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Hypereosinophilic syndrome

Subtypes of Hypereosinophilic syndrome

Eosinophilic pneumonia 1

3 published articles · Updated continuously

Clinical Trial Landscape

Clinical Trials for hypereosinophilic syndrome

7 trials tracked for hypereosinophilic syndrome: 4 in phase 3 or 4 and 3 with published results. The most-cited published study has 44 citations.

7Trials tracked
4Phase 3 & 4
0Recruiting
3With published results
Phase distribution
Phase 4 1 Phase 3 3 Phase 2 2 Other / NA 1
  1. Phase 3 Efficacy and Safety Study of Mepolizumab in Subjects With Severe Hypereosinophilic Syndrome (HES) Completed · 44 cited
  2. Phase 3 A Multi-center, Open-label Extension, Safety Study of Mepolizumab in Subjects With Hypereosinophilic Syndrome (HES) From Study 200622 Completed · 44 cited
  3. Phase 4 Steroid Treatment for Hypereosinophilic Syndrome Completed · 12 cited
  4. Phase 3 Study in Pediatrics With HypEREosinophilic Syndrome (SPHERE) Completed
  5. Phase 2 A Study of Oral AMN107 in Adults With Chronic Myelogenous Leukemia (CML) or Other Hematologic Malignancies Completed
  6. Phase 2 Dasatinib as Therapy for Myeloproliferative Disorders (MPDs) Completed
Show 1 more trials
  1. N/A Therapy of HES, PV, Atypical Chronic Myelocytic Leukemia (CML) or Chronic Myelomonocytic Leukemia (CMML), and Mastocytosis With Imatinib Mesylate Completed

Showing the 7 most-cited and recently-updated of 7 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found Updated — new results For clinicians

Hypereosinophilic syndrome: what the trials found

Mepolizumab has demonstrated efficacy in managing hypereosinophilic syndrome (HES). In a Phase 3 trial, Mepolizumab was associated with significant improvements in clinical stability; specifically, the percentage of participants experiencing an HES flare or withdrawing from the study was significantly lower in the treatment group compared to the control group over a 32-week period (56% vs. 28%, p=0.002) and during the final weeks of the study (35% vs. 17%, p=0.020). Additionally, Mepolizumab was associated with a significantly longer time to first HES flare 4.

Mepolizumab also showed utility in reducing corticosteroid requirements. Data indicates that patients treated with Mepolizumab experienced reductions in mean daily oral corticosteroid (OCS) doses over 52 weeks, with several participants achieving an OCS dose of less than or equal to 7.5 mg during the final phase of treatment 1.

Glucocorticoid challenge was shown to result in a mean percent change in eosinophil count of -69.6% and -13.6% respectively 2.

Recent results — preliminary, needs further review

  • Nilotinib has been investigated for HES, but results are not yet corroborated 5.
  • Dasatinib (BMS-354825) has been investigated for HES, but results are not yet corroborated 6.
  • Imatinib Mesylate (Gleevec) has been investigated for HES, but results are not yet corroborated 7.

For the clinician treating this condition

  • Mepolizumab is associated with a significantly lower rate of HES flares and study withdrawals compared to control groups over 32 weeks 4.
  • Mepolizumab treatment may facilitate a reduction in the required daily dose of oral corticosteroids for patients with HES 1.
  • Glucocorticoid challenge can result in significant reductions in eosinophil counts 2.

AI synthesis of 6 cited trials, updated Jun 29, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.