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Sep 30, 2022

Atea Q3 2022 Earnings Report

Atea Pharmaceuticals reported financial results for Q3 2022 and provided a business update.

Key Takeaways

Atea Pharmaceuticals reported on their progress in advancing clinical candidates, with expectations of pivotal developments in 2023. They anticipate imminent enrollment into the SUNRISE-3 trial for COVID-19, completion of enrollment in the AT-752 challenge study and the first cohort of DEFEND-2, and submission of clinical trial applications for a Hepatitis C study.

Enrollment of patients into SUNRISE-3 evaluating bemnifosbuvir for COVID-19 is expected imminently.

Completion of enrollment is anticipated around the end of the year for the AT-752 challenge study and the first cohort of DEFEND-2, with initial data to follow.

Clinical trial applications for the bemnifosbuvir and ruzasvir combination hepatitis C study are expected to be submitted around year-end, leading to Phase 2 initiation.

Atea continues to progress its second-generation protease inhibitor discovery program for COVID-19, focused on candidates for combination therapy with bemnifosbuvir.

EPS
-$0.1
Previous year: -$0.34
-70.6%
Cash and Equivalents
$665M
Previous year: $840M
-20.8%
Free Cash Flow
-$21.3M
Total Assets
$687M
Previous year: $844M
-18.6%

Atea

Atea

Forward Guidance

Atea Pharmaceuticals anticipates several key milestones in the near future, including the start of patient enrollment for the SUNRISE-3 trial, completion of enrollment for the AT-752 challenge study and DEFEND-2 trial's first cohort, and submission of clinical trial applications for the combination study of bemnifosbuvir and ruzasvir for Hepatitis C.

Positive Outlook

  • Expect imminent enrollment of patients into SUNRISE-3 evaluating bemnifosbuvir for COVID-19.
  • Anticipate completing enrollment in the AT-752 challenge study around the end of the year.
  • Expect to complete enrollment in the first cohort of DEFEND-2 around the end of the year.
  • Initial data from AT-752 challenge study and DEFEND-2 trial's first cohort is expected to follow completion of enrollment.
  • Expect to submit clinical trial applications for the bemnifosbuvir and ruzasvir combination hepatitis C study around the end of the year, leading to Phase 2 initiation.

Challenges Ahead

  • Uncertainty around and costs associated with the clinical development of bemnifosbuvir as a potential treatment for COVID-19.
  • Uncertainty around and costs associated with the clinical development of bemnifosbuvir as a potential treatment for HCV.
  • Uncertainty around and costs associated with the clinical development of AT-752 for dengue.
  • Risks and uncertainties that may cause actual results to differ from forward-looking statements.
  • Factors discussed under the caption “Risk Factors” in the Annual Report on Form 10-K could cause actual results to differ materially.