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Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC) Compared to Placebo and Best Available Care (BAT), for the Treatment of Moderate to Severe COVID-19 Patients.

Primary Purpose

Covid19

Status
Unknown status
Phase
Phase 1
Locations
Israel
Study Type
Interventional
Intervention
AMOR 18 Powder & Inhalation
Placebo
Sponsored by
Amorphical Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Males and females of age ≥ 18 years and ≤ 80 years
  2. Signed an Informed Consent
  3. Agree to undergo blood tests as per protocol
  4. Diagnosed with COVID-19
  5. Evidence of lung involvement (by chest X rays or lung US)
  6. May or may not need for Supplemental Oxygen at enrollment
  7. Hospitalized

Exclusion Criteria:

  1. Pregnant or breast-feeding females
  2. Patients with non-COVID19 related Pneumonia
  3. Any pulmonary disease not related to COVID19
  4. Tracheostomy
  5. High flow oxygen or non-invasive ventilation (Bipap) or Mechanical ventilation
  6. Hypercalcemia defined as calcium or corrected calcium > 10.5mg/dL
  7. Hyperphosphatemia defined as > 4.5mg/dL
  8. Urine calcium to creatinine ratio >0.14
  9. Participating in another clinical study

Sites / Locations

  • Shamir MCRecruiting
  • Tel-Aviv Sourasky MCRecruiting
  • Ziv MCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

AMOR 18 Powder & Inhalation

Placebo

Arm Description

AMOR_inhaled Double Pack- Each kit contains two tubes that after mixing result with 1.14 % ACC in 10 ml suspension. AMOR_powder- ACC in a dry powder (up to 2000mg Calcium/day sublingually).

Placebo_Inhaled Double Pack - Each kit contains two tubes of saline at different volumes (similar to investigational product) after mixing the results remains saline at a final volume of 10ml. Placebo_Powder: Each sachet contains powder at the same particle size and weight as the powder of the investigational product.

Outcomes

Primary Outcome Measures

Change of Severity rating of Disease using an 8-point ordinal scale on days 7, 14, 21, measured as improvement greater than or equal to 1 point from baseline score.
Ordinal 8 points scale: Not hospitalized and no limitations of activities. Not hospitalized, with limitation of activities, home oxygen requirement, or both. Hospitalized, not requiring supplemental oxygen and no longer requiring ongoing medical care (used if hospitalization was extended for infection-control or other nonmedical reasons). Hospitalized, not requiring supplemental oxygen but requiring ongoing medical care (related to Covid-19 or to other medical conditions). Hospitalized, requiring any supplemental oxygen. Hospitalized, requiring noninvasive ventilation or use of high-flow oxygen devices. Hospitalized, receiving invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO). Death.

Secondary Outcome Measures

Duration of Hospital stay
Time to discharge from hospital
Duration of ICU stay
Time patient is hospitalized in ICU, if applicable.
Duration of Mechanical Ventilation Use
Time the patient requires Mechanical Ventilation (if needed)
Duration of Oxygen Supplementation
Time the patient requires Oxygen Supplementation (if needed)
Duration of No Oxygen use
Time the patient does not require Oxygen Supplementation
% of patients to meet ordinal scale of 3 or less
Proportion of subjects hospitalized, not requiring supplemental oxygen and no longer requiring ongoing medical care (used if hospitalization was extended for infection-control or other nonmedical reasons).
% of death
Proportion of subjects died during the study, if any.
Frequency and severity of adverse events
Number and percent of patients with hypercalcemia

Full Information

First Posted
May 19, 2021
Last Updated
May 23, 2021
Sponsor
Amorphical Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04900337
Brief Title
Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC) Compared to Placebo and Best Available Care (BAT), for the Treatment of Moderate to Severe COVID-19 Patients.
Official Title
A Phase 1/2 Prospective Randomized Placebo Controlled Study to Assess the Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC) Administered Sublingual and in Inhalation Concomitantly With BAT (Best Available Care) as Compared to Placebo and BAT for the Treatment of Moderate to Severe COVID-19 Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 9, 2021 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Amorphical Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a phase I/II study with Amorphous Calcium Carbonate (ACC) administered sublingual and in Inhalation concomitantly with BAT (Best Available Care) as Compared to Placebo and BAT for the treatment of Moderate to Severe COVID-19 patients. The purpose of this study is to assess the Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC).
Detailed Description
This study includes two parts: Part 1 - A training period of a single arm active treatment open label, to assess the optimal method of study drug administration, as well as the safety of the combined administration, on 5 patients. Following DSMB review of the data collected in part 1 and the DSMB approval to proceed to next part, part 2 will be initiated. Part 2 - A randomized (1:1) placebo controlled 2 arms study. Additional 95 patients will be recruited to this arm. Patients who are hospitalized due to moderate or severe COVID-19 will be recruited to this study. The following elements are the main elements that will be assessed: Confirmation SARS-CoV-2 infection Respiratory Function (breathing rate, SpO2 Oxygen Saturation Vital Signs (BP, HR), Temperature Blood Tests Disease Severity Scale (8 points ordinal scale) The whole study period per patient will be 22 days (21 treatment days) or until the patient has recovered and/or is discharged from the hospital, whichever comes first.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
AMOR 18 Powder & Inhalation
Arm Type
Experimental
Arm Description
AMOR_inhaled Double Pack- Each kit contains two tubes that after mixing result with 1.14 % ACC in 10 ml suspension. AMOR_powder- ACC in a dry powder (up to 2000mg Calcium/day sublingually).
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo_Inhaled Double Pack - Each kit contains two tubes of saline at different volumes (similar to investigational product) after mixing the results remains saline at a final volume of 10ml. Placebo_Powder: Each sachet contains powder at the same particle size and weight as the powder of the investigational product.
Intervention Type
Drug
Intervention Name(s)
AMOR 18 Powder & Inhalation
Intervention Description
AMOR Inhalation x 3 times a day, via Circulaire® II AMOR Powder x 4 times a day, sublingual
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo Inhalation x 3 times a day, via Circulaire® II Placebo Powder x 4 times a day, sublingual
Primary Outcome Measure Information:
Title
Change of Severity rating of Disease using an 8-point ordinal scale on days 7, 14, 21, measured as improvement greater than or equal to 1 point from baseline score.
Description
Ordinal 8 points scale: Not hospitalized and no limitations of activities. Not hospitalized, with limitation of activities, home oxygen requirement, or both. Hospitalized, not requiring supplemental oxygen and no longer requiring ongoing medical care (used if hospitalization was extended for infection-control or other nonmedical reasons). Hospitalized, not requiring supplemental oxygen but requiring ongoing medical care (related to Covid-19 or to other medical conditions). Hospitalized, requiring any supplemental oxygen. Hospitalized, requiring noninvasive ventilation or use of high-flow oxygen devices. Hospitalized, receiving invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO). Death.
Time Frame
Treatment Day 1 to Day 21 or discharge from hospital, the earliest.
Secondary Outcome Measure Information:
Title
Duration of Hospital stay
Description
Time to discharge from hospital
Time Frame
Date of hospitalization to treatment day 21 or discharge, whichever comes first.
Title
Duration of ICU stay
Description
Time patient is hospitalized in ICU, if applicable.
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
Duration of Mechanical Ventilation Use
Description
Time the patient requires Mechanical Ventilation (if needed)
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
Duration of Oxygen Supplementation
Description
Time the patient requires Oxygen Supplementation (if needed)
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
Duration of No Oxygen use
Description
Time the patient does not require Oxygen Supplementation
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
% of patients to meet ordinal scale of 3 or less
Description
Proportion of subjects hospitalized, not requiring supplemental oxygen and no longer requiring ongoing medical care (used if hospitalization was extended for infection-control or other nonmedical reasons).
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
% of death
Description
Proportion of subjects died during the study, if any.
Time Frame
Treatment Day 1 to treatment day 21 or discharge, whichever comes first.
Title
Frequency and severity of adverse events
Time Frame
Screening to End of treatment day 21 or discharge, whichever comes first.
Title
Number and percent of patients with hypercalcemia
Time Frame
Treatment days 4, 7, 11, 17 and 21.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females of age ≥ 18 years and ≤ 80 years Signed an Informed Consent Agree to undergo blood tests as per protocol Diagnosed with COVID-19 Evidence of lung involvement (by chest X rays or lung US) May or may not need for Supplemental Oxygen at enrollment Hospitalized Exclusion Criteria: Pregnant or breast-feeding females Patients with non-COVID19 related Pneumonia Any pulmonary disease not related to COVID19 Tracheostomy High flow oxygen or non-invasive ventilation (Bipap) or Mechanical ventilation Hypercalcemia defined as calcium or corrected calcium > 10.5mg/dL Hyperphosphatemia defined as > 4.5mg/dL Urine calcium to creatinine ratio >0.14 Participating in another clinical study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yehudit Natan
Phone
08-6115024
Email
dity@amorphical.com
Facility Information:
Facility Name
Shamir MC
City
Be'er Ya'aqov
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ronit Zaidenstein, Dr.
Phone
08-9779999
Email
ronitz@shamir.gov.il
Facility Name
Tel-Aviv Sourasky MC
City
Tel Aviv
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Zeltser, Prof.
Phone
03-6974093
Email
Davidz@tlvmc.gov.il
Facility Name
Ziv MC
City
Tsefat
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kamal Abu-Jabal, Dr.
Phone
077-3631261
Email
kamala@ziv.gov.il

12. IPD Sharing Statement

Learn more about this trial

Safety, Tolerability and Efficacy of Amorphous Calcium Carbonate (ACC) Compared to Placebo and Best Available Care (BAT), for the Treatment of Moderate to Severe COVID-19 Patients.

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