Oncopeptides AB (publ)
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About the company
Oncopeptides AB (publ) is a biotechnology company focused on developing pharmaceutical therapies to combat cancer. The firm's therapeutic innovations are intended for markets across the United States, Europe, and internationally. Its flagship product candidate, melflufen, is an advanced anti-cancer peptide drug conjugate specifically designed to treat adult patients afflicted with relapsed refractory multiple myeloma.
- CEO
- Sofia Heigis
- IPO
- 2020
- Employees
- 80
- HQ
- Stockholm, SE
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- Market Cap
- $55.98M
- P/E
- -2.58
- PEG
- -0.05
- P/S
- 5.12
- P/B
- 30.83
- EV/EBITDA
- -2.44
- Div Yield
- 0.00%
- Gross Margin
- 96.40%
- Op Margin
- -211.09%
- Net Margin
- -223.55%
- ROE
- -1725.84%
- ROIC
- -120.56%
Latest fiscal year · YoY change
- Revenue
- $31.65M-10.1%
- Gross Profit
- $28.98M-20.1%
- Op Income
- $-283,498,000
- Net Income
- $-284,607,000-14.2%
- EPS
- $-1.87+32.2%
- OCF Growth
- +6.8%
- FCF Growth
- +6.8%
- 52W High
- $0.27
- 52W Low
- $0.27
- 50D MA
- $0.27
- 200D MA
- $0.27
- Beta
- -0.55
- RSI (14)
- 0
- Avg Volume
- 8
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Oncopeptides posted 62% Q2 revenue growth, improved first-half margins and losses, and reiterated a path to cash flow positivity during 2027 while pushing a European label expansion and new pipeline work.· August 27, 2026
- Q2 net sales were SEK 31.1 million, up 62% year over year; first-half sales rose 74% to SEK 56.5 million.
- Gross margin for the first half was 98%, and first-half operating expenses fell 2% to SEK 146.9 million.
- EBIT loss improved to SEK 86.2 million from SEK 116.1 million, helped by revenue growth and tighter cost control.
- Cash ended Q2 at SEK 158 million after the March rights issue, which added SEK 167 million after transaction costs.
- Management said it remains on track for positive cash flow during 2027 and expects full-year operating expenses to be around SEK 300 million.
Net sales in Q2 2026 were SEK 31.1 million, up 62% versus Q2 2025. First-half net sales were SEK 56.5 million, up 74% year over year, and first-half gross margin was 98%. First-half operating expenses declined 2% to SEK 146.9 million, and EBIT loss improved to SEK 86.2 million from SEK 116.1 million. Cash was SEK 158 million at the end of Q2, following a March rights issue that contributed SEK 167 million after transaction costs. Management reiterated that it expects positive cash flow during 2027 and said full-year operating expenses should be around SEK 300 million, with Q3 slightly lower than Q2.
Sofia Heigis framed the quarter as evidence that the company is executing across commercial, regulatory, clinical, and partnership fronts despite a lean organization. She emphasized Pepaxti’s European growth, the EMA Type II variation to move into third-line multiple myeloma, the first patient dosed in the glioblastoma study, and the Salus distribution deal covering 11 Central and Eastern European countries. Her tone was upbeat but practical, repeatedly stressing external validation, peer-to-peer advocacy, and the need to keep working market by market.
Henrik Bergentoft highlighted that sales growth is translating efficiently into gross profit, citing a 98% gross margin for the first half. He pointed to disciplined spending, with first-half operating expenses down 2% to SEK 146.9 million and G&A down to SEK 16.7 million from SEK 18.6 million in the quarter, while R&D was SEK 23.5 million and sales and marketing was SEK 40.8 million. He said the rights issue materially strengthened liquidity, leaving SEK 158 million in cash, and reiterated the goal of cash flow positivity during 2027; he also guided full-year operating expenses to roughly SEK 300 million.
Analyst questions focused on Spain, the timing of revenue from the Salus CEE partnership, operating expense trends, Japan, Greece, the U.S., and Q3. Management said Spain improved late in Q2 but second-half access remains uncertain because of possible strikes and limited HCP availability; in CEE, they expect first sales from Salus sometime in 2027 after price/listing steps, starting with Slovenia. They also said Q3 expenses should be slightly lower than Q2, Japan remains in partner discussions due to delays with the prior exclusive partner, Greece did not contribute in Q2 because of budget constraints, and the U.S. is not currently a focus.
The bull case is that Oncopeptides is showing real commercial traction in Europe, with 62% Q2 growth, broadening prescriber adoption in core markets, and improving profitability metrics. The company also has multiple potential catalysts: the EMA review of its third-line expansion, further CEE rollout through Salus, and early clinical work in glioblastoma that management believes could create additional long-term options.
The main risks are that growth still depends heavily on a handful of European markets, with Spain facing uncertain HCP access and Greece contributing nothing in Q2 due to budget issues. The U.S. is not a near-term focus, Japan is delayed, and the CEE partnership may not generate sales until 2027, so several promised expansions remain a ways off. Management also did not give quarter-specific guidance for Q3, and success depends on regulatory timing from EMA and local pricing/reimbursement steps.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 86.8%
- Shares Outstanding
- 211.26M
- Float Shares
- 183.31M
Our ONPPF coverage
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Generate ONPPF report →Oncopeptides AB (publ) (ONPPF) Q4 2025 Sales/Trading Call Transcript
seekingalpha.com · Jan 16
Oncopeptides AB (publ) (ONPPF) Q3 2025 Earnings Call Transcript
seekingalpha.com · Nov 5
Oncopeptides presents new data from OCEAN and PORT study - abstracts online
prnewswire.com · Aug 27
After Second Look Oncopeptides' Melflufen Wins Head-To-Head Myeloma Trial, But Difference In OS Triggers FDA Hold
benzinga.com · Jul 8
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