NewAmsterdam Pharma Company (NAMS) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
5 Aug, 2026Executive summary
Positive CHMP opinion recommending marketing authorization for obicetrapib and its fixed-dose combination in Europe, with potential launches in Germany and UK in Q4 2026 and a final decision expected later in 2026.
Focused on late-stage development of obicetrapib, with positive Phase 3 results in BROADWAY, BROOKLYN, and TANDEM trials, and ongoing PREVAIL, REMBRANDT, and RUBENS trials targeting cardiovascular and Alzheimer's disease.
Statistically significant reductions in plasma p-tau217, an Alzheimer's biomarker, observed in BROADWAY Phase 3 trial, supporting expansion into neurodegenerative disease.
U.S. commercialization to be pursued independently, with Menarini partnership for European commercialization and additional partnerships considered for other regions.
Pipeline expansion includes trials in diabetes and Alzheimer's disease, with new studies planned for 2026.
Financial highlights
Revenue for Q2 2026 was $3.7M, down 81% year-over-year due to non-recurring milestone payments; six-month revenue was $6.7M, down 70%.
Net loss for Q2 2026 was $64.1M, up from $17.4M in Q2 2025; six-month net loss was $112.6M, up from $56.9M.
R&D expenses rose to $41.7M in Q2 2026, driven by clinical trials and increased personnel costs.
SG&A expenses were $26.9M in Q2 2026, slightly down year-over-year, reflecting lower marketing and IP costs offset by higher share-based compensation.
Cash, cash equivalents, and marketable securities totaled $678.3M as of June 30, 2026.
Outlook and guidance
Awaiting regulatory decisions on EU marketing applications for obicetrapib and FDC; potential launches in late 2026.
PREVAIL interim analysis expected in Q4 2026, with DSMB recommendation in Q1 2027; topline data from RUBENS Phase 3 trial expected by year-end 2026.
Sufficient liquidity to fund operations and obligations, with no sales under the $250M at-the-market program in H1 2026.
Additional analyses from BROOKLYN and BROADWAY studies to be presented throughout 2026.
New clinical trial for Alzheimer's prevention with obicetrapib planned for 2026.
Latest events from NewAmsterdam Pharma Company
- PREVAIL’s interim review could accelerate a trial backed by 18%-22% modeled risk reduction.NAMS
Stifel 2026 Healthcare Conference 2026 - PREVAIL interim is on track for end-2026 as European launch preparations advance.NAMS
3rd Annual Guggenheim Healthcare Innovation Conference - EU approvals and Q3 revenue lift; PREVAIL and RUBENS readouts are ahead.NAMS
Q3 2026 - 2024 pivotal readouts and $500M pro forma cash underpin the obicetrapib program.NAMS
Q4 2023 - PREVAIL trial data and European launch of obicetrapib set the stage for major milestones in 2026-2027.NAMS
12th Annual Cantor Fitzgerald Global Healthcare Conference - PREVAIL’s interim analysis and upcoming RUBIN data position obicetrapib for a differentiated launch.NAMS
Wells Fargo 21st Annual Healthcare Conference - PREVAIL targets a 15% MACE reduction, with strong data and new trials driving global launch momentum.NAMS
Investor Day 2026 - Obicetrapib delivers robust LDL and Lp(a) reductions with strong safety, with pivotal data ahead.NAMS
Jefferies London Healthcare Conference 2024 - Obicetrapib cut LDL-C by 41.5% at one year with strong safety in HeFH patients.NAMS
Study Update