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MT

Molecular Templates, Inc. (MTEM)·Q3 2023 Earnings Summary

Executive Summary

  • Q3 2023 delivered YoY revenue growth to $6.80M (+61% YoY) and a sharply lower net loss of $4.20M vs. $24.6M in Q3 2022, driven by collaboration revenue (BMS) and CPRIT grants and reduced R&D/G&A spend .
  • Liquidity improved sequentially with cash and equivalents of $15.81M and runway guided to the end of Q2 2024; prior quarter guidance was to Q3 2024, implying a modest shortening of runway versus Q2 guidance .
  • Clinical updates were constructive: MT-6402 showed monotherapy activity in heavily pre-treated head & neck cancer; MT-8421 first patient dosed; MT-0169 continuing with activity and acceptable safety profile in lower-dose cohorts .
  • Catalysts: continued data flow across MT-6402/MT-8421/MT-0169, advancement of the BMS collaboration, and conference participation (Stifel, Evercore ISI), with management highlighting ETBs’ differentiated biology and potential best-in-class approach to PD-1/PD-L1 axis .
  • Wall Street consensus estimates from S&P Global were unavailable for MTEM this quarter; therefore, no beat/miss assessment versus Street figures can be made (S&P Global consensus unavailable due to mapping issue).

What Went Well and What Went Wrong

What Went Well

  • Strong YoY improvement: revenue rose to $6.80M from $4.20M, and net loss narrowed to $4.20M from $24.6M in Q3 2022; lower R&D ($7.6M vs. $22.0M) and G&A ($4.3M vs. $5.9M) drove improved operating loss .
  • Clinical signals: MT-6402 showed partial responses and durable disease control in heavily pre-treated head & neck cancer patients at 63 and 83 mcg/kg; no Grade 4/5 AEs or CLS were observed with next-gen ETBs .
  • Strategic progress: BMS collaboration continues; MT-8421 first patient dosed; MT-0169 patient remains in stringent CR into cycle 16, underscoring program activity .

Management quotes:

  • “ETBs represent a new approach to oncology drug development...updates throughout this year and into 2024” — Eric Poma, PhD (CEO/CSO) .
  • “We are very excited to see responses...monotherapy activity of long duration...potentially best-in-class approach to targeting the PD-1-PD-L1 axis” — Eric Poma .
  • “MT-6402 appears generally well-tolerated...no instances of CLS seen at any dose” — Dr. Maurizio Voi (CMO) .

What Went Wrong

  • Liquidity remains a watch-point: cash of $15.81M and runway guided to end of Q2 2024 implies remaining financing needs absent non-dilutive inflows .
  • Contingent liabilities persist: a contingent value right liability of $3.975M remains on the balance sheet following debt restructuring earlier in 2023 .
  • Estimates unavailable: With S&P Global consensus inaccessible due to mapping, investors lack a standardized benchmark for EPS/revenue vs. Street expectations this quarter (S&P Global consensus unavailable).

Financial Results

Quarterly Financial Summary (Q1–Q3 2023)

MetricQ1 2023Q2 2023Q3 2023
Revenue ($USD Millions)$36.629 $6.865 $6.796
Net Income (Loss) ($USD Millions)$10.845 $(10.868) $(4.153)
EPS (Basic/Diluted, $USD)$0.19 $(0.19) $(0.82)
R&D Expense ($USD Millions)$19.042 $13.413 $7.624
G&A Expense ($USD Millions)$5.802 $5.195 $4.309
Cash & Equivalents ($USD Millions)$38.782 $4.952 $15.811

Notes:

  • Q3 balance sheet footnote indicates prior period amounts were retrospectively adjusted for the 1-for-15 reverse stock split in certain balance sheet items; EPS comparability across periods may be affected by share changes and corporate actions .

Q3 2023 vs. Q3 2022

MetricQ3 2022Q3 2023
Revenue ($USD Millions)$4.200 $6.800
Net Loss ($USD Millions)$(24.600) $(4.200)
R&D Expense ($USD Millions)$22.000 $7.600
G&A Expense ($USD Millions)$5.900 $4.300

Drivers:

  • Q3 revenue composition: BMS collaboration and CPRIT grants .
  • Operating expense reductions YoY reflect strategic reprioritization and restructuring earlier in 2023 .

KPIs (Clinical Program Highlights)

ProgramKPIQ1–Q2 MentionsQ3 2023 Highlights
MT-6402 (PD-L1 ETB)Dose levels studiedEscalation through 16–100 mcg/kg; PD effects observed Expansion at 63 & 83 mcg/kg; Part A completed
MT-6402 (PD-L1 ETB)Efficacy signalsPRs and tumor regression in NSCLC and nasopharynx; durable responses In H&N cancer, 2 PRs (1 unconfirmed), 1 tumor regression; multiple stable diseases
MT-6402 SafetyCLSNo CLS across next-gen ETBs No Grade 4/5 AEs and no CLS; irAE profile consistent with checkpoint therapies
MT-8421 (CTLA-4 ETB)Clinical initiationIND accepted; start planned mid-year 2023 First patient dosed; enrollment commenced
MT-0169 (CD38 ETB)Regulatory/safetyFDA partial hold in April; lifted May 31; cohorts resumed Ongoing; ≥Grade 3 AEs not observed; patient in stringent CR continues at cycle 16

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
Cash RunwayQ2 2023 vs. Q1 2023Into Q1 2024 To Q3 2024 Raised/Extended
Cash RunwayQ3 2023 vs. Q2 2023To Q3 2024 To end of Q2 2024 Lowered/Shortened

No explicit quantitative guidance for revenue, margins, OpEx, OI&E, tax rate, or dividends was provided in Q3 materials .

Earnings Call Themes & Trends

TopicPrevious Mentions (Q-2 and Q-1)Current Period (Q3 2023)Trend
R&D ExecutionMT-6402 dose escalation (16–100 mcg/kg) with PD effects; MT-8421 IND accepted; MT-0169 partial hold lifted; durable PRs reported MT-8421 first patient dosed; MT-6402 expansion at 63/83 mcg/kg; H&N monotherapy activity Improving/progressing
Regulatory/LegalMT-0169 partial hold (Apr) lifted (May 31) No new regulatory setbacks disclosed; continued development Improving
Financing/LiquidityK2 loan context and strategic review (Q1); private placement $20M initial tranche; debt discharged via CVR agreement (Q2) Cash $15.81M; runway to end Q2 2024; CVR liability present Stabilized but moderate runway
Collaboration (BMS)Ongoing research collaboration; expansion across targets Continued progress; $70M upfront referenced in upcoming milestones Ongoing
Safety ProfileNo CLS with next-gen ETBs across programs No CLS; no Grade 4/5 AEs with MT-6402; irAE profile consistent with checkpoints Consistently favorable

Management Commentary

  • “ETBs represent a new approach to oncology drug development that continue to show unique biology and monotherapy activity in heavily pre-treated patients. We expect to see substantial additional data across all three of our clinical programs with updates throughout this year and into 2024.” — Eric Poma, PhD (CEO/CSO) .
  • “We are very excited to see responses in heavily pre-treated, checkpoint-experienced, head and neck cancer patients...monotherapy activity of long duration and monotherapy activity in a patient refractory to checkpoint therapy...potentially best-in-class approach to targeting the PD-1-PD-L1 axis.” — Eric Poma .
  • “MT-6402 appears generally well-tolerated at the 63 and 83 mcg/kg doses with no Grade 4 or Grade 5 adverse events and no instances of CLS...irAE profile...consistent with other checkpoint therapies.” — Dr. Maurizio Voi (CMO) .

Q&A Highlights

  • No Q3 2023 earnings call transcript was available in the document set; therefore, Q&A highlights could not be assessed this quarter (no earnings-call-transcript documents found).

Estimates Context

  • S&P Global consensus estimates for MTEM were unavailable due to a CIQ mapping issue, preventing EPS/revenue beat/miss analysis versus Street expectations this quarter (S&P Global consensus unavailable).
MetricQ3 2023 ConsensusNotes
Primary EPS Consensus MeanN/AS&P Global consensus unavailable
Revenue Consensus MeanN/AS&P Global consensus unavailable
Primary EPS - # of EstimatesN/AS&P Global consensus unavailable
Revenue - # of EstimatesN/AS&P Global consensus unavailable

Key Takeaways for Investors

  • Revenue mix is collaboration/grant-driven; continued BMS activities and CPRIT grant support underpin near-term revenue visibility .
  • Operating discipline is evident: YoY reductions in R&D and G&A materially narrowed the quarterly net loss in Q3 .
  • Clinical momentum: MT-6402 monotherapy signals in H&N cancer at mid-dose levels, MT-8421 dosing start, and MT-0169 activity at lower doses de-risk platform efficacy across IO/hematologic indications .
  • Safety profile remains supportive for next-generation ETBs with no CLS reported; MT-6402 irAEs consistent with checkpoints, which may aid combination potential .
  • Liquidity improved sequentially, but runway to end of Q2 2024 keeps financing needs on the horizon; watch for non-dilutive funding or additional equity measures .
  • Strategic collaboration with BMS continues to be a key asset and potential long-term value driver through discovery across multiple targets .
  • Near-term trading implications: sensitivity to clinical update cadence, financing signals, and any Street estimate availability; medium-term thesis hinges on converting differentiated biology into repeatable efficacy signals and partnering leverage .