Saturday, March 28, 2020

Roche says its kit will give results in 3 hrs


‘Made in India’ kit by Mylab Discovery

The kits developed by the Pune-based firm are claimed to be completely made in India. “The kits will eliminate the requirement of two tests — screening and confirmatory testing. Rather, it will give the results within two-and-a-half hours of loading the samples on the machine,” Mylab Discovery managing director Hasmukh Rawal told ThePrint.
Dr Gautam Wankhede, director of medical affairs at Mylab, said, “Since the test is based on the sensitive PCR technology, even early stage infection can be detected with our kits. Per day, over 10,000 tests can be done and capacity can be increased.”
Mylab, in 2019, was recognised as India’s first FDA-approved molecular diagnostics company for the RT-PCR-based kits for testing HIV, Hepatitis B and C.
“With our expertise in the field of molecular diagnostics, the cost of testing will be much lesser with our kits in comparison to the foreign made kits. Their price of testing per sample is more than twice our price,” Wankhede said, without disclosing the price.
Mylab is the first company in Asia and second in the world to manufacture ID-NAT kits, which check blood samples to reduce risk of transfusion-transmitted infections in recipients.

Also Read: Why doctors in Italy are letting some coronavirus patients die to save others

Trivitron can produce 7.5 lakh kits every day

Trivitron Healthcare also calls its diagnostic test kits for COVID-19 the country’s first indigenous kit.
“The kit can be used in all five sample types recommended by ICMR and WHO. The costs are still being worked out. We have allocated Rs 4 to 5 crore emergency funds to upgrade our R&D infrastructure for launching hand sanitisers and COVID-19 kits,” Dr G.S.K. Velu, Chairman & Managing Director, Trivitron Healthcare Group, told ThePrint.
“The standard turnaround time is normally 2-3 days, but Trivitron is trying to reduce (the time) to 3-5 hours for generating results.”
“The kits by our joint venture company in China, Labsystems Diagnostics Shandong, are approved and sold there. China and we are planning to use that expertise and components to make them in India,” he said.
The company is waiting for approvals from the National Institute of Virology for validation protocols and positive samples. “In the next two to three weeks, as long as we complete our validation in government-approved institutions, 500 to 750,000 test kits can be produced per day.”

Roche says its kit will give results in 3 hrs

Roche, Swiss diagnostic and pharma giant, has received emergency use authorisation from the United States’ regulator Food and Drug Administration (FDA) for its SARS-CoV-2 test.
“Roche Diagnostics India is keen to partner with the Government’s efforts in their drive to manage the COVID-19 infection situation. We have the potential to offer 3 types of test kits that can be used to screen and further diagnose COVID-19 infections on our existing systems that run other infectious disease panels. These systems are installed across India’s 15 major cities,” Dr Shravan Subramanyam, Managing Director, India and Neighbouring Markets, Roche Diagnostics India Private Limited, told ThePrint in an email.
According to the company’s media release, the test kits — Roche’s cobas 6800/8800 Systems, which are used to perform the cobas SARS-CoV-2 Test — “provide test results in three and a half hours”.
The company also claims it provides up to 96 results in about three hours and a total of 384 results for the cobas 6800 System technology whereas 960 results are produced for the cobas 8800 System in eight hours.

Friday, March 27, 2020

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11 hours ago - U.S. DEPARTMENT of STATE — BUREAU of CONSULAR AFFAIRS ... State.Gov > U.S. Visas News > Update on H and J Visas for Medical ...

Last Updated: March 26, 2020
We encourage medical professionals seeking to work in the United States on a work or exchange visitor, particularly those working to treat or mitigate the effects of COVID-19, to reach out to the nearest embassy or consulate to request a visa appointment.



Meeting coronavirus warrior Dr Raman Sharma

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Friday, March 20, 2020

Japanese flu drug 'clearly effective' in treating coronavirus, says China

Shares in Fujifilm Toyama Chemical, which developed favipiravir, surged after praise by Chinese official following clinical trials
A laboratory technician prepares Covid-19 patient samples for semi-automatic testing
Patients given the medicine in Shenzhen turned negative in a median of four days Photograph: John Minchillo/AP
Medical authorities in China have said a drug used in Japan to treat new strains of influenza appeared to be effective in coronavirus patients, Japanese media said on Wednesday.
Zhang Xinmin, an official at China’s science and technology ministry, said favipiravir, developed by a subsidiary of Fujifilm, had produced encouraging outcomes in clinical trials in Wuhan and Shenzhen involving 340 patients.
“It has a high degree of safety and is clearly effective in treatment,” Zhang told reporters on Tuesday.
Patients who were given the medicine in Shenzhen turned negative for the virus after a median of four days after becoming positive, compared with a median of 11 days for those who were not treated with the drug, public broadcaster NHK said.
In addition, X-rays confirmed improvements in lung condition in about 91% of the patients who were treated with favipiravir, compared to 62% or those without the drug.
Coronavirus: the week explained - our expert correspondents put a week’s worth developments in context in one email newsletter
Fujifilm Toyama Chemical, which developed the drug – also known as Avigan – in 2014, has declined to comment on the claims.
Shares in the firm surged on Wednesday following Zhang’s comments, closing the morning up 14.7% at 5,207 yen, having briefly hit their daily limit high of 5,238 yen.
Doctors in Japan are using the same drug in clinical studies on coronavirus patients with mild to moderate symptoms, hoping it will prevent the virus from multiplying in patients.
But a Japanese health ministry source suggested the drug was not as effective in people with more severe symptoms. “We’ve given Avigan to 70 to 80 people, but it doesn’t seem to work that well when the virus has already multiplied,” the source told the Mainichi Shimbun.
The same limitations had been identified in studies involving coronavirus patients using a combination of the HIV antiretrovirals lopinavir and ritonavir, the source added.
In 2016, the Japanese government supplied favipiravir as an emergency aid to counter the Ebola virus outbreak in Guinea.
Favipiravir would need government approval for full-scale use on Covid-19 patients, since it was originally intended to treat flu.
A health official told the Mainichi the drug could be approved as early as May. “But if the results of clinical research are delayed, approval could also be delayed.”

Thursday, March 19, 2020

Today’s #GoogleDoodle honours Ignaz Semmelweis, a Hungarian physician and an early pioneer of antiseptic procedures.
He was the first person to suggest that hand-washing would prevent the spread of life-threatening germs.
🙌goo.gle/2IOToBh