Company Description
Absci Corporation (Nasdaq: ABSI) is a clinical-stage biopharmaceutical and biotechnology company that applies generative artificial intelligence and synthetic biology to discover and design new protein-based therapeutics. The company describes its approach as Integrated Drug Creation™, combining advanced AI models with a synthetic biology data engine and wet lab validation to accelerate the design of biologic drug candidates that address challenging therapeutic targets.
According to Absci, its Integrated Drug Creation platform uses a continuous feedback loop between AI algorithms and laboratory experiments. Data generated in the lab are fed back into its models, which are then refined to improve the precision and speed of therapeutic design. This platform underpins both Absci’s internal pipeline of AI-designed antibodies and its collaborations with pharmaceutical, biotechnology, technology, and academic partners.
Business focus and therapeutic pipeline
Absci identifies itself as a clinical-stage company, with internal programs built on AI-designed antibodies. A central focus of its current pipeline is ABS-201™, an investigational anti-prolactin receptor (PRLR) antibody. ABS-201 is being developed for androgenetic alopecia, commonly known as male- or female-pattern hair loss, and is also being investigated as a potential therapy for endometriosis, a chronic inflammatory condition affecting women of reproductive age. Absci reports that ABS-201 is designed using its generative AI platform and that preclinical studies have shown hair regrowth activity and support a PRLR-targeting mechanism.
Absci has initiated a Phase 1/2a HEADLINE™ clinical trial of ABS-201 for androgenetic alopecia. The study is described as a randomized, double-blind, placebo-controlled first-in-human trial in healthy volunteers with or without androgenetic alopecia. It is intended to evaluate safety, tolerability, immunogenicity, pharmacokinetics, pharmacodynamics, and early efficacy measures such as target area hair count, hair width, pigmentation, and patient- and investigator-reported outcomes. The company has stated that the multiple ascending dose portion of the trial is designed to demonstrate human proof-of-concept for hair regrowth.
In addition to androgenetic alopecia, Absci is planning development of ABS-201 in endometriosis. The company describes endometriosis as an inflammatory disease characterized by endometrial-like lesions outside the uterine lining, associated with pelvic pain, heavy bleeding, infertility, and ovarian cysts, and notes that there is no medical or surgical cure. Absci indicates that safety, tolerability, and pharmacokinetic data from the ABS-201 androgenetic alopecia trial are expected to support Phase 2 clinical development in endometriosis.
Beyond ABS-201, Absci reports additional internal antibody programs. ABS-101 is described as an anti-TL1A antibody program with interim Phase 1 data showing extended half-life compared to first-generation anti-TL1A competitor programs and a favorable safety profile in the reported trial. Absci has indicated that it is exploring partnership and out-licensing opportunities for ABS-101 rather than advancing later-stage trials internally. The company has also disclosed preclinical programs such as ABS-301, a fully human antibody targeting an undisclosed immuno-oncology pathway discovered through its Reverse Immunology platform, and ABS-501, an AI-designed anti-HER2 antibody candidate with preclinical characteristics reported by the company, including novel epitope interactions and activity in trastuzumab-resistant models.
Technology platform and partnerships
Absci emphasizes that its generative AI Drug Creation platform is central to both its internal pipeline and its partnered programs. The platform combines large-scale AI models, a synthetic biology data engine, and high-throughput wet lab capabilities. The company has described using large-scale molecular dynamics simulations and end-to-end antibody design workflows, supported by external cloud and hardware collaborations, to accelerate biologics design cycles and reduce computational costs.
In its public communications, Absci notes that it works alongside pharmaceutical, biotech, technology, and academic organizations on drug creation partnerships. These collaborations are intended to apply Absci’s AI and synthetic biology capabilities to partner-defined targets while Absci continues to advance its own internal assets. The company has also highlighted expectations around signing additional drug creation partnerships, including with large pharmaceutical companies, as part of its business strategy.
Industry classification and listing
Absci is classified in the Professional, Scientific, and Technical Services sector, within an industry category that includes testing laboratories. Its operations, however, are described in its own materials as focused on biopharmaceutical research and development using AI and synthetic biology. The company’s common stock is listed on The Nasdaq Global Select Market under the trading symbol ABSI, as confirmed in multiple Form 8-K filings that identify its registered securities.
Geographic footprint
Absci states that it is headquartered in Vancouver, Washington. It also reports operating an AI Research Lab in New York City and an Innovation Center in Switzerland. These locations support its AI model development, data generation, and wet lab validation activities that feed into its Integrated Drug Creation platform.
Approach to drug discovery
According to company descriptions, Absci’s approach to drug discovery relies on the interplay between AI model design and experimental validation. The platform generates candidate biologics, which are then tested in the lab. The resulting data are used to refine the models, creating a feedback loop that the company believes improves the quality and speed of candidate optimization. This methodology is applied to internal programs such as ABS-201 and to partnered programs where Absci works on targets selected by collaborators.
Absci’s communications highlight the use of generative design for biologics, in contrast to traditional trial-and-error approaches. The company positions its technology as a way to address targets that are considered challenging for conventional drug discovery methods, and to design antibodies with properties such as affinity, potency, and developability that are informed by large datasets and AI-driven predictions.
Capital markets and corporate activity
Absci files periodic and current reports with the U.S. Securities and Exchange Commission as a public company. Recent Form 8-K filings describe activities such as underwritten equity offerings, the appointment of new board members, and the release of quarterly financial results. For example, the company has reported entering into an underwriting agreement for a public offering of common stock under an effective shelf registration statement, with stated intentions to use net proceeds to fund internal asset development, invest in its Integrated Drug Creation platform, and for working capital and general corporate purposes.
The company also uses investor presentations and webcasts to provide updates on its pipeline, platform, and financial position. These materials are referenced in its Form 8-K filings and are described as including internal pipeline program updates and strategic priorities.
Position within the biopharmaceutical ecosystem
Absci’s public materials present it as a biotech company applying generative AI to biologic drug discovery. Its work spans early-stage design, preclinical research, and progression into clinical trials for its lead programs. By combining AI, synthetic biology, and wet lab experimentation, Absci aims to create new therapeutic antibodies and to work with partners on drug creation projects. Investors and analysts following ABSI typically evaluate the company based on the progress of its clinical-stage programs such as ABS-201, the performance and adoption of its AI-driven platform, and its ability to secure and advance collaborations.