Fortress Biotech Files 8-K

Ticker: FBIOP · Form: 8-K · Filed: Dec 16, 2024 · CIK: 1429260

Fortress Biotech, INC. 8-K Filing Summary
FieldDetail
CompanyFortress Biotech, INC. (FBIOP)
Form Type8-K
Filed DateDec 16, 2024
Risk Levellow
Pages2
Reading Time2 min
Sentimentneutral

Sentiment: neutral

Topics: 8-K, regulatory-filing

Related Tickers: FBIO

TL;DR

FBIO filed an 8-K, no major news yet.

AI Summary

Fortress Biotech, Inc. filed an 8-K on December 13, 2024, reporting an "Other Event." The filing does not contain specific details about the event, dollar amounts, or new developments, but it confirms the company's reporting status.

Why It Matters

This filing indicates that Fortress Biotech, Inc. has made a regulatory submission, which is a standard procedural step for public companies.

Risk Assessment

Risk Level: low — The filing is a routine 8-K for an 'Other Event' and does not disclose any new material information that would immediately impact risk.

Key Players & Entities

FAQ

What specific event is Fortress Biotech, Inc. reporting in this 8-K filing?

The filing is categorized under 'Other Events' and does not specify the exact nature of the event.

When was the earliest event reported in this 8-K filing?

The earliest event reported was on December 13, 2024.

What is the principal executive office address for Fortress Biotech, Inc.?

The principal executive offices are located at 1111 Kane Concourse, Suite 301, Bay Harbor Islands, FL 33154.

What is the Commission File Number for Fortress Biotech, Inc.?

The Commission File Number is 001-35366.

In which state is Fortress Biotech, Inc. incorporated?

Fortress Biotech, Inc. is incorporated in Delaware.

Filing Stats: 473 words · 2 min read · ~2 pages · Grade level 12.7 · Accepted 2024-12-16 16:50:22

Filing Documents

01. Other Events

Item 8.01. Other Events . On December 13, 2024, Checkpoint Therapeutics (" Checkpoint "), a majority-controlled subsidiary of Fortress Biotech, Inc. (the " Company " or " Fortress "), announced that the U.S. Food and Drug Administration (the " FDA ") approved UNLOXCYT (cosibelimab-ipdl) for the treatment of adults with metastatic or locally advanced cutaneous squamous cell carcinoma (" cSCC ") who are not candidates for curative surgery or curative radiation. UNLOXCYT is the first and only programmed death ligand-1 (PD-L1) blocking antibody to receive FDA marketing approval for this indication. The FDA approval for UNLOXCYT was granted based on clinically meaningful objective response rates and duration of response data, as assessed by an independent central review committee, from Study CK-301-101 (NCT03212404), a multicenter, multicohort, open-label study of UNLOXCYT in adults with advanced solid tumor cancers, including cSCC. 99

SIGNATURES

SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized. Fortress Biotech, Inc. (Registrant) Date: December 16, 2024 By: /s/ David Jin David Jin Chief Financial Officer

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