EoE – Eosinophilic Esophagitis Study


Viable Clinical Research is conducting a clinical research study for FLUTicasone in Eosinophilic Esophagitis (FLUTE): A Randomized, Double-blind, Placebo-controlled, Dose-ranging, and Maintenance Study of APT-1011 in Subjects With Eosinophilic Esophagitis.

Ages Eligible for Study: 18 Years to 75 Years
Genders Eligible for Study: Both
Conditions: Eosinophilic Esophagitis, Esophageal Disorders


Inclusion Criteria:

  1. Evidence of EoE defined by > 15 peak eosinophils per HPF as measured from proximal and distal biopsies
  2. Subject-reported history of < 3 episodes of dysphagia in the 7 days prior to Screening
  3. 7-day Global EoE Symptom Score > 3 at baseline and at screening
  4. Willing and able to adhere to study-related treatment regiments, procedures, and visit schedule

Exclusion Criteria:

  1. Have known contraindication, hypersensitivity, or intolerance to corticosteroids;
  2. Have any physical, mental, or social condition or history of illness or laboratory abnormality that in the Investigator’s judgement might interfere with study procedures or the ability of the subject to adhere to and complete the study;
  3. Presence of oral or esophageal mucosal infection of any type;
  4. Have any mouth or dental condition that prevents normal eating;
  5. Have any condition affecting the esophageal mucosa or altering esophageal motility other than EoE;
  6. Use of systemic corticosteroids within 60 days prior to Screening, use of inhaled/swallowed corticosteroids within 30 days prior to Screening, or extended use of high-potency dermal topical corticosteroids within 30 days prior to Screening;
  7. Initiation of an elimination diet or elemental diet within 30 days before Screening (diet must remain stable after signing ICF);
  8. Morning serum cortisol level ≤5 µg/dL (138 nmol/L);
  9. Use of biologic immunomodulators in the 24 weeks prior to Screening;
  10. Use of calcineurin inhibitors or purine analogues, or potent cytochrome P450 (CYP) 3A4 inhibitors in the 12 weeks prior to Screening;
  11. Have a contraindication to or factors that substantially increase the risk of EGD or esophageal biopsy or have narrowing of the esophagus that precludes EGD with a standard 9 mm endoscope;
  12. Have a history of an esophageal stricture requiring dilatation within the previous 12 weeks prior to Screening;
  13. Have initiated, discontinued or changed dosage regimen of PPIs, H2 antagonists, antacids or antihistamines for any condition such as GERD or allergic rhinitis within 4 weeks prior to qualifying endoscopy. These drugs must remain constant throughout the study.
  14. A serum cortisol level >18 µg/dL (497 nmol/L) at 60 minutes with adrenocorticotropic hormone (ACTH) stimulation test using 250 µg cosyntropin (i.e., a positive result on the ACTH stimulation test).

Contact the Viable Clinical Research team regarding this study.