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Iovance Biotherapeutics, Inc.
NASDAQ: IOVA Healthcare Pharma 🔎 Screen
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$3.0B
Market Cap
P/E
PEG
-13.3%
ROCE
-11.9%
ROE
0.01
D/E
-153.1%
OPM
-10.1%
% from 52W High
97
α RS
🔍 IOVA is showing a momentum setup because RS Rating is 97 (top decile vs market), it matches 2 of 37 tracked screener presets, and an ECS of 63.5 last quarter. Net: Broad signal stack, not a recommendation. ? RS Rating Conviction ECS
Sources
RS Rating 97 · Conviction 2/37 · ECS 63.5
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📈 Price History
Ratio Health
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About

Iovance Biotherapeutics, Inc., a commercial-stage biopharmaceutical company, develops and commercializes cell therapies using autologous tumor infiltrating lymphocyte for the treatment of metastatic melanoma and other solid tumor cancers in the United States and internationally.

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📊 MIXED Iovance Q1'26: AMTAGVI rev $60M, guides full year $350-370M, cash to 2028.
Revenue & Profitability
First quarter 2026 total revenue was $71 million, a 45% year-over-year increase. AMTAGVI revenue was $60 million (up 38% year-over-year), and Proleukin revenue was $11 million (nearly doubled year-over-year). Gross margin was about 41%, impacted by one-time non-recurring facility upgrade costs. The company had approximately $319 million in cash and equivalents as of March 31, 2026, and expects to fund operations into 2028. Research and development expenses declined for the third consecutive quarter, down 18% year-over-year.
Outlook
Management noted strong demand trends for AMTAGVI, with March 2026 being the largest reported revenue month to date. They expect continued growth driven by ATC network expansion, earlier patient referrals, and increasing physician awareness. The company sees significant unmet need in second-line metastatic serous endometrial cancer (response rates below 15%) and in non-small cell lung cancer (a market about seven times larger than the advanced melanoma opportunity). Ex-U.S., regulatory decisions are anticipated in Australia (first half 2026) and Switzerland (2027).
Growth Drivers
Key growth levers include expanding the ATC network to over 110 by year-end (with a growing mix of community ATCs), driving earlier referrals with real-world evidence and five-year durability data, and increasing the field sales force. Pipeline expansion into new indications such as metastatic serous endometrial cancer (40% confirmed ORR), non-small cell lung cancer (Fast Track designation), and soft tissue sarcomas (IOV-SAR-201 trial starting Q3 2026) also supports long-term growth. Next-generation programs (IOV-5001, IOV-3001, IOV-4001) target larger patient populations.
Balance Sheet & CapEx
Not discussed in this earnings call beyond the completed maintenance upgrades at the internal manufacturing facility (ICTC), which were described as one-time non-recurring costs that should not recur. No specific CapEx guidance or future infrastructure investments were mentioned.
Margins
First quarter gross margin was about 41%, absorbing one-time non-recurring costs related to facility upgrades. Management expects margins to trend higher for the rest of 2026 as in-house manufacturing scales and operational efficiencies improve. Cost of sales is expected to benefit from exclusive in-house production, economies of scale, and targeted operational excellence projects in the plant. The company is on a clear path to profitability.
Key Risks
No specific risks were flagged by management in the prepared remarks or Q&A beyond the standard forward-looking statement disclaimer about risks and uncertainties in SEC filings. Analysts did not raise risk-related questions.
Generated by AI · Q1 2026 results · Not investment advice
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✓ 📞 Earnings Call Transcripts (5 quarters) submit a missing quarter
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📞 Earnings Call Transcripts (5)
Q2 2026 Q2 2026 2026-08-06
Record Q2 revenue and margin were driven by robust Amtagvi demand, expanding ATC network, and operational efficiencies. Pipeline advanced with key regulatory milestones and international approvals, while strong cash reserves support ongoing growth and R&D.
Q1 2026 Q1 2026 2026-05-07
Q1 2026 revenue grew 45% year-over-year, driven by strong AMTAGVI demand and operational efficiencies. Guidance for Q2 and full-year 2026 remains robust, with margins expected to improve and a broadening pipeline targeting multiple solid tumor indications.
Q4 2025 Q4 2025 2026-02-24
Q4 and full-year 2025 saw 61% revenue growth, record gross margins, and strong AMTAGVI adoption. Pipeline advances include FDA Fast Track for lifileucel in lung cancer and positive sarcoma data, with global expansion and further revenue growth expected in 2026.
Q3 2025 Q3 2025 2025-11-06
Q3 revenue rose 13% sequentially to $68M, with gross margin improving to 43% due to cost reductions. Amtagvi and Proleukin sales drove growth, and strong clinical data in NSCLC support future expansion. Revenue guidance of $250–300M for 2025 is reaffirmed.
Q2 2025 Q2 2025 2025-08-07
Q2 2025 revenue grew 22% sequentially to $60M, driven by record Amtagvi infusions and strong demand. Strategic restructuring is set to deliver $100M+ in annual savings and margin improvement, with guidance reaffirmed at $250–$300M for the year.
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Financial Model
Projections are built from each company's audited annual financials (Income Statement, Balance Sheet, Cash Flow) over the last 5 fiscal years. Forward assumptions — revenue growth %, EBITDA margin, D&A (USD millions), interest expense, tax rate, and capex — are AI-generated using historical context and refreshed twice a year: after the December results season and after the September/Q4 results season.

DCF Valuation
Fair Value = Σ(FCFt / (1+WACC)t) + Terminal Value. Terminal Value uses the Gordon Growth Model: FCF5 × (1+g) / (WACC−g). Default WACC: 10% (US risk-free ~4.5%, equity risk premium ~5.5%). Default terminal growth: 3% (long-run US nominal GDP proxy).

CAGR Tracker
Expected 5-year CAGR = (DCF Fair Value / Current Price)1/5 − 1. Assumes fair value is reached in exactly 5 years — a mechanical estimate only.

Data Sources & Limitations
Financial statements sourced from public filings. Prices updated daily. Forward assumptions are AI-generated. All monetary values in USD millions. Non-US ADR companies may have currency conversion inaccuracies. Models are point-in-time and do not update intra-quarter or account for M&A, macro shocks, or extraordinary items.

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Investment Risk:
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No Investment Recommendation:
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Information Sources:
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