Jun 30, 2021

Altimmune Q2 2021 Earnings Report

Altimmune reported financial results for Q2 2021 and provided a corporate update.

Key Takeaways

Altimmune reported a revenue of $0.1 million and a net loss of $24.8 million, or $0.60 net loss per share for the three months ended June 30, 2021. The company's cash, cash equivalents, short-term investments and restricted cash totaled $217.9 million at June 30, 2021.

Reported encouraging 6-week interim data from the ongoing Phase 1 clinical trial of ALT-801 in Australia, with a placebo-adjusted weight loss of 6.3% achieved at 6 weeks of treatment with 1.8 mg once weekly dose.

Advancing to ALT-801 12-week data readout on three cohorts, expected in September 2021.

Filing of ALT-801 investigational new drug (IND) application for non-alcoholic steatohepatitis (NASH) on track for Q3 2021, which will be followed by the initiation of a clinical trial in non-alcoholic fatty liver disease (NAFLD).

Altimmune had cash, cash equivalents, short-term investments and restricted cash totaling $217.9 million at June 30, 2021.

Total Revenue
$138K
Previous year: $722K
-80.9%
EPS
-$0.41
Previous year: -$0.94
-56.4%
Gross Profit
-$13.1M
Cash and Equivalents
$174M
Previous year: $64.7M
+168.9%
Free Cash Flow
-$26.6M
Total Assets
$257M
Previous year: $103M
+150.9%

Altimmune

Altimmune

Forward Guidance

Altimmune is focused on advancing its NASH and obesity pipeline, with key milestones expected in the coming quarters, including data readouts and IND filings.

Positive Outlook

  • ALT-801 12-week data readout expected in September 2021.
  • Potential start of the ALT-801 12-week NAFLD trial in September 2021.
  • Potential start of the ALT-801 drug/drug interaction trial and Type 2 diabetes trial by year end 2021.
  • Potential filing of a NASH IND in Q3 2021.
  • Potential filing of an obesity IND in Q4 2021.

Challenges Ahead

  • Potential impacts due to the COVID-19 pandemic such as delays in regulatory review.
  • Manufacturing and supply chain interruptions.
  • Access to clinical sites, enrollment, adverse effects on healthcare systems and disruption of the global economy.
  • The reliability of the results of studies relating to human safety and possible adverse effects resulting from the administration of the Company’s product candidates.
  • The Company’s ability to manufacture clinical trial materials and commercial supply on the timelines anticipated.