While it’s all hands on deck in the COVID-19 battle, we want to continue to raise awareness about the other diseases that continue to affect millions of Americans. So, today, we want to recognize Hepatitis Awareness Month and the biotech industry’s good work to combat—and yes, even cure—this virus, too.
Millions of Americans of all walks of life are living with viral hepatitis—which can cause chronic pain and discomfort as well as serious complications like cirrhosis, liver cancer, and liver failure.
But thanks to biotech innovations, many cases of hepatitis are treatable and even preventable. There are safe, effective vaccines for hepatitis A and B and treatments for hepatitis C, as the CDC explains.
In fact, next-generation hepatitis C drugs have cure rates of 90% and higher—including Gilead’s Sovaldi, which has kept many patients from progressing to liver failure, and Harvoni, which likewise reduces the risk of liver cancer and transplants.
Why it matters right now: While we’re still learning more about the coronavirus and how it affects us, we do know that people with underlying medical conditions are at greater risk of the most serious COVID-19 complications. This is why, as we continue our R&D on COVID-19 vaccines and therapeutics as quickly as possible, it’s equally important that the industry is able to continue to invest in cures for other diseases, too, now and in the future.
Andrew Adds: Hepatitis Awareness Month is an important reminder that researchers and scientists can beat the world’s most deadly and debilitating diseases—like they did with hepatitis C. If anyone can solve the COVID-19 crisis, it’s America’s resilient biotech industry, which continues to discover innovations that are beyond our imagination. – Andrew Segerman, BIO's Director of Health Communications
Learn more about Hepatitis Awareness Month.
More Health Care News:
CNBC: Moderna’s experimental coronavirus vaccine gets FDA’s ‘fast track’ status
“A vaccine or treatment that gets the ‘fast track’ designation is eligible for the agency’s ‘priority review’ status, under which the FDA aims to take a decision on approving the drug within six months.”
Regulatory Focus: FDA issues two guidances to accelerate COVID-19 treatments
“The first of the two guidances focuses on walking drugmakers through the pre-IND process to provide them with feedback and help them get their products into clinical trials in a quick and efficient manner…In the second guidance, FDA provides recommendations for clinical trial design for Phase 2 and 3 clinical trials intended to establish safety and efficacy for therapeutic or prophylactic drugs and biologics for COVID-19.”
STAT: Deluge of genome editing therapies end research drought for sickle cell disease
The “intense activity” on sickle cell disease is a “dramatic turnaround.”