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Dose Escalation Study to Evaluate an Experimental New Treatment (CALY-002) in Healthy Subjects and Subjects With Celiac Disease and Eosinophilic Esophagitis

Primary Purpose

Eosinophilic Esophagitis, Celiac Disease

Status
Recruiting
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
CALY-002
Placebo
Sponsored by
Calypso Biotech BV
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Eosinophilic Esophagitis focused on measuring anti IL-15, CalypsoBiotech, Calypso Biotech, Celiac Disease, Eosinophilic Esophagitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Part A. Healthy Subjects:

    1. Male or female aged between 18 and 50 years (both inclusive)
    2. Must be healthy on the basis of the physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead electrocardiogram [ECG] results) performed at screening, in the opinion of the investigator
  • Part B. Subjects with Celiac Disease (CeD):

    1. Male or female ≥ 18 years of age.
    2. Diagnosis of CeD by intestinal biopsy at least 12 months prior to screening as confirmed by medical records.
    3. No histological signs of active CeD at screening
    4. Gluten-free diet (GFD) for at least 12 consecutive months prior to screening
    5. Willing to undertake a gluten challenge (intake of approximately 3 g of gluten daily) for 56 consecutive days
    6. Must be healthy on the basis of physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead ECG results) performed at screening, in the opinion of the investigator.
  • Part C. Subjects with Eosinophilic Esophagitis (EoE):

    1. Male or female ≥ 18 years of age.
    2. Must have endoscopically confirmed and documented diagnosis of EoE
    3. Should exhibit active symptoms of dysphagia with more than 3 episodes of dysphagia during a period of 2 weeks during screening.
    4. Must have clinically active disease
    5. Must have had a relapsed EoE or did not respond after first line therapy
    6. Subject must be healthy on the basis of physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead ECG results) performed at screening, in the opinion of the investigator.

Exclusion Criteria:

  • Part A. Healthy Subjects excluded:

    1. Any significant medical condition, laboratory abnormality, or psychiatric illness
    2. Any condition that confounds the ability to interpret data from the study.
    3. Currently receiving or has been previously treated with a biologic agent.
    4. History of anaphylactic reactions to protein therapeutics.
    5. Has current or recent (within 4 weeks prior to screening) signs or symptoms of infection that require parenteral antibiotic administration.
    6. Has evidence of SARS-CoV-2 infection and/or subject Is deemed at risk for the coronavirus disease (COVID-19)
    7. Has had major surgery (including joint surgery) within 8 weeks prior to screening and hospitalisation for a clinically relevant event within the 4 weeks prior to screening.
  • Part B. Subjects with Celiac Disease (CeD) excluded:

    1. A concurrent active autoimmune disease (other than CeD) that requires systematic treatment with immunosuppressants.
    2. Has severe complication of CeD such as refractory CeD.
    3. Has active (microscopic) colitis with clinical signs of diarrhoea and abdominal pain.
    4. Is currently receiving or has been previously treated with a biologic agent.
    5. Has a history of anaphylactic reactions to protein therapeutics.
    6. Subject has evidence of SARS-CoV-2 infection and/or subject is deemed at risk for the coronavirus disease (COVID-19).
  • Part C: Subjects with Eosinophilic Esophagitis (EoE) excluded:

    1. Has a hyper-eosinophilic syndrome.
    2. Has a concurrent active autoimmune disease (other than EoE) that requires treatment with immunosuppressants.
    3. Has active (microscopic) colitis with clinical signs of diarrhoea and abdominal pain.
    4. Currently receiving or has been previously treated with a biologic agent.
    5. Has a history of anaphylactic reactions to protein therapeutics.
    6. Subject has evidence of SARS-CoV-2 infection and/or subject is deemed at risk for the coronavirus disease (COVID-19).

Sites / Locations

  • Cliniques Universitaires Saint-Luc - HospitalRecruiting
  • UZ LeuvenRecruiting
  • Tampere University HospitalRecruiting
  • ChariteRecruiting
  • Universitatsklinikum Erlangen - HospitalRecruiting
  • Universitätsklinikum Freiburg - HospitalRecruiting
  • Universitätsmedizin der Johannes Gutenberg-Universität Mainz - HospitalRecruiting
  • Klinikum rechts der Isa der Technischen Universitaet Muenchen - HospitalRecruiting
  • AMCRecruiting
  • Ziekenhuis Rijnstate - HospitalRecruiting
  • Maastricht University Medical Center - HospitalRecruiting
  • Oslo University Hospital HFRecruiting
  • Alesund HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

CALY-002

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Incidence of treatment-emergent adverse event

Secondary Outcome Measures

Full Information

First Posted
October 13, 2020
Last Updated
March 3, 2023
Sponsor
Calypso Biotech BV
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1. Study Identification

Unique Protocol Identification Number
NCT04593251
Brief Title
Dose Escalation Study to Evaluate an Experimental New Treatment (CALY-002) in Healthy Subjects and Subjects With Celiac Disease and Eosinophilic Esophagitis
Official Title
A Multicentre, SAD, and MAD Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IV Treatment of CALY-002 in Healthy Subjects and Subjects With Celiac Disease and Eosinophilic Esophagitis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 28, 2020 (Actual)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Calypso Biotech BV

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
This is a single and multiple ascending study to characterize the safety, PK, PD and clinical effect in healthy volunteers and participants with Celiac Disease and Eosinophilic Esophagitis.
Detailed Description
This is a multi-site, randomized, placebo controlled single and multiple dose escalation study of an anti-IL-15 mAb (CALY-002). The study initiates as placebo controlled, randomized trial with a single ascending dosing part in healthy subjects and commences with a multiple ascending dosing part in participants with Celiac Disease undergoing a gluten challenge and includes open label multiple dose expansion cohorts in participants with Eosinophilic Esophagitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eosinophilic Esophagitis, Celiac Disease
Keywords
anti IL-15, CalypsoBiotech, Calypso Biotech, Celiac Disease, Eosinophilic Esophagitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
95 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CALY-002
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Biological
Intervention Name(s)
CALY-002
Intervention Description
1-hour intravenous infusion
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
1-hour intravenous infusion
Primary Outcome Measure Information:
Title
Incidence of treatment-emergent adverse event
Time Frame
through study completion, an average of 3 months post last dose

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Part A. Healthy Subjects: Male or female aged between 18 and 50 years (both inclusive) Must be healthy on the basis of the physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead electrocardiogram [ECG] results) performed at screening, in the opinion of the investigator Part B. Subjects with Celiac Disease (CeD): Male or female ≥ 18 years of age. Diagnosis of CeD by intestinal biopsy at least 12 months prior to screening as confirmed by medical records. No histological signs of active CeD at screening Gluten-free diet (GFD) for at least 12 consecutive months prior to screening Willing to undertake a gluten challenge (intake of approximately 3 g of gluten daily) for 56 consecutive days Must be healthy on the basis of physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead ECG results) performed at screening, in the opinion of the investigator. Part C. Subjects with Eosinophilic Esophagitis (EoE): Male or female ≥ 18 years of age. Must have endoscopically confirmed and documented diagnosis of EoE Should exhibit active symptoms of dysphagia with more than 3 episodes of dysphagia during a period of 2 weeks during screening. Must have clinically active disease Must have had a relapsed EoE or did not respond after first line therapy Subject must be healthy on the basis of physical examination findings, clinical laboratory tests, medical history, vital signs, and cardiac monitoring (normal 12 lead ECG results) performed at screening, in the opinion of the investigator. Exclusion Criteria: Part A. Healthy Subjects excluded: Any significant medical condition, laboratory abnormality, or psychiatric illness Any condition that confounds the ability to interpret data from the study. Currently receiving or has been previously treated with a biologic agent. History of anaphylactic reactions to protein therapeutics. Has current or recent (within 4 weeks prior to screening) signs or symptoms of infection that require parenteral antibiotic administration. Has evidence of SARS-CoV-2 infection and/or subject Is deemed at risk for the coronavirus disease (COVID-19) Has had major surgery (including joint surgery) within 8 weeks prior to screening and hospitalisation for a clinically relevant event within the 4 weeks prior to screening. Part B. Subjects with Celiac Disease (CeD) excluded: A concurrent active autoimmune disease (other than CeD) that requires systematic treatment with immunosuppressants. Has severe complication of CeD such as refractory CeD. Has active (microscopic) colitis with clinical signs of diarrhoea and abdominal pain. Is currently receiving or has been previously treated with a biologic agent. Has a history of anaphylactic reactions to protein therapeutics. Subject has evidence of SARS-CoV-2 infection and/or subject is deemed at risk for the coronavirus disease (COVID-19). Part C: Subjects with Eosinophilic Esophagitis (EoE) excluded: Has a hyper-eosinophilic syndrome. Has a concurrent active autoimmune disease (other than EoE) that requires treatment with immunosuppressants. Has active (microscopic) colitis with clinical signs of diarrhoea and abdominal pain. Currently receiving or has been previously treated with a biologic agent. Has a history of anaphylactic reactions to protein therapeutics. Subject has evidence of SARS-CoV-2 infection and/or subject is deemed at risk for the coronavirus disease (COVID-19).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jos Houbiers, MD, PhD
Phone
+41 225523307
Email
info@calypsobiotech.com
Facility Information:
Facility Name
Cliniques Universitaires Saint-Luc - Hospital
City
Brussel
Country
Belgium
Individual Site Status
Recruiting
Facility Name
UZ Leuven
City
Leuven
Country
Belgium
Individual Site Status
Recruiting
Facility Name
Tampere University Hospital
City
Tampere
Country
Finland
Individual Site Status
Recruiting
Facility Name
Charite
City
Berlin
Country
Germany
Individual Site Status
Recruiting
Facility Name
Universitatsklinikum Erlangen - Hospital
City
Erlangen
Country
Germany
Individual Site Status
Recruiting
Facility Name
Universitätsklinikum Freiburg - Hospital
City
Freiburg
Country
Germany
Individual Site Status
Recruiting
Facility Name
Universitätsmedizin der Johannes Gutenberg-Universität Mainz - Hospital
City
Mainz-GE
Country
Germany
Individual Site Status
Recruiting
Facility Name
Klinikum rechts der Isa der Technischen Universitaet Muenchen - Hospital
City
Munich
Country
Germany
Individual Site Status
Recruiting
Facility Name
AMC
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Name
Ziekenhuis Rijnstate - Hospital
City
Arnhem
Country
Netherlands
Individual Site Status
Recruiting
Facility Name
Maastricht University Medical Center - Hospital
City
Maastricht
Country
Netherlands
Individual Site Status
Recruiting
Facility Name
Oslo University Hospital HF
City
Oslo
Country
Norway
Individual Site Status
Recruiting
Facility Name
Alesund Hospital
City
Ålesund
Country
Norway
Individual Site Status
Recruiting

12. IPD Sharing Statement

Learn more about this trial

Dose Escalation Study to Evaluate an Experimental New Treatment (CALY-002) in Healthy Subjects and Subjects With Celiac Disease and Eosinophilic Esophagitis

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