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ACET

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

ACET evidence brief

What we can confirm

BioSniper Score:
7.0 / 10
Market Cap:
$59.4M
Lead Asset:
ADI-001 (Phase 1)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $59.4M · Lead Asset: ADI-001 (Phase 1)
BioSniper AIPage evidence connected

Prepared research question

What matters most for ACET—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ACET

Adicet Bio is a clinical-stage biotechnology company developing allogeneic gamma delta CAR-T cell and in vivo CAR-T therapies for autoimmune diseases, hematologic malignancies, and solid tumors [news · published 2026-09-25].

Key risk: Cash burn rate

7.0/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$59.4M

Cash Runway

—

Lead Asset

ADI-001 (Phase 1)

Next Catalyst

—

Financial data as of Jun 30, 2026.

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

Similar companies

AI OverviewAI overview is shown in English only.

Adicet Bio is a clinical-stage biotechnology company developing allogeneic gamma delta CAR-T cell and in vivo CAR-T therapies for autoimmune diseases, hematologic malignancies, and solid tumors [news · published 2026-09-25].

  • Reported 12-month DORIS remission in 54% of evaluable SLE patients and complete renal response in 50% of evaluable lupus nephritis patients from the prula-cel Phase 1 study [news · published 2026-09-28].
  • FDA cleared the IND for ADI-212, a CAR targeting PSMA with IL-12 armoring and CRISPR/Cas9 MED12 disruption, for metastatic castration-resistant prostate cancer; Phase 1 enrollment expected to begin in Q4 2026 [news · published 2026-08-27].
  • Cash and equivalents of $33.1M as of 2026-06-30 [sec].
  • Pipeline includes prula-cel (Phase 1 for lupus nephritis, SLE, and other autoimmune indications), ADI-212 (Phase 1 for mCRPC), and ADI-270 (Phase 1 for renal cell carcinoma) [pipeline].
  • Prula-cel has received Fast Track designation from the FDA [pipeline].

What works

  • Prula-cel Phase 1 data showed 54% 12-month DORIS remission in SLE and 50% complete renal response in lupus nephritis, supporting plans for pivotal study start-up in Q4 2026 [news · published 2026-09-28].
  • The company has a differentiated allogeneic gamma delta CAR-T platform that may enable off-the-shelf use, potentially reducing manufacturing complexity and cost [news · published 2026-08-11].
  • ADI-212 IND clearance for mCRPC expands the pipeline into a large oncology market with a novel mechanism (PSMA CAR, IL-12 armoring, MED12 disruption) [news · published 2026-08-27].

What to weigh

  • The company reported a net loss of $21.4M for the period ending 2026-06-30, indicating ongoing cash burn [sec].
  • ADI-212 faces a competitive landscape with 22 competitors including major pharma (Merck, AstraZeneca) in mCRPC [pipeline].
  • Prula-cel is still in Phase 1; pivotal data and regulatory approval remain uncertain and years away [news · published 2026-09-28].

From the filings

Quoted directly from source documents.

  • Prula-cel Phase 1 efficacy results

    “Adicet Bio (NASDAQ:ACET) reported 12-month DORIS remission in 54% of evaluable systemic lupus erythematosus patients and complete renal response in 50% of evaluable lupus nephritis patients”

    News · September 28, 2026

  • ADI-212 IND clearance and planned Phase 1 start

    “the U.S. Food and Drug Administration (FDA) has cleared the Company’s Investigational New Drug (IND) application for ADI-212 for the treatment of patients with metastatic castration-resistant prostate cancer”

    News · August 27, 2026

  • Prula-cel Fast Track designation

    “Regulatory Status: Fast Track”

    Pipeline

Risks & what to watch (3)›

Key risks

  • Cash burn rate — Net loss of $21.4M in the period ending 2026-06-30; cash of $33.1M may not sustain operations beyond 2027 without additional financing [sec].
  • Competitive mCRPC landscape — ADI-212 enters a field with 22 competitors including Merck and AstraZeneca, many with later-stage assets [pipeline].
  • Early-stage pipeline — All programs are Phase 1; no approved products; pivotal data for prula-cel not yet available [news · published 2026-09-28].

What to watch

  • Initiation of prula-cel pivotal study start-up activities in Q4 2026 [news · published 2026-09-28].
  • Phase 1 enrollment for ADI-212 in mCRPC expected to begin in Q4 2026 [news · published 2026-08-27].
  • Future financing or partnership announcements given cash runway concerns [sec].
  • Additional prula-cel data in other autoimmune indications (SSc, AAV, IIM, RA) listed in pipeline [pipeline].

Sources: News · Pipeline · Generated October 5, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.7

D/E 0.23 · 0% dilution

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

47

Total value held

$42.4M

Showing top 10 of 47 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 is a clinical-stage biotechnology company developing allogeneic gamma delta CAR-T cell and in vivo CAR-T therapies for autoimmune diseases, hematologic malignancies, and solid tumors [news · published 2026-09-25].

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.

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.

What therapeutic areas does Adicet Bio, Inc. focus on?

Adicet Bio, Inc. develops therapies across Oncology, Gene Therapy, Immunology, Nephrology, Musculoskeletal.

923 companies304,846 SEC filings22,720 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.