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Panbela Therapeutics (PBLA) investor relations material
Panbela Therapeutics Q3 2024 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Secured up to $12M in strategic financing from Nant Capital, with $2.85M funded and $9.15M pending, supporting clinical and operational activities and enabling potential immunotherapy collaborations.
Advanced multiple clinical programs, including the pivotal Phase 3 ASPIRE trial in metastatic pancreatic cancer, and initiated a Phase I study in STK11 mutant NSCLC.
Achieved milestones such as FDA approval of Aflornithine for pediatric neuroblastoma and completion of enrollment in the Phase 3 PACE's trial for colorectal cancer prevention.
Delisted from Nasdaq in April 2024; shares now quoted on OTCQB, with relisting application pending.
CRO for ASPIRE trial terminated in August 2024 due to payment delays; company assumed direct trial management.
Financial highlights
Q3 2024 net loss was $7.2M ($1.48 per share), compared to $7.8M ($53.74 per share) in Q3 2023; nine-month net loss was $21.4M, up from $18.8M year-over-year.
R&D expenses for Q3 2024 were $6.0M–$6.1M, down from $6.7M in Q3 2023; G&A expenses were flat at $1.1M.
Cash as of September 30, 2024, was $142K–$0.1M, not including Nant Capital funding; current assets $5.2M, current liabilities $20.1M.
Cash used in operations for the nine months ended September 30, 2024, totaled $12.5M, down from $22.2M in the prior year.
Net loss per share for nine months ended September 30, 2024, was $(5.00), reflecting a higher share count.
Outlook and guidance
Full enrollment of the Phase 3 ASPIRE trial (~600 patients) expected by Q2 2025; interim analysis planned for Q1 2025 due to lower-than-expected event rates.
Data readout for the Phase 3 PACE's trial anticipated in the second half of 2026.
Interim analysis for the Type 1 diabetes trial expected next year; Phase 2 ovarian cancer and neoadjuvant pancreatic trials to open in early 2025.
Company expects to continue incurring substantial losses and negative cash flows as it advances clinical programs; additional capital is required to fund operations.
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