Vor Biopharma/$VOR
1D1W1MYTD1Y5YMAX
Capital at risk
About Vor Biopharma
Vor Biopharma Inc is a clinical-stage biopharmaceutical company focused on developing novel therapies for the treatment of autoimmune diseases. Its program, telitacicept, is a potential first- and best-in-class dual BAFF/APRIL inhibitor designed to suppress the signaling pathways that drive the maturation, proliferation, and survival of harmful B cells, including self-reactive B cells, thereby reducing autoantibody production and preventing downstream tissue damage.
- Ticker
- $VOR
- Sector
- Health
- Primary listing
- NASDAQ
- Employees
- 76
- Headquarters
- Boston, United States
- Website
- www.vorbio.com
Vor Biopharma Metrics
BasicAdvanced
$1.1B
0.91
$20.19
1.72
-
Price and volume
Market cap
$1.1B
Beta
1.72
52-week high
$49.95
52-week low
$6.50
Average daily volume
1.1M
Financial strength
Current ratio
19.147
Quick ratio
18.785
Long term debt to equity
-0.013
Total debt to equity
-0.014
Profitability
EBITDA (TTM)
-117.285
Management effectiveness
Return on assets (TTM)
-21.37%
Return on equity (TTM)
-73.60%
Valuation
Price to earnings (TTM)
0.907
Price to book
-4.98
Price to tangible book (TTM)
-4.98
Price to free cash flow (TTM)
-4.043
Free cash flow yield (TTM)
-24.74%
Free cash flow per share (TTM)
-4.529
Growth
Earnings per share change (TTM)
-105.89%
3-year earnings per share growth (CAGR)
-19.81%
Bulls say / Bears say
Telitacicept has a credible efficacy base rather than being an early discovery bet: Vor says its China Phase 3 gMG trial produced statistically significant, clinically meaningful MG-ADL and QMG improvements at week 24, with improvement continuing through week 48. Vor has now completed global UPSTREAM MG enrolment, with topline data due in H1 2027. (GlobeNewswire)
The asset is being built as a multi-indication franchise: telitacicept has secured additional China commercial approvals for Sjögren’s disease and IgA nephropathy, while Vor’s global SjD Phase 3 is on track and a global ocular MG Phase 3 is planned for H1 2027. Success in one indication could therefore support a broader commercial platform rather than a single-label product. (BioSpace, GlobeNewswire)
Near-term financing risk is lower than for many clinical biotechs: Vor reported $466.1m of cash, equivalents and marketable securities at 30 June, plus $48.4m of net July ATM proceeds, and expects this to fund operations into early 2029. That should cover the H1 2027 MG readout and ongoing SjD work without an obvious forced raise before the key catalyst. (BioSpace)
The investment case remains a binary test of whether Chinese efficacy translates to a Western trial. Management said it expects the global effect size to compress, especially because of the placebo arm, so a statistically positive result could still be less differentiated than the China data imply. (StockAnalysis)
Vor is effectively a single-asset clinical-stage company: its value is concentrated in telitacicept, with no established commercial revenue to cushion a failed Phase 3 outcome. The planned ocular MG expansion also adds execution and trial-cost demands before the lead readout. (Simply Wall St)
Even if telitacicept succeeds, the licence economics are heavy: RemeGen can receive up to $330m in regulatory milestones, up to $3.775bn in sales milestones and tiered royalties from high single digits to mid-teens on net sales. Those obligations could reduce the value retained by Vor and make commercial success more expensive to scale. (StockTitan)
Data summarised monthly by Lightyear AI. Last updated on 19 Sept 2026.
Upcoming events
No upcoming events
Funds containing Vor Biopharma
AllUSDGBPEUR
Fund name | Fund size | $VOR weighting |
|---|---|---|
iShares Nasdaq US Biotechnology$BTEC | $1.2B | 0.07% |
iShares Nasdaq US Biotechnology£BTEK | £865M | 0.07% |
SPDR Russell 2000 US Small Cap€R2US | €4.8B | 0.03% |
SPDR Russell 2000 US Small Cap£R2SC | £4.1B | 0.03% |
SPDR MSCI All Country World IM€SPYI | €7.5B | 0.00% |
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