Atea Pharmaceuticals, Inc.
NASDAQ•AVIR
CEO: Dr. Jean-Pierre Sommadossi Ph.D.
Sector: Healthcare
Industry: Biotechnology
Listing Date: 2020-10-30
Atea Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, discovers, develops, and commercializes antiviral therapeutics for patients with viral infections. Its lead product candidate is AT-527, an oral antiviral candidate that is in Phase 3 SUNRISE-3 clinical trial for the treatment of patients with COVID-19. The company also develops bemnifosbuvir in combination with ruzasvir, which is in Phase 2 clinical trial, for the treatment of hepatitis C virus (HCV); and a protease inhibitor for the treatment of COVID-19. It has a license agreement with MSD International GmbH for the development, manufacture, and commercialization of Ruzasvir, an NS5A inhibitor, for the treatment of HCV. Atea Pharmaceuticals, Inc. was incorporated in 2012 and is headquartered in Boston, Massachusetts.
Contact Information
Market Cap
$476.57M
P/E (TTM)
-3.0
17.9
Dividend Yield
--
52W High
$6.45
52W Low
$2.46
52W Range
Rank45Top 56.8%
3.6
F-Score
Modified Piotroski Analysis
Based on 7-year fundamentals
Weak • 3.6 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2019-2025
Financial Dashboard
Q4 2025 Data
Revenue
$0.00+0.00%
4-Quarter Trend
EPS
-$0.57+0.00%
4-Quarter Trend
FCF
-$28.22M+0.00%
4-Quarter Trend
2025 Annual Earnings Highlights
Key Highlights
HCV Phase 3 Trials Progressing C-BEYOND fully enrolled; C-FORWARD enrollment expected complete YE 2026; NDA targeted March 2027.
Net Loss Narrows Significantly Net loss decreased $10.0 M to $(158.3) M in 2025; R&D spend increased slightly to $148.0 M.
Cash Position Strong Cash, equivalents, and securities totaled $301.8 M on December 31, 2025, sufficient through 2027.
Workforce Reduction Completed 25% workforce reduction in Q1 2025 expected to yield $15.0 M aggregate cost savings through 2027.
Risk Factors
High Dependence on HCV Candidate Business highly dependent on successful HCV regimen development, approval, and commercialization; failure causes significant harm.
Need Substantial Future Financing Expect substantial operating expenses; failure to obtain necessary capital could delay or terminate product development efforts.
Regulatory Approval Unpredictable Regulatory approval processes are lengthy, expensive, and inherently unpredictable; failure to obtain approval seriously harms business.
Intellectual Property Litigation Risk Facing patent challenges from Gilead Sciences regarding bemnifosbuvir; adverse ruling requires licensing or halts commercialization.
Outlook
Targeting HCV NDA Submission Targeting submission of HCV regimen NDA to FDA in March 2027, pending successful completion of Phase 3 trials.
Initiate HEV Phase 1 Study Anticipate initiating clinical development of AT-587 for chronic HEV with a first-in-human Phase 1 study mid-2026.
Cash Funds Operations Through 2027 Current cash position of $301.8 M is expected to fund planned operations through the end of 2027.
Merck Milestone Payment Anticipated Next $10.0 M Merck milestone payment anticipated due upon acceptance of HCV regimen NDA in H1 2027.
Peer Comparison
Revenue (TTM)
$216.11M
$74.12M
$66.98M
Gross Margin (Latest Quarter)
100.0%
100.0%
93.3%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| VTYX | $1.00B | -9.4 | -48.1% | 4.7% |
| OMER | $793.38M | -6.1 | 57.3% | 103.2% |
| ALLO | $539.35M | -2.8 | -57.1% | 18.0% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
N/M
Revenue Volatile
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
0%
Cash Flow Needs Attention
Deep Research
Next earnings:May 11, 2026
EPS:-$0.56
|Revenue:-
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
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No Data