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Spots Global Cancer Trial Database for Real-world Usage of HyQvia in Multiple Myeloma Adults With Secondary Immunodeficiency

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Trial Identification

Brief Title: Real-world Usage of HyQvia in Multiple Myeloma Adults With Secondary Immunodeficiency

Official Title: A Prospective, Observational Study to Assess the Real-World Usage and Outcomes of HyQvia in Patients With Multiple Myeloma (MM) Diagnosed With Secondary Immunodeficiency (SID)

Study ID: NCT05879757

Interventions

No Intervention

Study Description

Brief Summary: In this study, multiple myeloma participants with secondary immunodeficiency (SID) will be treated with HyQvia according to their clinic's standard practice. The study's main aim is to look into infusion parameters of HyQvia administration.

Detailed Description: This is a prospective, observational study of adults having multiple myeloma (MM) with SID treated with HyQvia as part of routine clinical care. This study will characterize the real-world infusion parameters of HyQvia administration. The study will enroll approximately 100 participants. Study data will be requested through participants' routine clinic visits and patient-reported outcome (PRO)s are voluntary. This multi-center trial will be conducted in selected European and Latin American countries. The overall time of this study is 38 months. Participants will make multiple visits to the clinic 12 days after last dose of study drug for a follow-up assessment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Centro de investigaciones Clinicas Cordoba, Cordoba, , Argentina

Fakultni nemocnice Plzen, Pilsen, , Czechia

Vseobecna fakultni Nemocnice, Praha 2, , Czechia

UH Amiens CEDEX 1, Amiens Cedex 1, , France

CHU Dijon - Hopital du Bocage, Dijon, , France

Hopital Prive du Confluent, Nantes, , France

Hopital de la Source - CHR Orleans, Orleans, , France

CHU Bordeaux - Hopital Haut-Leveque, Pessac, , France

MHP-Muenchner Haematologiepraxis, Berlin, , Germany

Alexandra General Hospital, Athens, , Greece

G. Papanikolaou Hospital, Thessaloniki, , Greece

A.O.U.C Policlinico di Bari, Bari, , Italy

AOU Policlinico Rodolico San Marco, Catania, , Italy

Azienda Ospedale Universita Padova, Padova, , Italy

University of Padova, Treviso, , Italy

Lubin Region St. Jana z Dukli, Lublin, , Poland

Institutul Clinic Fundeni, Bucharest, , Romania

Ion Chiricuta Oncology Institute, Cluj Napoca, , Romania

Spitalul Clinic Municipal Filantropia Craiova, Craiova, , Romania

Clinical Emergency Hospital Sibiu, Sibiu, , Romania

Hospital Clinico San Carlos, Madrid, , Spain

H12 de Octubre, Madrid, , Spain

Hospital Universitari Son Espases, Palma, , Spain

SUS, Lund, Lund, , Sweden

Uppsala UH, Uppsala, , Sweden

Ankara University, Ankara, , Turkey

Antalya Training and Research Hospital, Antalya, , Turkey

Istanbul Universitesi, Istanbul, , Turkey

Medipol Istanbul University, Istanbul, , Turkey

Contact Details

Name: Study Director

Affiliation: Takeda

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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