Effectiveness and Safety of Rhea Health Tone® as add-on Therapy for COVID-19 in Hospitalized Adults in Indonesia (RHEA-COVID19)

June 7, 2021 updated by: Keri Lestari, Universitas Padjadjaran

A Multicenter, Randomized, Open-label, Controlled Trial to Assess Effectiveness and Safety of Rhea Health Tone® as add-on Therapy for COVID-19 in Hospitalized Adults in Indonesia

This is a multicenter, randomized, open-label, controlled trial to evaluate the effectiveness and safety of Rhea Health Tone® as add-on therapy in hospitalized adults with COVID-19.

The study is a multi-center trial that will be conducted in up to approximately 2 sites nationally. New sites may be added as needed after appropriate assessment. Interim monitoring will be conducted to evaluate the arms and for safety and effectiveness. Any change would be accompanied by updated sample size.

Subjects will be assessed while hospitalized. All subjects will undergo a series of laboratory (inflammatory biomarkers (IL-6, hs-CRP, IFNγ), SGOT, SGPT and Creatinine, conversion rate by PCR, QTc prolongation by ECG, chest X-ray), clinical (clinical assessment, vital sign, concomitant medication, other medical conditions) and safety assessment (serious adverse event).

Randomization will be performed 1:1 for each arm. Arm 1 = Standard of Care (SoC) alone, arm 2 = SoC + Rhea Health Tone®.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

This is a multicenter, randomized, open-label, controlled trial to evaluate the effectiveness and safety of Rhea Health Tone® in hospitalized adults with COVID-19 confirmed by PCR.

The study is a multi-center trial that will be conducted in up to approximately 2 sites nationally. Interim monitoring will be conducted to evaluate the arms and for safety and effectiveness. Any change would be accompanied by an updated sample size.

Eligible patients are male or female adults (age ≥ 18 years up to 50 years old) recently admitted as in-patients, with mild to moderate COVID-19 confirmed by positive PCR that fulfill the inclusion and exclusion criteria stated in the protocol. Laboratory assessment include SGOT, SGPT and Creatinine at screening. The subjects must sign their consent in writing electronically beforehand. Total subjects = 69.

Subjects with any of these conditions will be excluded:

  • Any allergy to any composition of Rhea Health Tone;
  • Pregnant and breast feeding;
  • History and co-morbid of severe underlying disease where treatment and follow up is not likely to be beneficial to the patient based on physician judgement (e.g. retinopathy, cardiovascular disease (QTc > 500 mdet (narrow QRS); QTc ≥ 550 mdet (wide QRS)), heart arrythmia, uncontrolled diabetes mellitus, hypertension, chronic pulmonary disease, asthma, chronic kidney disease (Creatinine > 2x upper limit of normal), liver disease (SGOT/SGPT > 2x upper limit of normal), chronic neurological disease, or etc.). This includes people requiring care in designated supported living facilities and severe dementia;
  • Possibility of being transferred to a non-study-hospital within 72 hours.
  • History of autoimmune disease, cancer, HIV AIDS

Any suspected serious adverse event reaction is reported to CRO/Sponsor and EC within 24 hours, using patient's study ID.

During the study conduct, the study team shall keep all the relevant source documents and transcribe the data in case report form (CRF). The study team should also update study essential document (e.g. subject log, investigational product accountability log, etc.) and keep the copy captured by scan/camera for monitoring/audit/inspection purpose.

The study is expected to be finished in 2 months.

Standard of Care (SoC) treatment is based on COVID-19 Treatment Protocol (1st edition, 2020) published by Medical Associations (PDPI, PERKI, PAPDI, PERDATIN, IDAI).

Arm 1: SoC alone for 9 days Arm 2: SoC + Rhea Health Tone 2 ml twice a day after meal (every 12 hours) for 9 days.

It is anticipated that patients with COVID-19 will present to participating hospitals, and that no external recruitment efforts towards potential subjects are needed. Recruitment efforts may also include dissemination of information about this trial to other medical professionals/hospitals.

The Ethics Committee will approve the recruitment process and all materials prior to any recruitment to prospective subjects directly.

Screening will begin with a brief discussion with study staff. Some will be excluded based on demographic data and medical history (i.e., pregnant, < 18 years of age, severe COVID-19, etc.). Information about the study will be presented to potential subjects (or legally acceptable representative) and questions will be asked to determine potential eligibility. Screening procedures can begin only after informed consent is obtained.

To evaluate the effectiveness of Rhea Health Tone® in the therapy of mild to moderate hospitalized adults with confirmed COVID-19 based on length of stay in hospital (after subject received randomization code until subject discharge/death/recovered). Secondary parameters will be Incidence and duration of Oxygenation (days of oxygenation), incidence is defined as number of days from randomization until the subject received oxygenation, duration is defined as total days of the use of oxygenation; incidence of Ventilation (days to receiving ventilation).

Incidence is defined as number of days from randomization until the subject received ventilation; inflammatory biomarkers (IL-6, hs-CRP and IFNγ).

Analyses relate outcome to the randomly allocated treatment (e.g. intent-to-treat). The primary analyses assess any effects of treatment allocation on length of hospitalization, analyzing separately people who already at mild and moderate level at entry and by age. Interim analysis will be carried out after 50% subject enrolled. The results will be monitored by monitor assigned by the Sponsor to ensure subject well-being and safety as well as study integrity. The monitor will evaluate the study safety parameter after 50% subject enrolled in the study.

The main secondary analyses assess any effects of treatment allocation on:

  1. Incidence and duration of Oxygenation (days of oxygenation, days of free oxygenation);
  2. Incidence of Ventilation (days to receiving ventilation);
  3. Inflammatory biomarkers (IL-6, hs-CRP , IFNγ );
  4. Conversion rate from positive to negative by PCR result;
  5. Percentage of improvement of patients' clinical
  6. Percentage of improvement of patients based on chest X-ray; and
  7. QTc prolongation by ECG.

Study related data will be recorded. All the data in the source documents shall be collected by the study team to be transcribed in the electronic case report form (eCRF). Once the document recorded, the electronic data will be automatically available for monitoring/audit/inspection purpose. All the electronic system used and data recording in the study must be conducted in compliance to Good Clinical Practice.

The investigator must assure that subjects' anonymity will be maintained and that their identities are protected from unauthorized parties. On CRFs or other documents submitted to the sponsor, subjects should not be identified by their names, but by an identification code. The investigator should keep a subject enrolment log showing codes, names and addresses. The investigator should maintain documents not for submission to Sponsor, e.g. subjects' written consent forms, in strict confidence.

The investigator shall ensure the quality control and quality assurance of the data generated during the study and how the data will be handled, including providing access to monitoring activities, audit and inspection and source documents which will be used in the study. Investigator will permit monitoring, audits and inspections by Sponsor/CRO, EC, and regulatory bodies.

All source records including electronic data (if any) will be stored in secured systems in accordance with institutional policies and locally applicable regulation. All the essential documents should be retained until at least 5 years after the study ended or based on the applicable regulatory requirements or based on the agreement with the funder.

The Drug Safety Monitoring Board (DSMB) is an Independent Data Monitoring Committee consisting of doctors who are experienced in clinical trials, statisticians, and other members who do not direct involvement with this study. The DSMB responsible for the ongoing review of a clinical trial and for making recommendations to the sponsor concerning the continuation, modification, and termination of the trial as it is being conducted. The DSMB will be the only committee that is allowed to review the confidential data in the study. The statistician will analyze the subject's security data and report to DSMB to be evaluated more closely. The key responsibilities of the DSMB are to ensure patient safety by routine review of overall safety data including all SAEs, SUSARs, all severe AEs and AEs leading to drug or study discontinuation and, where applicable, literature cases and information from Competent Authorities (CAs) and by judging the relevance of the events for patients' safety. The DSMB will review the results of data that has been analyzed in accordance with SAP and consider other evidence arising from other studies and will provide advice to the Trial Steering Committee (TSC) (the research committee and national coordinator) regarding the sustainability of this study. The DSMB may recommend the TSC to the recruitment or study termination or provide recommendations related to alternatives treatment (if any).

Study Type

Interventional

Enrollment (Actual)

85

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Indonesia
    • DKI Jakarta
      • Jakarta, DKI Jakarta, Indonesia, 14360
        • Rumah Sakit Darurat Penanganan Covid-19 Wisma Atlet Kemayoran (RSDCWA)
    • West Java
      • Bandung, West Java, Indonesia, 40161
        • Dr. Hasan Sadikin Central General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 50 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Male and female patients aged ≥ 18 years to 50 years old, who recently admitted as in-patients and have not received any standard of care yet, with COVID-19 confirmed by PCR with mild to moderate symptoms.
  2. Female subjects of child-bearing age agree to take effective contraceptive measures during the study until seven days of the last oral medication of study product;
  3. Willing to receive a random assignment to any designated treatment group and not participating in another study at the same time;
  4. Willing for not using any other immunomodulator or treatment that might bias the study
  5. Patient willing to provide informed consent.

Exclusion Criteria:

  1. Any allergy to any composition of Rhea Health Tone®;
  2. Pregnant and breastfeeding;
  3. History and co-morbid of severe underlying disease where treatment and follow up is not likely to be beneficial to the patient based on physician judgment (e.g. retinopathy, cardiovascular disease (QTc > 500 mdet (narrow QRS); QTc ≥ 550 mdet (wide QRS)), heart arrhythmia, uncontrolled diabetes mellitus, hypertension, chronic pulmonary disease, asthma, chronic kidney disease (Creatinine > 2x upper limit of normal), liver disease (SGOT/SGPT > 2x limit of normal), chronic neurological disease, or etc.). This includes people requiring care in designated supported living facilities and severe dementia;
  4. Possibility of being transferred to a non-study-hospital within 72 hours.
  5. History of autoimmune disease, cancer, HIV AIDS.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: SoC alone
Standard of Care alone (days 1 to 9)
EXPERIMENTAL: Rhea Health Tone®
Rhea Health Tone® 2 ml twice daily after meal (every 12 hours) for 9 days to be provided together with Standard of Care.
Dietary supplement: Rhea Health Tone®
Rhea Health Tone® 2 ml twice daily after the meal (every 12 hours)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Length of stay
Time Frame: From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Total days the subjects were hospitalized
From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Duration of oxygenation
Time Frame: From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Total days of oxygen supplementation
From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Duration of ventilation
Time Frame: From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Total days of receiving ventilation
From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
PCR conversion
Time Frame: Will be examined at days 1st , 7th, and 10th.
Total days of conversion rate from positive to negative by PCR result
Will be examined at days 1st , 7th, and 10th.
Inflammatory biomarkers 1
Time Frame: Will be examined at days 1st and 10th.
IL-6 (pg/mL)
Will be examined at days 1st and 10th.
Inflammatory biomarkers 2
Time Frame: Will be examined at days 1st and 10th.
hs-CRP (mg/L)
Will be examined at days 1st and 10th.
Inflammatory biomarkers 3
Time Frame: Will be examined at days 1st and 10th.
IFNγ (pg/mL)
Will be examined at days 1st and 10th.
Percentage of improvement of subjects' clinical status
Time Frame: From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Daily measurement of temperature, heart rate, respiratory rate, blood pressure, oxygen saturation, capillary filling time >2 seconds
From the date of randomization until the date of first documented subject discharge or death from any cause, assessed up to 10 days
X-Ray
Time Frame: From the date of informed consent signed by subject, until the date of first documented subject discharge or death from any cause, assessed up to 10 days
Percentage of improvement of subjects based on chest X-ray
From the date of informed consent signed by subject, until the date of first documented subject discharge or death from any cause, assessed up to 10 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Universitas Padjadjaran

Collaborators

PT. Rhea Pharmaceutical Sciences Indonesia
Prodia Diacro Laboratories P.T.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

December 9, 2020

Primary Completion (ACTUAL)

May 19, 2021

Study Completion (ANTICIPATED)

September 1, 2021

Study Registration Dates

First Submitted

November 10, 2020

First Submitted That Met QC Criteria

November 12, 2020

First Posted (ACTUAL)

November 13, 2020

Study Record Updates

Last Update Posted (ACTUAL)

June 10, 2021

Last Update Submitted That Met QC Criteria

June 7, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Pharm-202010.01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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