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BioLineRx (BLRX) investor relations material
BioLineRx Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Formed a joint venture with Hemispherian to develop GLIX1, a first-in-class oral small molecule targeting glioblastoma and other cancers, with a phase I/II-A trial set to begin in Q1 2026 and leveraging complementary expertise in clinical development and small molecule discovery.
GLIX1's IND was cleared by the FDA in August, with initial phase 1 data expected in H1 2027.
Retained rights to develop metixafortide in pancreatic cancer (PDAC) and continue to support its development through the CheMo4METPANC phase II-B trial in collaboration with Columbia University and Regeneron.
Maintains a cash runway into the first half of 2027, with $25.2 million in cash and equivalents as of September 30, 2025.
Financial highlights
Q3 2025 total revenues were $0.4 million, reflecting royalties from APHEXDA commercialization.
Research and development expenses were $1.7 million, down from $2.6 million in Q3 2024, mainly due to lower metixafortide-related costs, out-licensing, and reduced headcount.
No sales and marketing expenses in Q3 2025, compared to $5.5 million in Q3 2024, following the shutdown of U.S. commercial operations.
General and administrative expenses were $0.8 million, down from $1.4 million year-over-year.
Net loss for Q3 2025 was $1 million, compared to $5.8 million in Q3 2024.
Outlook and guidance
GLIX1 phase I/II-A trial in glioblastoma to start in Q1 2026, with phase 1 data anticipated in H1 2027 and potential periodic updates before then.
Plans to expand GLIX1 development into additional cancer indications after establishing safety and dosing.
Ongoing support for metixafortide in PDAC and sickle cell disease, with key data presentations expected at upcoming conferences and interim analysis planned at 40% PFS events.
Cash runway expected to last into the first half of 2027.
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