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Adlai Nortye (ANL) investor relations material
Adlai Nortye Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Achieved significant progress in clinical pipeline, with ongoing enrollment in global Phase I trials for multiple oncology assets and first regulatory approval for a new ADC candidate.
Expanded clinical and operational capabilities in the US and Singapore to accelerate RAS program development and global growth.
Appointed two leading oncologists to the Scientific Advisory Board to strengthen expertise.
Financial highlights
Cash and cash equivalents plus short-term investments reached $231.9M as of June 30, 2026, up from $8.1M at December 31, 2025, driven by two oversubscribed private placements totaling $290M.
Revenue for the first half of 2026 was $13.1M, compared to nil in the prior year period, mainly from an exclusive license agreement for AN9025.
Net loss decreased by 70.9% to $5.3M for the six months ended June 30, 2026, from $18.3M in the same period last year.
Research and development expenses decreased 4% year-over-year to $14.6M, while general and administrative expenses rose 43.1% to $5.8M due to higher share-based compensation.
Outlook and guidance
Initial Phase Ia clinical data for AN9025 expected in 1H27; early QW arm data possible.
First patient dosing for AN4035 Phase I trial anticipated in 2H26, with initial data in 2H27.
AN8025 Phase I dose escalation completion targeted by year-end 2026.
Topline results for AN0025 Phase II ARTEMIS study expected in 1H27.
- RAS inhibitor and ADC programs advance with innovative dosing and combination strategies.ANL
Jefferies Global Healthcare Conference 2026 - Shelf registration enables flexible issuance of up to $600M in securities with strong governance.ANL
Registration filing - Global oncology innovator offers $600M in securities, advancing RAS and immunotherapy pipeline.ANL
Registration filing - 2025 net loss narrowed, R&D costs fell, and new PIPE and licensing deals boosted liquidity.ANL
Q4 2025 - Shelf registration enables up to $600M equity offering to fund oncology R&D and growth.ANL
Registration Filing - AN0025 plus chemoradiotherapy achieved high response and disease control rates with good tolerability.ANL
Investor Presentation - AN4005 demonstrated promising safety and efficacy signals in advanced solid tumors.ANL
Investor Presentation - Tri-specific AN8025 delivers coordinated immune stimulation and strong preclinical anti-tumor efficacy.ANL
Investor Presentation - Net loss improved to $51.9M in 2024; cash $60.9M; AN2025 Phase III topline data due Q2 2025.ANL
Q4 2024
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