BioLineRx Ltd.
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About the company
BioLineRx Ltd. , a commercial stage biopharmaceutical company, develops and commercializes therapeutics for oncology and rare diseases. The company's pipeline includes APHEXDA (motixafortide), a peptide that is in Phase 1 clinical trial for the treatment of sickle cell disease, and Phase 2b clinical trial for the treatment of pancreatic cancer, as well as completed Phase 3 clinical trial for the treatment of multiple myeloma.
- CEO
- Philip A. Serlin
- IPO
- 2007
- Employees
- 22
- HQ
- Hevel Modi'in, HM, IL
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- Market Cap
- $41.77M
- P/E
- -1.49
- PEG
- 0.00
- P/S
- 9.94
- P/B
- 0.85
- EV/EBITDA
- -1.83
- Div Yield
- 0.00%
- Gross Margin
- 74.67%
- Op Margin
- -780.21%
- Net Margin
- -633.83%
- ROE
- -47.86%
- ROIC
- -36.68%
Latest fiscal year · YoY change
- Revenue
- $1.28M-95.6%
- Gross Profit
- $462.21K-97.7%
- Op Income
- $-11,135,376
- Net Income
- $-1,271,903+86.2%
- EPS
- $-0.00+93.5%
- OCF Growth
- +80.1%
- FCF Growth
- +80.0%
- 52W High
- $2.40
- 52W Low
- $1.10
- 50D MA
- $1.51
- 200D MA
- $1.52
- Beta
- 0.71
- RSI (14)
- 62
- Avg Volume
- 3.00M
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
BioLineRx highlighted early progress for GLIX1, stronger APHEXDA royalties, and cash runway into the first half of 2027.· May 27, 2026
- GLIX1 moved into a Phase I/IIa first-in-human GBM study, with the first patient dosed at NYU Langone and additional sites at Northwestern and Moffitt expected to open soon.
- Management said preclinical data were encouraging, including dose-dependent tumor growth inhibition and survival benefit in GBM models, plus a synergistic rationale for combining GLIX1 with PARP inhibitors.
- APHEXDA sales at Ayrmid rose to $2.5 million in Q1 2026 from $1.4 million in Q1 2025, generating $0.5 million of royalty revenue for BioLineRx.
- Cash and equivalents ended the quarter at $17.4 million, which management said funds the operating plan into the first half of 2027.
- In PDAC, the CheMo4METPANC trial remains on track for an interim futility analysis later this year, while management noted the treatment landscape may be changing.
For the 3 months ended March 31, 2026, revenues were $0.5 million versus $0.3 million in the prior-year quarter, driven by higher APHEXDA royalties. R&D expense was $2.5 million versus $1.6 million year over year, and G&A was $0.9 million versus $1.0 million. Net loss was $2.6 million versus net income of $5.1 million in Q1 2025, while net nonoperating income was $0.5 million versus $7.6 million a year earlier. Cash and equivalents were $17.4 million at quarter-end, and management said this supports the operating plan into the first half of 2027. No formal next-quarter or full-year revenue guidance was given; the company said it expects periodic GLIX1 updates in the second half of 2026 and full dose-escalation results in 2027.
Phil Serlin framed GLIX1 as the quarter’s main strategic focus, emphasizing that GBM is a wide-open area with high unmet need and limited effective therapies. He highlighted the trial’s launch, the addition of multiple academic centers, and the company’s confidence in the program based on preclinical data and blood-brain-barrier penetration. He also pointed to APHEXDA royalty growth as evidence of improving commercial traction and said he remains very optimistic about BioLineRx’s prospects this year and beyond.
Mali Zeevi focused on the financial recap: revenues of $0.5 million were up from $0.3 million a year ago, mainly due to APHEXDA royalties; R&D rose to $2.5 million from $1.6 million, primarily because of GLIX1; and G&A was $0.9 million versus $1.0 million. She noted net nonoperating income of $0.5 million versus $7.6 million last year, largely tied to noncash fair value changes in warrant liabilities. Cash and equivalents of $17.4 million were said to be sufficient to fund operations into the first half of 2027.
Analysts focused on GBM trial recruitment, site activation, APHEXDA commercialization progress, and GLIX1 dosing. Management said recurrent GBM has little real recruitment competition and that NYU is active, while Northwestern and Moffitt should open shortly, but they would not disclose more site-by-site detail or initial safety observations yet. On APHEXDA, Phil said BioLineRx has limited visibility into Ayrmid’s marketing tactics, but sales growth from about $1.3 million-$1.4 million to $2.5 million suggests momentum. On PDAC, he said the interim futility analysis for CheMo4METPANC is still expected later this year, but changing competitive data could affect the pathway forward.
The company now has a live clinical program in GLIX1, with management citing encouraging preclinical results, a novel mechanism, and the ability to cross the blood-brain barrier. APHEXDA royalties also improved meaningfully year over year, and BioLineRx says cash is sufficient into the first half of 2027, reducing near-term financing pressure.
GLIX1 is still very early, with no disclosed clinical doses, no initial safety readout, and efficacy still unproven in patients. Management also acknowledged that the PDAC landscape may be shifting, which could complicate how motixafortide is positioned in that indication, and APHEXDA commercialization remains dependent on Ayrmid’s execution over which BioLineRx has limited control.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 96.1%
- Shares Outstanding
- 2.61B
- Float Shares
- 2.51B
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