A Study to Investigate the Efficacy and Tolerability of ESO-101 in Patients With Eosinophilic Esophagitis

Eosinophilic Esophagitis Clinical Trial

Official title:

A Randomized, Placebo-controlled, Double-blind Trial Evaluating the Efficacy, Tolerability and Safety of ESO-101 in Adult Patients With Active Eosinophilic Esophagitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04849390
• Other study ID #: ACESO
• Secondary ID: 2020-000082-16
• Status: Completed
• Phase: Phase 2
• Start date: June 29, 2021
• Est. completion date: October 9, 2023

Study information

• Verified date: November 2023
• Source: EsoCap AG
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized, placebo-controlled, double-blind trial to evaluate the efficacy, tolerability, and safety of ESO-101 in adult patients with active eosinophilic esophagitis (EoE). Patients will be screened at 2 visits (Visit 1 and Visit 2) during which their eligibility will be assessed based on endoscopy-independent criteria (Visit 1) and based on the histologic assessment of esophageal biopsy samples taken during the screening endoscopy (Visit 2). Eligible patients will be randomized 2:1 to once-daily treatment with ESO-101 or placebo and treated for 28 days starting on Day 0. Further clinic visits will be performed at Day 14 (Visit 4) and Day 28 (Visit 5, end of treatment) to assess the efficacy, tolerability, and safety. In addition, a safety follow-up call will be scheduled 2 weeks after the end of treatment (Day 42, Visit 6).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 43
• Est. completion date: October 9, 2023
• Est. primary completion date: October 9, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Adult patients aged 18-70 years;

2. Confirmed clinicopathological diagnosis of EoE (eosinophilic esophagitis);

3. Active and symptomatic EoE, defined as:

1. peak eosinophil count =15 eosinophils/high-powered field (hpf) at 2 levels of the esophagus at the screening endoscopy (Visit 2) as measured in a total of 6 hpfs derived from 6 biopsies, 2 each from the proximal, mid, and distal segment of the esophagus;

2. either a dysphagia or odynophagia severity sore of =4 on a 11-point numeric rating scale for =1 day during the 7 days before Screening (Visit 1);

4. Written informed consent;

5. Willingness and ability to comply with the protocol for the duration of the trial;

6. Negative pregnancy test at Screening (Visit 1) and Day 0 (Visit 3) in women of childbearing potential (i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy);

7. Women of childbearing potential must be willing to use (for a least 3 monthly cycles before the screening endoscopy [Visit 2] and until 4 weeks after the last intake of IMP) a highly effective method of contraception or birth control (failure rate less than 1% per year when used consistently and correctly). Reliable methods for this trial are:

1. combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal);

2. progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable);

3. intrauterine device or intrauterine hormone-releasing system;

4. bilateral tubal occlusion;

5. a vasectomized sexual partner;

6. sexual abstinence (only accepted as true abstinence when this is in line with the preferred and usual lifestyle of the patient; periodic abstinence [e.g. calendar, ovulation, symptothermal, post-ovulation methods, and withdrawal] is not an acceptable method of contraception).

Exclusion Criteria:

1. Women who are pregnant, lactating, possibly pregnant or planning a pregnancy during the trial period;

2. Current or past (within the last 3 months) alcohol or drug abuse;

3. Initiation of a diet-modifying food restriction within 4 weeks before the screening endoscopy (Visit 2) until EOT (end of treatment);

4. Use of systemic corticosteroids or biologic immunomodulators within 3 months before the screening endoscopy (Visit 2) until the EOT;

5. History of non-response to treatment of EoE with topical corticosteroid drugs (defined as no improvement of clinical symptoms of EoE after a minimum of 4 weeks corticosteroid therapy used at appropriate doses according to the investigator's judgment) or requirement of cessation of corticosteroid therapy for EoE treatment due to oral candidiasis or systemic corticosteroid side effects;

6. Use of corticosteroids for treatment of EoE within 4 weeks before the screening endoscopy (Visit 2) until the EOT;

7. Use of inhalable (pulmonary or nasal) corticosteroids within 4 weeks before the screening endoscopy (Visit 2) until the EOT;

8. Asthma requiring corticosteroid therapy in the seasonal allergy period according to the investigator's judgment based on anamnesis until the EOT;

9. Change in proton pump inhibitor (PPI) dosing regimen within 4 weeks before the screening endoscopy (Visit 2) until the EOT;

10. Use of systemic leukotriene receptor antagonists, immunosuppressant therapy, or chronic oral or systemic anticoagulants (such as coumarin derivates, novel oral and subcutaneous anticoagulants) within 2 weeks before Screening (Visit 1) until the EOT;

11. Unable to swallow a test tablet of about the size of the IMP capsule used in the trial;

12. History of diabetes mellitus;

13. Other severe comorbid condition, concurrent medication, or other issue that renders the patient unsuitable to participate in the trial in the judgment of the investigator, including but not limited to: comorbid condition with an estimated life expectancy of =12 months, dialysis, severe pulmonary (requiring home oxygen, uncontrolled chronic obstructive pulmonary disease Gold III/IV) or cardiovascular conditions (heart failure New York Heart Association III and IV, uncontrolled hypertension systolic blood pressure by repeated measurement >180mmHg);

14. History of cancer (except non-melanoma skin cancer, or carcinoma in situ of cervix) or treatment with anticancer therapy (chemotherapy, immunotherapy, radiotherapy, hormone therapy for cancer treatment, targeted therapy or gene therapy) within 12 months before Screening (Visit 1) until the EOT;

15. Known intolerability or hypersensitivity to mometasone furoate or any of the IMP excipients (e.g. bovine gelatin, polyvinyl alcohol, polyvinyl acetate, glycerol, sorbitol);

16. Systemic autoimmune disorders or any condition requiring immunosuppression (e.g. methotrexate, cyclosporine, interferon alpha, tumor necrosis factor alpha inhibitors, antibodies to immunoglobulin E) within 3 months before Screening (Visit 1);

17. Mental condition rendering the patient unable to understand the nature, scope, and possible consequences of the trial or presence of any condition that impacts compliance with the trial procedures;

18. Use of any investigational or non-registered product (medicinal product or medical device) within 4 weeks before the screening endoscopy (Visit 2) until the EOT;

19. Employee at the trial center, spouse, partner or child of investigators or sub-investigators or employee of the sponsor.

20. History of or active eosinophilic gastroenteritis and colitis, inflammatory bowel disease, celiac disease, oral or esophageal mucosal infection of any kind, and esophageal varices;

21. Gastroesophageal reflux disease with Los Angeles Grade B or higher, or erosive esophagitis Grade 2 or above;

22. Presence of Barrett's esophagus with a maximum length of =3 cm with intestinal metaplasia or dysplasia, peptic stricture, achalasia, significant hiatal hernia >3 cm, esophageal scleroderma, or diagnosis of Lichen planus;

23. Emergency endoscopy for bolus impaction within 2 weeks before Screening (Visit 1);

24. Any mouth or dental condition that prevents normal eating;

25. History of (dilation within the previous 8 weeks) or current severe endoscopic structural abnormality in esophagus (e.g. high-grade stenosis where an 8-10 mm endoscope cannot pass without dilatation at the screening endoscopy [Visit 2]);

26. Diagnosed liver cirrhosis or portal hypertension;

27. History of upper gastrointestinal bleeding within 8 weeks before Screening (Visit 1);

28. Known allergy to ß-lactoglobulin (cow milk protein).

Related Conditions & MeSH terms

• Eosinophilic Esophagitis
• Esophagitis

Intervention

Drug:
• ESO-101
Daily administration in the evening at bedtime for 28 days
• Placebo
Daily administration in the evening at bedtime for 28 days

Locations

Country	Name	City	State
Germany	Facharztzentrum Eppendorf	Hamburg
Germany	Universitätsklinikum Leipzig AöR	Leipzig
Germany	Otto-von-Guericke-Universität Medizinische Fakultät Universitätsklinikum Magdeburg A. ö. R.	Magdeburg
Germany	Klinikum rechts der Isar der TUM	München
Netherlands	Amsterdam University Medical Center	Amsterdam
Netherlands	Albert Schweitzer Ziekenhuis	Dordrecht
Poland	Centrum Medyczne Med-GASTR Sp. z o.o.	Lódz
Poland	Centrum Medyczne Sonomed Sp. z o.o.	Szczecin
Spain	Hospital Universitario Vall d' Hebrón	Barcelona
Spain	Hospital Universitario de La Princesa	Madrid
Spain	Hospital Universitario Fundación Jiménez Díaz	Madrid
Spain	Hospital Universitario Central De Asturias	Oviedo
Spain	Hospital de Navarra	Pamplona
Spain	Hospital General de Tomelloso	Tomelloso
Spain	Hospital Universitario Rio Hortega	Valladolid
Spain	Hospital de Viladecans	Viladecans
Switzerland	Universitätsspital Zürich	Zürich

Sponsors (3)

Lead Sponsor	Collaborator
EsoCap AG	FGK Clinical Research GmbH, FGK Representative Service B.V.

Countries where clinical trial is conducted

Germany,  Netherlands,  Poland,  Spain,  Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Absolute change in peak eosinophil count from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with histological remission, defined as the reduction of peak eosinophil count in all esophageal samples to <15 eosinophils/hpf at end of treatment, overall and determined differentially in each of the 3 esophageal segments	Biopsy samples will be taken at Visit 2 and end of treatment (Visit 5). At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields (hpfs) with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with a peak eosinophil count in all esophageal samples of <6 eosinophils/hpf at end of treatment, overall and determined differentially in each of the 3 esophageal segments	Biopsy samples will be taken at Visit 2 and end of treatment (Visit 5). At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields (hpfs) with the highest density of eosinophils will be counted.	End of treatment (Visit 5 = day 28)
Secondary	Proportion of patients with an improvement in the dysphagia severity score from Baseline to end of treatment	Patients will rate the dysphagia severity score daily on a 11-point NRS (numeric rating scale): 0 = 'no symptoms' to 10 = 'worst possible symptoms'. At Visit 3 (Day 0) and Visit 5 (end of treatment), the worst severity scores out of the 7 days preceding the respective visit will be used for the assessment. The score assessed at Visit 3 (Day 0) at the center before IMP intake will serve as baseline score. Patients will additionally assess the severity score of the actual day in the patient diary daily after IMP intake starting on Day 0.	From Baseline (Visit 3) to end of treatment (Visit 5 = 28 days after Visit 3)
Secondary	Absolute change in mean eosinophil count from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Relative change in mean eosinophil count from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with a relative reduction in peak eosinophil count of =30 percent from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with a relative reduction in peak eosinophil count of =50 percent from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with a relative reduction in peak eosinophil count of =75 percent from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Histology results of the biopsies at Visit 2 will be considered baseline values. For the peak number of eosinophils, hematoxylin and eosin stained esophageal biopsy specimen will be assessed and the high-powered fields with the highest density of eosinophils will be counted.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Proportion of patients with histological remission AND improvement in the dysphagia severity score from Baseline to end of treatment	The processing and analysis of biopsy samples taken at Visit 2 and end of treatment (Visit 5) will be performed blinded at a central laboratory according to a laboratory manual. At both visits, 6 biopsy samples will be taken, 2 each from the proximal, mid, and distal segment of the esophagus. Additionally, patients will rate the dysphagia and odynophagia severity score daily on a 11-point NRS (numeric rating scale): 0 = 'no symptoms' to 10 = 'worst possible symptoms'. Patients will assess the severity score of the actual day in the patient diary daily after IMP intake starting on Day 0.	From Baseline (Visit 2 + 3) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Absolute change in dysphagia and odynophagia severity scores from Baseline	Patients will rate the dysphagia and odynophagia severity score daily on a 11-point NRS (numeric rating scale): 0 = 'no symptoms' to 10 = 'worst possible symptoms'. Patients will assess the severity score of the actual day in the patient diary daily after IMP intake starting on Day 0.	From Baseline (Visit 3) to end of treatment (Visit 5 = 28 days after Visit 3)
Secondary	Relative change in dysphagia and odynophagia severity scores from Baseline	Patients will rate the dysphagia and odynophagia severity score daily on a 11-point NRS (numeric rating scale): 0 = 'no symptoms' to 10 = 'worst possible symptoms'. Patients will assess the severity score of the actual day in the patient diary daily after IMP intake starting on Day 0.	From Baseline (Visit 3) to end of treatment (Visit 5 = 28 days after Visit 3)
Secondary	Time to achieve symptom relief (defined as 50 percent improvement in the dysphagia or odynophagia symptoms on an NRS compared to Baseline)	Patients will rate the dysphagia and odynophagia severity score daily on a 11-point NRS (numeric rating scale): 0 = 'no symptoms' to 10 = 'worst possible symptoms'. Patients will assess the severity score of the actual day in the patient diary daily after IMP intake starting on Day 0.	From Baseline (Visit 3) to end of treatment (Visit 5 = 28 days after Visit 3)
Secondary	Change in the EREFS from Baseline to end of treatment	The EREFS score (Eosinophilic esophagitis endoscopic reference score) is a classification and grading system for the endoscopic assessment of the esophageal features of eosinophilic esophagitis. The grading is used either to assess the severity of endoscopic findings from 0=´none´ to 2 or 3=´severe´ or to classify 0=´absent´ or 1=´present´.The total score will be calculated and compared between Baseline and end of treatment. A higher score correlates with more severe eosinophilic esophagitis symptoms.	From Baseline (Visit 2) to end of treatment (Visit 5 = 4-7 weeks after Visit 2)
Secondary	Incidence of treatment-emergent Adverse Events	All Adverse Events occurring from the first investigational medicinal product administration onwards are defined as treatment-emergent Adverse Events.	Visit 3 (Day 0) to day 42
Secondary	Incidence of treatment-emergent Serious Adverse Events	All Serious Adverse Events occurring from the first investigational medicinal product administration onwards are defined as treatment-emergent Serious Adverse Events.	Visit 3 (Day 0) to day 42
Secondary	Incidence of AESI	The following AEs are defined as AEs of special interest (AESI), if these events were not already present at Visit 2: Oral candidiasis; Oropharyngeal candidiasis.	Visit 2 (day -21 to -1) to Visit 6 (day 42)
Secondary	Local tolerability	The local tolerability of the IMP administration will be evaluated daily throughout the treatment period in the patient diary. Patients should indicate whether they had any discomfort in mouth, throat or esophagus while taking IMP on a VAS (Visual analog scale) ranging from 'no discomfort' to 'the worst imaginable discomfort'. The first assessment on Day 0 recorded in the patient diary after IMP intake will be considered Baseline.	From Baseline (Visit 3) to end of treatment (Visit 5 = 28 days after Visit 3)
Secondary	Patient-reported treatment satisfaction at end of treatment based on questions about handling, taste, and time necessary for administration	Patients will be asked to answer a questionnaire about their satisfaction with the IMP treatment at Visit 5. Questions will cover the general satisfaction with the IMP, the swallowability of the IMP, and the frequency of administration. Answers involve gradings from 0 (the best outcome) to 3 or 4 (the worst outcome) plus an indication for the preference of single or multiple administrations of the investigated product.	At end of treatment (Visit 5 = day 28)