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NCT06764511Possibly a fitRecruiting

Biosimilar EPO for anemia in low-risk MDS

Myelodysplastic Syndromes (MDS)

Part of Blood & lymphatic clinical trials.

This trial tests how well a biosimilar version of erythropoietin (a drug that boosts red blood cells) works in people with low-risk myelodysplastic syndrome (MDS) who have anemia. It aims to see if this treatment can safely improve low hemoglobin levels without needing more intensive therapies.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
60 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must have a diagnosis of myelodysplastic syndrome (MDS), which is a bone marrow disorder that can cause low blood counts.
  • Your MDS must be considered lower-risk, meaning it has a low, very low, or intermediate IPSS-R score.
  • Before starting treatment, your hemoglobin (red blood cell count) must have been less than 10 grams per deciliter (g/dL), showing signs of anemia.
  • Your erythropoietin (EPO) level before treatment must have been less than 500 U/L. (EPO is a hormone that signals your body to make red blood cells.)
  • You must have started treatment with a biosimilar form of erythropoietin alfa between June 2018 and December 2021 at the IRCCS hospital in Bologna.
  • You are 18 years or older and willing to give consent.
  • You do not have other serious health problems, such as severe immune system weakness (ECOG >3) or other causes of anemia (like chronic inflammation, internal bleeding, or a type of anemia called hemolysis).
  • You are not currently receiving other cancer chemotherapy drugs.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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