Poolbeg Pharma PLC
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About the company
Poolbeg Pharma plc operates as a clinical-stage pharmaceutical company, headquartered in London, United Kingdom, with a focus on developing treatments for infectious diseases. Its current product pipeline includes: POLB 001: A p38 MAP Kinase inhibitor being advanced for the treatment of severe influenza. POLB 002: An innovative, first-in-class RNA-based immunotherapy, acquired through a licensing agreement, designed for intranasal administration to combat various respiratory viral infections.
- CEO
- Jeremy Skillington
- IPO
- 2022
- Employees
- 15
- HQ
- London, GL, GB
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- Market Cap
- $73.14M
- P/E
- -9.68
- PEG
- -0.07
- P/S
- 0.00
- P/B
- 7.36
- EV/EBITDA
- -10.11
- Div Yield
- 0.00%
- Gross Margin
- 0.00%
- Op Margin
- 0.00%
- Net Margin
- 0.00%
- ROE
- -55.47%
- ROIC
- -73.60%
Latest fiscal year · YoY change
- Revenue
- $0+0.0%
- Gross Profit
- $-58,989+0.0%
- Op Income
- $-6,416,959
- Net Income
- $-5,694,077+1.7%
- EPS
- $-0.01+19.0%
- OCF Growth
- +3.0%
- FCF Growth
- -1.4%
- 52W High
- $0.12
- 52W Low
- $0.04
- 50D MA
- $0.10
- 200D MA
- $0.07
- Beta
- 1.81
- RSI (14)
- 65
- Avg Volume
- 1.15K
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Poolbeg said 2025 was a transformative year, with POLB 001 moving into the clinic, a cash runway into 2027, and management leaning heavily on partnering potential ahead of summer data.· April 28, 2026
- Cash ended the year at GBP 7.7 million, and management says that funds operations into 2027.
- POLB 001’s TOPICAL trial is ready to start: protocol finalized, MHRA approval received, ACT appointed, and 6 U.K. cancer centers lined up.
- Johnson & Johnson agreed to supply teclistamab at no cost, underscoring external interest in the program.
- The company says it secured FDA Orphan Drug designation and new patent grants, including cancer-immunotherapy CRS coverage in Australia.
- Management expects interim POLB 001 data in summer 2026 and wants to use that readout to drive partnering or licensing discussions.
Poolbeg reported ending 2025 with GBP 7.7 million in cash and said it has financial runway into 2027. Management also said it raised GBP 4.865 million from the market during the year. No revenue, EPS, or gross margin figures were provided in the call. For guidance, the company expects POLB 001 interim CRS-prevention data in the summer of 2026, with patient recruitment and dosing to begin shortly after site initiation; the oral GLP-1 clinical trial is now expected to start in the second half of 2026 because of revised manufacturing lead times.
Jeremy Skillington framed the year as a major de-risking period for the company, emphasizing that Poolbeg is now in “execution mode” with POLB 001 and has built a strong partnering backdrop. He repeatedly pointed to the combination of regulatory progress, IP protection, payer interest, and a large unmet need as reasons he sees meaningful transaction potential. His tone was upbeat and persistent, but he stressed that the real value inflection point will be the upcoming clinical data.
No separate CFO remarks were included in the transcript. The financial commentary came from Jeremy Skillington, who said the company finished 2025 with GBP 7.7 million in cash, had raised GBP 4.865 million during the year, and believes the cash position supports operations into 2027. He tied that runway to the ability to reach multiple clinical milestones before needing to secure a partner-led transaction.
Analysts focused on the timing and sufficiency of the TOPICAL trial, asking whether summer 2026 means June, July, or August, whether the trial would trigger a clear go/no-go decision, and whether 30 patients is enough for a commercial outcome. Management said the exact summer timing depends on enrollment speed, but the open-label design should allow rapid readout, and 30 patients was described as ample for establishing effect size and informing later-stage trial design. They also said a positive interim readout could be enough for some potential partners to transact, while others may want more data or another study before moving ahead.
The bullish case from this call is that POLB 001 now has the key operational pieces in place: regulatory approval, a clinical executor, major-site support, and free drug supply from J&J. Management also said payers see a willingness to reimburse a commercially meaningful solution for CRS, and they believe the market opportunity could exceed USD 10 billion across the initial target settings.
The main risk is that the company still has no human efficacy data in the target indication, so the investment case remains dependent on the summer 2026 readout. Management also acknowledged that commercialization likely depends on a partner and could still be “a few years down the line,” while the oral GLP-1 program has already slipped to the second half of 2026 because of manufacturing lead times.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 67.6%
- Shares Outstanding
- 763.44M
- Float Shares
- 515.91M
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Generate POLBF report →Poolbeg wins Israeli patent nod for lead cancer immunotherapy drug
proactiveinvestors.co.uk · Jul 21
Poolbeg Pharma raises £3.5m to support key trial and GLP-1 progress
proactiveinvestors.co.uk · Jul 14
Cavendish sees multi-billion-dollar prize as Poolbeg begins pivotal trial
proactiveinvestors.co.uk · Jul 13
Poolbeg doses first patient in cancer immunotherapy safety trial
proactiveinvestors.co.uk · Jul 13
Poolbeg Pharma secures South African patent for lead drug candidate
proactiveinvestors.co.uk · Jun 30
Poolbeg's European patent win bolsters partnering case before summer trial data, says Cavendish
proactiveinvestors.co.uk · Jun 16
European patent boosts Poolbeg Pharma's POLB 001 IP portfolio
proactiveinvestors.co.uk · Jun 16
Poolbeg Pharma has begun an exciting new clinical trial - ICYMI
proactiveinvestors.co.uk · Jun 13
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