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Aura Biosciences, Inc. (AURA)·Q1 2024 Earnings Summary

Executive Summary

  • Aura reported no product revenue as a clinical-stage biotech; Q1 2024 operating loss was driven by higher R&D spend, with net loss of $19.7M and diluted EPS of $(0.40) .
  • Cash and marketable securities totaled $202.9M at March 31, 2024; management reiterated cash runway into the second half of 2026 .
  • Clinical execution advanced: global Phase 3 CoMpass trial in early-stage choroidal melanoma continued enrolling, and Phase 1 bladder cancer early data is expected mid-2024, creating upcoming catalysts .
  • Consensus estimates (EPS, revenue) via S&P Global were unavailable; comparisons to Street for Q1 2024 cannot be made. Aura has no revenue and analysts typically focus on cash runway and clinical timelines .

What Went Well and What Went Wrong

What Went Well

  • Continued enrollment and site activation in the global Phase 3 CoMpass trial in early-stage choroidal melanoma under an SPA with FDA, reinforcing regulatory alignment and trial momentum . CEO: “Enrollment continues in our global Phase 3 CoMpass trial in early-stage choroidal melanoma…” .
  • Strong balance sheet with $202.9M in cash and marketable securities; runway guided into 2H 2026, supporting multiple programs through inflection points . CEO (prior quarter context): “Our financial strength allows us to fund multiple clinical programs through major inflection points…” .
  • Early bladder cancer signal: Phase 1 trial ongoing; preliminary first patient data in the light-activated cohort showed a clinical complete response with histopathologic evidence of necrosis and immune activation; early data expected mid-2024 .

What Went Wrong

  • Operating losses widened y/y: net loss increased to $19.7M from $17.5M in Q1 2023, reflecting elevated clinical, CRO, and personnel costs as programs advance .
  • R&D expense rose to $17.1M from $14.4M y/y, driven by Phase 2 progression, Phase 3 trial advancement, and personnel, highlighting ongoing cash burn until potential approvals .
  • General & administrative expense increased to $5.3M from $5.0M y/y, including higher stock-based compensation ($1.4M vs $1.1M), underscoring organizational growth costs .

Financial Results

MetricQ1 2023Q4 2023Q1 2024
Revenues ($USD Millions)$0.0 $0.0 $0.0
Research & Development Expense ($USD Millions)$14.4 $20.3 $17.1
General & Administrative Expense ($USD Millions)$5.0 $4.5 $5.3
Total Operating Expenses ($USD Millions)$19.4 $24.8 $22.3
Net Loss ($USD Millions)$(17.5) $(22.1) $(19.7)
Diluted EPS ($USD)$(0.46) $(0.40)
Cash & Marketable Securities ($USD Millions)$226.2 $202.9

Notes:

  • Aura is pre-revenue; management states no product revenue and does not expect near-term product revenue .

Segment breakdown and KPIs:

  • Cash runway guidance: “sufficient to fund operations into the second half of 2026” .
  • Phase 3 CoMpass enrollment target: ~100 patients; 2:1:2 randomization (high dose, low dose bel-sar, sham); primary endpoint time to tumor progression at 15 months under SPA .
  • Bladder cancer Phase 1 expected to enroll ~21 patients; histopathological evaluation planned; early data mid-2024 .

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
Cash RunwayMulti-yearInto 2H 2026 (as of FY/Q4 2023) Into 2H 2026 (affirmed Q1 2024) Maintained
Bladder Cancer Phase 1 Early DataMid-2024Mid-2024 (Q4 2023) Mid-2024 (Q1 2024) Maintained
CoMpass Phase 3 Enrollment/Activation2024U.S. sites activated; global rollout in 2024 (Q4 2023) Continued U.S. activation; global enrollment ongoing (Q1 2024) Maintained
Choroidal Metastasis Phase 2 Initiation2024On track for 2024 (Q4 2023) On track for 2024 (Q1 2024) Maintained

No revenue, margin, OpEx, OI&E, tax rate, or dividend guidance is provided given clinical-stage status .

Earnings Call Themes & Trends

Note: A Q1 2024 earnings call transcript was not available in the document catalog; this section reflects press-release themes.

TopicPrevious Mentions (Q-2: Q3 2023; Q-1: Q4 2023)Current Period (Q1 2024)Trend
Regulatory alignment (SPA)Highlighted SPA for Phase 3 design and endpoints ; Phase 3 startup progress Phase 3 CoMpass enrolling under SPA; design reiterated Stable positive
Phase 3 CoMpass trial progressStartup/global activation; dosing expected 2H 2023 Continued enrollment, U.S. site activations; global target ~100 patients Advancing
Bladder cancer Phase 1 programOngoing; data expected 2024 Ongoing; early data mid-2024; preliminary complete response in first light-activated patient Strengthening
Pipeline expansion (choroidal metastasis, ocular surface)Plan to initiate Phase 2 in 2024; multi-billion TAM On track to initiate Phase 2 in 2024; ocular surface preclinical data presented (ARVO) Consistent progress
R&D execution and spendingR&D increased with CRO/manufacturing as trials scale R&D up y/y to $17.1M; drivers consistent (clinical, CRO, personnel) Elevated investment
Cash runway and financingRaised $99M gross in Nov 2023 follow-on; runway to 2H 2026 Runway to 2H 2026 reiterated Stable funding

Management Commentary

  • CEO Elisabet de los Pinos emphasized focus on ocular and urologic oncology: “Aura is committed to changing the treatment paradigms in ocular and urologic oncology… novel therapies that can effectively treat the tumor and also preserve the function of the organ with cancer” .
  • On Phase 3 progress: “Enrollment continues in our global Phase 3 CoMpass trial in early-stage choroidal melanoma” .
  • On pipeline breadth and funding (Q4 context): “Bel-sar is a potential vision-and-organ sparing therapy… This is a multi-billion dollar market… Our financial strength allows us to fund multiple clinical programs through major inflection points…” .

Q&A Highlights

  • A Q1 2024 earnings call transcript was not available in the document catalog; no Q&A content could be reviewed after searching for “earnings-call-transcript” across Q1 2024. We searched company filings and press releases for Q1 2024 and found none beyond the 8-K and Exhibit 99.1 press release ; ListDocuments returned zero earnings-call transcripts for 2024 [earnings-call-transcript search result].

Estimates Context

  • S&P Global consensus estimates for Q1 2024 EPS and revenue were unavailable through our data access; Aura is a pre-revenue clinical-stage company, and most Street focus is on clinical timelines and cash runway rather than quarterly revenue/EPS .
  • Without available consensus, we cannot assess “beat/miss” versus Wall Street for Q1 2024; we note results in the Financial Results table and maintain qualitative context from management disclosures .

Key Takeaways for Investors

  • Near-term catalysts: early Phase 1 bladder cancer data mid-2024, with preliminary complete response signal already observed; additional ocular oncology data and continued Phase 3 enrollment could drive sentiment and stock reactions as milestones approach .
  • Funding runway into 2H 2026 supports continued execution across Phase 3 (choroidal melanoma), Phase 1 (bladder cancer), and planned Phase 2 (choroidal metastasis), reducing financing overhang near term .
  • Clinical rationale strengthening: SPA-backed Phase 3 design and Phase 2 SC data support efficacy and vision preservation endpoints, anchoring bel-sar’s potential differentiation versus radiotherapy (no drugs approved in early-stage disease) .
  • Expense trajectory: R&D and G&A increases reflect scaling trials and team; monitor quarterly burn versus runway and trial timelines for funding risk assessment .
  • Market opportunity: ocular oncology indications (~60,000 combined US/EU incidence) and bladder cancer (~80,000 US annually) present sizable addressable markets for organ/vision-sparing therapies, if clinical success and approvals are achieved .
  • Data dependency: Stock likely to be data-driven; watch mid-2024 bladder data and any Phase 3 enrollment/operational updates for inflection; lack of transcripts limits tone assessment, but press releases convey confident execution .
  • Regulatory path: SPA alignment with FDA for Phase 3 endpoints and design lowers regulatory uncertainty around pivotal trial read-throughs; continued adherence to agreed endpoints is critical .

Appendix: Prior Two Quarters’ Earnings (Trend Context)

MetricQ3 2023Q4 2023
Research & Development Expense ($USD Millions)$15.4 $20.3
General & Administrative Expense ($USD Millions)$5.06 $4.5
Net Loss ($USD Millions)$(18.5) $(22.1)
Diluted EPS ($USD)$(0.48)
Cash & Marketable Securities ($USD Millions)$162.0 $226.2

Search and document notes:

  • Q1 2024 8-K 2.02 press release (Exhibit 99.1) read in full .
  • Q4 2023 8-K 2.02 press release read in full .
  • Q2 2023 8-K 2.02 press release read in full for trend and pipeline context .
  • Q3 2023 10-Q read for quarterly detail (expenses, EPS, “no revenue”) .