Fundraising Fox

Autotelicbio

4 known investors

Korean biotech developing antisense oligonucleotide and other new drugs for CNS and rare incurable diseases.

Also known as Autotelic Bio · Autotelic Bio Inc. · Autotelic Korea · Autotelic.bio · 오토텔릭바이오

Investors · 4

Also in the syndicate · 3

Mega InvestmentST PharmUTC Investment

Company profile

researched Aug 2026

Autotelic Bio Inc. (Korean: 오토텔릭바이오) is a South Korean biotechnology company developing innovative new drugs, with a stated focus on treatments for central nervous system (CNS) disorders and rare, incurable diseases. Its scientific approach centers on antisense oligonucleotide (ASO) therapeutics, which the company describes as inhibiting production of disease-associated target proteins by blocking disease-expressing genes at the mRNA level, positioning the platform as a means of addressing targets considered undruggable by conventional modalities.

The company's pipeline is identified by ATB-series program codes, including ATB-101, ATB-301, ATB-320, ATB-610 and ATB-810. A clinical development registry lists five trials associated with the organization across six trial active ingredients, with a highest development phase of Phase 3; Phase 3 ingredients listed include atb-1013 and dapagliflozin, and Phase 1 ingredients include aldesleukin, atb-320, olmesartan and taso-001. The registry records the first clinical trial in 2021 and no marketed drug or NDA approval to date.

Autotelic Bio is headquartered in Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do, with an R&D center in Suji-gu, Yongin-si, Gyeonggi-do. The company states core values of innovation, shared growth and transparency, and describes governance through a board of directors and a steering committee with communication to investors.

Founding story

The company was established in November 2015 as Autotelic Korea and received corporate R&D center accreditation in September 2017. In January 2018 it changed its name from Autotelic Korea to Autotelic Bio, and in February 2018 received venture designation from the Korea Technology Finance Corporation.

Business model

The company develops proprietary drug candidates and monetizes them through out-licensing, technology transfer and co-development arrangements with pharmaceutical partners in specific territories, supplemented by government and public-foundation R&D grants and equity investment from venture and strategic corporate investors.

Revenue arises from licensing and technology transfer agreements with pharmaceutical partners (for example, exclusive license and supply agreements for ATB-101 in Mexico and Brazil) and from co-development agreements, alongside non-dilutive public R&D grant funding.

Traction

A clinical registry records five trials with six trial active ingredients, a highest phase of Phase 3, a first clinical trial in 2021 and no marketed drug or NDA approval; last known activity is recorded as 2025. Company-reported milestones include Phase 1 IND approvals for ATB-101 and ATB-301 (2021), successful completion of an ATB-101 Phase 1 DDI/PK study (2021), Phase 3 IND approval for ATB-101 (2022), multiple government R&D grants, and licensing deals for ATB-101 with Chinoin (Mexico, 2024) and Aché (Brazil, 2025).

Latest developments

In June 2025 Autotelic Bio signed an exclusive license and technology transfer agreement with Aché of Brazil for ATB-101. In January 2026, ATB-810 was selected for the Ministry of SMEs and Startups' Deep Tech Challenge Project.

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

Market position

Autotelic Bio positions its ASO platform technology as enabling the drugging of undruggable targets, combined with a pipeline that has advanced a lead asset (ATB-101) into Phase 3-stage development and generated out-licensing deals in Latin America.

Technology

Autotelic Bio's core platform is antisense oligonucleotide (ASO) therapeutics, delivered by injection, which act on mRNA to inhibit production of disease-associated proteins and block expression of disease-causing genes. The company presents this platform as a route to drugging undruggable targets, and applies it toward CNS and rare incurable disease indications.

Go-to-market

Patients with CNS disorders and rare, incurable diseases are the intended beneficiaries; commercial counterparties are pharmaceutical companies that license, co-develop or supply Autotelic Bio's candidates in their territories, including Jeil Pharm, Youngjin Pharm, Clinigen in the UK, Chinoin in Mexico and Aché in Brazil.

Geography

Headquarters in Cheongju-si, Chungcheongbuk-do, South Korea, with an R&D center in Yongin-si, Gyeonggi-do (previously a Pankyo R&D center). Partnerships extend to the United Kingdom (Clinigen), Mexico (Chinoin), Brazil (Aché) and China-based CRO Tigermed for global development of ATB-101.

History

Autotelic Korea was founded in November 2015 in Cheongju-si, Korea, and secured its first government R&D grant for ATB-101 from the Ministry of SMEs and Startups in 2017 alongside corporate R&D center accreditation. Renamed Autotelic Bio in January 2018, the company signed a TIPS investment agreement and received angel investment that year and established a Pankyo R&D center in September 2018, which was expanded and relocated in September 2019. In 2019 it completed a technology transfer and investment agreement with Jeil Pharm for ATB-101, a CMO agreement with ST Pharm for TASO, and an investment agreement with Aju Pharm and KODIT, and ATB-301 was selected for the MFDS "Pharm Navi" project. Series A rounds were recorded in January 2019 (Mega Investment, UTC Investment) and February 2020 (Stonebridge Ventures), followed by a strategic investment from ST Pharm and two other pharmaceutical companies in August 2020 and a Series B round in March 2022. Clinically, ATB-301 and ATB-101 received Phase 1 IND approvals in February 2021, ATB-101's Phase 1 DDI/PK study completed in August 2021, and ATB-101 received Phase 3 IND approval in May 2022. Subsequent milestones include a co-development agreement with Youngjin Pharm (March 2023), an MOU with Dream CIS and Tigermed for global development of ATB-101 (June 2023), an exclusive license and supply agreement for ATB-101 with Chinoin in Mexico (April 2024), an exclusive license and technology transfer agreement with Aché of Brazil for ATB-101 (June 2025), and selection of ATB-810 for the Deep Tech Challenge Project in January 2026.

Compiled by commissioned research from 5 cited public sources — announcements, filings, and press listed under research sources below.

Key figures

latest reported
Clinical trials (registry count)Jan 20255 trials
First clinical trialJan 20212021 (NCT04862767)
Highest clinical phaseJan 2025Phase 3
Marketed drugsJan 20250 drugs
NDA approvalsJan 20250 approvals
Trial active ingredientsJan 20256 ingredients

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

Timeline · 24

launches, deals, and filings
Jan 2026
ATB-810 selected for Ministry of SMEs and Startups' Deep Tech Challenge Project

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Jun 2025
Exclusive license and technology transfer agreement with Aché (Brazil) for ATB-101

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Apr 2024
ATB-101 exclusive license and supply agreement with Chinoin in Mexico

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Jun 2023
MOU with Dream CIS and Tigermed for global development of ATB-101

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Apr 2023
ATB-101 R&D grant from Ministry of SMEs and Startups

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Mar 2023
Co-development agreement with Youngjin Pharm

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Sep 2022
ATB-610 R&D grant from Korea Drug Development Fund

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May 2022
ATB-101 receives IND approval for Phase 3 study

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Jan 2022
ATB-320 R&D grant from Ministry of Trade, Industry and Energy

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Aug 2021
ATB-101 Phase 1 (DDI, PK) study completed

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Feb 2021
Phase 1 IND approvals for ATB-101 and ATB-301

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Jan 2021
ATB-301 agreement with Clinigen (UK)

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Jan 2020
Inno-biz certification (technology and innovation-oriented SME)

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Oct 2019
Investment agreement with Aju Pharm and KODIT

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Sep 2019
Pankyo R&D Center expansion and relocation

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May 2019
TASO CMO agreement with ST Pharm

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Apr 2019
ATB-301 selected for MFDS "Pharm Navi" project

ATB-301 was selected in the MFDS "Pharm Navi" project, described as similar to the US FDA fast track regulatory system.

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Jan 2019
ATB-101 technology transfer and investment agreement with Jeil Pharm

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Sep 2018
Pankyo R&D Center established

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Jul 2018
TIPS investment agreement and ATB-301 R&D grant

Signed an investment agreement under the TIPS program; ATB-301 received an R&D grant from the Ministry of SMEs and Startups.

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Feb 2018
Venture designation from Korea Technology Finance Corporation

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Jan 2018
Company name changed from Autotelic Korea to Autotelic Bio

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Sep 2017
Corporate R&D center accreditation and ATB-101 R&D grant

Received corporate R&D center accreditation and an R&D grant for ATB-101 from the Ministry of SMEs and Startups.

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Nov 2015
Autotelic Korea established

The company was founded as Autotelic Korea in Cheongju-si, Republic of Korea.

source ↗

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

Research sources · 5

primary sources listed

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

Frequently asked questions

What does Autotelicbio do?
Korean biotech developing antisense oligonucleotide and other new drugs for CNS and rare incurable diseases.
Who are Autotelicbio's investors?
Autotelicbio's investors include Colopl Next.