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Adicet Bio, Inc. (ACET)·Q3 2024 Earnings Summary

Executive Summary

  • Q3 showed operational progress as ACET expanded ADI-001 to six autoimmune indications, opened enrollment for lupus nephritis (LN) in Q4, and reiterated first data for LN and ADI-270 in 1H25; cash stood at $202.1M with runway into 2H26 .
  • P&L remained in line with a clinical-stage profile: Net loss was $30.5M (EPS $(0.34)), modestly higher vs Q2 on slightly higher R&D, and improved YoY due to the absence of a non‑cash 2023 goodwill impairment; interest income provided a partial offset .
  • Guidance/timing shifts: non‑LN autoimmune preliminary data moved from 1H25 to 2H25; LN enrollment slipped to Q4 from prior Q3 target; ADI-270 timelines (start in Q4, data in 1H25) maintained .
  • Near-term stock catalysts: continued site activations and patient accrual, ADI-270 trial initiation, and preliminary data in 1H25 (LN/ADI-270); mechanistic biomarker data (tissue trafficking and complete B‑cell depletion) reinforce the platform narrative .

What Went Well and What Went Wrong

What Went Well

  • Expanded ADI-001 autoimmune footprint from four to six indications (added IIM and SPS) and activated sites; CEO: “We are now investigating ADI-001 across six autoimmune indications…” .
  • Platform validation: biomarker data demonstrated robust tissue trafficking and complete CD19+ B‑cell depletion in secondary lymphoid tissue, supporting best‑in‑class potential in autoimmune diseases .
  • Solid tumor program momentum: ADI-270 received FDA Fast Track in ccRCC; company reiterated plan to open enrollment in Q4’24 and share preliminary data in 1H25 .

What Went Wrong

  • Autoimmune timelines partially pushed: non‑LN preliminary data moved to 2H25 from 1H25, and LN enrollment opened in Q4 vs earlier aim to start in Q3 .
  • Cash balance trended lower with ongoing development (Mar 31: $247.6M; Jun 30: $224.1M; Sep 30: $202.1M) despite runway maintained into 2H26, reinforcing continued cash burn as trials scale .
  • YoY net loss improvement is flattered by a non‑recurring 2023 goodwill impairment ($19.5M); underlying OpEx otherwise steady to slightly up YoY in R&D and G&A .

Financial Results

Metric ($USD Millions, except per-share)Q3 2023Q1 2024Q2 2024Q3 2024
Revenue
R&D Expense26.167 23.897 25.901 26.253
G&A Expense6.633 6.974 6.948 6.900
Goodwill Impairment19.462
Total Operating Expenses52.262 30.871 32.849 33.153
Interest Income2.520 2.918 2.999 2.730
Net Loss(49.885) (28.016) (29.901) (30.478)
Net Loss per Share (EPS)(1.16) (0.35) (0.33) (0.34)
Stock-based Compensation (included)5.6 5.7 6.0 6.8

Notes: “—” indicates not reported; ACET reported no revenue line items in these periods .

Cash and Balance Highlights

Metric ($USD Millions)Q1 2024 (Mar 31)Q2 2024 (Jun 30)Q3 2024 (Sep 30)
Cash & Cash Equivalents / ST Investments247.589 224.069 202.065
Working Capital232.889 210.449 186.922
Total Stockholders’ Equity258.804 235.111 211.531

Segment breakdown and margins: Not applicable; ACET is a pre‑revenue, clinical-stage biotech with no reported segment revenues or gross/operating margins in the period .

Key Operating KPIs

KPIQ1 2024Q2 2024Q3 2024
ADI-001 autoimmune indications includedPlanning expansion beyond LN LN, SLE, SSc, AAV (4) LN, SLE, SSc, AAV, IIM, SPS (6)
Autoimmune trial statusPlan LN Phase 1 in 2Q24 Plan LN enrollment in Q3’24 LN enrollment opened in Q4’24; additional sites scaling
ADI-270 regulatory statusPlan IND 2Q24 IND cleared; Fast Track granted Fast Track reiterated; enrollment planned Q4’24
Preliminary data timingLN: 4Q24/1Q25 window LN/SLE/SSc/AAV: 1H25 LN: 1H25; other autoimmune: 2H25; ADI‑270: 1H25

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
Cash runwayCorporateInto 2H 2026 Into 2H 2026 Maintained
ADI-001 LN – start/enrollment2024Begin LN enrollment in Q3’24 Enrollment opened in Q4’24 Lowered (timing slip)
ADI-001 LN – preliminary data20251H25 1H25 Maintained
ADI-001 SLE/SSc/AAV – preliminary data20251H25 2H25 Lowered (pushed out)
ADI-270 – trial initiation2024Initiate in Q4’24 Open enrollment in Q4’24 Maintained
ADI-270 – preliminary data20251H25 1H25 Maintained

Drivers: management cited site activation and enrollment pacing for autoimmune timelines; broader program scope (six indications) also adds operational complexity .

Earnings Call Themes & Trends

No Q3’24 earnings call transcript was available in our document set; themes are synthesized from company press releases.

TopicPrevious Mentions (Q1 & Q2)Current Period (Q3)Trend
Autoimmune expansionPlan to expand beyond LN (Q1); IND clearances for SLE/SSc/AAV and Fast Track for LN (Q2) Expanded to six indications adding IIM and SPS; sites activated; LN enrollment opened Q4 Expanding scope; operational ramp; some timing slippage
ADI-270 solid tumor programPlan IND 2Q (Q1); IND cleared + Fast Track; start Q4, data 1H25 (Q2) Fast Track reiterated; enrollment opening Q4; data 1H25; conference presentations On track; added visibility via presentations
Platform validationBiomarker data show robust tissue trafficking and complete B‑cell depletion Strengthened mechanistic support
Cash runwayInto 2H26 (Q1, Q2) Into 2H26 (Q3) Maintained runway despite cash utilization

Management Commentary

  • “We are now investigating ADI-001 across six autoimmune indications… This progress highlights the broad and important potential applications of our gamma delta platform.” — Chen Schor, President & CEO .
  • “We expect to have several additional sites open for enrollment by the end of the fourth quarter of 2024… Our sites are open to enroll patients with LN, and we plan to initiate enrollment of patients with SLE, SSc, and AAV in the fourth quarter of this year.” — Francesco Galimi, M.D., Ph.D., SVP & CMO .
  • “These results clearly support the potential of ADI-001… demonstrating robust trafficking and complete B cell depletion in tissue…” — Blake Aftab, Ph.D., Chief Scientific Officer .

Q&A Highlights

  • No earnings call transcript was available in the source documents for Q3’24; therefore no Q&A highlights or clarifications can be provided from a call transcript [List: 0 found for earnings-call-transcript].

Estimates Context

  • Wall Street consensus (S&P Global) for Q3’24 EPS and revenue was unavailable via our tool at the time of analysis; as a clinical-stage biotech, revenue is not reported in ACET’s quarterly statements and EPS is driven by OpEx/interest items .
  • Implication: With no revenue and minimal non-operating items, estimate revisions (if any) would likely reflect updated OpEx spend trajectory and timing of trial starts rather than top-line changes; we cannot assess beats/misses vs consensus without S&P Global figures (unavailable).

Key Takeaways for Investors

  • Platform momentum: Expansion to six autoimmune indications and strong biomarker data (tissue trafficking, complete B‑cell depletion) reinforce the differentiated gamma delta approach and potential for durable tissue-level impact in autoimmune disease .
  • Execution path: LN enrollment opened in Q4 and additional sites expected to come online; preliminary LN data in 1H25 remains the pivotal readout for the autoimmune thesis .
  • Solid tumor optionality: ADI-270 (Fast Track) set to open enrollment in Q4 with first data in 1H25; positive signals could broaden the narrative beyond autoimmune to CD70+ solid tumors .
  • Cash runway into 2H26 provides funding visibility through initial data catalysts across both ADI-001 (autoimmune) and ADI-270 (ccRCC), though cash levels are trending down as trials ramp .
  • Near-term trading catalysts: site activation/enrollment updates; conference disclosures; confirmation of ADI-270 trial start; any early safety/kinetics updates in autoimmune cohorts .
  • Watch for timeline risk: non‑LN data pushed to 2H25 and LN enrollment slipped to Q4; further delays could pressure sentiment; conversely, clean execution on enrollment and early signals could be stock‑positive .
  • P&L steady-state: With no revenue line and OpEx largely in R&D, quarterly EPS movements are modest and driven by spend/timing and interest income; YoY comparison is affected by a non‑recurring 2023 goodwill impairment .

Additional Source Documents (Q3-related and prior-quarter context)

  • Q3’24 results press release and 8‑K: financials and operational updates .
  • Q2’24 results press release and 8‑K: prior guidance and timelines .
  • Q1’24 results 8‑K: early 2024 guidance and cash .
  • Q3‑period press releases: ADI‑270 Fast Track (Jul 8), ADI‑001 biomarker data (Sep 19), autoimmune trial enrollment opening (Sep 30) .