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Brief Title: A Study of Epoetin Beta (NeoRecormon) in Participants With Solid Tumors
Official Title: An Open-Label Study of the Safety Of NeoRecormon in Patients With Solid Tumors Being Treated With Platinum Capable of Inducing Anemia
Study ID: NCT02554942
Brief Summary: This study will evaluate the safety of subcutaneous (SC) epoetin beta (NeoRecormon) in adults with solid tumors being treated with platinum-based chemotherapy capable of inducing anemia. The anticipated time on study treatment is 16 weeks, and the target sample size is approximately 208 individuals.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, Alcoy, , Spain
, Barakaldo, , Spain
, Barcelona, , Spain
, Barcelona, , Spain
, Barcelona, , Spain
, Caceres, , Spain
, El Palmar Murcia, , Spain
, La Laguna, , Spain
, Manresa, , Spain
, Salamanca, , Spain
, Valencia, , Spain
, Valencia, , Spain
, Zaragoza, , Spain
Name: Clinical Trials
Affiliation: Hoffmann-La Roche
Role: STUDY_CHAIR