Vir Biotechnology Files 8-K
Ticker: VIR · Form: 8-K · Filed: Jun 26, 2024 · CIK: 1706431
| Field | Detail |
|---|---|
| Company | Vir Biotechnology, Inc. (VIR) |
| Form Type | 8-K |
| Filed Date | Jun 26, 2024 |
| Risk Level | low |
| Pages | 3 |
| Reading Time | 4 min |
| Key Dollar Amounts | $0.0001 |
| Sentiment | neutral |
Sentiment: neutral
Topics: sec-filing, 8-k, routine-reporting
TL;DR
Vir Bio filed a routine 8-K, no major news.
AI Summary
Vir Biotechnology, Inc. filed an 8-K on June 26, 2024, to report other events and financial statements/exhibits. The filing does not detail specific transactions or events beyond its routine reporting nature.
Why It Matters
This 8-K filing indicates routine corporate reporting by Vir Biotechnology, Inc. to the SEC, without disclosing specific material events.
Risk Assessment
Risk Level: low — The filing is a standard 8-K for reporting events and exhibits, not indicating any specific negative or positive material changes.
Key Players & Entities
- Vir Biotechnology, Inc. (company) — Registrant
- Delaware (jurisdiction) — State of incorporation
- 001-39083 (company_id) — Commission File Number
- 81-2730369 (company_id) — IRS Employer Identification No.
- 1800 Owens Street, Suite 900 (address) — Principal executive offices
- San Francisco, California 94158 (address) — Principal executive offices
- 415-906-4324 (phone_number) — Registrant's telephone number
- June 26, 2024 (date) — Date of earliest event reported
FAQ
What is the primary purpose of this 8-K filing for Vir Biotechnology, Inc.?
The primary purpose of this 8-K filing is to report "Other Events" and "Financial Statements and Exhibits" as of June 26, 2024.
When was this 8-K filing submitted?
This 8-K filing was submitted on June 26, 2024.
What is Vir Biotechnology, Inc.'s state of incorporation?
Vir Biotechnology, Inc. is incorporated in Delaware.
What is the address of Vir Biotechnology, Inc.'s principal executive offices?
The address of Vir Biotechnology, Inc.'s principal executive offices is 1800 Owens Street, Suite 900, San Francisco, California 94158.
Does this 8-K filing disclose any specific material events or transactions?
Based on the provided text, this 8-K filing is for routine reporting of "Other Events" and "Financial Statements and Exhibits" and does not detail specific material events or transactions.
Filing Stats: 987 words · 4 min read · ~3 pages · Grade level 14.4 · Accepted 2024-06-26 08:15:29
Key Financial Figures
- $0.0001 — nge on which registered Common Stock, $0.0001 par value VIR Nasdaq Global Select
Filing Documents
- d835539d8k.htm (8-K) — 28KB
- d835539dex991.htm (EX-99.1) — 14KB
- g835539g0626060813808.jpg (GRAPHIC) — 2KB
- 0001193125-24-168554.txt ( ) — 172KB
- vir-20240626.xsd (EX-101.SCH) — 3KB
- vir-20240626_lab.xml (EX-101.LAB) — 18KB
- vir-20240626_pre.xml (EX-101.PRE) — 11KB
- d835539d8k_htm.xml (XML) — 4KB
Forward-Looking Statements
Forward-Looking Statements This disclosure, including the press release filed herewith as Exhibit 99.1, contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as "may," "will," "plan," "potential," "aim," "expect," "anticipate," "promising" and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Vir's expectations and assumptions as of the date of this Current Report on Form 8-K. Forward-looking statements contained herein include, but are not limited to, statements regarding the Company's strategy and plans, the potential clinical effects, benefits, safety and efficacy of tobevibart and elebsiran, the timing, nature and significance of data from the Company's multiple ongoing trials evaluating tobevibart and elebsiran, including the previously announced Phase 2 SOLSTICE data, the timing of any further releases of data or of any presentations or investor conference calls, the Company's plans and expectations for its chronic hepatitis delta and chronic hepatitis B programs, the Company's ability to realize the benefits from receiving the Fast Track Designation from the FDA, and risks and uncertainties associated with drug development and commercialization. Many factors may cause differences between current expectations and actual results, including that the Fast Track Designation might not result in a more expedited development or regulatory review process, and such a designation does not increase the likelihood that the combination of tobevibart and elebsiran for the treatment of chronic hepatitis delta infection will receive marketing approval in the United States; the Fast Track Designation does not change the standards for regulatory approval; the FDA may later decide that the combination of tobevibart and elebsiran for the treatment o
Financial Statements and Exhibits
Financial Statements and Exhibits. (d) Exhibits Exhibit No. Description 99.1 Press Release of the Company, dated June 26, 2024 104 Cover Page Interactive Data File (embedded within the Inline XBRL document)
SIGNATURES
SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized. VIR BIOTECHNOLOGY, INC. Date: June 26, 2024 By: /s/ Marianne De Backer Marianne De Backer, M.Sc., Ph.D., MBA Chief Executive Officer