MARKET

CYCCP

CYCCP

Cyclacel Phar Pr
NASDAQ
10.20
+0.95
+10.27%
Closed 15:55 07/26 EDT
OPEN
9.00
PREV CLOSE
9.25
HIGH
10.35
LOW
8.82
VOLUME
16.75K
TURNOVER
0
52 WEEK HIGH
22.20
52 WEEK LOW
5.25
MARKET CAP
3.42M
P/E (TTM)
-0.4639
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at CYCCP last week (0715-0719)?
Weekly Report · 4d ago
Weekly Report: what happened at CYCCP last week (0708-0712)?
Weekly Report · 07/15 09:37
Weekly Report: what happened at CYCCP last week (0701-0705)?
Weekly Report · 07/08 09:37
Weekly Report: what happened at CYCCP last week (0624-0628)?
Weekly Report · 07/01 09:37
CYCLACEL PHARMACEUTICALS: GOT NOTICE FROM EUROPEAN PATENT OFFICE OF INTENTION TO GRANT PATENT COVERING PLOGOSERTIB PHARMACEUTICAL COMPOSITIONS
Reuters · 06/26 13:20
Cyclacel Announces Notice of Intention to Grant New European Patent Covering Plogosertib Pharmaceutical Compositions
Cyclacel Pharmaceuticals, Inc. Has received a notice from the European Patent Office of the intention to grant a patent. The European patent will provide exclusivity until August 2040. The Company is developing innovative medicines based on cancer cell biology. The patent includes claims to novel pharmaceutical compositions of plogosertib.
Barchart · 06/26 08:15
Weekly Report: what happened at CYCCP last week (0617-0621)?
Weekly Report · 06/24 09:39
Weekly Report: what happened at CYCCP last week (0610-0614)?
Weekly Report · 06/17 09:37
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About CYCCP
Cyclacel Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on developing cancer medicines based on cell cycle, transcriptional regulation and mitosis control biology. The transcriptional regulation program is evaluating fadraciclib, a Cyclin-dependent kinase 9 (CDK9) inhibitor, in solid tumors and hematological malignancies. The epigenetic/anti-mitotic program is evaluating plogosertib, in solid tumors and hematological malignancies. The Company's Plogosertib is a novel, small molecule, selective and potent Polo-like kinase 1 (PLK1) inhibitor, which has demonstrated potent and selective target inhibition (PLK1 IC50 approximately 3 nM) and efficacy in human tumor xenografts at non-toxic doses. Its translational biology program supports the development of plogosertib in solid tumor and hematological malignancy indications.

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