10-Q · May 7, 2026
Absi Corporation's Q4 2026 results reveal significant challenges, marked by a revenue decline to $0.65 million from $2 million in the same quarter last year, leading to an EPS of -$0.20, which was worse than analysts'…
Earnings analysis · 10-Q
Filed August 11, 2026 · Our reading of the company's report
The latest report
Absci’s Q2 2026 revenue of $318,000 improved sequentially from $215,000 but declined from $593,000 a year earlier and significantly missed the $1.27 million consensus estimate; EPS of negative $0.21 also missed the…
Absci’s Q2 2026 revenue of $318,000 improved sequentially from $215,000 but declined from $593,000 a year earlier and significantly missed the $1.27 million consensus estimate; EPS of negative $0.21 also missed the negative $0.19 estimate. Losses continued to expand, with a six-month net loss of $62.8 million versus $56.9 million in the prior-year period, while R&D expense remained high at $22.6 million for the quarter. Liquidity was strengthened by approximately $93.6 million of net equity proceeds and $201.1 million of cash, cash equivalents and marketable securities, but the absence of downstream licenses, milestone or royalty revenue remains a material business-model risk.
How much of each revenue dollar the business keeps.
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Q2 2026 revenue was $318,000, up 47.9% from $215,000 in Q1 2026 but down 46.4% from $593,000 in Q2 2025. Revenue was also below the $1.27 million consensus estimate.
Cash, cash equivalents and marketable securities totaled $201.1 million as of June 30, 2026. Management said these resources and anticipated operating cash flows should fund needs for at least the next 12 months.
The company reported $62.8 million of net losses for the six months ended June 30, 2026, compared with $56.9 million in the prior-year period, an increase of $5.9 million or 10.4%.
R&D expense was $22.6 million in Q2 2026, reflecting continued investment in internally developed programs, including ABS-201, and the Integrated Drug Creation platform.
The company reported that 13,495,277 shares were issued and sold for net proceeds of approximately $93.6 million, while an additional $84.0 million remained available for future sale under its $100.0 million ATM facility as of June 30, 2026.
ABS-201 was being evaluated in a Phase 1/2a clinical trial, with planned single ascending dose cohorts completed and multiple ascending dose cohorts continuing as of the filing.
As of August 11, 2026, no partner had entered into a license for clinical or commercial use of intellectual property related to a product candidate or cell line, and the company had received no milestone or royalty revenue to date. This leaves revenue dependent on drug-creation activity and partner timing.
The BIOSECURE Act was enacted in December 2025, the Department of Defense added WuXi AppTec to its Section 1260H list in June 2026, and the OMB is required to publish its initial biotechnology companies of concern list no later than December 2026. A designation could cause supply-chain disruption, delays and higher costs.
ABS-201 is being evaluated in Australia, and the company stated that the FDA may not accept foreign clinical-trial data without meeting specified conditions. Rejection of the data could require additional trials and delay commercialization.
Significant provisions of the EU Artificial Intelligence Act are expected to become effective in August 2026, potentially imposing additional data-quality, transparency, monitoring and human-oversight obligations on the company’s AI activities.
No numeric revenue or EPS guidance was provided. Management stated that $201.1 million of cash, cash equivalents and marketable securities, together with anticipated operating cash flows, should fund working capital and capital expenditure needs for at least the next 12 months; the earnings update indicated operating plans are funded into the second half of 2028.
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