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Vor Biopharma Inc. logo

Vor Biopharma Inc.

VOR
NASDAQ: VOR Delayed
14.03USD -2.4%
As of 13 June 2026, Vor Biopharma Inc. has a market cap of $760.77M USD, ranking #12385 globally and #2349 in the United States. It ranks #1132 in the Healthcare sector, and #209 in the Biotechnology industry.
Global Rank
12385
Country Rank
2349
Sector Rank
1132
Industry Rank
209
Key Stats
Market Cap
$760.77MUSD
Enterprise Value
$308.56MUSD
EBITDA (TTM)
-$339.05MUSD
Net Income (TTM)
-$695.98MUSD
Company Profile
Country (HQ)
Sector
Healthcare
Industry
Biotechnology
CEO
Jean-Paul Kress open_in_new
Employees
76
Founded
2015
IPO
05 Feb 2021
Website
vorbio.com open_in_new
warningChart data may be delayed
1d 1w 1m 3m 6m 1y
-2.4% -8.4% -3.1% 2.1% -48% 0.5%

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Markets

Exchange Ticker Price
NASDAQ
MIC: XNAS
PRIMARY
VOR
Vor Biopharma Inc Ordinary Shares
ISIN: US9290332074
Shares Out.:
54.186M1 Shares Float: 54.186M2
TV:
SA:
YF:
VOR
GF:
NQ:
VOR
BA:
VOR
MS:
14.03 USD
1Market cap is calculated using shares outstanding.
2Float shares are publicly tradable shares, excluding insider-held stock.

About Vor Biopharma Inc.

Vor Biopharma Inc. operates as a clinical-stage cell and genome engineering company. The company offers the Vor Bio platform, a technology platform for the treatment of acute myeloid leukemia (AML) and other blood cancers. It develops tremtelectogene empogeditemcel (trem-cel), a genome-edited hematopoietic stem and progenitor allogeneic donor product candidate to treat acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and other blood cancers; trem-cel in combination with Mylotarg to treat patients in VBP101, which is in phase 1 / 2; and VCAR33, a CAR-T therapy designed to target CD33, which is under preclinical studies to treat AML post-transplant. The company also develops trem-cel + VCAR33 treatment system, CD33-directed CAR-T program, which is under pre-clinical studies for the treatment of AML; VADC45 for the treatment of hematologic malignancies, conditioning, and immune reset, which is under preclinical studies; and CD33-CLL1 treatment system made with CD33-CLL1 multiplex-edited HSC therapy and a CD33-CLL1 multi-specific CAR-T therapy, which is under preclinical studies for the treatment of AML. It has a license agreement with Columbia University and the National Institutes of Health for patents; and with Editas Medicine, Inc. for ex-vivo Cas9 gene-edited HSC therapies for the treatment and/or prevention of hematological malignancies. The company was incorporated in 2015 and is headquartered in Cambridge, Massachusetts.

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