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Autolus 2026 AGM passes all resolutions, re-elects directors and approves auditors
Adopted 2025 annual accounts: 165,846,326 for, 2,895,344 against.
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Autolus files UK annual report highlighting AUCATZYL launch, pipeline progress, and EU sales delay
AUCATZYL launched in US (Jan 2025) and UK (Jan 2026) for r/r B-ALL; conditional EU approval but no 2026 sales planned.
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Autolus Q1 2026: AUCATZYL net revenue $26.2M; positive gross margin; reaffirms FY revenue $120-135M
Net product revenue $26.2M (vs $9.0M Q1 2025); gross profit $1.6M, first positive quarter for ALL business.
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Autolus cuts workforce 13%; expects $8M restructuring charge, $15M annualized savings
Reduces workforce ~13% as part of operational efficiency plan; impacted employees receive severance and benefits.
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Autolus Therapeutics dismisses EY UK and appoints EY US as independent auditor
Audit committee dismissed EY UK on April 14, 2026; no disagreements or reportable events in prior two fiscal years.
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Autolus hosts ALL Business investor event; presentation lacks specific financial data
Virtual investor event held on April 8, 2026, titled 'Spotlight on the Acute Lymphoblastic Leukemia (ALL) Business'.
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Autolus reports FY2025 AUCATZYL net revenue $74.3M; guides FY2026 $120-135M
Q4 2025 AUCATZYL net revenue $23.3M; full-year $74.3M, primarily from U.S. sales.
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Autolus enters 10-year lentiviral vector supply deal with AGC Biologics
Master Service Agreement with AGC Biologics for lentiviral vector, critical for CAR-T production.
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Autolus reports preliminary 2025 AUCATZYL rev $75M; guides FY2026 $120-135M
Preliminary unaudited AUCATZYL net product revenue: Q4 2025 ~$24M, full year 2025 ~$75M.
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Autolus appoints former BioNTech CSO Ryan Richardson to Board
Ryan Richardson appointed as Class I director effective Dec 1, 2025; served as BioNTech CSO (2018–2025).
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Autolus Q3 net product revenue $21.1M; RMAT for pediatric ALL; lupus data show 83% remission
Q3 2025 net product revenue of $21.1M and deferred revenue of $7.6M; net loss of $79.1M ($0.30 per share).
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Autolus reports Q2 AUCATZYL revenue $20.9M; EU/UK approvals secured but Germany launch on hold
Net product revenue $20.9M in Q2, $29.9M H1 2025; 46 U.S. centers activated, >90% medical lives covered.
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Autolus Therapeutics announces results of 2025 Annual General Meeting, all resolutions passed
Resolution 1 (adopt 2024 accounts): 219,809,664 for, 97,503 against, 477,332 abstain.
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Autolus sets AGM for June 26; two directors to step down; new equity plan proposed
AGM on June 26, 2025; resolutions include adoption of 2024 accounts, auditor reappointment (EY LLP), and director re-elections.
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Autolus directors Anderson and Murphy will not stand for re-election at 2025 AGM
Joseph Anderson and Martin Murphy notified the board on May 23, 2025, of their decision.
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Autolus reports Q1 AUCATZYL revenue $9.0M; UK MHRA approval for r/r B-ALL
Q1 2025 AUCATZYL net product revenue $9.0M, first quarter of launch.
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Autolus schedules R&D investor event with corporate update; no specific data disclosed
Corporate update presented at R&D investor event on April 23, 2025.
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Autolus Therapeutics VP Finance resigns; CFO Dolski appointed PAO
Andrew Mercieca resigned as VP Finance & PAO on Feb 24, 2025, effective August 2025; not due to any disagreement.
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Autolus reports FY2024 net loss $220.7M; AUCATZYL launch on track with 33 U.S. centers
Net loss $220.7M ($0.86 per share) vs $208.4M ($1.20) in 2023; revenue $10.1M (up from $1.7M).
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Autolus presents at JPM Health Conference; no material news in 8-K
Autolus presented corporate update at J.P. Morgan Health Conference on Jan 13, 2025.
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FDA approves Autolus' AUCATZYL (obe-cel) for adult r/r B-ALL; no REMS required
Approval based on FELIX trial: 63% overall complete remission (CR/CRi) in efficacy-evaluable patients (n=65); median DOR 14.1 months.
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Autolus Therapeutics Q3 net loss $82M; FDA approval of AUCATZYL triggers $30M milestone
FDA approved AUCATZYL (obe-cel) for adult r/r B-ALL on Nov 8, 2024, ahead of PDUFA date.
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Autolus presents corporate update at KBC Life Sciences Conference; limited exhibit provided
Corporate presentation made at KBC Life Sciences Conference on September 26, 2024.
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Autolus Therapeutics appoints Matthias Will, M.D. as Chief Development Officer
Dr. Will joins as CDO effective September 30, 2024.
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Autolus secures up to £18.5M landlord funding for Nucleus facility clean rooms
Landlord provides up to £18.5M for improvements to Stevenage manufacturing facility.
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Autolus Q2 net loss $58.3M; cash $705.9M; obe-cel PDUFA Nov 16, 2024 on track
Net loss $58.3M ($0.22/sh) vs $45.6M ($0.26/sh) in Q2 2023; cash $705.9M up from $239.6M at Dec 31, 2023.
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Autolus Therapeutics shareholders approve all nine resolutions at 2024 AGM
Adoption of 2023 annual accounts passed with 190.78M votes for, 35.8K against.
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Autolus publishes UK Annual Report; provides obe-cel BLA status, PDUFA date Nov 16, 2024
BLA for obe-cel accepted by FDA; PDUFA target action date set for 16 November 2024.
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Autolus presents FELIX update: 78% ORR, 40% ongoing remission without SCT, median OS 23.8 months
ORR 78% (99/127); median EFS 11.9 months, median OS 23.8 months; 12-month OS rate 61.1%.
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Autolus reports Q1 2024 net loss of $52.7M; cash $758.5M; obe-cel PDUFA Nov 16
Net loss $52.7M ($0.24 diluted EPS) vs $39.8M loss year ago; license revenue $10.1M.
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Autolus Therapeutics delays Q1 2024 filing; cancels May 14 earnings call, reschedules to May 17
Plans to file Form 12b-25 for automatic 5-day extension of Q1 2024 10-Q due May 15.
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Autolus appoints Mike Bonney as Chair and Ravi Rao as director; John Johnson resigns effective April 1, 2024
John H. Johnson steps down as Chairman and Non-Executive Director; departure not due to disagreements.
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Autolus restates 2021-2022 financials on R&D tax credit classification error
Error: UK SME R&D tax credits previously classified as income tax benefit should reduce R&D expense instead.
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Autolus files 8-K/A to furnish Q4 2023 earnings call transcript; no new financial details
Amendment filed solely to furnish transcript of March 14, 2024 FY2023 earnings call.
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Autolus FY2023 net loss $208.4M; raises $600M via BioNTech deal and offering; CDO resigns
Net loss for FY2023 was $208.4M ($1.20 diluted EPS) vs $148.8M in 2022; cash at year-end $239.6M.
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Autolus posts updated corporate presentation; no material new details available
Company posted updated corporate presentation to its website on February 13, 2024.
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Autolus enters $200M equity deal and strategic CAR-T collaboration with BioNTech
BioNTech invests $200M in Autolus ADS at $6.00 per share, plus $50M upfront under license agreement.
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Autolus prices $350M ADS offering at $6.00 per ADS for obe-cel development
Offering of 58,333,336 ADSs at $6.00/ADS for gross proceeds of $350 million.
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Autolus Therapeutics announces FDA acceptance of BLA for obe-cel; PDUFA date Nov 16, 2024
FDA accepted BLA for obe-cel in relapsed/refractory Adult B-ALL; PDUFA target action date November 16, 2024.
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Autolus appoints Robert Azelby to Board, commercial focus as BLA for obe-cel submitted
Robert W. Azelby appointed Class II director effective Jan 9, 2024; brings 30+ years biopharma commercial experience.
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Autolus appoints Elisabeth Leiderman to board; Kapil Dhingra resigns
Kapil Dhingra resigned from Board effective Dec 31, 2023; not due to any disagreement with company.
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Autolus obe-cel FELIX pooled analysis: 78% CR/CRi, 12-mo EFS 50%, low immunotoxicity; BLA filed for r/r B-ALL
Pooled FELIX Phase Ib/II (n=127): CR/CRi rate 78%; grade ≥3 CRS 2%, ICANS 7%; median follow-up 16.6 months.
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Autolus submits BLA to FDA for cell therapy obe-cel in r/r adult B-ALL
BLA for obecabtagene autoleucel (obe-cel) submitted to FDA for relapsed/refractory adult B-cell ALL.
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Autolus voluntarily elects U.S. domestic issuer reporting, no change to Q3 2023 financials
Autolus will file periodic reports on Forms 10-K, 10-Q, and 8-K instead of foreign private issuer forms.