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Pharma Giant Zydus Cadila Initiates Clinical Study On 1,048 Volunteers For Potential COVID-19 Vaccine

Potential coronavirus vaccine’s clinical trial will be conducted in two phases during which the volunteers have to comply with trial procedures and shall remain available for the duration of follow-up

Pharma Giant Zydus Cadila Initiates Clinical Study On 1,048 Volunteers For Potential COVID-19 Vaccine
  • Zydus Cadila has initiated phase 1, 2 clinical trial of vaccine candidate
  • Phase 1: Healthy males, females between 18-55 years have been selected
  • Phase 2: Healthy volunteers of either gender aged 12/above will be selected

New Delhi: Indian pharmaceutical giant Zydus Cadila has initiated the phase 1, 2 clinical trial to evaluate the safety and immunogenicity of coronavirus vaccine candidate by intradermal (injection) route in 1,048 subjects after the pharma company got approval from Drugs Controller General of India (DCGI) earlier this month. According to the Clinical Trial Registry- India (CTRI), the clinical study is based on two criteria — inclusion and exclusion. The inclusion criteria is divided into two phases.

In phase 1, the company has selected healthy males and females (non-pregnant and non-lactating) between 18-55 years of age.

Also Read: India ‘Pharmacy Of The World’, On Fast-Track Mode To Develop COVID-19 Vaccine: Indian Council of Medical Research

The volunteers have to comply with trial procedures and should remain available for the duration of follow-up. The participants should be able and willing to complete an informed consent process with an understanding of the purpose and procedures of the study, it said.

For phase 2, healthy volunteers of either gender aged 12 or above will be selected.

The company has to get informed consent from the adult subjects or from the parents of pediatric subjects.

The next is the exclusion criterion which is also divided into phase 1 and 2, respectively.

Also Read: Researchers Identify Targets For COVID-19 Vaccine Using Cancer Immunotherapy Tools

In the exclusion criteria — subjects are not allowed having — febrile illness (temperature >= 38degC or 100.4degF) or any acute illness or infection within four weeks of enrolment, having story of confirmed coronavirus case or history of contact with a COVID-19 confirmed patient within 14 days or history of SARS/MERS infection, individual positive for antibody and antigen against coronavirus, person who has previously participated in any clinical trial of a COVID candidate vaccine, history of hepatitis C, B infection or human immunodeficiency virus I or II, history or presence of significant smoking (>10 cigarettes per day), past history of hypersensitivity reaction or any serious adverse event after any vaccination and subjects with thrombocytopenia or any coagulation disorder, or subjects on anticoagulation therapy, it stated.

Also Read: Fight Against COVID-19: Human Trials For The Country’s First Covid-19 Vaccine Candidate ‘COVAXIN’ To Start In July

The phase 1 trials, from Day 0 to 84, will be conducted to evaluate the safety of the COVID-19 vaccine candidate by intradermal route in healthy subjects. In phase 2, which will run from 0 to 224 days, the immunogenicity of COVID-19 vaccine candidates by intradermal route in healthy subjects compared to placebo will be evaluated.

The World Health Organisation (WHO) said that the coronavirus outbreak was first reported in China last late December in 2019. Being a highly transmissible virus between humans, it took the shape of a pandemic. As of July 15, globally there have been 13,119,239 confirmed cases of COVID-19, including 573,752 deaths reported to the global health body.

In the absence of effective prevention measures, current management to control the epidemic is the enforcement of quarantine, isolation and physical distancing. Effective vaccines against COVID-19 are urgently needed to reduce the enormous burden of mortality and morbidity associated with the infection.

The number of deaths due to COVID-19 rose to 24,309 and the total number of cases climbed to 9,36,181 in India, after it registered 582 fatalities and a record single-day spike of 29,429 cases till Wednesday 8 am, according to the Union Health Ministry.

Also Read: COVID-19 Fatality Rate Is 2.6 Per Cent And Rapidly Coming Down: Health Ministry

NDTV – Dettol Banega Swasth India campaign is an extension of the five-year-old Banega Swachh India initiative helmed by Campaign Ambassador Amitabh Bachchan. It aims to spread awareness about critical health issues facing the country. In wake of the current COVID-19 pandemic, the need for WASH (WaterSanitation and Hygiene) is reaffirmed as handwashing is one of the ways to prevent Coronavirus infection and other diseases. The campaign highlights the importance of nutrition and healthcare for women and children to prevent maternal and child mortality, fight malnutrition, stunting, wasting, anaemia and disease prevention through vaccines. Importance of programmes like Public Distribution System (PDS), Mid-day Meal Scheme, POSHAN Abhiyan and the role of Aganwadis and ASHA workers are also covered. Only a Swachh or clean India where toilets are used and open defecation free (ODF) status achieved as part of the Swachh Bharat Abhiyan launched by Prime Minister Narendra Modi in 2014, can eradicate diseases like diahorrea and become a Swasth or healthy India. The campaign will continue to cover issues like air pollutionwaste managementplastic banmanual scavenging and sanitation workers and menstrual hygiene.

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