Gilead Earnings Beat Estimates As Biotech Awaits Liver Disease Drug Ruling

The drug maker reported Q2 product sales of $6.9bn, more than analyst consensus for the quarter, and raised its full-year guidance.

• Source: Shutterstock

Gilead Sciences, Inc.’s second quarter 2024 earnings beat expectations, despite declines for some products, during a quarter in which it unveiled positive data for a long-acting drug for pre-exposure prophylaxis (PrEP) of HIV and later revealed that its chief medical officer plans to step down. Looking ahead, the company awaits an “imminent” US Food and Drug Administration ruling on a drug for primary biliary cholangitis (PBC).

The Foster City, CA-based drug maker announced its earnings on 8 August, reporting that total product sales were $6.9bn, up by 5% from the comparable period last year. Excluding the COVID-19 drug Veklury (remdesivir), total product sales were $6.7bn, up 6% from Q2 of 2023

Key Takeaways
  • Gilead reported second quarter earnings of $6.9bn, which was 6% more than in Q2 2023 and beat analyst forecasts.

  • The company saw sales increase across its HIV, oncology and liver disease franchises

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Earnings

Takeda Plans US Investment But Sees Little Impact From Tariffs

 

The Japanese drug maker is on track for three pivotal Phase III readouts and two regulatory submissions in 2025.

Q1 S&E In Brief: Tracking New Launches And Catalysts In Biopharma

 

Neurocrine, Madrigal and Vanda updated investors on new drug launches, while Cytokinetics talked to investors about an FDA extension for aficamten.

Viatris Will File ‘Fast-Acting’ Meloxicam For FDA Approval This Year

 
• By 

Seven years after acquiring it, Viatris will seek approval of a meloxicam formulation for acute pain backed by data from two Phase III studies in post-surgical pain settings.

Sarepta Slammed By Double Blow: Elevidys Sales Miss, Prasad’s CBER Appointment

 
• By 

Sarepta’s stock price was battered after Vinay Prasad was appointed to lead the US FDA’s CBER, then the company’s shares were bruised when Q1 Elevidys sales came in below consensus.

More from Business

Finance Watch: Deerfield Closes $600m-Plus VC Fund; Gates Speeds Up Health Investments

 
• By 

Private Company Edition: Deerfield’s third innovations fund will back therapeutics and other opportunities, the Gates Foundation – a sometimes funder of biotech firms – will spend $200bn over the next 20 years, and NewLimit raised a $130m series B round, among other financings.

Pharma Left Hanging After US/UK Trade Pact

 
• By 

An ‘historic economic prosperity deal’ does not include the sector.

Viatris Will File ‘Fast-Acting’ Meloxicam For FDA Approval This Year

 
• By 

Seven years after acquiring it, Viatris will seek approval of a meloxicam formulation for acute pain backed by data from two Phase III studies in post-surgical pain settings.