GBAF Logo
Global Banking & Finance Awards® 2026 Nominations open, free to enter Nominate now →
V

Vor Biopharma VOR · USD

Health Care · US listing · 🇺🇸 United States

Compare

19.98

+0.50%

Close of 9 Nov 2026, in USD

Search any instrument

Reference data, closing prices and charts across 45,000 companies, plus crypto, commodities and currencies.

About Vor Biopharma

From its filings with the US Securities and Exchange Commission

SEC filings

Vor Biopharma is based in Boston, Massachusetts. Its shares trade on Nasdaq under the ticker VOR. The SEC classifies its business as biological products, (no diagnostic substances). In the fiscal year to 31 December 2025, it reported a net loss of $696.0m. At that date it held total assets of $464.1m and shareholders' equity of −$164.3m.

In its own words

Vor Biopharma, Inc. ("Vor Bio") is a clinical-stage biopharmaceutical company focused on developing a novel therapy in the treatment of autoimmune diseases. In June 2025, we in-licensed telitacicept from RemeGen Co., Ltd. (“RemeGen”). Pursuant to our license agreement with RemeGen, we were granted an exclusive license to develop and commercialize telitacicept outside of the Greater China region, which includes mainland China, Hong Kong, Macau and Taiwan. RemeGen retains development and commercialization rights in Greater China.

Telitacicept is approved in China for the treatment of systemic lupus erythematosus (“SLE”), rheumatoid arthritis (“RA”), and generalized myasthenia gravis (“gMG”), and has two Biologics License Applications ("BLAs") filed and pending in China for the treatment of Sjögren’s disease (“SjD”) and IgA nephrapathy (“IgAN”). Our global Phase 3 clinical trial in gMG is currently underway across the United States, Europe, South America, and Asia to support potential approval in the United States, Europe, and Japan. We have recently initiated a global Phase 3 clinical trial in SjD, with the first patient dosing in March 2026, and anticipate enrolling at clinical sites across the United States, Europe, South America, and Asia to support potential approval in the United States, Europe, and Japan.

Quoted from its 10-K, filed 30 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
5 Feb 2021
Employees
76
Website
vorbio.com ↗
Head office
500 BOYLSTON STREET, BOSTON, MA, 02116
Classification
Biological Products, (No Diagnostic Substances)
Filer status
Non-accelerated filer<br>Smaller reporting company<br>Emerging growth company

Leadership

Pay as last reported

  • Dr. Jean-Paul KressChairman of the Board, Chief Executive Officer, since 2025
  • Mr. Sandesh MahatmeChief Financial Officer, Chief Business Officer
  • Mr. Dallan MurrayChief Commercial Officer
  • Dr. Qing ZurawChief Development Officer
  • Ms. Daniella BeckmanIndependent Director$94,800
  • Mr. Erez KalirIndependent Director
  • Dr. Fouad NamouniIndependent Director$140,495
  • Ms. Sarah ReedIndependent Director

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
0
Environment
0
Social
0
Governance
0

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Vor Biopharma's eHSC platform leverages HSC biology for cancer treatment solutions.
  • Trem-cel targets acute myeloid leukemia with a novel engineering approach.
  • VBP101 Phase I/II study demonstrates clinical progress in AML treatment.

Weaknesses

  • The company employs 76 full-time employees, which is below industry standards.
  • Vor Biopharma's IPO date of 5 February 2021 is relatively recent.
  • The company's focus on hematological malignancies limits market diversity.

Opportunities

  • Expanding VBP101 study to additional AML patient segments increases market reach.
  • Collaborations with US healthcare providers could enhance treatment adoption.
  • Growing demand for cell therapies in the US Health Care sector presents growth potential.

Threats

  • Competition from established biotech firms in the US Health Care sector.
  • Regulatory hurdles for novel cell therapies may delay product approval.
  • High costs associated with developing targeted cancer treatments pose financial risks.

Sources and methodology

Data on this tab
Our data supplier
Chart on the Overview
TradingView

Nothing here is investment advice. Prices can be delayed or wrong, so check with the exchange before relying on them. Data for this page. How we cover markets.