MARKET

FULC

FULC

Fulcrum Therapeutics
NASDAQ
6.73
-0.21
-3.03%
After Hours: 6.73 0 0.00% 17:20 03/27 EDT
OPEN
6.93
PREV CLOSE
6.94
HIGH
7.00
LOW
6.68
VOLUME
390.89K
TURNOVER
--
52 WEEK HIGH
15.74
52 WEEK LOW
2.315
MARKET CAP
448.22M
P/E (TTM)
-5.6942
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at FULC last week (0316-0320)?
Weekly Report · 6d ago
Fulcrum Extends Pociredir Program With Long-Term Sickle Cell Study
TipRanks · 03/20 16:32
Analysts Offer Insights on Healthcare Companies: Taysha Gene Therapies (TSHA) and Fulcrum Therapeutics (FULC)
TipRanks · 03/20 12:51
Fulcrum Therapeutics enters partnership for emergency sickle cell disease care
TipRanks · 03/19 12:26
MedicAlert Foundation, SCDAA And Fulcrum Therapeutics Partner To Help Streamline And Expedite ED Care For People Living With Sickle Cell Disease Through Rapid Access To Patient-Specific Care Plans
Benzinga · 03/19 12:26
Weekly Report: what happened at FULC last week (0309-0313)?
Weekly Report · 03/16 10:20
Weekly Report: what happened at FULC last week (0302-0306)?
Weekly Report · 03/09 10:20
Fulcrum Therapeutics grants 34,000 inducement stock options to new employee
Reuters · 03/06 21:30
More
About FULC
Fulcrum Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases in areas of high unmet medical need. The Company's lead clinical program is pociredir, a small molecule designed to increase expression of fetal hemoglobin for the treatment of sickle cell disease (SCD). It uses technology to identify drug targets that can modulate gene expression to treat the known root cause of gene mis-expression. In addition to its product candidates, the Company has developed a discovery approach that it employs to systematically identify and validate cellular drug targets that can potentially modulate gene expression to treat known root causes of genetically defined rare diseases. The Company continues to advance its program for the potential treatment of inherited aplastic anemias, such as Diamond-Blackfan anemia (DBA), Shwachman-Diamond syndrome, and Fanconi anemia.

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