| 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
|
|
|
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)
|
|
|
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. |