BREAKING — Aqtual raises oversubscribed $31M Series B to scale its cfDNA platform PRIMA-102 trial surpasses 1,300 patients enrolled One blood draw reads 1,000,000+ transcription-factor binding sites First cfDNA assay to integrate DNA, epigenetics & protein-DNA binding ~$47M raised total across seed, Series A and Series B BREAKING — Aqtual raises oversubscribed $31M Series B to scale its cfDNA platform PRIMA-102 trial surpasses 1,300 patients enrolled One blood draw reads 1,000,000+ transcription-factor binding sites First cfDNA assay to integrate DNA, epigenetics & protein-DNA binding ~$47M raised total across seed, Series A and Series B

Company Profile · Precision Medicine · Hayward, CA

Aqtual, Inc. logo

The AQTUAL wordmark, its “Q” drawn as a strand of DNA — a quiet nod to the company’s former name, BloodQ. Hayward, California, 2025.

AQTUAL

Reading the blood’s hidden signal — epigenetics, gene regulation and transcriptomics from a single draw.

Founded 2018 ~32 Employees Series B · $31M Liquid Biopsy cfDNA Platform
The Story

The company that decided the noise was the signal

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.

$47M
Total raised
1M+
Binding sites read
1,300+
Trial patients
6
Therapeutic areas
1
Blood draw
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.
— Diana Abdueva, PhD · Founder & CEO
Under the Hood

One draw, a genome’s worth of context

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.

What a single Aqtual assay surveys

Regulatory elements read from circulating chromatin in one blood draw

200K
Gene promoters
400K
Enhancers
50K
Insulators
20K
Silencers
1M
TF binding sites
The Problem & The Edge

Ending trial-and-error medicine

The problem it solves

  • Chronic-disease treatment is often educated guessing — patients try drug after drug.
  • In rheumatoid arthritis, finding an effective biologic can take months of failed attempts.
  • Failed therapies mean cost, side effects and disease progression.
  • Existing liquid biopsy mostly detects cancer, not which treatment will work.

How Aqtual is different

  • Amplifies the cfDNA “noise” competitors filter out.
  • Reads epigenetics, gene regulation and transcriptomics — not just sequence.
  • First to combine DNA, epigenetic regulation and protein-DNA binding in one assay.
  • Starts with autoimmune disease, then extends across six therapeutic areas.
  • Aims to predict therapy response, not merely diagnose.
Products & Services

A platform, not a single test

Core Technology

Active Chromatin cfDNA Platform

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.

Flagship Product

RA Therapy Response Test

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).

Pipeline

Oncology & Chronic Disease

Biomarker discovery and disease-monitoring assays extending the platform across oncology, immunology, cardiovascular, metabolic and neurological conditions for detection, monitoring and stratification.

The Money

Roughly $47M, three rounds

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.

Seed · 2019
$8.5M
Series A · 2023
$16M
Series B · 2025
$31M
Lead Investors

The syndicate

Genoa Ventures · Manta Ray Ventures · Yu Galaxy · Bold Capital · Bold Longevity Growth Fund

Stage

Pre-commercial

Scaling toward launch of its first diagnostic test; PRIMA-102 expected to complete in Q4 2025.

Expertise

Built by scientists, run as a platform

Diana Abdueva, PhD

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.

Rich Rava, PhD

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.

Where It Fits

The market and the alternatives

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.

Timeline

From BloodQ to Series B

2018

Founded as BloodQ

Launched in the San Francisco Bay Area to build a cfDNA-based precision-medicine platform.

2019

Seed financing

Raised roughly $8.5M to develop its circulating-chromatin technology.

2023

Emerges from stealth · $16M Series A

Rebranded as Aqtual with a round co-led by Genoa Ventures, Manta Ray Ventures and Yu Galaxy.

2024

Clinical & executive expansion

Launched its rheumatoid arthritis trial and appointed new medical and research executives.

2025

$31M Series B & trial milestone

Oversubscribed round; PRIMA-102 surpassed 1,300 patients, targeting Q4 2025 completion.

Good to Know

Frequently asked

What does Aqtual do?

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.

What is Aqtual’s first product?

A blood test that predicts which therapy will work for rheumatoid arthritis patients, validated through the PRIMA-102 clinical trial (NCT05936970).

Who founded Aqtual and where is it based?

Founded in 2018 (formerly BloodQ) by CEO Diana Abdueva, PhD and CTO Rich Rava, PhD, and headquartered in Hayward, California.

How much has Aqtual raised?

Roughly $47M total — an ~$8.5M seed, a $16M Series A in 2023 and an oversubscribed $31M Series B in July 2025.

How is it different from other liquid-biopsy companies?

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.