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Adicet Bio, Inc.

Biopharma developer (SEC filing verified)·Phase 1·Boston, MA, United States·CEO: Mr. Chen Schor BA, CPA, M.B.A.
OncologyGene TherapyImmunologyNephrologyMusculoskeletal

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BioSniper AI · ACET

Adicet Bio, Inc. is a clinical-stage biotechnology company developing allogeneic gamma-delta T cell therapies for autoimmune diseases and cancer, with lead candidate ADI-001 in Phase 1 and Phase 2 studies across multiple indications.

Key risk: Capital needs

5.5/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$84.8M

Cash Runway

17.7 mo

Lead Asset

ADI-001 (Phase 1)

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 2 clinical trials · 2 catalysts for Adicet Bio, Inc..

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AI OverviewAI overview is shown in English only.

Adicet Bio, Inc. is a clinical-stage biotechnology company developing allogeneic gamma-delta T cell therapies for autoimmune diseases and cancer, with lead candidate ADI-001 in Phase 1 and Phase 2 studies across multiple indications.

  • Lead product candidate ADI-001 is being evaluated in Phase 1 and Phase 2 studies for autoimmune indications including systemic lupus erythematosus (SLE), lupus nephritis (LN), systemic sclerosis, idiopathic inflammatory myopathy, stiff person syndrome, ANCA-associated vasculitis, and rheumatoid arthritis [sec · filed 2025-10-07].
  • The company plans to meet with the FDA in Q1 2026 to inform Phase 2 pivotal trial design, with a study anticipated to commence in Q2 2026 [sec · filed 2025-10-07].
  • Cash and equivalents were $36.0M as of 2026-06-30, with a net loss of -$21.4M for the quarter, shareholders' equity of $133.4M, and no long-term debt [sec].
  • The company anticipates needing substantial additional capital to fund operations and development, and may seek financing through equity, debt, or collaborations [sec_mda · as of 2026-08-05].
  • More than 25 clinical sites globally are open for enrollment for the Phase 1 study of ADI-001 in autoimmune indications [sec · filed 2025-10-07].

What works

  • ADI-001 is being studied across a broad range of autoimmune indications, potentially addressing large patient populations [sec · filed 2025-10-07].
  • The company has established a global clinical footprint with over 25 sites open for enrollment [sec · filed 2025-10-07].
  • Adicet has no debt and a manageable cash burn, with $36.0M in cash as of 2026-06-30 [sec].

What to weigh

  • The company has a history of net losses, reporting a -$21.4M net loss for the quarter ended 2026-06-30 [sec].
  • Adicet will require substantial additional capital to continue development, with no guarantee of securing financing [sec_mda · as of 2026-08-05].
  • All product candidates are in clinical or preclinical stages, with no approved products or revenue from product sales [sec_mda · as of 2026-08-05].

From the filings

Quoted directly from source documents.

  • Phase 1 enrollment is open for multiple autoimmune indications

    The Phase 1 program is now open for enrollment of patients with systemic sclerosis (SSc), idiopathic inflammatory myopathy, stiff person syndrome, anti-neutrophil cytoplasmic autoantibody associated vasculitis and rheumatoid arthritis (RA).

    SEC filings · October 7, 2025

  • Company plans FDA meeting in Q1 2026 for Phase 2 pivotal trial design

    The Company plans to request a meeting with the U.S. Food and Drug Administration (FDA) in first quarter of 2026 to inform Phase 2 pivotal trial design with a study anticipated to commence in second quarter of 2026.

    SEC filings · October 7, 2025

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · adi-212 — Phase 2 Readout: adi-212Topline data from the Phase 2 study of adi-212 is expected, which will inform further development.
  • 2027-02-15 · Phase3_Topline — Phase 3 Topline: A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Bendamustine and RituxTopline results from a Phase 3 study of bendamustine and rituximab are anticipated.
Risks & what to watch (3)

Key risks

  • Capital needsAdicet will require substantial additional capital to fund operations and development; no assurance of raising funds [sec_mda · as of 2026-08-05].
  • Clinical-stage onlyAll product candidates are in clinical or preclinical stages; no approved products or revenue [sec_mda · as of 2026-08-05].
  • Regulatory uncertaintyPhase 2 pivotal trial design depends on FDA feedback; delays or changes could impact timelines [sec · filed 2025-10-07].

What to watch

  • FDA meeting in Q1 2026 to discuss Phase 2 pivotal trial design for ADI-001 [sec · filed 2025-10-07].
  • Phase 2 pivotal study initiation anticipated in Q2 2026 [sec · filed 2025-10-07].
  • Enrollment progress across multiple autoimmune indications in Phase 1 [sec · filed 2025-10-07].
  • Future financing events to support ongoing operations [sec_mda · as of 2026-08-05].

Sources: SEC filings · SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway4.9

17.7 months

Financial Health9.7

D/E 0.23 · 0% dilution

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth7.2

4 candidates

Catalyst Momentum5.0

2 upcoming, next in ~123d

Insider Signal2.2

0 buys · 4 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

46

Total value held

$41.7M

Showing top 10 of 46 institutional holders of Adicet Bio, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 20, 2026
% of float
8.1%
Days to cover
5.9
Shares short
656,546
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ACET short interest

Governance

Frequently asked questions

What is the AI investment thesis for Adicet Bio, Inc.?

Adicet Bio, Inc. is a clinical-stage biotechnology company developing allogeneic gamma-delta T cell therapies for autoimmune diseases and cancer, with lead candidate ADI-001 in Phase 1 and Phase 2 studies across multiple indications.

What is Adicet Bio, Inc.'s lead drug candidate?

Adicet Bio, Inc.'s most advanced tracked candidate is ADI-001 (Phase 1) for Lupus Nephritis; Lymphoma, Follicular.

What is Adicet Bio, Inc.'s next catalyst?

Adicet Bio, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: adi-212" — expected December 31, 2026.

Who is the CEO of Adicet Bio, Inc.?

Mr. Chen Schor BA, CPA, M.B.A. is the chief executive officer of Adicet Bio, Inc. (ACET).

Where is Adicet Bio, Inc. headquartered?

Adicet Bio, Inc. (ACET) is headquartered in Boston, MA, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.