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CTRI Number  CTRI/2020/10/028335 [Registered on: 09/10/2020] Trial Registered Prospectively
Last Modified On: 11/11/2020
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   A clinical study to assess the efficacy and safety of Tinefcon in patients with moderate COVID-19 infection 
Scientific Title of Study   A multi-centric, open-labeled, prospective, comparative study to evaluate the efficacy and safety of Tinefcon and standard of care versus standard of care alone in patients of moderate COVID-19 
Trial Acronym  TINEFCON 
Secondary IDs if Any  
Secondary ID  Identifier 
Tinefcon/01/20 Final dated 30 June 2020  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Mala Kaneria 
Designation  Professor 
Affiliation  TN Medical College & BYL Nair Hospital 
Address  Department of Medicine, TN Medical College & BYL Nair Hospital, Dr. AL Nair Road, Mumbai Central, Mumbai
same as above
Mumbai
MAHARASHTRA
400008
India 
Phone  02223027122  
Fax    
Email  kaneriamala@rediffmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Rajiv Salvi 
Designation  Marketing Manager 
Affiliation  Piramal Enterprises Limited 
Address  Gopikrishna Memorial Hospital, Ganpatrao Kadam Marg, Lower Parel, Mumbai 400013
same as above
Mumbai
MAHARASHTRA
400013
India 
Phone  9920526213  
Fax    
Email  rajiv.salvi@piramal.com  
 
Details of Contact Person
Public Query
 
Name  Mridul Sharma 
Designation  Vice President, Strategic Business 
Affiliation  Piramal Enterprises Limited 
Address  Gopikrishna Memorial Hospital, Ganpatrao Kadam Marg, Lower Parel, Mumbai 400013
same
Mumbai
MAHARASHTRA
400013
India 
Phone  9643010000  
Fax    
Email  mridul.sharma@piramal.com  
 
Source of Monetary or Material Support  
Piramal Enterprises Limited Gopikrishna Memorial Hospital, Ganpatrao Kadam Marg, Lower Parel, Mumbai 400013 
 
Primary Sponsor  
Name  Piramal Enterprises Limited 
Address  Gopikrishna Memorial Hospital Ganpatrao Kadam Marg, Lower Parel, Mumbai 400013. 
Type of Sponsor  Pharmaceutical industry-Indian 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 4  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Rahul Tambe  Nanavati Super Specialty Hospital  A unit of Dr Balabhai Nanavati Hospital SV Rd, Suresh Colony, Vile Parle West, Mumbai, 400056
Mumbai
MAHARASHTRA 
9820192401

rahul.tambe@nanavatihospital.org 
Dr Alben Sigamani  Narayana Hrudayalaya Limited  NH Health City, Bommasandra Industrial Area, Anekal Taluk Bangalore 560105
Bangalore
KARNATAKA 
8884431444

alben.sigamani.dr@narayanahealth.org 
Dr Mehul Shah   Sir H N Reliance Foundation Hospital  Prarthana Samaj, Raja Rammohan Roy Rd, Charni Road East, Khetwadi, Girgaon, Mumbai 400004
Mumbai
MAHARASHTRA 
91-22-61305757

Mehul.S.Shah@rfhospital.org 
Dr Mala Kaneria  TN Medical College & BYL NAir Hospital  Department of Medicine 1st floor College bldg Dr. AL Nair Road Mumbai Central Mumbai
Mumbai
MAHARASHTRA 
9820210926

kaneriamala@rediffmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 4  
Name of Committee  Approval Status 
Ethics Committee, Nanavati Super Specialty Hospital  Submittted/Under Review 
Ethics Committee, Sir H N Reliance Foundation Hospital  Submittted/Under Review 
Institutional Ethics Committee (IEC), TNMC & BYL Nair Hospital, Mumbai  Approved 
Narayana Health Medical Health Committee  Approved 
 
Regulatory Clearance Status from DCGI
Modification(s)  
Status 
Approved/Obtained 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: B972||Coronavirus as the cause of diseases classified elsewhere,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Standard of Care   Tab. Ivermectin 12 mg single dose Tab. Hydroxychloroquine 400 mg twice daily on Day 1, then 400 mg OD for 5 days 
Intervention  Tinefcon   2.8g/day (four tablets of 700 mg/day) orally once a day for 10 days 
 
Inclusion Criteria
Modification(s)  
Age From  18.00 Year(s)
Age To  75.00 Year(s)
Gender  Both 
Details  1. Subjects who are able to provide a written informed consent or have a legally accepted representative to provide the same.
2. Subjects who are proven to be positive for SARS-CoV-2 infection, as confirmed by the RT-PCR test.
3. Subjects who are admitted with moderate COVID-19 (MOFHW criteria) for treatment at the hospital having the following clinical criteria: pneumonia with no signs of severe disease; peripheral capillary oxygen saturation (SPO2) between 90 and 94% on room air and respiratory rate between 15 and 30 breaths per minute.
4. Subjects with arterial partial pressure of oxygen/fraction of inspired oxygen (PaO2/FiO2) between 200 and 300 mm/Hg.
5. Female subjects with a negative urine pregnancy test at screening.
6. Subjects who are able to take the study drug orally and comply with the study procedures 
 
ExclusionCriteria 
Details  1. Subjects who are participating in any other clinical trial or experimental treatment for COVID-19.
2. Subjects with persistent vomiting (more than three episodes of vomiting in 12 hours) and who cannot tolerate oral drugs.
3. Subjects requiring concomitant use of invasive or non-invasive mechanical ventilation.
4. Subjects requiring vasopressors or ionotropic medications.
5. Subjects requiring anti-viral drugs like ritonavir, favipirir, lopinavir or monoclonal antibodies like tocilizumab at hospitalization, in the opinion of the Investigator.
6. Female subjects who are pregnant or lactating.
7. Subjects who are known to be HIV positive or positive for Hepatitis B or C. (The same may be noted based on history given by the subject or standards of care followed at the individual sites.)
8. Subjects with history of retinopathy or macular degeneration.
9. Subjects with prolonged QTc interval at screening (>450 ms in males and >470 ms in females).
10. Subjects with liver enzymes (namely alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST)) > 5x upper limit of normal.
11. Subjects with creatinine clearance <50 ml/min (using Cockgroft-Gault formula).
12. Subjects who are not deemed fit as per the investigator for any other medical reason 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Case Record Numbers 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Clinical response: Resolution of fever
Clinical Improvement Scale
Overall survival of the subjects
Progression of COVID-19 associated pneumonitis
Cytokine levels 
Clinical response: Resolution of fever - measured daily for 10 days
Clinical Improvement Scale:measured at baseline and days 3, 7 and 10
Overall survival of the subjects: at 14 days
Progression of COVID-19 associated pneumonitis: measured daily for 10 days
Cytokine levels at baseline and on days 7 and 10 
 
Secondary Outcome  
Outcome  TimePoints 
A.Overall survival
B.Survival to hospital discharge
C.Progression of COVID-19 associated pneumonitis
D.Number of ICU days
E. Duration of Increased Supplemental Oxygen Requirement from Baseline 
Day 0 to Day 21 
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3 
Date of First Enrollment (India)   12/10/2020 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="8"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   none yet 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

COVID-19 disease features range from minor upper respiratory tract infections, mild (fever myalgia) to severe symptoms like the cytokine storm syndrome/cytokine release syndrome or even death. Patients with known corona virus infection have raised IL-6, IL-10, IL-12, IL-14, TNFα and INFg levels, 4-10 days after onset of disease (Huang C et al, 2020; Ren L et al, 2020.)

Clinical data from China showed that approximately 17.7% - 32% of patients required intensive care with evidence suggesting that cytokine release syndrome (CRS) plays a major role in the COVID-19 progression (Liu et al, 2020).

 

Due to the lack of a specific treatment or vaccine against the SARS-CoV-2 infection, several agents are in clinical evaluation for the same, including agents targeting IL-6 and anti-viral agents. Recombinant monoclonal antibodies like Tocilizumab and Sarilumab and anti-viral agents like remdesivir have shown promising results in COVID-19 infection and are being evaluated further.

 

Sphaeranthus indicus is a freely available, weed-like plant growing across India in the hillocks and stony areas along river banks. It is also known as Gorakhmundi, Mundi or Munditika. It has been demonstrated to have immune-modulatory and anti-inflammatory properties. Extract of S. indicus fruiting and flowering heads [standardized for 7- hydroxy frullanolide (7-HF) contained not less than 5% w/w-Tinefcon] has been tested ‘in vitro’ and ‘in vivo’ for inhibitory effect on cytokine (TNF - a, IL – 1b, IL-6, IL-8, IL-12/23) release  with positive results. It has been extensively studied in animal models for efficacy; has undergone toxicity studies and clinical studies with patients of rheumatoid arthritis and psoriasis. Tinefcon has been found to show efficacy in the pre-clinical species studies and did not show any major toxicological effect in the toxicity studies conducted. There was reasonable safety and tolerability with efficacy demonstrated in the clinical studies up to a dose of 2.8 g/day of Tinefcon. Currently, it has been approved in several countries including India for marketing and is widely used.

 

Given the action of Tinefcon on inhibition of LPS-induced release of TNF-α, IL-1β, IL-6 and IL-8 in human peripheral blood mono-nuclear cells (hPBMCs) in vitro and LPS-induced TNF-α release in BALB/c mice when given orally, it is anticipated to show benefits in symptomatic patients with the SARS-CoV-2 infection and halt the progression of the disease towards the cytokine release syndrome or worsening disease.

 

With anticipated suppression of the acute inflammatory response in terms of cytokine release, Tinefcon will be effective in reducing the clinical signs and symptoms and should be evaluated in hospitalized, non-critically ill patients who are SARS-CoV-2 positive.

 
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