Celldex Therapeutics, Inc.
NASDAQ•CLDX
CEO: Mr. Anthony S. Marucci M.B.A.
Sector: Healthcare
Industry: Biotechnology
Listing Date: 1986-05-15
Celldex Therapeutics, Inc., a biopharmaceutical company, engages in developing therapeutic monoclonal and bispecific antibodies for the treatment of various diseases. Its drug candidates include antibody-based therapeutics to treat patients with inflammatory, allergic, autoimmune, and other devastating diseases. The company's clinical development programs CDX-0159, a Phase II monoclonal antibody that binds the receptor tyrosine kinase KIT and inhibits its activity. It has research collaboration and license agreements with Yale University. The company was incorporated in 1983 and is headquartered in Hampton, New Jersey.
Contact Information
Perryville III Building, Suite 220 53 Frontage Road, Hampton, NJ, 08827, United States
908-200-7500
Market Cap
$2.30B
P/E (TTM)
-8.9
18.2
Dividend Yield
--
52W High
$35.29
52W Low
$17.85
52W Range
Rank55Top 80.0%
2.6
F-Score
Modified Piotroski Analysis
Based on 10-year fundamentals
Weak • 2.6 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2016-2025
Financial Dashboard
Q4 2025 Data
Revenue
$75.00K+0.00%
4-Quarter Trend
EPS
-$1.23+0.00%
4-Quarter Trend
FCF
-$64.93M+0.00%
4-Quarter Trend
2025 Annual Earnings Highlights
Key Highlights
Barzolvolimab Phase 3 Enrollment Complete Phase 3 CSU studies enrollment finished February 2026; topline data expected Q4 2026. PN/AD Phase 2 enrollment also complete.
R&D Spending Increased 50% Research and development expenses reached $245.1M in 2025, up 50% from $163.6M in 2024, funding clinical advancement.
Net Loss Widened Significantly Net loss increased 64% to $258.8M in 2025 versus $157.9M in 2024, driven by higher R&D costs.
Cash Position Remains Adequate Total cash and securities stood at $518.6M on December 31, 2025, funding operations through 2027.
Risk Factors
Need Capital To Fund Operations Company has no product revenue and requires substantial financing to complete clinical trials and achieve regulatory approval.
Clinical Development Failure Risk Drug candidates face risk of clinical failure at any stage, potentially precluding commercial revenue generation despite significant investment.
Regulatory Approval Uncertainty FDA review process is lengthy and uncertain; approval delays or limitations could severely restrict market potential and profitability.
Reliance on Third-Party Manufacturers Dependence on single-source CDMOs for manufacturing exposes operations to supply chain delays, quality issues, and compliance risks.
Outlook
Advance Barzolvolimab Phase 3 Data Expect topline data from EMBARQ-CSU1/2 trials in Q4 2026; PN Phase 2 data expected Summer 2026.
CDX-622 Data Anticipated Q3 2026 Multiple ascending dose data for bispecific candidate CDX-622 anticipated in third quarter 2026, supporting further development.
Expect Continued Operating Losses Anticipate incurring operating losses in 2026 and beyond due to planned significant costs for drug candidate development.
Prepare For Future Capital Raising Company plans further capital raising activities including licensing, debt issuance, or equity offerings to meet long-term liquidity needs.
Peer Comparison
Revenue (TTM)
$868.45M
$247.00M
$90.49M
Gross Margin (Latest Quarter)
100.0%
100.0%
99.0%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| CELC | $5.92B | -36.3 | -203.2% | 41.9% |
| SYRE | $4.41B | -162.8 | -29.4% | 0.0% |
| EWTX | $3.69B | -21.1 | -32.0% | 0.7% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
-52.4%
Growth Under Pressure
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
0%
Cash Flow Needs Attention
Deep Research
Next earnings:Apr 30, 2026
EPS:-$1.20
|Revenue:$795.36K
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
|---|
No Data