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UPTRAVI® (selexipag) Receives FDA Approval for Intravenous Use in Adult Patients with Pulmonary Arterial Hypertension (PAH)

UPTRAVI® (selexipag) Receives FDA Approval for Intravenous Use in Adult Patients with Pulmonary Arterial Hypertension (PAH)
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All You Need To Know About Johnson & Johnson's Covid-19 Vaccine Trial In India

All You Need To Know About Johnson & Johnsonâs Covid-19 Vaccine Trial In India
by Bhaswati Guha Majumder - Apr 10, 2021 11:46 AM
(A picture of vaccine vials from Johnson and Johnson)
American pharma giant Johnson & Johnson is in talks with the Indian government to conduct an early-stage clinical trial of its single-dose Covid-19 vaccine in the country.
According to Reuters, the company said: We are in discussions with the Government of India with the objective of starting a bridging clinical study of our Janssen Covid-19 vaccine candidate in India, subject to local regulatory approvals.
The news comes at a time when India is wrestling with time to boost its vaccine distribution program, which has received worldwide appreciation. But due to the current surge in Covid-19 cases, the vaccine demand is rising. ....

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US DFC announces support for city-based vaccine maker

To help Biological E make 1 billion COVID doses
The U.S. International Development Finance Corporation (DFC) has said it will assist vaccine maker Biological E scale up to produce at least one billion doses of COVID-19 vaccines by 2022, including Johnson & Johnson vaccines.
“It is hard to conceive of an investment with a greater developmental impact than using our financial tools to increase the capacity of vaccine manufacturing to help developing countries in Asia and around the world respond to COVID-19 and other diseases,” DFC COO David Marchick said in a statement. It seeks to invest $5-500 million on each eligible project, pertaining to COVID vaccines, through a range of financial tools, which includes equity and debt financing, political risk insurance, and technical development. ....

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From recognition to response: A COVID-19 timeline

2019
Dec. 31: The World Health Organization China Country Office is informed of strange cases of pneumonia from an unknown cause in Wuhan City, Hubei Province of China. This is the first report to WHO, though the virusâs origin could later be traced to late November or early December 2019.
2020
Jan. 11: Chinese state media report the first known death of the 2019 novel coronavirus, according to The New York Times.
Jan. 17: The Centers for Disease Control and Prevention and the Department of Homeland Securityâs Customs and Border Protection announce health screenings at three major airports in San Francisco, New York and Los AngelesÂ to screen for the novel coronavirus. ....

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Beyond Batten Disease Foundation Announces Agreement with Actelion [...]

02 marzo 2021 17:14
Fonte: Adnkronos
#salute-e-benessere
AUSTIN, Texas, March 2, 2021 /PRNewswire/ Beyond Batten Disease Foundation (BBDF) is pleased to announce an agreement with Actelion Pharmaceuticals Ltd, a Janssen Pharmaceutical Company of Johnson & Johnson, to provide Zavesca® (miglustat) for the development of BBDF-101, a proprietary combination of miglustat and trehalose to treat juvenile Batten disease (CLN3). Janssen will provide drug supply for the clinical trials and Extended Access Program, and right of reference to data within the Zavesca New Drug Application (NDA) to support the development of BBDF-101.
CLN3, one of a group of disorders known as neuronal ceroid lipofuscinoses (NCLs), is a rare, fatal, inherited, neurodegenerative disease for which there is no treatment. Since it was founded in 2008, BBDF has spearheaded the development of BBDF-101. ....

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