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In reply to the discussion: Merck says a trial shows it has produced the first effective antiviral pill for Covid. [View all]BumRushDaShow
(165,183 posts)5. As I was following the vaccine development efforts over the past year
Merck decided to go on and drop their vaccine development and instead opted to go with this anti-viral treatment.
However this past spring, they made an agreement with Biden to assist in manufacturing vaccines through a partnership with Janssen (J&J) since they have a huge vaccine manufacturing complex in NC.
- https://www.hhs.gov/about/news/2021/03/02/biden-administration-announces-historic-manufacturing-collaboration-between-merck-johnson-johnson-expand-production-covid-19-vaccines.html
FOR IMMEDIATE RELEASE
March 2, 2021
Contact: HHS Press Office
202-690-6343
media@hhs.gov
Biden Administration Announces Historic Manufacturing Collaboration Between Merck and Johnson & Johnson to Expand Production of COVID-19 Vaccines
President Biden Invokes Defense Production Act to Support Measures to Accelerate Vaccine Development
President Biden announced today that his Administration has helped forge a historic manufacturing collaboration between two of the largest U.S. health care and pharmaceutical companies, Merck and Johnson & Johnson (J&J), to expand production of J&s COVID-19 vaccine. The collaboration will increase manufacture of vaccine drug substance, as well as its fill-finish capacity two of the biggest bottlenecks facing J&J in the production of its vaccine.
The U.S. Department of Health and Human Services (HHS) will collaborate with Merck to repurpose some of its existing Merck facilities for rapid large-scale manufacturing of vaccines and therapeutics for use in public health emergencies including the current pandemic. The facilities will be available to private sector partners working with the federal government on the COVID-19 response or to produce Merck products against COVID-19. Janssen Pharmaceuticals, part of Johnson & Johnson, will be the first federal partner to use repurposed Merck facilities to manufacture COVID-19 vaccine. Merck will use two of its facilities to produce drug substance, formulate and fill vials of J&Js vaccine.
Consistent with the Administrations mission to ensure that the United States has sufficient long term sustainable capacity to manufacture vaccines, the Biomedical Advanced Research and Development Authority (BARDA), part of the HHS Office of the Assistant Secretary for Preparedness and Response (ASPR), will leverage the Defense Production Act to provide an initial investment of $105 million in funding for Merck, at the Administrations request, to convert, upgrade and equip Merck facilities to the standards necessary to safely manufacture the vaccine. The company will address all the necessary qualification and validation activities needed for the facilities to be used for large-scale manufacturing.
To further accelerate production of the J&J vaccine, President Biden also announced he has invoked the Defense Production Act to expedite materials in vaccine production, such as equipment, machinery and supplies like single use bags, and he has directed the Department of Defense (DOD) to provide daily logistical support to strengthen J&Js efforts. With the urging and assistance of the Administration, J&J also will begin operating its manufacturing facilities 24/7 to maximize production output.
These efforts will contribute to J&Js ability to accelerate delivery of their vaccine doses from 100 million doses by the end of June to at or near 100 million doses by the end of May. In the long term, these actions will ultimately double J&Js U.S. capacity to produce drug substance and increase the U.S. capacity for fill-finish.
About HHS, ASPR, and BARDA:
HHS works to enhance and protect the health and well-being of all Americans, providing for effective health and human services and fostering advances in medicine, public health, and social services. The mission of ASPR is to save lives and protect Americans from 21st century health security threats. Within ASPR, BARDA invests in the innovation, advanced research and development, acquisition, and manufacturing of medical countermeasures vaccines, drugs, therapeutics, diagnostic tools, and non-pharmaceutical products needed to combat health security threats. To date, BARDA-supported products have achieved 59 FDA approvals, licensures or clearances. For more on BARDAs portfolio for COVID-19 diagnostics, vaccines and treatments and about partnering with BARDA, visit medicalcountermeasures.gov. To learn more about coronavirus, visit cdc.gov/coronavirus.
###
March 2, 2021
Contact: HHS Press Office
202-690-6343
media@hhs.gov
Biden Administration Announces Historic Manufacturing Collaboration Between Merck and Johnson & Johnson to Expand Production of COVID-19 Vaccines
President Biden Invokes Defense Production Act to Support Measures to Accelerate Vaccine Development
President Biden announced today that his Administration has helped forge a historic manufacturing collaboration between two of the largest U.S. health care and pharmaceutical companies, Merck and Johnson & Johnson (J&J), to expand production of J&s COVID-19 vaccine. The collaboration will increase manufacture of vaccine drug substance, as well as its fill-finish capacity two of the biggest bottlenecks facing J&J in the production of its vaccine.
The U.S. Department of Health and Human Services (HHS) will collaborate with Merck to repurpose some of its existing Merck facilities for rapid large-scale manufacturing of vaccines and therapeutics for use in public health emergencies including the current pandemic. The facilities will be available to private sector partners working with the federal government on the COVID-19 response or to produce Merck products against COVID-19. Janssen Pharmaceuticals, part of Johnson & Johnson, will be the first federal partner to use repurposed Merck facilities to manufacture COVID-19 vaccine. Merck will use two of its facilities to produce drug substance, formulate and fill vials of J&Js vaccine.
Consistent with the Administrations mission to ensure that the United States has sufficient long term sustainable capacity to manufacture vaccines, the Biomedical Advanced Research and Development Authority (BARDA), part of the HHS Office of the Assistant Secretary for Preparedness and Response (ASPR), will leverage the Defense Production Act to provide an initial investment of $105 million in funding for Merck, at the Administrations request, to convert, upgrade and equip Merck facilities to the standards necessary to safely manufacture the vaccine. The company will address all the necessary qualification and validation activities needed for the facilities to be used for large-scale manufacturing.
To further accelerate production of the J&J vaccine, President Biden also announced he has invoked the Defense Production Act to expedite materials in vaccine production, such as equipment, machinery and supplies like single use bags, and he has directed the Department of Defense (DOD) to provide daily logistical support to strengthen J&Js efforts. With the urging and assistance of the Administration, J&J also will begin operating its manufacturing facilities 24/7 to maximize production output.
These efforts will contribute to J&Js ability to accelerate delivery of their vaccine doses from 100 million doses by the end of June to at or near 100 million doses by the end of May. In the long term, these actions will ultimately double J&Js U.S. capacity to produce drug substance and increase the U.S. capacity for fill-finish.
About HHS, ASPR, and BARDA:
HHS works to enhance and protect the health and well-being of all Americans, providing for effective health and human services and fostering advances in medicine, public health, and social services. The mission of ASPR is to save lives and protect Americans from 21st century health security threats. Within ASPR, BARDA invests in the innovation, advanced research and development, acquisition, and manufacturing of medical countermeasures vaccines, drugs, therapeutics, diagnostic tools, and non-pharmaceutical products needed to combat health security threats. To date, BARDA-supported products have achieved 59 FDA approvals, licensures or clearances. For more on BARDAs portfolio for COVID-19 diagnostics, vaccines and treatments and about partnering with BARDA, visit medicalcountermeasures.gov. To learn more about coronavirus, visit cdc.gov/coronavirus.
###
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Merck says a trial shows it has produced the first effective antiviral pill for Covid. [View all]
BumRushDaShow
Oct 2021
OP
I wonder also, if this will lead to "spin-off" drugs/therapies/treatments...
NurseJackie
Oct 2021
#3
Why would they spend money to make a drug for a disease for which the whole "disease"
3Hotdogs
Oct 2021
#4
Thank for the information. Think this new age of misinformation mandates a Ministry of Information.
Alexander Of Assyria
Oct 2021
#6
It is good news, but people still need to get the vaccine. It cuts deaths by half, so preventive
JohnSJ
Oct 2021
#7
In Memoriam: For the 8 who died from getting the placebo instead of the real thing
Submariner
Oct 2021
#11
You realize in clinical trials the patients are fully informed if they choose to take part
JohnSJ
Oct 2021
#36
That's a really small sample size- most drug trials are in the 10's of thousands. Nt
Fiendish Thingy
Oct 2021
#23
Every time I see news like this, I check out what the RWNJ have to say about it
MissMillie
Oct 2021
#26
Do as Canada will do by end of this month...Vaccinated? If not, no planes trains and ships for you!
Alexander Of Assyria
Oct 2021
#42
Merck says there is a chance of "genetic mutations" with molnupiravir. Get vaccinated instead.
PSPS
Oct 2021
#45