Iovance Biotherapeutics Earnings Calls
| Release date | Nov 06, 2025 |
| EPS estimate | -$0.290 |
| EPS actual | -$0.250 |
| EPS Surprise | 13.79% |
| Revenue estimate | 82.287M |
| Revenue actual | 67.455M |
| Revenue Surprise | -18.02% |
| Release date | Aug 07, 2025 |
| EPS estimate | -$0.290 |
| EPS actual | -$0.330 |
| EPS Surprise | -13.79% |
| Revenue estimate | 78.321M |
| Revenue actual | 59.952M |
| Revenue Surprise | -23.45% |
| Release date | May 08, 2025 |
| EPS estimate | -$0.250 |
| EPS actual | -$0.360 |
| EPS Surprise | -44.00% |
| Revenue estimate | 82.374M |
| Revenue actual | 49.324M |
| Revenue Surprise | -40.12% |
| Release date | Feb 27, 2025 |
| EPS estimate | -$0.260 |
| EPS actual | -$0.260 |
| Revenue estimate | 72.174M |
| Revenue actual | 73.694M |
| Revenue Surprise | 2.11% |
Last 4 Quarters for Iovance Biotherapeutics
Below you can see how IOVA performed 4 days prior and 4 days after releasing the earnings report. Also, you can see the pre-estimates and the actual earnings. This information can give you a slight idea of what you might expect for the next quarter's release.
| Release date | Feb 27, 2025 |
| Price on release | $5.26 |
| EPS estimate | -$0.260 |
| EPS actual | -$0.260 |
| Date | Price |
|---|---|
| Feb 21, 2025 | $5.78 |
| Feb 24, 2025 | $5.55 |
| Feb 25, 2025 | $5.34 |
| Feb 26, 2025 | $5.35 |
| Feb 27, 2025 | $5.26 |
| Feb 28, 2025 | $4.24 |
| Mar 03, 2025 | $4.04 |
| Mar 04, 2025 | $3.92 |
| Mar 05, 2025 | $4.05 |
| 4 days before | -9.00% |
| 4 days after | -23.00% |
| On release day | -19.49% |
| Change in period | -29.93% |
| Release date | May 08, 2025 |
| Price on release | $3.17 |
| EPS estimate | -$0.250 |
| EPS actual | -$0.360 |
| EPS surprise | -44.00% |
| Date | Price |
|---|---|
| May 02, 2025 | $3.50 |
| May 05, 2025 | $3.50 |
| May 06, 2025 | $3.10 |
| May 07, 2025 | $3.13 |
| May 08, 2025 | $3.17 |
| May 09, 2025 | $1.75 |
| May 12, 2025 | $1.93 |
| May 13, 2025 | $1.79 |
| May 14, 2025 | $1.71 |
| 4 days before | -9.43% |
| 4 days after | -46.21% |
| On release day | -44.79% |
| Change in period | -51.29% |
| Release date | Aug 07, 2025 |
| Price on release | $2.64 |
| EPS estimate | -$0.290 |
| EPS actual | -$0.330 |
| EPS surprise | -13.79% |
| Date | Price |
|---|---|
| Aug 01, 2025 | $2.68 |
| Aug 04, 2025 | $2.83 |
| Aug 05, 2025 | $2.75 |
| Aug 06, 2025 | $2.58 |
| Aug 07, 2025 | $2.64 |
| Aug 08, 2025 | $2.11 |
| Aug 11, 2025 | $1.97 |
| Aug 12, 2025 | $2.23 |
| Aug 13, 2025 | $2.45 |
| 4 days before | -1.49% |
| 4 days after | -7.20% |
| On release day | -20.08% |
| Change in period | -8.58% |
| Release date | Nov 06, 2025 |
| Price on release | $2.31 |
| EPS estimate | -$0.290 |
| EPS actual | -$0.250 |
| EPS surprise | 13.79% |
| Date | Price |
|---|---|
| Oct 31, 2025 | $1.97 |
| Nov 03, 2025 | $1.95 |
| Nov 04, 2025 | $1.82 |
| Nov 05, 2025 | $1.81 |
| Nov 06, 2025 | $2.31 |
| Nov 07, 2025 | $2.30 |
| Nov 10, 2025 | $2.37 |
| Nov 11, 2025 | $2.65 |
| Nov 12, 2025 | $2.54 |
| 4 days before | 17.26% |
| 4 days after | 9.96% |
| On release day | -0.433% |
| Change in period | 28.93% |
Iovance Biotherapeutics Earnings Call Transcript Summary of Q3 2025
Iovance reported Q3 2025 progress including 13% quarter-over-quarter revenue growth to roughly $68M (Amtagvi ~$58M; Proleukin ~$10M) and an improved gross margin of ~43% following restructuring and cost-optimization measures. Management announced centralization of all manufacturing to its internal Iovance Cell Therapy Center (iCTC) in early 2026 to lower cost of sales, improve margins and scale capacity. The company reiterated full-year 2025 revenue guidance of $250M–$300M and reported cash of ~$307M, expected to fund operations into Q2 2027. Commercial expansion is focused on broadening adoption of Amtagvi across academic and community Authorized Treatment Centers (ATCs); real-world data show a 60% response rate in second-line melanoma. Interim registrational LUN-202 lung cancer data (n=39) for Lifileucel showed an objective response rate of 26%, disease control rate of 72%, and median duration of response not reached at >25 months — management plans to enroll ~80 patients in 2026 to support an accelerated approval pathway with a potential U.S. launch in H2 2027. International filings/approvals are underway (Canada approved; UK, Australia, Switzerland pending; EU resubmission planned). Company emphasized continued expense discipline, manufacturing quality improvements (write-offs down ~40% since start of year), and efforts to drive profitability. Key risks remain regulatory timelines, enrollment execution, and typical commercial ramp uncertainties.
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