MARKET

SHPH

SHPH

SHUTTLE PHARMACTCLS HLDGS INC
NASDAQ
1.630
-0.540
-24.88%
After Hours: 1.630 0 0.02% 19:58 09/06 EDT
OPEN
2.070
PREV CLOSE
2.170
HIGH
2.118
LOW
1.590
VOLUME
968.38K
TURNOVER
--
52 WEEK HIGH
6.80
52 WEEK LOW
1.280
MARKET CAP
3.63M
P/E (TTM)
-0.4299
1D
5D
1M
3M
1Y
5Y
1D
Why Shuttle Pharmaceuticals (SHPH) Is Extremely Volatile Today
Benzinga · 2d ago
Shuttle Pharma Issued U.S. Patent For Selective Histone Deacetylase Inhibitors For Treatment Of Human Disease
Benzinga · 2d ago
SHUTTLE PHARMA ANNOUNCES ISSUANCE OF U.S. PATENT FOR SELECTIVE HISTONE DEACETYLASE INHIBITORS FOR THE TREATMENT OF HUMAN DISEASE
Reuters · 2d ago
Why Modular Medical Shares Are Trading Higher By Around 29%; Here Are 20 Stocks Moving Premarket
Benzinga · 2d ago
Shuttle Pharmaceuticals Files Delayed Financial Statements, Reports Progress on Drug Study
Dow Jones · 3d ago
SHUTTLE PHARMA PROVIDES SECOND QUARTER 2024 CORPORATE UPDATE
Reuters · 3d ago
US Stocks Mixed; Trade Gap Widens In July
Benzinga · 3d ago
BUZZ-U.S. STOCKS ON THE MOVE-PagerDuty, AMD, Athira Pharma
Reuters · 3d ago
More
About SHPH
Shuttle Pharmaceuticals Holdings, Inc. is a discovery and development stage specialty pharmaceutical company. The Company is focused on improving the outcomes of cancer patients treated with radiation therapy (RT). It is developing a pipeline of products designed to address cancer therapies as well as to extend to the new applications of radiation therapy. Its product candidates include Ropidoxuridine (IPdR), Ropidoxuridine and Tipracil (IPdR/TPI), SP-1-161, SP-2-225, and SP-1-303. Ropidoxuridine (IPdR) is its lead candidate radiation sensitizer for use in combination with RT to treat brain tumors (glioblastoma) and sarcomas. Ropidoxuridine and Tipracil (IPdR/TPI) is undergoing preclinical development for use as a radiation sensitizer for rectal cancers. SP-1-161 is a pre-clinical candidate lead histone deacetylase (HDAC) inhibitor, a radiation sensitizing candidate product. SP-2-225 is a pre-clinical class II b selective HDAC inhibitor that affects histone deacetylase HDAC6.

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