Ollin Biosciences, Inc.
Austin, US · Founded 2022 · 9 known investors
A clinical-stage biotechnology company focused on therapies for vision-threatening conditions including wet AMD and diabetic macular edema.
Also known as Ollin · Ollin Bio
Founders & leadership
Board
Investors · 9
Also in the syndicate · 5
Funding
SEC filings, press & company announcements$486.2M disclosed across 2 of 4 rounds · 2025–2026
- $330MSeries BJun 2026 · 3 sourcesSource ↗
▶$156.2MraisedJun 2026 · 32 investors · BiotechnologyRule 506(b)
- Travis MurdochDirector
- Fred CohenDirector
- Alaa HalawaDirector
- Cariad ChesterDirector
- Jason EhrlichExecutive Officer, Director
- Paul BernsDirector
- Jason ColomaDirector
- Offering amount
- $330M
- Amount sold
- $156.2M
- First sale
- May 2026
- Incorporated
- Corporation, Delaware, 2022
- Federal exemptions
- 06b
Source: SEC EDGAR Form D. Amounts as filed; amended filings shown once at their latest values.
Company profile
researched Aug 2026Ollin Biosciences, Inc. is an Austin, Texas-based clinical-stage biopharmaceutical company established in 2023 and publicly launched in September 2025. It describes itself as an asset-centric company that acquires and develops therapies for vision-threatening diseases, combining ophthalmology drug development expertise with data science and ophthalmic image analysis tools.
Its lead program, OLN324, is a VEGF/Ang2 bispecific antibody engineered for substantially higher Ang2 potency than faricimab, a smaller protein format, and higher molar dosing than both faricimab and aflibercept (including Eylea HD). It targets wet (neovascular) age-related macular degeneration and diabetic macular edema. OLN324 was discovered by Innovent Biologics (HKEX: 01801, R&D code IBI324) and is being developed in collaboration with Innovent. A prior Phase 1 single- and multiple-ascending-dose study in DME patients was conducted in China. The randomized, U.S.-based Phase 1b JADE proof-of-concept study (NCT07484074, started February 2025) enrolled 164 patients and compared OLN324 head-to-head with faricimab; the company reported faster and greater improvements in retinal anatomy in both DME and wAMD and numerically greater vision gains, with final data announced in March 2026 and presentations at the ASRS annual meeting in July 2026.
A second program, OLN102 (also referenced as VBS-102), is a TSHR/IGF-1R bispecific antibody for thyroid eye disease and the underlying autoimmune condition of Graves' disease, discovered by and developed in collaboration with VelaVigo. As of the Series B announcement it was expected to enter clinical development in 2026.
Founding story
The company was established in 2023 and emerged publicly in September 2025 with an initial $100 million financing. It was co-founded by Jason Ehrlich, M.D., Ph.D., who serves as chief executive officer and previously was chief medical officer and chief development officer at Kodiak Sciences; Travis Murdoch, M.D., is also identified in later coverage as a co-founder of Ollin. ARCH Venture Partners managing director Paul Berns serves as board chair, and ARCH is described as a founding investor alongside co-founding investors Mubadala Capital and Monograph Capital. Management has characterized the company as "purpose-built" to acquire and advance next-generation ophthalmology product candidates rather than to originate discovery-stage assets internally.
Business model
Ollin operates as an asset-centric biopharmaceutical developer that in-licenses or acquires clinical- and late-preclinical-stage ophthalmology candidates originated by other organizations (Innovent Biologics for OLN324, VelaVigo for OLN102) and advances them through clinical development and regulatory approval. Operations are funded by venture and institutional equity financing rather than product revenue.
Traction
Completed the 164-patient randomized Phase 1b JADE head-to-head study versus faricimab with reported anatomic and numerical vision advantages; completed an FDA End-of-Phase 2 meeting and received EMA scientific advice; raised approximately $430 million across a $100 million launch financing and a $330 million Series B; data selected for oral presentation at the ASRS 44th Annual Scientific Meeting in July 2026. Third-party data indicates a headcount range of 10-50.
Latest developments
On June 24, 2026 Ollin announced an oversubscribed $330 million Series B co-led by TCGX and ARCH Venture Partners, with TCGX Managing Partner Cariad Chester joining the board. Proceeds are earmarked for global Phase 3 trials of OLN324 in DME and wAMD starting in the second half of 2026 and for moving OLN102 into clinical development. In July 2026 the company announced oral presentations of JADE Phase 1b results at the ASRS annual meeting.
▸Full profile — market position, technology, go-to-market, geography, history, risks & controversies
Market position
Positions itself as a challenger in retinal vascular disease against the established VEGF/Ang2 inhibitor faricimab (Genentech's Vabysmo) and anti-VEGF agents including aflibercept/Eylea HD, in what the company describes as a $15 billion retina market. Investors and management describe OLN324 as a potential best-in-class therapy, though these are forward-looking claims based on Phase 1b data.
Stated differentiation rests on molecular engineering of OLN324 (higher Ang2 potency versus faricimab, smaller protein format, higher molar dose) and on generating randomized head-to-head comparative data against the market leader at an early stage, plus an acquisition-led pipeline strategy that pairs in-licensed assets from Innovent Biologics and VelaVigo with an experienced ophthalmology development team.
Technology
Bispecific antibody therapeutics for ocular disease. OLN324 is an intravitreally administered VEGF/Ang2 bispecific antibody with higher Ang2 potency than faricimab, a smaller protein format, and higher molar dosing, intended to improve target coverage and treatment durability. OLN102 is a TSHR/IGF-1R bispecific antibody designed to block both clinically validated TED targets for more precise tissue targeting and a wider therapeutic index. The company also states it uses advanced ophthalmic image analysis and data science tools in development.
Go-to-market
Development-stage; the company frames its strategy around leveraging validated biology and clear regulatory pathways, running head-to-head comparative trials against the market-leading VEGF/Ang2 inhibitor faricimab to establish differentiation with retina specialists, and pursuing registrational Phase 3 programs in the U.S. and internationally following FDA and EMA interactions.
Patients with retinal vascular diseases (diabetic macular edema and wet age-related macular degeneration) and thyroid eye disease/Graves' disease, reached through retina specialists and ophthalmologists.
Geography
Headquartered in Austin, Texas, United States. The JADE Phase 1b study was U.S.-based; an earlier Phase 1 dose-escalation study of OLN324 was conducted in DME patients in China. Planned Phase 3 programs are described as global, with regulatory engagement in both the U.S. (FDA) and Europe (EMA). Development partners Innovent Biologics and VelaVigo are China-based.
History
Established in 2023, Ollin operated without a public profile until its September 17, 2025 launch announcement, which disclosed $100 million in initial financing and two bispecific antibody programs. The Phase 1b JADE trial of OLN324 began in February 2025 and was fully enrolled at launch, with final data reported in March 2026. In June 2026 the company announced an oversubscribed $330 million Series B, bringing disclosed financing to approximately $430 million, and stated it had completed an End-of-Phase 2 meeting with the FDA and obtained EMA scientific advice ahead of global Phase 3 studies planned for the second half of 2026.
Risks & controversies
The lead asset has only Phase 1b proof-of-concept and earlier dose-escalation data; reported vision gains versus faricimab were numerical rather than statistically demonstrated, and registrational Phase 3 studies had not begun as of the latest sources. The company has no approved products or disclosed revenue and depends on equity financing. Both lead programs are in-licensed from third-party originators (Innovent Biologics, VelaVigo), creating partner dependency, and OLN324 would enter a market with entrenched approved competitors.
Compiled by commissioned research from 8 cited public sources — announcements, filings, and press listed under research sources below.
Key figures
latest reportedCompany-reported or press-reported figures, each dated to when it was claimed — not independently audited.
Timeline · 9
launches, deals, and filingsOllin announced upcoming oral presentations of Phase 1b JADE results comparing OLN324 with faricimab in DME and wAMD at the ASRS annual meeting, July 15-18 in Montreal, Canada.
Series B co-led by new investor TCGX and founding investor ARCH Venture Partners, with a16z Bio+Health, Blackstone Multi-Asset Investing, Commodore Capital, CPP Investments, RA Capital Management, accounts advised by T. Rowe Price Investment Management, an unnamed sovereign wealth fund, Mubadala Capital and Monograph Capital. Proceeds fund global Phase 3 development of OLN324 and advancement of OLN102 into the clinic.
$330M source ↗
Cariad Chester, Managing Partner of TCGX, joined Ollin's Board of Directors in connection with the Series B financing.
Company stated it completed an End-of-Phase 2 meeting with the FDA and received EMA scientific advice on the OLN324 Phase 3 program, with global Phase 3 trials in DME and wAMD planned for the second half of 2026.
Ollin reported final results of the randomized 164-patient JADE study comparing OLN324 with faricimab (Vabysmo), reporting faster and greater improvements in retinal anatomy in both DME and wAMD and numerically greater vision gains.
Company publicly launched as an Austin, Texas-based clinical-stage biopharmaceutical company with $100 million in initial financing led by ARCH Venture Partners, Mubadala Capital and Monograph Capital, disclosing two bispecific antibody programs (OLN324, OLN102).
$100M source ↗
OLN324 (Innovent R&D code IBI324) was discovered by Innovent Biologics (HKEX: 01801) and is being developed in collaboration with Ollin.
OLN102 (VBS-102) was discovered by VelaVigo and is being developed in collaboration with Ollin; expected to enter clinical development in 2026.
Ollin-sponsored Phase 1b study assessing safety, tolerability, pharmacokinetics and exploratory efficacy of two formulations of intravitreal OLN324 in adults with wet AMD or DME; listed as completed.
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
- Ollin Biosciences Raises $330M in Series B Fundingfinsmes.com · web
8 public sources were cited for this profile; the first-party ones are listed here.
Frequently asked questions
- What does Ollin Biosciences, Inc. do?
- Austin-based clinical-stage biotech developing in-licensed bispecific antibodies for retinal and thyroid eye disease.
- Who are Ollin Biosciences, Inc.'s investors?
- Ollin Biosciences, Inc.'s investors include Monograph Capital Partners, ARCH Venture Partners, MC Healthcare Ventures, TCG Crossover.
- How much funding has Ollin Biosciences, Inc. raised?
- Ollin Biosciences, Inc. has disclosed $486.2M raised across 2 of its 4 known rounds.
- Where is Ollin Biosciences, Inc. headquartered?
- Ollin Biosciences, Inc. is headquartered in Austin, US.