Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT04872686 |
| Other study ID # |
BRiCM LABS BANGASAFE SPRAY |
| Secondary ID |
|
| Status |
Completed |
| Phase |
Phase 3
|
| First received |
|
| Last updated |
|
| Start date |
April 10, 2021 |
| Est. completion date |
May 30, 2021 |
Study information
| Verified date |
January 2022 |
| Source |
Bangladesh Reference Institute of Chemical Measurements (BRICM) |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The COVID-19 pandemic is the defining global health crisis of our time and the greatest
challenge we have faced since World War-II.Corona virus is transmitted via respiratory
droplets or aerosol, produced from sneezing or coughing of infected persons to healthy
individual through mouth, nose and eye. PVP-I gargle/spray used in throat and nose are shown
to have broad spectrum antimicrobial activity and may have preventive effect on SARS-CoV-2.
0.6% PVP-I oro-nasal spray phase 3 clinical trial will be conducted in three dedicated
Covid-19 hospitals namely Dhaka Medical College Hospital, Kurmitola General Hospital,
Kuwait-Moitree Hospital. Chemical compound of the oro-nasal spray which was developed and
tested at Bangladesh Reference Institute for Chemical Measurements, for its quality control/
quality assurance, shelf life and related stability following GLP guideline.
This study aims to evaluate virucidal efficacy of 0.6% PVP-I against SARS-CoV-2 along with
its safe uses in oronasal mucosa of healthy and SARS-CoV-2 exposed persons.
The participant will be divided into three groups: Group A 768 COVID-19 positive, moderately
ill admitted patient who will receive intervention once. Group B 20 asymptomatic to mild
COVID-19 patients having multiple comorbidity will receive intervention 4 times hourly and
Group C 10 healthy individual who accept intervention 0.6% PVP-I oronasal spray 3-4 times
interval in a day for 30 days. Placebo will be used among control group for better
comparison.
The chemical which will be used in this study is available inside the country and also
registered to open use in Bangladesh. BRiCM ensures raw material & impurities
characterization as per BP 2019, AOAC and AWWA and determination of shelf life by performing
the stability studies will be conducted according to Stability Zone Iva and ICH guidelines.
A written consent will be taken by concern participant and a short interview will be taken on
the spot prior to intervention. Participant's medical documents will be used and swab from
nasopharynx & oropharynx will be taken for performing necessary test (RT-PCR) to confirm
viral presence.
There is no potential risk for application of this oro-nasal spray. Even though if any
adverse reaction occur while using the oro-nasal spray, necessary medical management will be
carried out in the respected hospital.
Description:
Introduction:
COVID-19 pandemic is the defining global health crisis of our time and the greatest challenge
we have faced since World War Two. We have now reached the tragic milestone of two million
deaths, and the human family is suffering under an almost intolerable burden of loss.
Background Information:
1. Description of Bangasafe (proposed name) Oro-Nasal Spray: The spray contains PVP-I is a
water-soluble iodophor that consists of a complex between iodine and a solubilizing
polymer carrier, polyvinylpyrrolidone. In aqueous solution, a dynamic equilibrium occurs
between free iodine, the active virucidal agent, and the PVP-I-complex.
2. Composition: Oro-Nasal spray contains 0.6% PVP-I as an Active Pharmaceutical Ingredients
(API) in sterile de-ionized water.
3. Product Development, Quality Control and Quality Assurance: Following aspects of raw
materials including API, manufacturing in-process steps, finished product are to be real
time monitored and produced in Bangladesh Reference Institute for Chemical Measurements,
- Raw materials characterization: Appearance, solubility, identification, nitrogen
content, iodide value, loss on drying, pH, sulphated ash and available iodine.
- Solvent/diluent characterization: pH, conductivity, total organic carbon, heavy
metal (Pb, As), endotoxin, microbial count.
- Quality testing in several stages during product development: pH, available iodine,
iodide, UV absorbance, potency.
- Impurity profile testing: 1-Vinyl-2-pyrrolidinone, 2-Pyrrolidinone, heavy metal
(Pb)
- Accelerated & real time stability study and shelf-life determination: pH, available
iodine, iodide, UV absorbance Up to 3 (three) month at 25C, 30C and 35C
4. Mode of Action: PVP itself has no microbicidal activity but rather delivers the free
iodine to target cell membranes. The basic mechanism leads to strong microbicidal
activity expressed by multiple modes of action as oxidation of amino acids and nucleic
acids that disrupt the microbial metabolic pathways, as well as destabilization of the
structural components of cell membranes, causing irreversible damage to the pathogen.
5. Dosage and Administration: Mouth & Nostril: 2 puffs, in 3-4 hours interval not more than
4 times a day.
6. How Supplied: Oro-nasal spray aqueous solution containing 0.6%PVP-I is supplied in 30ml
amber color High Density Poly Ethylene (HDPE) bottle designed for pharmaceutical
packaging to provide adequate protection against sun light.
Objectives of the study
1. Primary Objective
To assess the virucidal efficacy of 0.6% PVP-I against SARS-CoV-2 in nasopharynx and
oropharynx in order to use:
- To prevent viral infection before exposure while visiting and treating COVID-19
patients, attending public gatherings, using public transport etc.
- To prevent viral infection after exposure to COVID-19 patients
- To reduce viral load in nasopharynx and oropharynx of COVID-19 patients which is
supposed to reduce viral transmission through respiratory route
2. Secondary Objectives
- To assess the viral load in the nasopharynx and oropharynx before and after
application of 0.6% PVP-I of participants of this study.
- To assess the duration of effectivity of 0.6% PVP-I on mucosal surface of
participating COVID-19 patients by testing consecutive sample hourly upto 4hr .
- To estimate the shelf-life and stability of 0.6 % PVP-Ioronasal spray.
- To characterize raw materials and impurities for product development and quality
control/ assurance
- To measure the safety level of 0.6% PVP-Ioronasal sprayby biochemical analysis of
participants blood & urine This study aims to evaluate virucidal efficacy of 0.6%
PVP-I against SARS-CoV-2 amongst humans and its safety that is expected to
contribute to save lives during this COVID-19 pandemic.
Methodology Study design It will be a Multicentre, Single blind, Randomized Controlled
Trial.The participant will be divided into three groups namely Group A : 768 (384
intervention group and 384 control group) COVID-19 positive, moderately ill admitted patient
will receive intervention once (2 puff 0.6% PVP-I in each nostril and mouth).
Step 1: Enrollment of the study populations by applying inclusion and exclusion criteria Step
2: Randomization to allocate experimental and controlled group by using table of random
number Step 3: Application of 0.6% PVP-I spray to experimental group and distilled water to
control group Step 4: Follow up (waiting for 2-5 minutes) Step 5: Collection of
nasopharyngeal and oropharyngealsawab for RT-PCR test for both group Step 6: Observation of
the patients for 30 minutes for possible early adverse effects (if any) and subsequent
management (if needed).
Step 7: Data collection, processing and analysis by SPSS software.
Group B : 20 asymptomatic to mild Covid -19 patients having multiple comorbidity will receive
intervention 4 times (2 puff 0.6% PVP-I containing oronasal spray in to each nostril and
mouth).
Step 1: Selection of 20 patients randomly with no or mild symptoms and obtain their consent
for the further tests.
Step 2: Collection of 2nd, 3rd and 4th sample from nasopharynx and oropharynx hourly Step 3:
Data collection, processing and analysis by SPSS software
Group C : 10 healthy individual who accept intervention 0.6% PVP-I oronasal spray 3-4 times
interval but not more than 4 time a day for 30 days.
Step 1: Selection of 10 healthy volunteers randomly for using 0.6% PVP-I Oro-Nasal spray 2
puff inside both nostrils and mouth 3 to 4 times a day for one month.
Step 2: Collection of blood & urine of participants on day 0, 10, 20, 30 for determination of
any change in biochemical marker (thyroid, kidney and liver functions will be done) Step 3:
Data collection, processing and analysis by SPSS software
Raw material & impurities characterization
- PVP-I collection from approved vendor with certificate of analysis (CoA)
- Characterization tests of PVP-I such as appearance, identification, solubility, nitrogen
content, iodide value, loss on drying, pH, sulphated ash and available iodine as per BP
2019 are performed in well-equipped lab of BRiCM to review the test results with the
acceptance criteria stated in the specification.
- Impurity testing of PVP-I as 1-Vinyl-2-pyrrolidinone, 2-Pyrrolidinone according to
British Pharmacopeia (BP) 2019 and heavy metal (Pb) as per AOAC is carried out using
HPLC, LC-MS-MS, AAS & ICPMS.
- Sterile water, the diluent of 0.6% PVP-I solution is characterized by performing the
tests of pH, conductivity, total organic carbon, heavy metal (Pb, As) as per AWWA,
endotoxin as per EU 85 and microbial count as per AOAC in the well-equipped Microbiology
Lab of BRiCM.
- Production of 0.6% PVP-I Oro-nasal spray solution from batch dispensing to final product
packing is carried out following the norms of cGMP
- In-process quality assurance/control of the product is done at real time by performing,
volume check, pH of the solution, available iodine, UV absorbance as per BP 2019 and
packing integrity with necessary primary and secondary packing materials.
Stability Study & Shelf-life estimation
- Stability studies of the product are carried out at both accelerated condition as well
as real time condition as per ICH guidelines applicable for Stability Zone IVa.
- Stability studies at accelerated condition is carried out at 40 deg. C up to 12 months
in 2 months interval and stability studies at real time condition is carried out at 25
deg. C up to two years in three months interval.
- Stability indicting parameters such as appearance, pH, available iodine, UV absorbance
are included in both stability studies.
- Findings of both accelerated and real time stability studies are used to predict the
shelf-life of the product up to two years.
Period of study The study will be carried out during the period of May 2020 to June 2021.
Place of study Dhaka Medical College Hospital, Kurmitola General Hospital and Kuwait Moytree
Hospital including product development & quality assurance will be held at Bangladesh
Reference Institute for Chemical Measurements (BRiCM) Sampling Technique: Random sampling
procedure will be followed using table of random numbers admitted patients of dedicated
Covid-19 hospital like KGH, KMH and DMCH will be taken after fulfilling of inclusion and
exclusion criteria. Then from interested participants written informed consent will be taken.
After ward randomization will be carried out to select intervention group and control group.
Sampling Unit: Individual study subject i.e. selected each participants will be considered as
a sample unit.
Data Collection instrument and Technique : After receiving written permission from respective
hospital authority face to face interview will also be taken. Study personnel at the site
will enter data from source documents corresponding to a subject's visit into the
protocol-specific paper CRF (Case report form). All data collected during the course of this
study must be reviewed and verified for completeness and accuracy by the Investigator.
Availability and Retention of Investigation Records: The Investigator must provide interim
study report with data at every three months interval to the principle investigator. As per
requirement study report and data may be provided to BMRC and DGDA. The Investigator must
ensure the reliability and availability of source documents from which the information on the
CRF will be derived. All study documents (patient files, signed informed consent forms,
copies of CRFs, Study File Notebook, etc.) must be kept secured for a period of five years.
Data safety & Monitoring: Monitoring visits will be conducted by principle investigator, co-
investigator as well as the representatives according to Guidelines for GCP. By signing this
protocol, the investigator grants permission to the appropriate regulatory authorities to
conduct on-site monitoring and/or auditing of all appropriate study documentation.
Subject Confidentiality:In order to maintain subject confidentiality, only a site number,
subject number and subject initials will identify all study subjects on CRFs and other
documentation submitted to the investigator. Additional subject confidentiality issues (if
applicable) are covered in the Clinical Study Agreement.
Risk Management Plan: Bangasafe (proposed name) oro-nasal spray containing comparatively very
low concentration (0.6% of PVP-I) is supposed to be safe in oro-nasal application. Moreover,
this oro-nasal spray is intended to be used in the selected hospitalized patients under the
direct supervision of doctors & nurses. Therefore, any adverse reaction risk if arises will
be managed accordingly with the available facilities in respective hospital without any cost.
- If any discomfort, irritation, burning sensation occur then nasal irrigation with
sterile plan water by 50 cc disposable syringe is to be given.
- If any hypersensitivity reaction occurs then anti-histamine and/or steroid is to be
given
Clinical Laboratory Measurements Blood Chemistry Profile Blood sample for Group - C
participants will be collected and sent to the respective hospitals/BRICM clinical chemistry
lab for determining of TSH, FT3, FT4, Serum creatinine, alanine aminotransferase (ALT/SGPT)
level including urine test.
Utilization of Results:By providing information and assurance about the efficacy and safety
of 0.6% PVP-I , we can inform and encourage people to use it as oronasal spray safely for
prevention of COVID-19, as an adjunct to PPE and reduce transmissibility of SARS Cov-2 virus.
