SLBT

SL Science Holding Limited Ordinary Shares
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$2.41B
P/E Ratio
EPS
$-0.01
Beta
52W High
$14.50
52W Low
$3.00
50-Day MA
$7.02
200-Day MA
$9.14
Dividend Yield
Profit Margin
0.00%
Forward P/E
PEG Ratio

About SL Science Holding Limited Ordinary Shares

SL Science Holding Limited is a dynamic company focused on leveraging advanced technologies to drive innovation in the scientific and healthcare sectors. With a commitment to developing cutting-edge solutions, SLBT is positioned to capitalize on emerging market trends and address critical challenges in biotechnology and life sciences. The company's strategic vision emphasizes research and development, fostering partnerships to enhance its product portfolio and expand its market presence. As an emerging player in this rapidly evolving industry, SLBT aims to deliver substantial long-term value for its stakeholders through sustainable growth and innovation.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)0
Gross Profit (TTM)0
EBITDA
Operating Margin0.00%
Return on Equity0.00%
Return on Assets0.00%
Revenue/Share (TTM)$0.00
Book Value
Price-to-Book1047.17
Price-to-Sales (TTM)1088.47
EV/Revenue1087.99
EV/EBITDA
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)0.00%
Shares Outstanding$560.76M
Float0
% Insiders59.55%
% Institutions0.39%

Historical Volatility

HV 10-Day
HV 20-Day
HV 30-Day
HV 60-Day
HV Rank

Latest News

SL Science Holding Limited Submits Orphan Drug Designation Request to the U.S. FDA for GDT Cell Therapy Targeting Glioblastoma

Taipei, TAIWAN, July 10, 2026 (GLOBE NEWSWIRE) -- SL Science Holding Limited (“SL Science” or the “Company”) (Nasdaq: SLBT), a Taiwan-headquartered biomedical company specializing in developing innovative cellular and gene therapies, today announced that the Company has submitted an Orphan Drug Designation (ODD) request to the U.S. Food and Drug Administration (FDA) for its Gamma Delta T (GDT) cell therapy product, Vdelta2+ Gamma Delta T Cells, for the treatment of glioblastoma multiforme (GBM). The FDA's Office of Orphan Products Development (OOPD) has formally acknowledged receipt of the request and is proceeding with review on additional files about the product

GlobeNewsWire7/10/2026Neutral

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Data last updated: 7/20/2026