Company Profile · Precision Medicine · Hayward, CA
The AQTUAL wordmark, its “Q” drawn as a strand of DNA — a quiet nod to the company’s former name, BloodQ. Hayward, California, 2025.
Reading the blood’s hidden signal — epigenetics, gene regulation and transcriptomics from a single draw.
For most of liquid biopsy’s history, the goal was to strip away background “noise” in a blood sample to catch a faint cancer signal. Aqtual, Inc. looked at that same discarded static and reached the opposite conclusion: it was information. The Hayward, California company built a platform to amplify it.
Aqtual is a precision-medicine company developing blood-based tests for chronic disease and oncology. Its proprietary active-chromatin cell-free DNA (cfDNA) platform measures epigenetics, gene regulation and transcriptomics from a single blood draw — capturing circulating chromatin rather than only the DNA sequence. According to the company, it is the first assay to integrate DNA, epigenetic regulation and protein-DNA binding in one blood-based test.
The practical promise is specific. Instead of detecting that disease exists, Aqtual aims to reveal how a given patient’s biology is behaving right now — which tissues are active, which regulatory switches are flipped, and, ultimately, which therapy is most likely to work. Its first commercial product targets rheumatoid arthritis, where patients can spend months cycling through biologics before finding one that helps.
Eliminating background noise has been the gold standard of liquid biopsy, but it turns out that ‘noise’ is a clinically relevant, information-rich radio frequency that Aqtual has learned to amplify.
Where a standard cfDNA test reads sequence, Aqtual reads regulation. By capturing active chromatin circulating in blood, a single assay surveys the control layer of the genome — the promoters, enhancers and binding sites that decide which genes are switched on. The scale of that survey is the platform’s core differentiator.
Regulatory elements read from circulating chromatin in one blood draw
Captures and analyzes circulating chromatin to measure epigenetics, gene regulation and transcriptomics from one blood draw — integrating DNA, epigenetic regulation and protein-DNA binding in a single assay.
A blood test to guide rheumatoid arthritis treatment by identifying biomarkers linked to drug response, aiming to predict the right drug class per patient. Validated via the PRIMA-102 trial (NCT05936970).
Biomarker discovery and disease-monitoring assays extending the platform across oncology, immunology, cardiovascular, metabolic and neurological conditions for detection, monitoring and stratification.
Aqtual’s July 2025 Series B was oversubscribed, drawing new investors Bold Capital and Bold Longevity Growth Fund alongside returning backers Genoa Ventures, Manta Ray Ventures and Yu Galaxy. The round funds the push to commercialize the rheumatoid arthritis test and scale the platform.
Genoa Ventures · Manta Ray Ventures · Yu Galaxy · Bold Capital · Bold Longevity Growth Fund
Scaling toward launch of its first diagnostic test; PRIMA-102 expected to complete in Q4 2025.
FOUNDER & CEO
Leads Aqtual’s vision of translating deep genomics research into practical clinical products, and its contrarian bet that discarded cfDNA signal carries clinical meaning.
CO-FOUNDER & CTO
Drives the technology behind the active-chromatin cfDNA platform, pairing molecular biology with a scalable, multi-omic assay design.
The team of roughly 32 spans molecular biology, data science and clinical development — a deliberately small group given the platform’s enormous surface area. In 2024 the company added medical, translational-research and data-integrity executives, including Maggie Louie, PhD as VP of Translational Research and Strategic Partnerships.
Aqtual sits at the intersection of liquid biopsy, epigenomics and precision medicine — a field crowded with cancer-detection players such as Guardant Health, Grail, Freenome and DELFI Diagnostics. Its differentiation is direction: rather than early cancer screening, Aqtual reads gene regulation to predict therapy response, and it opens in autoimmune disease rather than oncology.
The business model is B2B molecular diagnostics: clinically validated blood tests and biomarker classifiers sold to clinicians and health systems, with parallel potential in pharmaceutical partnerships for drug-response biomarkers. The wager is that a single platform reading the genome’s control layer can generalize across six disease areas — turning one assay into many products.
Launched in the San Francisco Bay Area to build a cfDNA-based precision-medicine platform.
Raised roughly $8.5M to develop its circulating-chromatin technology.
Rebranded as Aqtual with a round co-led by Genoa Ventures, Manta Ray Ventures and Yu Galaxy.
Launched its rheumatoid arthritis trial and appointed new medical and research executives.
Oversubscribed round; PRIMA-102 surpassed 1,300 patients, targeting Q4 2025 completion.
It reads epigenetics, gene regulation and transcriptomics from cell-free DNA in a single blood draw, using an active-chromatin cfDNA platform to build diagnostic and therapy-prediction tests.
A blood test that predicts which therapy will work for rheumatoid arthritis patients, validated through the PRIMA-102 clinical trial (NCT05936970).
Founded in 2018 (formerly BloodQ) by CEO Diana Abdueva, PhD and CTO Rich Rava, PhD, and headquartered in Hayward, California.
Roughly $47M total — an ~$8.5M seed, a $16M Series A in 2023 and an oversubscribed $31M Series B in July 2025.
Instead of filtering cfDNA “noise” to detect cancer, Aqtual amplifies it and integrates DNA, epigenetics and protein-DNA binding in one assay aimed at therapy prediction across multiple diseases.
Interview & product-demo videos: search “Aqtual liquid biopsy” on YouTube — the company has not published an official channel at time of writing.