•
Jun 30, 2024

Editas Q2 2024 Earnings Report

Reported a net loss with ongoing progress in clinical trials and preclinical development.

Key Takeaways

Editas Medicine reported a net loss of $67.6 million for the second quarter of 2024. The company is focused on advancing its reni-cel program and in vivo medicines, with key milestones expected by year-end. They have a strong financial position with a cash runway into 2026.

On track to present additional clinical data from the RUBY trial and the EdiTHAL trial by year-end.

Completed enrollment of the adolescent cohort of the Phase 1/2/3 RUBY trial for SCD.

Continue to dose adult patients in the RUBY trial and completed enrollment of the adult cohort.

On-track to establish in vivo preclinical proof-of-concept for an undisclosed indication by year-end.

Total Revenue
$513K
Previous year: $2.89M
-82.2%
EPS
-$0.82
Previous year: -$0.56
+46.4%
Gross Profit
-$907K
Previous year: $1.35M
-167.3%
Cash and Equivalents
$318M
Previous year: $480M
-33.7%
Free Cash Flow
-$60.6M
Previous year: -$40M
+51.2%
Total Assets
$385M
Previous year: $542M
-29.0%

Editas

Editas

Editas Revenue by Segment

Forward Guidance

Editas Medicine anticipates presenting additional clinical data from the RUBY and EdiTHAL trials by year-end 2024 and expects existing cash, cash equivalents, and marketable securities, together with near-term annual license fees and contingent upfront payment, to fund operating expenses and capital expenditures into 2026.

Positive Outlook

  • Presentation of substantive clinical data set of sickle cell patients with considerable clinical follow-up in the RUBY trial by year-end 2024.
  • Completion of enrollment of the adolescent cohort of the Phase 1/2/3 RUBY trial for SCD.
  • Manufacturing drug product for the initial adolescent cohort patients.
  • Continued dosing of adult patients in the RUBY trial, with completed enrollment of the adult cohort.
  • Presentation of additional clinical data from the EdiTHAL trial by year-end 2024.

Challenges Ahead

  • Uncertainties inherent in the initiation and completion of pre-clinical studies and clinical trials.
  • Availability and timing of results from pre-clinical studies and clinical trials.
  • Risk that interim results from a clinical trial will not be predictive of the final results of the trial or the results of future trials.
  • Expectations for regulatory approvals to conduct trials or to market products.
  • Availability of funding sufficient for the Company’s foreseeable and unforeseeable operating expenses and capital expenditure requirements.