Lifordi Immunotherapeutics
5 known investors
Lifordi Immunotherapeutics develops treatments for immunology and rare diseases through discovery, clinical development, and commercialization. The company serves patients with immunological disorders and rare genetic conditions.
Also known as Lifordi Β· Lifordi Immunotherapeutics, Inc.
Founders & leadership
Investors Β· 5
Also in the syndicate Β· 1
Funding
SEC filings, press & company announcements- Undisclosed amountSeries ANov 2025
5AM Ventures, ARCH Venture Partners, Atlas Venture
Source β
Source: company announcements and press reports β follow each round's link for the claim.
Company profile
researched Aug 2026Lifordi Immunotherapeutics, Inc. is a clinical-stage biotechnology company based in Burlington, Massachusetts, that applies antibody-drug conjugate (ADC) technology β an approach established in oncology β to autoimmune and inflammatory disorders. The company's stated aim is to deliver potent payloads selectively to immune cells so that therapeutic effect is achieved without the systemic toxicity that has historically limited chronic use of such agents.
The lead program, LFD-200, is a subcutaneously administered ADC that delivers a potent glucocorticoid (GC) payload directly to immune cells. It targets myeloid and lymphoid cells via VISTA, described by the company as a highly internalized cell-surface membrane protein; third-party pipeline data lists the target as GR x VISTA with a glucocorticoid receptor modulator mechanism. Preclinical in vitro and non-human primate studies reported by the company showed selective and sustained delivery of the GC payload to immune tissues, inhibition of ex vivo induced inflammatory cytokines, and no observed systemic toxicity at clinically relevant doses, including with weekly subcutaneous dosing for 13 weeks. A Phase 1a/1b randomized, double-blind, placebo- and active-controlled single- and multiple-ascending-dose study (NCT07207954) began on 6 October 2025, enrolling up to 66 healthy participants in the SAD portion, up to 40 healthy participants in a MAD portion of up to four weekly doses, and up to 70 participants with moderate to severe rheumatoid arthritis receiving up to 13 weekly doses.
Beyond LFD-200, Lifordi states that its targeted delivery platform has been applied to other payload classes, including small molecules, antisense oligonucleotides (ASOs) and siRNA. A third-party pipeline database also lists a discovery-stage VISTA-directed asset associated with patent WO2024254212.
Business model
Venture-funded therapeutics developer pursuing internal discovery and clinical development of ADC candidates for immune-mediated disease; the company references a partnering track record and has taken strategic corporate venture investment from Sanofi Ventures, but no revenue-generating products or specific licensing deals are described in the sources.
Traction
Initiated its first-in-human Phase 1 study of LFD-200 in October 2025; the trial was recruiting as of a February 2026 database update. The company presented preclinical data at EULAR 2025, additional non-human primate data at ACR Convergence 2025, and first-in-human Phase 1 data for LFD-200 at EULAR 2026. Total capital raised reached $112 million as of November 2025.
Latest developments
In November 2025, Lifordi announced a strategic investment from Sanofi Ventures alongside additional capital from existing investors ARCH Ventures, 5AM Ventures and Atlas Venture, reported as $42 million and bringing total funding to $112 million; proceeds support the ongoing Phase 1 study of LFD-200 in rheumatoid arthritis and CMC work to secure Phase 2 clinical supply. Christopher Gagliardi, Ph.D., Principal at Sanofi Ventures, joined Lifordi's Board of Directors as an observer. In June 2026 the company presented first-in-human Phase 1 data for LFD-200 at EULAR 2026.
βΈFull profile β market position, technology, go-to-market, geography, history, risks & controversies
Market position
Described in company materials as among the first companies to apply ADC technology, established in oncology, to autoimmune and inflammatory disorders. It was named a winner of Endpoints 11 in September 2024 as a developer of ADCs for autoimmune and inflammatory diseases and was profiled by BioCentury as an emerging company in February 2025 and by The Wall Street Journal in December 2025.
Positions targeted ADC delivery as a way to retain glucocorticoid efficacy while avoiding the systemic toxicity that has constrained long-term steroid use, potentially enabling less frequent dosing; preclinical non-human primate data reported sustained immune-tissue exposure without systemic toxicity signals. The platform is also described as extensible to ASO and siRNA payloads.
Technology
A targeted ADC delivery platform directed at VISTA, a highly internalized cell-surface membrane protein expressed on myeloid and lymphoid cells, used to internalize payloads into immune cells. The lead conjugate LFD-200 carries a potent glucocorticoid payload and is dosed subcutaneously. The company states the same delivery approach has been applied to other payload types including small molecules, antisense oligonucleotides and siRNA. Third-party pipeline classification lists Lifordi assets under antibody-drug conjugates and antibody fragment-drug conjugates (FDCs), with LFD-200 characterized as GR x VISTA targeting with a GR modulator mechanism.
Go-to-market
Patients with autoimmune and inflammatory disorders; the lead clinical indication is moderate to severe rheumatoid arthritis, with the Phase 1 program also enrolling healthy participants.
Geography
Headquartered in Burlington, Massachusetts, United States.
History
A third-party database lists the company as founded in 2023 in Massachusetts. Matthew W. McClure, M.D., was appointed Chief Medical Officer in January 2025. The company raised a $70 million Series A in 2024 and added $42 million in November 2025 with Sanofi Ventures joining, bringing total capital raised to $112 million. Its lead candidate entered clinical development in October 2025.
Risks & controversies
The company is clinical-stage with its lead asset only in Phase 1, so safety and efficacy in humans remain unproven; the FinSMEs report of the November 2025 financing states the deal amount was not disclosed, while other coverage cites $42 million, indicating some inconsistency in disclosed round size.
Compiled by commissioned research from 8 cited public sources β 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 β not independently audited.
Competitors Β· 2
by search overlapCompanies competing with Lifordi Immunotherapeutics for the same Google search keywords, organic and paid, via search-intersection analysis.
Timeline Β· 8
launches, deals, and filingsLifordi presented Phase 1 clinical data for LFD-200, its subcutaneously administered glucocorticoid antibody-drug conjugate, at EULAR 2026.
Sanofi Ventures made a strategic investment alongside existing investors ARCH Ventures, 5AM Ventures and Atlas Venture; reported at $42 million, bringing total raised to $112 million. Funds support the ongoing Phase 1 study of LFD-200 in rheumatoid arthritis and CMC preparations for Phase 2 clinical supply.
$42M source β
Christopher Gagliardi, Ph.D., Principal at Sanofi Ventures, joined Lifordi's Board of Directors as an observer as part of the investment.
Poster presentation reporting that LFD-200 selectively delivered its glucocorticoid payload to immune tissues with sustained anti-inflammatory effects and no observed systemic toxicity in non-human primates; the company also announced initiation of the Phase 1 rheumatoid arthritis study.
Start of a randomized, double-blind, placebo- and active-controlled single and multiple ascending dose study of subcutaneous LFD-200 in healthy adults and participants with moderate to severe rheumatoid arthritis; sponsor Lifordi Immunotherapeutics, status recruiting.
Lifordi presented preclinical data on glucocorticoid antibody drug conjugate LFD-200 for autoimmune and inflammatory diseases at EULAR 2025.
Lifordi appointed Matthew W. McClure, M.D., previously CMO of Aligos Therapeutics and Second Genome, as Chief Medical Officer.
Lifordi named a winner of Endpoints 11 as a developer of antibody drug conjugates for autoimmune and inflammatory diseases.
Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.
In the news
βΈResearch sources Β· 8
primary sources listed
- Lifordi Immunotherapeuticslifordi.com Β· web
8 public sources were cited for this profile; the first-party ones are listed here.
Frequently asked questions
- What does Lifordi Immunotherapeutics do?
- Clinical-stage biotech developing antibody-drug conjugates that deliver glucocorticoids to immune cells for autoimmune disease.
- Who are Lifordi Immunotherapeutics's investors?
- Lifordi Immunotherapeutics's investors include ARCH Venture Partners, Atlas Venture, Sanofi Ventures, 5AM Ventures.


