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Aura Q1 net loss $33.7M; Phase 3 CoMpass enrollment mid-2026; new CEO appointed
Net loss of $33.7M in Q1 2026; R&D expenses $28.0M (up from $23.3M) reflecting Phase 3 costs.
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Aura Biosciences raises ~$280.8M in public offering; to repurchase $39M in stock from Matrix Capital
Offering of 39,591,000 shares at $6.00 and 3,800,000 pre-funded warrants, net proceeds ~$280.8M.
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Aura Biosciences names Natalie Holles CEO; CoMpass trial enrollment at 86 patients, nearing completion
New CEO Natalie Holles, former CEO of Third Harmonic Bio and Audentes, appointed effective April 30, 2026.
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Aura Biosciences to repurchase ~6.9M shares from Matrix Capital at $5.64; reports preliminary cash of $114.7M
Enters stock purchase agreement to repurchase up to 6,922,870 shares from Matrix Capital Master Fund at $5.64 per share, matching equity offering price.
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Aura Biosciences reports 2025 net loss $106.2M; Phase 3 CoMpass enrollment to complete mid-2026
Cash and equivalents $144.2M as of Dec 31, 2025; sufficient to fund operations into Q1 2027.
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Aura Biosciences Q3 net loss $26.1M; Phase 3 CoMpass data expected Q4 2027
Net loss of $26.1M in Q3 2025 vs $21.0M in Q3 2024; R&D expenses rose to $22.2M from $17.0M.
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Aura Biosciences closes $69.9M public offering of common stock and warrants
Sold 11.7M shares, 3.6M pre-funded warrants, and 3.8M common stock warrants at $4.90 combined price.
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Aura Biosciences Q1 net loss $27.5M; appoints Tony Gibney as CFO; Phase 3 CoMpass enrollment may complete by end 2025
Net loss $27.5M for Q1 2025 vs $19.7M in Q1 2024; R&D expenses rose to $23.3M from $17.1M.
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Aura Biosciences Q4/FY2024 results: net loss $86.9M, cash $151.1M, Phase 3 CoMpass actively enrolling
Net loss $86.9M in FY2024 vs $76.4M in FY2023; R&D expenses $73.3M.
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Aura Biosciences Q3 net loss $21M; cash $174.4M; Phase 3 CoMpass authorized in Europe
Net loss $21.0M (Q3 2024) vs $18.5M YoY; cash $174.4M funds operations into 2H 2026.
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Aura Biosciences: 4 of 5 low-grade NMIBC patients achieve clinical complete response with single-dose bel-sar
Phase 1 trial of bel-sar in NMIBC: 4 of 5 low-grade patients had complete response (no tumor cells on histopathology).
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CFO Julie Feder to depart Oct 25; VP Finance Amy Elazzouzi named interim CFO
CFO Julie Feder will resign effective Oct 25, 2024; no dispute or disagreement with company.
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Aura reports positive Phase 2 bel-sar results: 80% tumor control, 90% vision preservation
Bel-sar achieved 80% tumor control rate in Phase 3-eligible patients (8/10); complete cessation of growth post-treatment.
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Aura Biosciences reports Q2 2024 net loss of $20.3M; cash $187.4M into H2 2026
Net loss of $20.3M in Q2 2024 vs $18.3M in Q2 2023; R&D spend $16.9M, G&A $5.9M.
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Aura Biosciences reports FY2023 net loss $76.4M; Phase 3 CoMpass trial enrolling with FDA SPA
Cash and equivalents $226.2M as of Dec 31, 2023; expected to fund operations into H2 2026.
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Aura Biosciences raises $99M in public offering; Q3 net loss $18.5M
Closed underwritten public offering of 11M shares at $9.00/share, gross proceeds $99.0M; net proceeds ~$92.6M.
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Aura Biosciences Receives FDA SPA Agreement for CoMpass Phase 3 Trial of Bel-sar in Choroidal Melanoma
FDA agreed under Special Protocol Assessment to design and planned analysis of CoMpass Phase 3 trial for bel-sar in early-stage choroidal melanoma.
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Aura Biosciences names new CMO/President of R&D and CTO; CMO Rich transitions to advisor
J. Jill Hopkins appointed CMO and President of R&D, effective Oct 16, 2023; prior roles at Novartis, Gyroscope, Roche-Genentech.
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Aura Biosciences reports Q1 2023 net loss of $17.5M; FDA backs Phase 3 trial design for choroidal melanoma
Cash and marketable securities $173.5M as of March 31, 2023; cash runway into 2025.
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Aura Biosciences Q4/Full Year 2022 Net Loss $58.8M; Phase 3 Trial on Track, FDA Fast Track for Choroidal Metastasis
Net loss of $58.8M for FY2022 vs $35.3M in 2021; cash & securities $188.8M sufficient into 2025.
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Phase 2 interim data: 100% tumor control, 88% vision preservation with bel-sar in early choroidal melanoma
100% tumor control (8/8) and 88% visual acuity preservation in patients receiving three cycles of bel-sar.
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Aura Biosciences raises $86.7M in public offering of 7.7M shares at $12.00/share
Net proceeds of ~$86.7M from 7.705M shares (including full overallotment) at $12.00 per share.
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Aura Biosciences reports Q3 2022 net loss of $15.9M; initiates global Phase 3 trial for bel-sar in choroidal melanoma
Net loss $15.9M for Q3 2022 vs $8.8M YoY; cash $111.5M sufficient into 2024.
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Aura reports Phase 2 interim data: 89% tumor control, significant growth rate reduction for choroidal melanoma
Interim Phase 2 data for belzupacap sarotalocan (AU-011) in early-stage choroidal melanoma show 88.9% (8/9) tumor control rate at therapeutic regimen.
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Aura Biosciences receives FDA Fast Track for belzupacap sarotalocan in NMIBC; Phase 1 trial H2 2022
FDA granted Fast Track designation for belzupacap sarotalocan (AU-011) for treatment of Non-Muscle Invasive Bladder Cancer.
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Aura Biosciences reports positive retrospective data for AU-011 in choroidal melanoma vs. radiotherapy
Belzupacap sarotalocan showed statistically significant vision preservation at 2 years vs. plaque radiotherapy (logMAR p=0.0094).
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Aura Biosciences Q1 2022 net loss $12.8M; cash $133.3M; AU-011 pivotal trial in 2H 2022
Net loss of $12.8M in Q1 2022 compared to $5.9M in Q1 2021; cash and marketable securities $133.3M, sufficient into 2024.
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Aura Biosciences reports FY2021 net loss $35.3M; cash $149.1M into 2024
Net loss for FY2021 was $35.3M, up from $22.2M in FY2020; R&D expenses rose to $25.2M.
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Aura Biosciences Q3 net loss $8.8M; AU-011 data and IPO highlight quarter
Net loss $8.8M for Q3 2021 vs $3.6M YoY; R&D expenses $6.4M (up from $2.9M).