EHA 2024: How Effective is Elritercept for Low-Risk MDS Patients?
At the European Hematology Association (EHA) 2024 conference, MDS specialists presented phase 2 trial updates on the FDA-approved medicine elritercept, focusing on its effectiveness in reducing MDS-related anemia and iron overload. Read the key findings below.
What Is Elritercept?
Elritercept (KER-050, Keros Therapeutics) is a recently FDA-approved medicine for low—to intermediate-risk MDS patients that helps improve anemia and iron overload. It works by limiting cell signals that cause low blood cell production, thereby increasing blood counts.
How Effective Is Elritercept for Low-Risk MDS?
The KER050-MD-201 study is still recruiting participants, but the first results in 60 low-risk MDS patients treated with elritercept over 24 weeks showed:
- Half of the patients experienced an improvement in their blood cell counts and/or no longer needed blood cell transfusions
- The side effects experienced by most patients were only mild-moderate cases of shortness of breath, diarrhea, fatigue, nausea, and headache.
Another interesting finding from this study was that elritercept helped reduce the amount of stored iron. This is beneficial because excess iron in the body negatively impacts the bones’ ability to make blood cells, potentially leading to bone loss.
Elritercept addresses this issue by promoting blood cell growth, such as red blood cells. Red blood cells use stored iron, mitigating iron overload.
Although elritercept is FDA-approved, further data from the study will help provide more information about how this medicine affects low-risk MDS patients. If you want to review your eligibility to join the ongoing KER050-MD-201 study, click here.
Conclusion
Early findings from the KER050-MD-201 study show that elritercept is generally safe for low-risk MDS patients. It also has the potential to improve patients’ blood cell counts, alleviate certain symptoms of anemia, and reduce iron overload. More research from this study will provide additional findings regarding elritercept’s effectiveness in myelodysplastic syndromes.
Join the HealthTree for MDS Newsletter to Learn More!
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Sources:
- Durable Clinical Benefit with Elritercept (KER-050) Treatment: Findings from an Ongoing Phase 2 Trial in Participants with Lower-Risk MDS
- Reduced Ferritin and Increased Bone Specific Alkaline Phosphatase in Participants with Lower-Risk MDS Treated with Elritercept (KER-050) Support Potential to Rebalance the Osteohematopoietic Niche
At the European Hematology Association (EHA) 2024 conference, MDS specialists presented phase 2 trial updates on the FDA-approved medicine elritercept, focusing on its effectiveness in reducing MDS-related anemia and iron overload. Read the key findings below.
What Is Elritercept?
Elritercept (KER-050, Keros Therapeutics) is a recently FDA-approved medicine for low—to intermediate-risk MDS patients that helps improve anemia and iron overload. It works by limiting cell signals that cause low blood cell production, thereby increasing blood counts.
How Effective Is Elritercept for Low-Risk MDS?
The KER050-MD-201 study is still recruiting participants, but the first results in 60 low-risk MDS patients treated with elritercept over 24 weeks showed:
- Half of the patients experienced an improvement in their blood cell counts and/or no longer needed blood cell transfusions
- The side effects experienced by most patients were only mild-moderate cases of shortness of breath, diarrhea, fatigue, nausea, and headache.
Another interesting finding from this study was that elritercept helped reduce the amount of stored iron. This is beneficial because excess iron in the body negatively impacts the bones’ ability to make blood cells, potentially leading to bone loss.
Elritercept addresses this issue by promoting blood cell growth, such as red blood cells. Red blood cells use stored iron, mitigating iron overload.
Although elritercept is FDA-approved, further data from the study will help provide more information about how this medicine affects low-risk MDS patients. If you want to review your eligibility to join the ongoing KER050-MD-201 study, click here.
Conclusion
Early findings from the KER050-MD-201 study show that elritercept is generally safe for low-risk MDS patients. It also has the potential to improve patients’ blood cell counts, alleviate certain symptoms of anemia, and reduce iron overload. More research from this study will provide additional findings regarding elritercept’s effectiveness in myelodysplastic syndromes.
Join the HealthTree for MDS Newsletter to Learn More!
We invite you to click the button below to subscribe to our newsletter and stay updated on the latest advancements in myelodysplastic syndromes.
JOIN THE HEALTHTREE FOR MDS NEWSLETTER
Sources:
- Durable Clinical Benefit with Elritercept (KER-050) Treatment: Findings from an Ongoing Phase 2 Trial in Participants with Lower-Risk MDS
- Reduced Ferritin and Increased Bone Specific Alkaline Phosphatase in Participants with Lower-Risk MDS Treated with Elritercept (KER-050) Support Potential to Rebalance the Osteohematopoietic Niche
about the author
Megan Heaps
Megan joined HealthTree in 2022. She enjoys helping patients and their care partners understand the various aspects of the cancer. This understanding enables them to better advocate for themselves and improve their treatment outcomes.
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