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Mar 31, 2024

Novocure Q1 2024 Earnings Report

Novocure reported strong execution with revenue growth and clinical trial progress.

Key Takeaways

Novocure reported a 13% year-over-year increase in net revenues to $139 million for Q1 2024. The company highlighted the growth in GBM active patients, positive results from the METIS Phase 3 clinical trial, and a productive Day-100 meeting with the FDA for the LUNAR PMA application.

Net revenues for the quarter were $138.5 million, a 13% increase compared to the same period in 2023, driven by successful launch in France and improved U.S. approval rates.

The METIS Phase 3 clinical trial met its primary endpoint, demonstrating a statistically significant extension in time to intracranial progression for patients with brain metastases from NSCLC.

1,643 prescriptions were received in the quarter, a 10% increase compared to the same period in 2023.

As of March 31, 2024, there were 3,845 active patients on therapy.

Total Revenue
$139M
Previous year: $122M
+13.4%
EPS
-$0.36
Previous year: -$0.5
-28.0%
Prescriptions Received
1.64K
Previous year: 1.5K
+9.8%
Gross Profit
$105M
Previous year: $92.6M
+13.3%
Cash and Equivalents
$454M
Previous year: $186M
+144.0%
Free Cash Flow
-$43.4M
Previous year: -$22.8M
+90.0%
Total Assets
$1.12B
Previous year: $1.17B
-4.5%

Novocure

Novocure

Forward Guidance

Novocure anticipates multiple milestones in 2024, including the PMA decision for Optune Lua in non-small cell lung cancer in the second half of 2024 and top-line data from the phase 3 PANOVA-3 clinical trial in locally advanced pancreatic cancer in H2 2024.

Positive Outlook

  • Anticipate PMA decision for Optune Lua in non-small cell lung cancer in the second half of 2024.
  • Top-line data from phase 3 PANOVA-3 clinical trial in locally advanced pancreatic cancer in H2 2024.
  • New five-year senior secured credit facility agreement with affiliates of Pharmakon Advisors for up to $400 million.
  • FDA approved the Investigational New Drug (IND) application for the randomized, Phase 3 KEYNOTE D58 trial.
  • The meeting with FDA was productive with no indication that the PMA will be referred to an advisory panel.