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GHTC signed on to letters from the tuberculosis (TB) advocacy community urging Congressional appropriators to provide additional resources for US TB programs in the next COVID-19 response legislation to reduce the detrimental impact of the pandemic on these programs.

Interested in more global health innovation news? Every week GHTC scours media reports worldwide to deliver essential global health R&D news and content to your inbox. Sign-up now to receive our weekly R&D News Roundup email.On Wednesday the National Institutes of Health (NIH) launched the Rapid Acceleration of Diagnostics (RADx) initiative, a US$1.5 billion effort to develop new diagnostic technologies for COVID-19 in partnership with the US Food and Drug Administration (FDA), the US Centers for Disease Control and Prevention (CDC), and the Biomedical Advanced Research and Development Authority (BARDA). As part of RADx, NIH will host a $500 million challenge seeking promising proposals for point-of-care and at-home diagnostic tests. "We need all innovators, from the basement to the boardroom, to come together to advance diagnostic technologies, no matter where they are in development," said NIH Director Francis Collins. Finalists who are awarded funding will be paired with technical, business, and manufacturing experts to complete develop their products.The NIH National Institute of Allergy and Infectious Diseases (NIAID) and Gilead announced hopeful results from separate clinical trials of Gilead's drug remdesivir, the broad-spectrum antiviral initially developed by Gilead to treat the Ebola and Marburg viruses, against COVID-19. According to NIAID, the drug compared to a placebo reduced median time to recovery from 15 to 11 days, and results suggest the drug had a small positive effect on survival rate. These results aren’t game-changing, but in combination with results reported from a separate trial run by Gilead with similar outcomes, were enough for FDA to grant an emergency use authorization for remdesivir last Friday.The Trump Administration is reportedly planning ways to drastically accelerate the development of a SARS-CoV-2 vaccine through a program called Operation Warp Speed. The program will convene pharmaceutical companies, government agencies, and the military with the audacious goal of cutting the development timeline of a vaccine by as much as 8 months and producing 300 million vaccine doses by the end of 2020. Through Operation Warp Speed the government will absorb the cost of evaluating several vaccine candidates simultaneously, first in animal models, then in one large human master protocol trial that will evaluate several candidates concurrently. After filtering the pipeline, top candidates will enter late-stage clinical trials while the government invests in advanced construction of manufacturing facilities to ramp up mass production of the vaccines before knowing if they are safe and effective.The Jenner Institute, a nonprofit vaccine developer based at Oxford University, has leaped ahead in the race to develop a SARS-CoV-2 vaccine. According to The New York Times, the Institute, having already shown in previous trials that similar inoculations are safe, plans to enroll 6,000 people in a clinical trial by the end of next month to test the vaccine’s efficacy, putting it ahead of other vaccine trials. Pending emergency approval from regulators, the developer say they could have several million doses available by September. The technology in use has been in development at the Jenner Institute for decades in attempts to create a malaria vaccine.

GHTC joined the Global Health Council (GHC) in urging Congress to provide additional funding to support COVID-19 response efforts in low- and middle-income countries. GHC sent a letter to appropriators signed by GHTC and other partners outlining a top-line ask for global health needs. A detailed supplement shared with the letter included specific recommendations from the global health community, including those from GHTC calling for supplemental resources of US$200 million for the US Agency for International Development to advance COVID-19 innovations for low-resource settings and $200 million to support the Coalition for Epidemic Preparedness Innovations.

Interested in more global health innovation news? Every week GHTC scours media reports worldwide to deliver essential global health R&D news and content to your inbox. Sign-up now to receive our weekly R&D News Roundup email. In the largest study yet of the malaria drug hydroxychloroquine’s effect on patients with COVID-19, there was a higher rate of deaths among those being treated with hydroxychloroquine and hydroxychloroquine plus the antibiotic azithromycin than those who received standard care. The study was a retrospective analysis of treatments for 368 patients rather than a rigorous, randomized controlled trial. It’s also important to note that patients who were treated with the drug were those who were the most sick. Yet, the study raises further questions about this treatment that has been widely used during the pandemic and promoted by President Trump. Reflecting on these findings, a panel of experts from the National Institutes of Health (NIH) released new COVID-19 treatment guidelines that specifically caution against the use of hydroxychloroquine and chloroquine, with and without azithromycin, outside of clinical trials.Dr. Rick Bright has been transferred from his position as director of the Biomedical Advanced Research Authority (BARDA)—a key agency involved in developing COVID-19 medical countermeasures—for a more narrowly focused position at NIH, just as BARDA has received supplemental funding more than ten times larger than its base funding of US $562 million to support coronavirus product development. Dr. Bright is asserting he was removed from his position because he pressed for rigorous vetting of hydroxychloroquine, an anti-malaria drug that has been frequently touted by President Trump as a potential treatment for COVID-19.The US Food and Drug Administration (FDA) approved under emergency use authorization the first of its kind at-home diagnostic test for COVID-19. Developed by LabCorp, the Pixel COVID-19 test includes an at-home collection kit, which will need to be ordered by a doctor, that provides patients with a nasal swab and saline solution for self-sampling. Patients will swab their noses, then mail their samples to LabCorp testing centers where LabCorp will use real-time PCR for diagnosis.