsed/Refractory Multiple Myeloma (rrMM) With Pomalidomide in Clinical Practice

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Trial Identification

Brief Title: Treatment of Relapsed/Refractory Multiple Myeloma (rrMM) With Pomalidomide in Clinical Practice

Official Title: Multicenter Non-interventional Study to Investigate Drug Utilization of Pomalidomide in Clinical Practice for the Treatment of Relapsed/Refractory Multiple Myeloma (rrMM)

Study ID: NCT02555839

Study Description

Brief Summary: There is a high unmet medical need for an anti-myeloma therapy for RRMM patients previously treated with Lenalidomide and Bortezomib, due to poor prognosis. This observational study focuses on the collection of data concerning the safe and optimal usage of Pomalidomide, a new therapy option for RRMM patients, thereby increasing the knowledge about optimal AE management. Beside this, further analysis of tolerability, dosage and efficacy will be performed. This knowledge could lead to a optimization of Pomalidomide usage and treatment.

Detailed Description: There is a high unmet medical need for further anti-myeloma therapy in patients with RRMM who have previously been treated with Lenalidomide and Bortezomib containing regimens that is both active and tolerable, as these patients have a poor prognosis. Hands-on experience with Pomalidomide is very limited in Austria and a non-interventional study enhances the attention paid to safe use and handling of the product as well as increase knowledge about optimal adverse event (AE) management substantially. A detailed record of the medical history including. co-morbidities and pre-treatment regimens will allow analysis of the impact there of on tolerability, dosage and efficacy. Beside the collection of data on efficacy and tolerability this observational drug utilization study could give insight into the clinical practice and the routine use of Pomalidomide.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

LKH Feldkirch, Intern E, Hämatologie, Feldkirch, , Austria

Medical University Graz, Graz, , Austria

KH der Elisabethinen Linz , 1. Interne Hämato-Onkologie, Linz, , Austria

Kepleruniversitätsklinikum GmbH, Hämatologie und Internistische Onkologie, Linz, , Austria

Krankenhaus der Barmherzigen Schwestern Ried, Innere Medizin I, Ried, , Austria

SCRI-CCCIT gemeinnßtzige GmbH & Universitätsklinikum der PMU Salzburg Gemeinnßtzige Salzburger Landeskliniken BetriebsgmbH, Salzburg, , Austria

LKH Steyr, Innere Medizin II, Steyr, , Austria

AKH, Innere Medizin I, Klin. Abt. f. Hämatologie, Vienna, , Austria

AKH, Universitätsklinik fßr Innere Medizin I /Klin. Abteilung fßr Onkologie, Vienna, , Austria

St. Josef Krankenhaus Wien,1. Abteilung fĂźr Innere Medizin Zentrum fĂźr Onkologie, Vienna, , Austria

Hanusch Krankenhaus Wien 3. Medizinische Abteilung Hämatolog, Vienna, , Austria

Wilhelminenspital, 1. Med.Abteilung, Zentrum fĂźr Onkologie, Vienna, , Austria

Salzkammergut-Klinikum VĂścklabruck, Abteilung Innere Medizin, VĂścklabruck, , Austria

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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