Search This Blog

Thursday, September 7, 2023

ChatGPT traffic slips again for third month in a row

 OpenAI's ChatGPT, the wildly popular artificial intelligence chatbot launched in November, saw monthly website visits decline for the third month in a row in August, though there are signs the decline is coming to an end, according to analytics firm Similarweb.

Worldwide desktop and mobile website visits to the ChatGPT website decreased by 3.2% to 1.43 billion in August, following approximately 10% drops from each of the previous two months. The amount of time visitors spent on the website has also been declining monthly since March, from an average of 8.7 minutes on site to 7 minutes on site in August.

But August worldwide unique visitors ticked up to 180.5 million users from 180 million.

School coming back into session in September may help ChatGPT's traffic and usage, and some schools have begun to embrace it. U.S. ChatGPT traffic in August rose slightly, in concert with American schools being back in session.

"Students seeking homework help appears to be part of the story: the percentage of younger users of the website dropped over the summer and is now starting to bounce back," said David F. Carr of Similarweb, who regularly tracks ChatGPT and its competitors.

ChatGPT set off a frenzied use of generative AI in daily tasks from editing to coding and reached 100 million monthly active users in January, two months after its launch. Generative AI technology uses past data to create new content, for instance to write essays or poems.

Before Meta’s Threads launch, it was the fastest-growing consumer application ever, and is now one of the top 30 websites in the world.

A few ChatGPT competitors, including Google's Bard chatbot, have been launched this year. Microsoft's search engine Bing also provides a chatbot powered by OpenAI for free.

OpenAI also released the ChatGPT app on the iOS system in May, which could sap some traffic from its website. ​ChatGPT is free to use but also provides a premium subscription for $20 a month.

Besides ChatGPT, OpenAI makes money by selling access to its AI models for developers and enterprises directly and through a partnership with Microsoft, which invested over $10 billion into the company.

https://finance.yahoo.com/news/exclusive-chatgpt-traffic-slips-again-183037303.html

News Corp in negotiations with AI companies over content usage - CEO

 News Corp is engaged in "various negotiations" with artificial intelligence companies over their use of its content, the company's chief executive said at an investor conference Thursday, adding it does not plan to pursue legal action against them at this stage.

"What you will see over time is a lot of litigation; some media companies have already begun those discussions," said News Corp Chief Executive Robert Thomson, speaking at the Goldman Sachs Communacopia + Technology Conference.

"Personally, we're not interested in that at this stage. We're much more interested in negotiation."

Publishers such as News Corp, which owns the Sunday Times and Wall Street Journal among other publications, are raising concerns about being compensated for content used to train Google’s generative AI chatbot Bard, as well as ChatGPT.

Launched by OpenAI in November, ChatGPT has become the world's fastest growing app to date, and its emergence has prompted the release of rivals such as Bard.

It's unclear whether more publishers will ultimately strike deals with the tech companies or pursue litigation related to the use of that content. The Associated Press struck a deal in July, licensing a part its archive of news stories to ChatGPT-owner OpenAI.

https://finance.yahoo.com/news/news-corp-negotiations-ai-companies-162807887.html

Cabaletta: Recent ratings, holder changes

 According to a recent report by Bloomberg, Cabaletta Bio, Inc. (NASDAQ:CABA) has received an average rating of “Buy” from seven research firms that are currently covering the company. These research analysts have unanimously given the stock a buy recommendation. Additionally, the average one-year price objective among brokers who have covered the stock in the past year is $17.88.

On Wednesday, Cabaletta Bio’s stock opened at $13.83. The company has a 50-day moving average of $12.95 and a 200-day moving average of $10.94. With a market capitalization of $550.57 million, Cabaletta Bio operates with a price-to-earnings ratio of -7.99 and a beta of 2.55. Its one-year low stands at $0.59, while its one-year high reaches $16.04.

In terms of shareholder activity, several institutional investors and hedge funds have recently made adjustments to their holdings in Cabaletta Bio (NASDAQ:CABA). Ameritas Investment Partners Inc., for example, acquired a new position in the company during Q2 with an estimated value of $27,000. UBS Group AG also obtained a new position in Q3 valued at approximately $33,000.

Barclays PLC increased its stake in shares of Cabaletta Bio by 239.6% during Q4 and now owns 4,146 shares worth $38,000 after acquiring an additional 2,925 shares during that period. Furthermore, Dynamic Technology Lab Private Ltd raised its holdings by 81.6% during Q1 to reach 19,250 shares valued at $39,000 after obtaining an additional 8,648 shares.

Lastly, Freedom Wealth Alliance LLC recently acquired a new stake in Cabaletta Bio during Q4 worth around $41,000.

https://beststocks.com/cabaletta-bio-receives-buy-rating-from-research-an/

NYC to stick with no-bid, $432M migrant contract, nixing comptroller's concerns

 Mayor Eric Adams said the city will continue with the award of a $432 million, no-bid contract to house and care for migrants across the state despite concerns raised by the city comptroller that the chosen company is ill-suited for the work.

“We're going to move forward with it,” Adams said of the contract awarded to DocGo, a medical services provider, during an unrelated press conference on Wednesday afternoon. “We can't change the rules in the middle of the game.”

In a letter returning the contract to the city department of Housing Preservation and Development, Comptroller Brad Lander said the agency provided “little evidence” to show that DocGo had sufficient experience or know-how to perform the contract.

“It is a medical services company, not a logistics company, social services provider or legal service provider,” Lander wrote. “Numerous reports of staff mistreating or misleading asylum-seekers, failing to properly respond to reported assault incidents, and inadequate service provision further exacerbate these concerns.”

Adams dismissed Lander's concerns. DocGo is already performing services under the agreement, including setting up migrant shelters in upstate hotels.

“I think the comptroller probably saw an opportunity to just get in the conversation,” Adams said.


Abigail Rush, a DocGo spokesperson, released a statement from the company on Thursday defending the company's work and disputing Lander's claims.

“DocGo, one of the nation's largest logistics companies in the mobile healthcare space, has been successfully providing critical services to asylum seekers ... for more than four months," the statement said. "We have thousands of asylum seekers currently in our care who rely on funding from the City for this program to receive case management, social work, food and housing. DocGo’s quick action to step up in the face of this crisis has been critical in helping the City meet the needs of the asylum seekers in our care."
Since 2015, according to the statement, DocGo has delivered services in over 7.5 million patient interactions. It has provided "social work services for underserved populations here in NYC for over two years, and have been working with NYC to provide services for asylees since this crisis began a year ago. We will continue to work with our partners at NYC to ensure that asylum seekers continue to receive these vital services.”

Last year, the comptroller granted the city the emergency authority to fast track contracts to house and care for the newly arrived migrants, thereby bypassing the normal approval process. City Hall said the comptroller’s further approval of the DocGo contract isn’t necessary, citing city charter rules on emergency procurement.

Lander also said HPD didn’t provide enough details to justify the price tag. He urged the city agency to reconsider hiring DocGo, but acknowledged in an interview that Adams could choose to “force the contract forward despite and over our concerns.”

"What I sincerely hope they do is answer the very reasonable questions and concerns," Lander later added.

HPD touted its own track record and DocGo's in a thread on X, formerly known as Twitter, beginning with "let's set the record straight."


The agency and company have "moved quickly" to care for the migrants, at times establishing emergency shelters with under 12 hours notice, the initial post said.

"The majority of the funds in the HPD contract with DocGo goes directly to local, community organizations to provide housing, meals, security and other needed services," the agency continued in a follow-up post.

Notwithstanding Lander's concerns, DocGo said in the statement, "we have received assurance from the mayor's office that NYC intends to fully pay DocGo for the services delivered under this contract, both historically and going forward."

New York Attorney General Letitia James has launched an investigation into allegations about DocGo deceiving and threatening migrants, following a New York Times report. A New York Department of State investigation found over 50 security guards hired by DocGo’s subcontractors lacked proper authorization.


https://gothamist.com/news/nyc-comptroller-rejects-432-million-migrant-contract-to-docgo

New drugs preserve vision but Florida leads US in eye degeneration disease

 Doctors told Gary Cartwright in 2002 that the vision in his left eye was deteriorating. Faces will start to blur, they said, and he could end up legally blind.

The problem was age-related macular degeneration, the result of wear-and-tear damage to the macula — the part of the eye that controls sharp, straight-ahead vision. The condition affects one in 10 Americans aged 50 and up and is one of the leading causes of irreversible blindness and visual impairment across the world.

The doctor who confirmed the diagnosis told Cartwright there was no treatment. Feeling distraught on the drive back home, he turned on the car radio and heard an advertisement for a medical trial. A deacon at the Holy Innocents’ Episcopal Church in Valrico, Cartwright thinks of it as a God moment.

The experimental drug, which was eventually approved by the Food and Drug Administration, required monthly injections in his eyeball. Two decades later, Cartwright, who now has the disease in both eyes, still has good vision.

But even with effective drugs, age-related macular degeneration remains a concern in Florida, which has the highest rate of the disease in the nation. Among the state’s over 40 population, 18.3% have some form of the disease, according to data from the Vision & Eye Health Surveillance System run by the Centers for Disease Control and Prevention.

Part of that is the consequence of Florida’s higher than average elderly population. But smoking and genetics are also risk factors for the disease that affects Caucasians more than minorities, said Jonathan Hu, an assistant professor in the University of Florida’s Department of Ophthalmology.

“The prevalence is getting higher because we live so much longer,” Hu said. “It’s not a disease we see in people in their 20′s and 30′s.”

Hu treats patients with the condition every day at the University of Florida’s eye clinic. Symptoms include blurry or wavy lines and blind spots in the center of a person’s vision. But early onset has few symptoms, which makes regular eye exams critical for detection, Hu said.

The most common form of the condition is known as dry macular degeneration. It is caused by cell deposits under the retina that can cut off oxygen and cause thinning of the macula. The condition tends to develop over several years.

In February, the Food and Drug Administration approved the use of SYFOVRE, the first medication for the dry form of the disease. A second medication has since also been approved.

About 20% of those with the condition progress toward the more serious wet macular degeneration, where abnormal blood vessels form in the eye and leak proteins and lipids. It can lead to vision impairment quickly if not treated.

Deacon Gary Cartwright helps conduct a church service at Holy Innocents’ Episcopal Church in Valrico. Cartwright suffers from age-related macular degeneration, or AMD. He receives quarterly injections into his eyeballs and without the treatment is at risk of ending up blind.
Deacon Gary Cartwright helps conduct a church service at Holy Innocents’ Episcopal Church in Valrico. Cartwright suffers from age-related macular degeneration, or AMD. He receives quarterly injections into his eyeballs and without the treatment is at risk of ending up blind. [ JEFFEREE WOO | Times ]
The drug trial that Cartwright participated in was for a medication that prevents the growth of those abnormal blood vessels. Administered through an injection directly into the eyeball, it improves vision in about one-third of patients, according to the American Academy of Ophthalmology.

Cartwright had monthly injections until about three years ago when he switched to VABYSMO, a medication produced by Genentech. He now only needs injections every three to four months, said retina specialist Ivan Suñer, who treats Cartwright at Retina Associates of Florida clinic.

The development of medications has revolutionized treatment, Suñer said. With increased education on the need for eye exams and early diagnosis, there is now a much higher chance of preserving a patient’s eyesight. Even when patients are not diagnosed until the disease has progressed, it can still be arrested, Suñer said.

“For these patients, most require lifelong therapy, he said. “It’s like when you have weeds in your front lawn. Think of these medications as weed killer.”

But education is still a concern, he said. More than 40% of U.S. adults said they had not had an eye exam in the previous two years, a 2017 survey by the Office of Disease Prevention and Health Promotion found.

Maintaining his eyesight has meant Cartwright, although retired, can still participate as a deacon at his church. His eyesight, roughly 20/30 means he can still drive legally and share the load when he and his wife make a road trip to visit their two sons in Atlanta or their daughter in Arkansas.

“Without that drug my life would have been very restricted,” he said..

He’s also had members of his congregation approach him with their vision problems. He encourages them to seek treatment.

“People get scared of a doctor making an injection in the eye,” he said. “It sounds scary but they first give you three numbing drops – I’ve never had any pain at all.”

https://www.tampabay.com/news/health/2023/09/06/new-drugs-preserve-vision-florida-leads-us-eye-degeneration-disease/

US quietly terminates a controversial $125m wildlife virus hunting program amid safety fears

 Two years after launching what officials hailed as a five year flagship project for hunting viruses among wildlife to prevent human pandemics, the US Agency for International Development is shuttering the enterprise. 

A flagship project for the controversial practice of hunting viruses among wildlife in South East Asia, Africa, and Latin America to prevent human outbreaks and pandemics is being quietly dropped by the United States Agency for International Development (USAID) after private and bipartisan criticism over the safety of such research, The BMJ has found.

For more than a decade the US government has been funding international projects engaged in identifying exotic wildlife viruses that might someday infect humans. Although critics have raised concerns over the potentially catastrophic risks of such virus hunting activities,1 hundreds of millions of dollars in unabated funding have symbolised a commitment to the effort.

The shuttering of the project, as described in a new congressional budget document and during interviews with scientists and federal policy makers, marks an abrupt retreat by the US government from wildlife virus hunting, an activity that has also been funded by the Department of Defense and the National Institutes of Health. The turnabout follows early warnings raised by sceptics—including officials in the Biden White House—that the $125m (£99m; €115m) “DEEP VZN” programme could inadvertently ignite a pandemic. The misgivings continue to resonate, as the cause of the SARS-CoV-2 pandemic, the world’s deadliest such event in a century, remains unproved.

When USAID, an arm of the US State Department, launched DEEP VZN (pronounced “deep vision”) in October 2021, the agency promoted it as “a critical next step . . . to understand and address the risks posed by zoonotic diseases that can be transmitted from animals to humans.”2 Short for “Discovery & Exploration of Emerging Pathogens—Viral Zoonoses,” DEEP VZN succeeded an earlier USAID programme called PREDICT and aimed to find previously unknown pathogens from three viral families: coronaviruses; filoviruses, such as Ebola; and paramyxoviruses, including Nipah virus. The aim was to help the world “be better prepared to detect, prevent and respond to future biological threats.”2

Officials at Washington State University, hired by USAID to help administer DEEP VZN, said in a submission to the agency that the university’s goal was to collect around 480 000 samples from wildlife, seeking out “previously unknown” viruses to “identify a subset that pose a significant pandemic threat.” The university said that the project aimed to “detect and characterize” as many as 12 000 novel viruses over the programme’s five years.3 Beginning in July of this year, however, officials at USAID quietly informed aides to Democratic and Republican members of two Senate committees with jurisdiction over DEEP VZN that it was being shut down. Apart from the Biden White House officials, several Republican senators had questioned the prudence of DEEP VZN, according to Senate letters and the interviews conducted for this article.

The previously unpublicised decision by USAID to terminate DEEP VZN comes amid heightened concerns over the many risks of working with exotic viruses—including unresolved questions about whether a research mishap or a naturally occurring spillover of virus from an animal species to humans caused the SARS-CoV-2 pandemic.4 In China, where a separate effort to catalogue viruses has been under way for years, scientists have described being bitten or scratched by bats or having bat urine or blood splashed into their eyes and faces.567

The closure of DEEP VZN was privately relayed to the Senate aides by the office of Atul Gawande, USAID’s assistant administrator for global health, said officials familiar with the matter. Gawande, an appointee of President Biden, was a general and endocrine surgeon and bestselling author before joining the administration in January 2022.

Weighing risks against potential benefits

The demise of DEEP VZN, despite its backing from proponents at USAID and the project’s grantees, validates the concerns of sceptics, including the handful of Biden White House officials who challenged the project.

In December 2021 two senior White House officials specialising in biosecurity and biosafety—Jason Matheny, deputy assistant to Biden for technology and national security, and Daniel Gastfriend, the National Security Council’s director for biodefence and pandemic preparedness—first privately shared their views with USAID’s administrator, Samantha Power, and advised her to shut down DEEP VZN. Those familiar with the matter said that another White House official, T Gregory McKelvey Jr, a physician and the assistant director for biosecurity with the Office of Science and Technology Policy, also privately raised concerns with USAID staff.

The White House officials’ remarks to Power in late 2021 and other details surrounding DEEP VZN were first reported by the Washington Post on 10 April this year.5 Power, a presidential appointee and Harvard trained lawyer, eventually told Matheny and Gastfriend that she would initiate a review of the project to ensure that DEEP VZN could be conducted in a way that adequately managed the risks, according to those with knowledge of the conversation. In March and November 2022 USAID directed its grantees to avoid collecting samples of viruses until safety protocols were reviewed anew. However, federal records state that through spring of this year USAID continued to fund the research while its project administrators lined up additional laboratories, technicians, and other support staff necessary to manage the expected volume of genetic samples.

The ultimate decision to terminate DEEP VZN reflected the Biden administration’s commitment to weigh more rigorously the risks and the potential benefits of research projects, according to interviews with present and former White House officials. They pointed to a policy recommendation issued in March by the National Science Advisory Board for Biosecurity, calling for such work to be approved only if “there are no feasible alternative methods of obtaining the relevant benefits from proposed research that pose less risk,” and after “unnecessary risks have been eliminated and the remaining risks are justified by the potential benefits.”8

In response to written questions, a USAID spokesperson confirmed on Wednesday 6 September that the agency has decided to close down DEEP VZN.

“USAID has determined that investments that focus on the search for and characterization of unknown viruses prior to spillover into humans are not an Agency global health security priority at this time. As a result, we will cease funding projects with this specific objective,” said the agency’s prepared statement.

Asked to what extent USAID leadership’s decision to shutter DEEP VZN hinged on concerns over its risks, the agency said that the decision reflected “the relative risks and impact of our programming.”

Instead of collecting viruses circulating exclusively among wildlife, USAID said that “the change in Agency priorities” would emphasise actions aimed at improving global “laboratory capacity, disease surveillance, human resources, biosafety and biosecurity, and risk communication and community engagement.” The agency said that it had informed Washington State University and other stakeholders beginning in July of USAID’s decision “to end the DEEP VZN” project.

Power did not respond to a request for her rationale with DEEP VZN. Gawande was described by an aide, Enam Hussain, as unavailable to speak on the record.

Matheny, who left the White House in mid-2022 to become president and chief executive officer of the RAND Corporation, told The BMJ he believed that USAID’s about-face with DEEP VZN stemmed from the newfound media scrutiny and serious safety considerations.

“It seems likely that the agency assessed that the risks exceeded the benefits of the programme,” said Matheny, noting that jettisoning DEEP VZN cut against USAID’s backing of such research, which has spanned three presidential administrations and surpassed $300m in funding. “USAID has consistently seen this viral discovery work as ‘part of our mission.’”

Although the agency has backed wildlife virus hunting since 2009, its historical and chief focus has been to mitigate suffering from disease, famine, and other natural disasters in resource challenged regions.

DEEP VZN’s grantees have included Washington State University, the University of Washington, Washington University in St Louis, PATH (formerly the Program for Appropriate Technology in Health), and FHI 360, a contractor based in Durham, North Carolina.9 On 1 October 2021 USAID awarded Washington State University $124.7m to provide overall support for DEEP VZN. The University of Washington was retained as a sub-grantee and was intended to provide expertise from five of its labs to build “capacity in other countries to be able to find new viruses and characterize them,” according to a university issued news item.10 In July 2022 USAID awarded an additional $1.1m to FHI 360, whose representative was installed as a project leader to help provide “expert technical guidance,” programme documents show.

Matheny and Gastfriend had first contacted Power at USAID on learning that Kevin Esvelt, a prominent Massachusetts Institute of Technology biotechnologist, was about to warn in public testimony to the House Foreign Affairs Committee on 8 December 2021 that pursuing novel, animal transmitted viruses could be exploited by terrorists and lead to a pandemic. That same day, coincidentally, the director of the White House Office of Science and Technology Policy, Eric S Lander, publicly discounted the benefits of wildlife virus hunting—a position at stark odds with the long running advocacy for such work from USAID, the Department of Defense, and leaders of the National Institutes of Health. Appearing before the privately funded Bipartisan Commission on Biodefense, Lander, appointed by Biden, was asked by the former Senate majority leader Tom Daschle, a Democrat, whether pandemics could be predicted or prevented.

“OK, I may get myself in trouble,” replied Lander, an expert on sequencing and interpreting the human genome. “I’m just not an optimist on the question, because nature is vast. There are viruses that can jump species—and we do not know how to take a virus from the animal kingdom and recognise when it is ready to jump species.”11

Research with a history of controversy

Well before the SARS-CoV-2 pandemic, other sceptics of wildlife virus hunting had dismissed such projects as unlikely to deliver lifesaving medicines or prevent pandemics. Writing for the journal Nature in June 2018, the biologists Edward Holmes, Andrew Rambaut, and Kristian Andersen said, “Making promises about disease prevention and control that cannot be kept will only further undermine trust.” They described assumptions that such virus hunting projects could succeed as “misguided” and “arrogant.”12

In the wake of the SARS-CoV-2 pandemic others have raised additional concerns, saying that the risks of collecting animal-to-animal transmitted viruses should not be dismissed lightly. Such research typically entails collecting biological specimens—such as excrement, blood, or saliva from bats dwelling in caves or tree groves—followed by shipments of the samples to one or more labs for analysis. A mishap at any stage of the work would, some experts warn,4 invite the risk of an outbreak or a pandemic (see box).


Unresolved questions over SARS-CoV-2’s origins

Concerns over the risks of research with exotic viruses have increased after revelations about the supervision of National Institutes of Health (NIH) funded lab experiments with genetic material harvested in the field from bats.13

In autumn 2021, responding to questions raised by some Republicans in Congress, Lawrence Tabak, then top deputy to the NIH director, described an inappropriate delay in tackling what he said had been unexpected results from experiments conducted on behalf of a grantee, EcoHealth Alliance. The efforts, carried out in China by a sub-grantee, the Wuhan Institute of Virology, involved work with several coronavirus strains derived from bats.14

The project, Understanding the Risk of Bat Coronavirus Emergence, had been approved after NIH grant administrators’ internal determination that it would not entail “gain of function” research—namely, work that would increase a pathogen’s transmissibility or lethality.

As a safeguard NIH had required EcoHealth, based in New York City, to “immediately stop all experiments with these viruses” and to promptly notify the agency if significant viral growth was observed in mice infected in the lab. In the grant terms specified by NIH, “no funds can be used to support gain-of-function research.”

But Tabak stated in letters on 10 October 2021 to several House Republicans that the work in Wuhan funded by NIH proceeded even though the evidence suggested that increased viral growth was recorded.14

“EcoHealth failed to report this finding right away, as was required by the terms of the grant,” wrote Tabak, then NIH’s principal deputy director. According to Tabak, the results in Wuhan remained unknown to NIH for about two years, until August 2021.15 (EcoHealth’s president, Peter Daszak, in written remarks to a government inspector general, disputed that his company had been required to immediately notify NIH of the concerns that the agency later identified, but he said that the company had “corrected certain procedures.”13)

As for what might have caused the pandemic, Tabak noted that the coronaviruses used during the NIH funded lab work were genetically divergent from SARS-CoV-2.16 US intelligence agencies, acting in response to requests from President Biden, have concluded that the pandemic was most likely caused by either an animal-to-human spillover or a research related mishap.16

Scrutiny had been building behind the scenes

In May of this year three leaders of the Republican controlled House Energy and Commerce Committee asked the Government Accountability Office to open a scientific audit to “assess the benefits and risks of conducting predictive field research programs for viruses.”17

The members cited research funded over the past decade by both USAID and the National Institute of Allergy and Infectious Diseases, an arm of NIH. Although such research, including USAID’S PREDICT programme (DEEP VZN’s predecessor), had “identified thousands of new viruses,” wrote the House members, “some researchers have questioned whether collecting and characterizing viruses found in animals can accurately predict those that may infect humans, or what the effect would be if and when humans are subsequently infected.”

Their letter continued, “Others have suggested these types of programs risk unintentional infection of field or laboratory workers that could result in an accidental outbreak.”

As part of the Government Accountability Office’s newly begun audit, its senior biological scientist, Michael Dickens, wrote a 22 July email to Thiravat Hemachudha, a former PREDICT programme leader in Bangkok, Thailand. In the email, obtained by The BMJ, Dickens noted the April report by the Washington Post, which revealed that Thiravat had decided to reject further US government funding for such research after coming to view it as unacceptably dangerous and because of the uncertain origin of the SARS-CoV-2 pandemic.5 Thiravat’s US funding had flowed from both the PREDICT programme and the Pentagon. He remains an advocate for surveillance of viruses that have emerged in humans.

The Government Accountability Office’s acting chief scientist, Karen Howard, estimated in an email to The BMJ that the audit would likely be completed during spring 2024; she declined to discuss any preliminary findings.

Meanwhile, interviews and documents show that USAID’s funding of the DEEP VZN programme has continued to draw scrutiny behind the scenes from members and staff at both the Senate foreign relations committee and the Senate appropriations committee. Beginning with a letter they wrote privately to USAID’s Power on 23 November 2021, the questions were spearheaded by the Republican senators Lindsey Graham of South Carolina, a member of the appropriations committee, and James Risch of Idaho, who serves on foreign relations.

“We are particularly concerned about . . . ‘DEEP VZN,’ aimed at discovering and studying unknown viruses in areas where there is high risk of animal to human spillover,” the senators wrote at that time. “Given all of the outstanding questions surrounding the origins of the covid-19 pandemic, it is critically important that this initiative be adequately vetted.”

Gawande, USAID’s assistant administrator, eventually responded. In an 11 page letter on 18 July 2022 he detailed planned, specific steps, including regularly scheduled visits to field sites and in-country partner labs, to confront the risks.

Power, in another letter conveyed privately to the senators dated 24 April 2023, further described the safeguards envisioned for DEEP VZN. But in a response to her on 16 May, Risch appeared unassuaged.

He wrote, “I remain deeply concerned that USAID does not yet exercise the level of oversight and control over its prime and sub-prime implementing partners that life sciences research . . . surely requires. Even if that level of control could be attained over the coming days, weeks, months, or years—which is highly unlikely—I remain unconvinced that hunting novel viruses would or should ever fall within the core competency of [USAID].”

The exchanges between the Senate and USAID culminated with a brief mention of the previously unreported termination of DEEP VZN in the State Department’s appropriation for the fiscal year 2024, dated 20 July of this year, stating, “The Committee notes the decision by USAID to cease funding for the exploration of unknown pathogens.”18