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Study to Assess the Safety of Ascending Doses of UNI911 INHALATION in Healthy Volunteers in Preparation for Evaluation in Adults With COVID-19

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ClinicalTrials.gov Identifier: NCT04576312
Recruitment Status : Active, not recruiting
First Posted : October 6, 2020
Last Update Posted : January 20, 2021
Sponsor:
Information provided by (Responsible Party):
UNION therapeutics

Brief Summary:
This is a Phase 1 Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study to Assess the Safety of Ascending Doses of UNI911 INHALATION in Healthy Volunteers in Preparation for Evaluation in Adults with COVID-19

Condition or disease Intervention/treatment Phase
COVID-19 Drug: UNI911 INHALATION Phase 1

Detailed Description:

This is a Phase 1 Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study to Assess the Safety of Ascending Doses of UNI911 INHALATION in Healthy Volunteers in Preparation for Evaluation in Adults with COVID-19

64 subjects will be sequentially enrolled to receive dosage of UNI911 INHALATION or placebo. 4 sentinel subjects (one per cohort 1, 2 ,3 and 4 ) will be treated in an open-label manner to confirm the safety of each dose sequentially. 40 subjects will be randomly assigned (3:1) to either active or placebo. For the last 2 cohorts, a total of 20 healthy volunteers will be enrolled to receive multiple doses of UNI911 INHALATION.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 64 participants
Allocation: Randomized
Intervention Model: Sequential Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Other
Official Title: Phase 1 Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study to Assess the Safety of Ascending Doses of UNI911 INHALATION in Healthy Volunteers in Preparation for Evaluation in Adults With COVID-19
Actual Study Start Date : June 29, 2020
Actual Primary Completion Date : December 31, 2020
Estimated Study Completion Date : April 30, 2021

Arm Intervention/treatment
Experimental: Cohort 1
IP Single and Total Dose* (Inhalation): 4 mL0.1% / 3.4 mg Duration of Treatment: 1 day
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 2
IP Single and Total Dose* (Inhalation): 1 mL1% /8.4 mg Duration of Treatment: 1 day
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 3
IP Single and Total Dose* (Inhalation): 3 mL1%/25.2 mg Duration of Treatment: 1 day
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 4
IP Single and Total Dose* (Inhalation): 6 mL 1% /50.5 mg Duration of Treatment: 1 day
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 5
IP Single and Total Dose* (Inhalation): 6 mL1% /50.5mg 30 mL/252mg Duration of Treatment: 2.5 days
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 6
IP Single and Total Dose* (Inhalation): 1 mL1% /8.4 mg Duration of Treatment: 7 days
Drug: UNI911 INHALATION
UNI911 INHALATION

Experimental: Cohort 7
IP Single and Total Dose* (Inhalation): 3 mL1%/25.2 mg Duration of Treatment: 7 days
Drug: UNI911 INHALATION
UNI911 INHALATION




Primary Outcome Measures :
  1. Assess safety of UNI911 INHALATION in healthy volunteers: AE frequency [ Time Frame: Up to Day 6 ]
    AE frequency in each cohort and treatment group


Other Outcome Measures:
  1. Pharmacokinetic Parameters: Cmax [ Time Frame: Up to Day 4 of participant treatment ]
    Maximum concentration of active drug molecules in blood (Cmax)

  2. Pharmacokinetic Parameters: Tmax [ Time Frame: Up to Day 4 of participant treatment ]
    Time to reach maximum level (Tmax)

  3. Pharmacokinetic Parameters: AUC [ Time Frame: Up to Day 4 of participant treatment ]
    Area Under the Curve of drug level in blood versus time (AUC)

  4. Pharmacokinetic Parameters: Half life [ Time Frame: Up to Day 4 of participant treatment ]
    Half life



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria (main ones):

  1. Signed Informed Consent Form (ICF)
  2. Male or non-pregnant and non-lactating female who is abstinent or agrees to use effective contraceptive methods throughout the course of the study. Females must have a negative urine beta-human chorionic gonadotropin hormone (hCG) pregnancy test prior to dosing. (Women who are postmenopausal or who had tubal ligation/hysterectomy do not need to have a pregnancy test done and do not need to agree to use contraception.)
  3. ECG without clinically significant abnormalities (including QTcF < 450 ms)
  4. Age ≥ 18 and < 65 years at the time of signing ICF
  5. Normally active and in good health by medical history and physical examination
  6. Minimum 80% of predicted lung function, including FEV1 after beta2-agonist, TLC, DCO, and CPET with pulse oximetry
  7. Chest X-ray without clinically significant abnormalities

Exclusion Criteria (main ones):

  1. Enrollment in an UNI911 study in the previous 6 months
  2. Clinically significant allergy (as judged by the investigator) or history of significant adverse reaction to niclosamide or related compounds, to any of the excipients used.
  3. Underlying condition that may interfere with inhalation of the IP
  4. Current acute or chronic condition (incl. COPD, asthma, or other severe respiratory disease, CV disease, diabetes mellitus, obesity, malignant and autoimmune diseases) unless considered clinically irrelevant and stable by the investigator
  5. Renal impairment (eGFR < 60 mL/min/1.73m2) or hepatic impairment (as judged by the investigator)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04576312


Locations
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Denmark
DanTrials
Copenhagen, Denmark
Sponsors and Collaborators
UNION therapeutics
Investigators
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Study Chair: Ulf Sjöbring, MD UNION therapeutics A/S
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Responsible Party: UNION therapeutics
ClinicalTrials.gov Identifier: NCT04576312    
Other Study ID Numbers: UNI911-101
First Posted: October 6, 2020    Key Record Dates
Last Update Posted: January 20, 2021
Last Verified: January 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Respiratory Aspiration
Respiration Disorders
Respiratory Tract Diseases
Pathologic Processes