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Experimental drug etavopivat may reduce pain and increase hemoglobin in sickle cell disease, study suggests.
A new study shows that etavopivat, an experimental drug, may reduce painful episodes in people with sickle cell disease.
The 52-week trial results indicate the drug could lower the frequency of pain crises and increase hemoglobin levels compared to a placebo.
These findings, presented at the American Society of Hematology meeting, suggest etavopivat could be a promising treatment, though further phase 3 trials are needed to confirm these results.
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El medicamento experimental etavopivat puede reducir el dolor y aumentar la hemoglobina en la enfermedad de células falciformes, sugiere el estudio.