Bayh-Dole Coalition Honors Emory Professor Behind Groundbreaking HIV and Covid-19 Treatments

ATLANTA, GA (August 21, 2023) —  Emory University Professor  Dennis Liotta  has been featured in the Bayh-Dole Coalition’s new  “Faces of American Innovation” report  for developing chemical compounds used in life-saving medicines.

The  Bayh-Dole Coalition  is a diverse group of innovation-oriented organizations and individuals committed to celebrating and protecting the Bayh-Dole Act, as well as informing policymakers and the public of its many benefits.

On September 13, Dr. Liotta and four other leading innovators will receive the inaugural Bayh-Dole Coalition American Innovator Award in Washington, D.C.

“This is a wonderful honor, and I am humbled to receive it,” said Dr. Liotta. “Although I had no prior experience in drug discovery and development, at age forty I made the fateful decision to radically change the focus of my research and began what became a three-decade pursuit of the discovery of new drugs to address unmet medical needs. Against all odds, I was successful!”

Dennis Liotta headshot

Dennis Liotta, PhD / Photo: Stephen Nowland

Dr. Liotta discovered  two chemical compounds  capable of stopping HIV replication. [1]  Emory later patented the molecules and licensed them to a drug company for further development. [2]  By 2003, the FDA had approved both of Dr. Liotta’s novel compounds to treat HIV. Dr. Liotta’s lab also invented  molnupiravir, which treats Covid-19. [3]

Dr. Deborah W. Bruner, Senior Vice President for Research at Emory University, commented, “Dr. Liotta has been at the forefront of bringing new research discoveries to market for over thirty years. His work bringing his  discovery of Emtricitabine  (in partnership with his two co-inventors) to market has provided a road map for other Emory researchers. He has blazed a trail for faculty and students to gain a deep understanding of pathways to engage with the entrepreneurial side of their research, and to fulfill our mission of doing good in the world by turning research into tangible benefits for humanity. As one of the top researchers of HIV antiretrovirals in the world, he is immensely deserving of this recognition.”

The Bayh-Dole Act was instrumental in bringing Dr. Liotta and his team’s technologies to the marketplace, said Joseph P. Allen, executive director of the Bayh-Dole Coalition.

“Without laws permitting universities to patent and license scientific discoveries made with the help of federal research funding, Dr. Liotta’s compounds may never have exited the lab and millions of people living with HIV/AIDS would not have healthy, productive lives today,” said Allen. “Thanks to the Bayh-Dole Act, private sector companies have a strong incentive to turn promising early-stage research into innovative therapies that save lives.”

“We’re thrilled for Dr. Liotta and this recognition,” said Todd Sherer, PhD, Associate Vice President for Research and Executive Director of  Emory University Office of Technology Transfer. “Dennis’ work has directly impacted millions of lives, as most Americans who have HIV – and many around the world – take at least one of the antiretroviral drugs invented at Emory.”

Pill Bottle

Emtriva, an HIV antiretroviral developed at Emory University by Drs. Dennis Liotta, Raymond Schinazi, and Woo-Baeg Choi.

Regarding his career, Dr. Liotta remarked, “Drug discovery is a team sport that requires synergistic interactions amongst multiple individuals with complementary skills. I have been fortunate to have many amazing co-workers and collaborators who have shared this journey with me. In particular, I want to acknowledge the important contributions of my friends and colleagues, Drs. Woo-Baeg Choi, Raymond Schinazi and George Painter.”

Emory signed a total of 10 exclusive and start-up patent licensing agreements in FY2022 alone, according to the Emory Office of Technology Transfer. [4]  In the same year, the U.S. Patent and Trademark Office issued 45 patents to Emory inventors, including jointly held patents. [5]  Over half of Emory-associated start-ups are working to discover new medicines. [6]  More than 60 life-changing products, from novel diagnostics to virtual reality solutions, have reached the market so far. [7]

###

October 5, 2026
Georgia Life Sciences has submitted written comments to the Georgia House Study Committee on Pharmacy Benefits Managers and Consumers’ Access to Prescription Medications, encouraging greater transparency, accountability, and a focus on measurable patient benefit across the prescription drug system. The comments address both pharmacy benefit manager practices and the federal 340B Drug Pricing Program, emphasizing the importance of understanding where prescription drug savings accrue and whether those savings ultimately benefit patients. The Study Committee continues its work this fall as it develops recommendations for the Georgia General Assembly. Read Georgia Life Sciences’ full comments →
September 22, 2026
Georgia Life Sciences (GLS) has joined more than 80 organizations from across industry, academia, public health and the biosecurity community in calling on congressional leaders to fully reauthorize the Pandemic and All-Hazards Preparedness Act (PAHPA) before the end of 2026. Led by the Johns Hopkins Center for Health Security, the coalition urged congressional leaders to advance a comprehensive reauthorization of PAHPA, the federal framework that supports the nation’s ability to prepare for and respond to public health emergencies and other health security threats. First enacted in 2006, PAHPA established and strengthened critical components of the nation’s health security infrastructure, including the Biomedical Advanced Research and Development Authority (BARDA). The law also supports public-private partnerships involved in the research, development, manufacturing and procurement of medical countermeasures, including vaccines, therapeutics and diagnostics. PAHPA’s authorization expired in 2023 and key provisions have since continued through short-term extensions. The coalition is calling for a comprehensive reauthorization that provides greater stability and ensures the nation’s preparedness infrastructure can continue adapting to emerging biological, infectious disease and other health security threats. For the life sciences industry, these programs are particularly important. Partnerships between government and industry can help move promising technologies from research through development and manufacturing while maintaining capabilities needed to respond quickly during an emergency. The Biotechnology Innovation Organization (BIO), also a signatory to the letter, has identified several priorities for reauthorization, including continued authorization of BARDA, the Strategic National Stockpile, Project BioShield and the Pandemic Influenza Program, as well as incentives supporting the development of medical countermeasures. Georgia Life Sciences is proud to join organizations across the country in supporting a strong and sustainable national framework for health security, preparedness and biomedical innovation. Read the coalition letter and view the full list of signatories.
September 14, 2026
Georgia Life Sciences has submitted comments to the Georgia Department of Community Health (DCH) regarding the Georgia Pathways to Coverage program and implementation of new federal Medicaid requirements. As Georgia prepares for these changes, Georgia Life Sciences is urging state leaders to prioritize continuity of care and minimize unnecessary administrative barriers that could delay or disrupt access to medically necessary treatment . This is particularly important for Georgians living with serious, chronic, rare, and medically complex conditions who may rely on ongoing medications, diagnostics, therapies, medical technologies, specialty care, and coordinated treatment plans. Even temporary disruptions in coverage can interrupt care and create additional challenges for patients and families. In its comments, Georgia Life Sciences encouraged DCH to protect continuity of coverage during eligibility and redetermination processes, provide patients and caregivers with clear and timely information, minimize unnecessary administrative burdens, and establish appropriate safeguards when a coverage disruption could interrupt an established course of treatment. “As Georgia implements these new federal requirements, we want to ensure that patients remain at the center of the process,” said Maria Thacker Goethe, MPH, President & CEO of Georgia Life Sciences. “Administrative changes should not become barriers between patients and the care they need. Protecting continuity of care is particularly important for Georgians managing serious and complex health conditions.” Read Georgia Life Sciences’ full comments to DCH here.
MORE POSTS