SGMT Sagimet Biosciences Inc. Series A Common Stock

Sector: Healthcare
Industry: Biotechnology
15 min delay
Today's News Sentiment
Loading...
Upcoming Earnings
Loading...
SGMT Fundamental Data
Loading...
Similar Companies
Loading...
SGMT Options Chain
Put/Call Ratio
-
-
Expected Move
-
-
Max Pain
-
-
ATM Call Break-even
-
-
ATM Put Break-even
-
-
Loading options…
CALLS
Strike Last Bid Ask Mark IV Volume OI Δ Delta Θ Theta
PUTS
Strike Last Bid Ask Mark IV Volume OI Δ Delta Θ Theta
SGMT Insider Transactions
Loading insider data…
SGMT News
Date Headline Sentiment
Sagimet Biosciences To Present 52-Week Results From Its Phase 3 ASC40-304 Open-Label Extension Of Denifanstat In Patients With Moderate To Severe Acne Vulgaris At The 2026 Fall Clinical Dermatology Conference, October 8-11
70.31%
HC Wainwright & Co. Reiterates Buy on Sagimet Biosciences, Maintains $29 Price Target
91.16%
Guggenheim Maintains Buy on Sagimet Biosciences, Raises Price Target to $26
84.53%
Oppenheimer Maintains Outperform on Sagimet Biosciences, Raises Price Target to $38
90.04%
Citizens Maintains Market Outperform on Sagimet Biosciences, Lowers Price Target to $27
96.09%
Sagimet Biosciences Surges Forward With Successful Acne Clinical Data and Capital Raise
86.43%
Sagimet Biosciences shares are trading higher after the company announced 52-week results from the Phase 3 ASC40-304 OLE trial of denifanstat for acne. The company suspended its at-the-market sale through Leerink Partners and announced the pricing of its $115 million offering of 8,750,010 shares at $10.00 per share.
91.7%
Sagimet Biosciences Prices $115M Offer Of Shares And Warrants At $10.00/Unit
92.72%
Sagimet Biosciences Suspends And Terminates August 14 Prospectus Supplement Regarding ATM Sales Agreement With Leerink
58.07%
Sagimet Biosciences Announces 52-week Results From The Phase 3 ASC40-304 OLE Trial Of Denifanstat In Patients With Moderate To Severe Acne Vulgaris; Denifanstat Showed Progressive And Sustained Improvements Across All Efficacy Endpoints In The OLE, Including Investigator's Global Assessment Success With A Response Rate Of 57%, 72% Reduction In Total Lesions, And 77% Reduction In Inflammatory Lesions, And Was Generally Well-Tolerated, With No Adverse Event-Related Permanent Discontinuations
83.65%