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India coronavirus vaccine candidate from Cadila Healthcare

SINGAPORE – Indian drug maker Cadila Healthcare is about to start a phase 3 clinical trial for a potential coronavirus vaccine, its chairman told CNBC.

“We are now entering the third phase, which will begin very, very soon,” Pankaj Patel told CNBC’s “Street Signs Asia” on Tuesday.

He said the process will involve around 30,000 volunteers and take around three to three and a half months.

The pharmaceutical company, also known as Zydus Cadila, announced on Sunday that it had received approval from India’s Medicines Agency to begin its Phase 3 clinical trial after previous studies found its DNA vaccine candidate was “safe, well tolerated and immunogenic “.

“We saw that the antibody response was very, very good, in the range of 20 to 80-fold increases in antibodies after the vaccine was given,” said Patel, adding studies that so far indicated that the volunteers the vaccine responded well to it. “We also saw good virus neutralization with it and we didn’t see any side effects to be concerned about.”

“Overall we have very good results and we believe that phase three should actually show us the exact effectiveness of the vaccine,” said Patel. Cadila’s candidate will likely become India’s second domestically developed Covid-19 vaccine when it receives regulatory approval following its phase three study.

Ground staff walk past a container that is being held at Freight Terminal 2 at Indira Gandhi International Airport and will be used as a COVID-19 center for vaccine handling and distribution on December 22, 2020 in New Delhi, India, according to officials becomes.

Anushree Fadnavis | Reuters

Unlike some other Covid-19 vaccines that require extremely cold storage temperatures, Cadila’s candidate can be kept stable at room temperature, according to Patel. That would make it easier to distribute to remote parts of India.

Patel stated that the company already has a distribution system in India and has invested in expanding its manufacturing capacity. He added that the company is also in advanced talks with several other countries to deliver the potential vaccine once it’s ready, but declined to name the nations.

South Asia’s largest country currently has more than 10.35 million reported cases of coronavirus infection, second only to the US. According to the Johns Hopkins University, almost 150,000 people in India are said to have died of Covid-19. However, official figures suggest that the number of cases of active infections is decreasing.

The Indian Medicines Agency on Sunday approved the restricted use of two coronavirus vaccines in emergency situations. One of them is a vaccine developed by AstraZeneca and Oxford University and made locally by the Serum Institute of India. The other was developed by India’s Bharat Biotech in partnership with the Indian State Council for Local Medical Research and received emergency approval if clinical trials continue.

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India Approves Oxford-AstraZeneca Covid-19 Vaccine and 1 Different

NEW DELHI – India announced on Sunday that it has approved two coronavirus vaccines, one made by AstraZeneca and Oxford University and the other developed in India for emergency use. This is an important step in stopping the coronavirus from spreading in one of the toughest in the world. countries hit.

The permits were announced at a press conference in New Delhi on Sunday. Dr. VG Somani, the Indian drug control officer, said the decision to approve the Oxford-AstraZeneca vaccine and a local vaccine developed by Bharat Biotech was made after “careful review” of both by the Central Drugs Standard Control Organization, India’s Indian medicines agency .

Indian regulators are still considering approvals for other vaccines. One made by Pfizer and BioNTech has already been approved in the US and Europe. Another, Russia’s Sputnik V, seems less far away.

The UK became the first country to issue emergency approval for the Oxford-AstraZeneca vaccine on Wednesday. Argentina soon followed.

Officials in India moved quickly for several reasons. The country ranks number 2 in confirmed infections behind the United States, and the outbreak is widely believed to be worse than official numbers suggest. The pandemic has devastated the economy and the unemployment rate is at a 45-year high. Education has been disrupted, leading to concerns about the long-term impact on the country’s youth.

India is now facing major challenges. Cans for more than 1.3 billion people have to be paid for and distributed over a vast country. Government officials may also have public doubts about the vaccine’s safety and effectiveness, partly due to the government’s lack of transparency about clinical trial protocols.

Criticism of the ambiguity of the data examined by the regulator came quickly after the two emergency vaccines were approved.

All India Drug Action Network, a public health watchdog, immediately issued a statement requesting more information on the scope of clinical trials and dosage regimens for both vaccines.

Regarding the Bharat biotech vaccine called Covaxin, the group said it was “baffled to understand the scientific logic that motivated the top experts” to approve a vaccine that is still in clinical trials.

Dr. Somani, the regulator, said the vaccine had been given to 22,500 study participants and “found safe” to date.

Both the AstraZeneca vaccine and the Bharat Biotech vaccine require two doses, said Dr. Somani. He did not state whether participants in Bharat Biotech’s ongoing clinical trials received both doses.

The effort has already been fraught with setbacks. The Serum Institute, an Indian drug company that had an agreement to make the Oxford vaccine before it was proven to be effective, has managed to produce only about a tenth of the 400 million doses it promised to make before the end of the year.

The government says it’s ready. To get the vaccine to a country known for its size and sometimes unreliable roads, officials will leverage knowledge from nationwide campaigns against polio and newborn vaccinations, as well as the skills and flexibility used in India’s mammoth general election where ballot boxes are delivered to the US furthest from the country.

The Serum Institute says it is on the right track to ramp up production of the vaccine known in India as Covishield. With $ 270 million of its own funds and $ 300 million from the Bill and Melinda Gates Foundation, Serum plans to increase production capacity to 100 million doses per month by February, said Mayank Sen, a company spokesman.

First, the Serum Institute signed a pact with AstraZeneca to manufacture one billion doses of the vaccine for low and middle income countries. The vaccine is attractive to developing countries because it is cheaper to manufacture and easier to transport than those which require colder temperatures during storage and transportation.

The Serum Institute experienced production delays when it built new facilities to manufacture the vaccine. It is said to have produced between 40 and 50 million cans for the world. The company’s chief executive Adar Poonawalla told reporters on Monday that the majority of the cans will be given to India.

Indian officials were unsure of how many doses to receive and when. Mr Sen said the Serum Institute had no firm agreement with the Government of India, but had committed to reserve most of its existing inventory for India.

“The government has not yet signed the papers and the final dotted line, but this is based on initial discussions we had because we have always said India will be the priority,” said Sen.

Until the vaccine is approved by the World Health Organization, serum will begin shipping doses at manufacturing cost to other developing countries, Sen said.

India’s approval process has also been delayed. The Serum Institute filed for emergency approval earlier last month, but regulators requested additional details from clinical trials, including whether any person involved in the trials had had any medical complications.

The details of this claim are not clear. After receiving the Covishield vaccine on October 1, a 40-year-old volunteer from Chennai, India, publicly reported neurological symptoms to the Serum Institute in a legal notice. The company threatened defamation lawsuits and required volunteers to pay approximately $ 13.7 million. While negative health effects from vaccine trials are rare, health professionals risked the Serum Institute promoting misinformation by punishing someone for speaking up.

Mr Poonawalla said Monday that the Serum Institute had submitted the additional information that regulators had requested. It has denied that the problems reported by the Chennai trial participant had anything to do with Covishield but refused to comment on allegations of intimidation.

Indian officials have drawn up an ambitious plan to vaccinate the country’s huge population. This is the greatest effort of this kind in the country’s history.

India plans to launch a vaccination campaign in the first three months of the year that will cover about a quarter of the population by August. The first 30 million people vaccinated will be health care providers, then police and other frontline workers. For the remaining 270 million people, authorities will focus on those over 50 who are suffering from conditions that may make them more vulnerable.

The rest of the population will be immunized based on the availability of vaccines and the latest scientific knowledge.

India has a long history of vaccinating its people. India’s first mass vaccination took place in 1802 to combat smallpox. Subsequent efforts suffered from misinformation and slow adoption.

The country has made progress in recent years. In the fight against polio, government officials ran informational campaigns to religious leaders to almost eradicate the disease. According to a study, a mass measles vaccination campaign between 2010 and 2013 saved the lives of tens of thousands of children.

For the coronavirus campaign, the national government has asked the states to prepare vaccination strategies. Some have established task forces at the state, district and block levels. To date, more than 20,000 health workers in around 260 districts have been trained to administer the vaccine, according to the Indian Ministry of Health.

The government plans to use the framework of its universal vaccination program for pregnant women and newborns – one of the largest and cheapest public health interventions in the world.

Indian civil aviation minister Hardeep Singh Puri said Tuesday that airlines, airports and ground handlers have been asked to develop plans to transport vaccine bottles in cold temperatures.

This week, health workers in four Indian states conducted an exercise to iron out wrinkles. Health officials in various locations distributed over 100 doses of placebo vaccine to trainers. They then tracked the temperature of the cans on the way from the train depot to the vaccination site, as well as the time and whether they reached the intended patient.

India has yet to improve its ability to store and transport vaccines under temperature controlled conditions known as the cold chain network, as well as improve distribution methods and train new workers.

India may need to double its health care workforce from its current 2.5 million, said Thekkekara Jacob John, a senior virologist in southern Tamil Nadu state.

“This is a Herculean task,” said John of the vaccination effort. “And the challenge is not in densely populated cities, but in rural areas – home of real India.”

Government officials must also stop the rumor, he said. Chat groups on WhatsApp, Facebook’s widespread messaging service in India, have already become misinformation about side effects.

A month ago, Prime Minister Narendra Modi urged citizens to look out for those trying to spread rumors about the vaccine, which he called “anti-national and anti-human” and urged politicians to help raise awareness .

Mr Modi renewed that appeal on Thursday, throwing the continued fight against the virus as one against an unknown enemy.

“Be careful of rumors,” he said, “and as a responsible citizen, you must not post messages on social media without checking.”

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Louis Kahn-Designed Dorms in India Could Be Razed

Controversy is brewing in India over the preservation of world-class architecture, where the administration of the Indian Institute of Management in Ahmedabad announced plans to demolish 14 of 18 student residences designed by architect Louis Kahn and built in the 1960s and 1970s were.

After local and international outcry, an online meeting was canceled to receive new offers for the demolition.

One of the most important American architects in history, Kahn is known for masterpieces such as the Salk Institute in La Jolla, California, the Kimbell Art Museum in Fort Worth, and the Philips Exeter Academy Library in Exeter, New Hampshire. and the First Unitarian Church in Rochester, NY (He also had three families, spoke with bricks, and died on the floor of the men’s room at Penn Station.)

The exposed red brick student dormitories in Ahmedabad are an integral part of the institute’s holistic campus design and are among the architect’s best works – with repetition, geometry, and manipulation of light and shadow. They illustrate Kahn’s ability to design buildings “in response to the cultures, climates, and traditions of their respective locations,” said historian William JR Curtis, who has contributed to Architectural Record and The Architectural Review on dormitory preservation support.

In a statement, the World Monuments Fund urged the institute’s administration to reconsider this, citing the project’s impact on the “modern development of Indian higher education” and environmentally conscious design, which continues to be an example of how to become a local climate builds. “The Kahn campus, designed as an ensemble, must be preserved in its entirety in order to protect the aesthetic, functional and symbolic values ​​it contains,” the statement said.

Supporters of the dormitories include the Council of Architecture, India, as well as architects and scholars, including the Pritzker Architecture Prize winners, Rafael Moneo, Alejandro Aravena, and Balkrishna Doshi (the architect who brought Kahn to India in the early 1960s) Letter. A Change.org petition had over 12,000 signatures on Thursday afternoon.

The director of the administrative institute, Errol D’Souza, defended the demolition plans in a letter to the alumni and called the structures “inanimate”, among other things because of “concrete and slabs falling from the roofs”. Brick deterioration causes cracks and water seepage; and structural problems following a 2001 earthquake.

The school had previously commissioned an extensive restoration project for the buildings, but reversed the course with the plan to rebuild.