“CNBC CURES: DEFYING RARE DISEASE” WITH BECKY QUICK TO PREMIERE ON THURSDAY, MARCH 19 AT 7PM ET
🎬 CNBC will debut a one-hour special titled "CNBC Cures: Defying Rare Disease" on Thursday, March 19 at 7PM ET.
👩💻 The program is hosted by Becky Quick, who shares her family's personal battle with her daughter's rare disease.
🧬 The special spotlights families affected by rare diseases and the innovators working to improve their futures.
💊 It highlights the gap between scientific advances and the ongoing issues of funding, access, and support for patients.
🗣️ Guests include GeneDx CEO Katherine Stueland, n-Lorem Founder Dr. Stanley Crooke, former FDA Commissioner Dr. Scott Gottlieb, and Biotechnology Innovation Organization President John Crowley.
🏥 Interviews also feature executives from Charles River Laboratories, Cure Rare Disease, physicians from the Children's Hospital of Philadelphia, and "Beast Games" winner Jeffrey Allen.
📺 CNBC is a global leader in business and financial news reaching half a billion people monthly across platforms.
💻 The network offers content through live TV, digital destinations like CNBC.com, and subscription services including CNBC+ and CNBC Pro.
📱 Audiences can access premium content via live events, podcasts, newsletters, and social media channels.
📩 CNBC is seeking confidential news tips from the public regarding rare disease developments.
- The special will premiere on Thursday, March 19 at 7PM ET, providing timely coverage of rare disease innovation.
- Hosted by Becky Quick, the program features exclusive interviews with leading industry leaders including GeneDx CEO Katherine Stueland and former FDA Commissioner Dr. Scott Gottlieb.
- CNBC reaches half a billion people every month across all platforms, offering broad reach for the in-depth reporting.
- The special highlights innovators fighting to change patient futures, showcasing positive progress in scientific advances.
- Audiences can access premium content through various CNBC+ and digital destinations to stay informed on market-moving forces.
- The special reveals stark reality of patients caught between groundbreaking scientific advances and persistent gaps in funding, access, and support, highlighting unresolved systemic challenges.
- Rising capital expenditure in medical research may be outpacing available funding for rare disease treatments as noted by the stark reality described in the program.