Mitapivat Improves Markers of Erythropoietic Activity in Long-Term Study of Adults with Alpha- or Beta-Non-Transfusion-Dependent Thalassemia
Bibliographic record
Abstract
Background: The thalassemias comprise a group of hemoglobinopathies characterized by ineffective erythropoiesis and hemolysis, which lead to chronic anemia and associated complications. Thalassemic red blood cells (RBCs) do not have sufficient levels of adenosine triphosphate (ATP) to meet their increased energy demands. Mitapivat is an allosteric activator of pyruvate kinase (PK), a key enzyme that regulates the final step of glycolysis responsible for ATP production in RBCs. We previously reported primary results of an open-label phase 2 study (NCT03692052) of mitapivat in pts with α- or β-non-transfusion-dependent thalassemia (NTDT) showing 80.0% (16/20) of pts achieved a hemoglobin (Hb) response of ≥1.0 g/dL increase from baseline at ≥1 assessments between Weeks (Wk) 4-12, inclusive. The increase in Hb was sustained, with a mean Hb (standard deviation) increase of 1.7 g/dL (0.5) at Wk 72; hemolysis markers were also improved. This analysis (data cutoff 27Mar22) evaluated the effect of mitapivat on markers of erythropoietic activity through Wk 72, along with Hb and markers of hemolysis and iron homeostasis. Methods: Eligibility criteria: ≥18 years (y) of age, known medical history of α- or β-thalassemia, Hb concentration ≤10.0 g/dL, and ≤5 RBC units transfused in the prior 24 wk and none in the 8 wk prior to study drug. Pts started mitapivat 50 mg twice daily (BID) and escalated to 100 mg BID based on individual safety and Hb assessments. Pts who completed the 24-wk core period and achieved a Hb response or a delayed Hb response (after Wk 12) were eligible to continue to the extension period (at Wk 24 dose) if they had no ongoing grade ≥3 treatment-emergent adverse events related to study drug. Study visits during the extension occur every 12 wk for up to 3 y. Assessments collected within 8 wk (56 days) after a transfusion were excluded from baseline derivation and analysis. Results: Nineteen of 20 pts completed the core period, 17 entered the extension period; 16 pts (4 with α- and 12 with β-thalassemia) were ongoing at the data cutoff date. At baseline, pts had biomarker levels consistent with ineffective erythropoiesis and hemolysis (Table). Changes from baseline showed a durable increase in Hb with a median (Q1, Q3) of 1.3 g/dL (0.60, 1.90) at Wk 12 and 1.2 g/dL (-0.03, 2.2) at Wk 72 (Table). Concurrently, there were trends for decreases in medians for erythropoietin, erythroferrone, soluble transferrin receptor, indirect bilirubin, and reticulocyte/erythrocyte fraction that were maintained over time. Median hepcidin levels remained relatively stable. Conclusions: These results indicate that mitapivat's mechanism ameliorates multiple aspects of the complex pathophysiology underlying α- and β-NTDT, including ineffective erythropoiesis, hemolysis, and anemia. The sustained long-term effects of mitapivat may offer a novel disease-modifying approach. Figure 1View largeDownload PPTFigure 1View largeDownload PPT Close modal
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".