Fundraising Fox

Sudo Bio

Menlo Park, US · Founded 2020 · 10 known investors

Sudo Biosciences develops small molecule therapeutics for neurological and immune-mediated inflammatory conditions. The company focuses on drug development and translational biology to address unmet medical needs.

Also known as Sudo · Sudo Biosciences · Sudo Biosciences, Inc.

Founders & leadership

JB
Jim BristolNamed on SEC filing
DE
Daniel EstesNamed on SEC filing
SB
Scott ByrdNamed on SEC filing

Investors · 10

Also in the syndicate · 4

Eventide Asset ManagementMonograph CapitalSurveyor Capital (a Citadel company)Velosity Capitallead

Funding

SEC filings, press & company announcements

$122.8M disclosed across 3 of 5 rounds · 2021–2024

$63.6MraisedFeb 2024 · 15 investors · Other Technology
Rule 506(b)
Officers, directors & promoters on the filing
  • Edd FlemingDirector
  • Chris GagliardiDirector
  • David JohnsonDirector
  • Scott ByrdExecutive Officer, Director
  • Shinichiro FuseDirector
  • Daniel EstesDirector
Offering amount
$161.8M
Amount sold
$63.6M
First sale
Dec 2023
Incorporated
Corporation, Delaware, 2020
Federal exemptions
06b
Full filing on SEC EDGAR ↗
$22.3MraisedMar 2022 · 6 investors · Other Technology
Rule 506(b)
Officers, directors & promoters on the filing
  • Jim BristolDirector
  • Daniel EstesDirector
  • Scott ByrdExecutive Officer, Director
Offering amount
$22.3M
Amount sold
$22.3M
First sale
Apr 2021
Incorporated
Corporation, Delaware, 2020
Federal exemptions
06b
Full filing on SEC EDGAR ↗

Source: SEC EDGAR Form D. Amounts as filed; amended filings shown once at their latest values.

Company profile

researched Aug 2026

Sudo Biosciences is a biopharmaceutical company designing and developing small-molecule precision inhibitors of tyrosine kinase 2 (TYK2), targeting the enzyme's regulatory pseudokinase (JH2) domain rather than the catalytic JH1 domain. TYK2 mediates signaling from cytokines including IL-12, IL-23 and type I interferons, pathways implicated in autoimmune, inflammatory and neuroinflammatory disease. The company positions allosteric pseudokinase-domain inhibition as a way to achieve TYK2 selectivity without the JAK1/JAK2 off-target effects that have limited the therapeutic window of earlier catalytic-domain JAK inhibitors.

The pipeline centers on two programs described at the time of the Series B: a brain-penetrant, oral CNS candidate for relapsing and progressive multiple sclerosis and for neurodegenerative conditions with underlying neuroinflammation such as Alzheimer's disease and ALS, and a topical TYK2 inhibitor for psoriasis and other immune-mediated dermatologic diseases. The lead CNS asset, SUDO-550, is a brain-penetrant, oral, selective TYK2 pseudokinase inhibitor; first participants were dosed in a Phase 1 trial in December 2024 and the company reported positive Phase 1 results in October 2025.

The company describes its approach as combining medicinal chemistry aimed at optimizing potency, pharmacokinetics and selectivity; translational biology grounded in human genetic data, proteomics and disease-relevant biomarkers with in vitro, in vivo and clinical work; and patient-centered clinical development with precision patient selection.

Business model

Venture-funded biopharmaceutical drug discovery and development; the company advances internally designed small-molecule TYK2 inhibitors through preclinical work into clinical trials, financed by equity rounds from life science investors, corporate venture arms and health-system venture funds.

Traction

Two development candidates were slated to enter clinical trials in 2024. First participants were dosed in a Phase 1 trial of SUDO-550 in December 2024, and the company announced positive Phase 1 results for SUDO-550 in October 2025. Funding totaled $157 million after the December 2023 Series B first close and $188 million after the January 2024 second close, according to company and investor announcements.

Latest developments

In October 2025 Sudo announced positive Phase 1 results for its brain-penetrant allosteric TYK2 inhibitor SUDO-550. In December 2025 it appointed Paul Bavier as Chief Legal Counsel; the leadership page lists him as Chief Legal Officer.

Full profile — market position, technology, go-to-market, geography, history

Market position

Sudo describes its candidates as potential first- and best-in-class within TYK2 inhibition, differentiating on brain penetrance for CNS indications and on topical delivery for dermatology. Its investors note that TYK2 inhibition has already shown benefit in psoriasis, psoriatic arthritis and lupus, and that Sudo is extending the mechanism into neuroinflammatory and neurodegenerative settings including MS, Alzheimer's disease and ALS.

Differentiation rests on targeting the TYK2 pseudokinase domain for selectivity over other JAK family members, and on fit-for-purpose molecule design: a fully CNS-penetrant oral candidate (SUDO-550) intended to treat both relapsing and progressive multiple sclerosis and neuroinflammatory neurodegeneration, alongside a topical candidate intended for dermatologic indications.

Technology

Sudo's compounds are highly potent small-molecule inhibitors that bind the TYK2 pseudokinase (JH2) regulatory domain, an allosteric mechanism intended to block TYK2-mediated IL-12, IL-23 and type I interferon signaling while avoiding inhibition of JAK1 and JAK2, whose catalytic domains are highly conserved across the JAK family. SUDO-550 is engineered for CNS penetration and oral dosing so that it can act on immune cells peripherally and on neurons and glial cells within the central nervous system, addressing both acute inflammatory relapse biology and chronic neuroinflammation. A separate program is formulated for topical dermal delivery. The company cites human genetic evidence—loss-of-function TYK2 variants that lower multiple sclerosis risk and reduce IL-12, IL-23 and type I IFN signaling responses—as target validation.

Go-to-market

Patients with immune-mediated inflammatory and neurological conditions, including multiple sclerosis (roughly one million people affected in the United States, per the company), psoriasis and other immune-mediated dermatologic diseases, and neurodegenerative diseases with neuroinflammatory components such as Alzheimer's disease, ALS and Parkinson's disease.

Geography

Company communications list Sudo Biosciences as based in Carmel, Indiana, with operations across the United States and the United Kingdom.

History

Sudo Biosciences was founded in 2020. It raised a $116 million Series B announced in December 2023, co-led by Enavate Sciences and TPG, then completed a second close of $30 million in January 2024 announced in February 2024, upsizing the round to $147 million. It dosed the first participants in a Phase 1 trial of SUDO-550 in December 2024, reported positive Phase 1 results in October 2025, and appointed a Chief Legal Officer in December 2025.

Compiled by commissioned research from 8 cited public sources — announcements, filings, and press listed under research sources below.

Key figures

latest reported
Total funding raised since foundingFeb 2024$188M
Total Series B round sizeFeb 2024$147M

Company-reported or press-reported figures, each dated to when it was claimed — not independently audited.

Founder mafia

3 people who came through Sudo Bio went on to found or lead other companies.

Timeline · 6

launches, deals, and filings
Dec 2025
Paul Bavier appointed Chief Legal Counsel

source ↗

Oct 2025
Positive Phase 1 results announced for SUDO-550

Sudo announced positive Phase 1 results for its brain-penetrant allosteric TYK2 inhibitor SUDO-550.

source ↗

Dec 2024
First participants dosed in Phase 1 trial of SUDO-550

Sudo announced that the first participants were dosed in a Phase 1 trial of its brain-penetrant allosteric TYK2 inhibitor SUDO-550.

source ↗

Feb 2024
Second close of upsized Series B brings round to $147M

Sudo completed a second close of its Series B during January 2024, raising an additional $30 million from new investors Dementia Discovery Fund, Leaps by Bayer and UPMC Enterprises; total raised since founding reported at $188 million.

$30M source ↗

Dec 2023
Sudo Biosciences raises $116M Series B

Series B financing co-led by Enavate Sciences and TPG (through TPG Life Sciences Innovations and The Rise Fund) to advance brain-penetrant and topical TYK2 candidates into the clinic; total raised since founding reported at $157 million.

$116M source ↗

Dec 2023
Edd Fleming, Shinichiro Fuse and Chris Gagliardi join Board of Directors

In conjunction with the Series B financing, Edd Fleming (Enavate Sciences), Shinichiro Fuse (TPG Life Sciences Innovations) and Chris Gagliardi (Sanofi Ventures) joined Sudo's Board of Directors.

source ↗

Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.

In the news

Research sources · 8

primary sources listed

8 public sources were cited for this profile; the first-party ones are listed here.

Frequently asked questions

What does Sudo Bio do?
Sudo Biosciences develops next-generation allosteric TYK2 inhibitors for multiple sclerosis, neurodegenerative and immune-mediated diseases.
Who are Sudo Bio's investors?
Sudo Bio's investors include Frazier Life Sciences, Monograph Capital Partners, Sanofi Ventures, SV Health Investors, Dementia Discovery Fund, TPG.
How much funding has Sudo Bio raised?
Sudo Bio has disclosed $122.8M raised across 3 of its 5 known rounds.
Where is Sudo Bio headquartered?
Sudo Bio is headquartered in Menlo Park, US.