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AKRO
Akero Therapeutics, Inc. Common Stock
stock NASDAQ

Market Open
Jul 14, 2025 11:22:40 AM EDT
53.05USD+2.870%(+1.48)214,560
52.98Bid   53.10Ask   0.12Spread
Pre-market
0.00USD-100.000%(-51.57)0
After-hours
Jul 11, 2025 4:00:30 PM EDT
51.57USD+0.049%(+0.03)0
OverviewOption ChainMax PainOptionsHistoricalExchange VolumeDark Pool LevelsDark Pool PrintsExchangesShort VolumeShort Interest - DailyShort InterestBorrow Fee (CTB)Failure to Deliver (FTD)ShortsTrendsNewsTrends
AKRO Reddit Mentions
Subreddits
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We have sentiment values and mention counts going back to 2017. The complete data set is available via the API.
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AKRO Specific Mentions
As of Jul 14, 2025 11:22:45 AM EDT (1 min. ago)
Includes all comments and posts. Mentions per user per ticker capped at one per hour.
13 days ago • u/WallstS • r/StockMarket • why_mash_is_not_easy • Discussion • B
Why #MASH is not easy ?
Boehringer Ingelheim terminated its second metabolic dysfunction-associated steatohepatitis (MASH) alliance back in March, ending an $870 million license agreement inked with Yuhan Corp. for dual GLP-1/FGF21 agonist, BI-3006337 (YH-25724)
$ALT Altimmune’s GLP-1/Glucagon
MASH candidate ‘Pemvidutide’ Ph2 data does not appear to have significant therapeutic benefits on fibrosis associated with MASH
$AKRO Though the ‘Efruxifermin’ Ph2 F4 MASH trial data showed significant results for 96 weeks, the study only randomized 182 patients which is literally a very small population. $MDGL has been working on same F4 trial with 700 patients
$VKTX Viking’s MASH candidate VK2809 Ph2 trial is completed back in Q2 2024, but no further progress has been reported by the company
$LLY Eli Lilly’s ‘tirzepatide’
Ph2 SYNERGY-NASH trial is completed back in Q2 2024, but no further updates have been provided by the company
Post Madrigal’s $MDGL Rezdiffra’s FDA approval back in March 2024, many companies are rethinking MASH strategy
$XBI #MASH #GLP1 #RareDisease
sentiment -0.44
13 days ago • u/WallstS • r/StockMarket • why_mash_is_not_easy • Discussion • B
Why #MASH is not easy ?
Boehringer Ingelheim terminated its second metabolic dysfunction-associated steatohepatitis (MASH) alliance back in March, ending an $870 million license agreement inked with Yuhan Corp. for dual GLP-1/FGF21 agonist, BI-3006337 (YH-25724)
$ALT Altimmune’s GLP-1/Glucagon
MASH candidate ‘Pemvidutide’ Ph2 data does not appear to have significant therapeutic benefits on fibrosis associated with MASH
$AKRO Though the ‘Efruxifermin’ Ph2 F4 MASH trial data showed significant results for 96 weeks, the study only randomized 182 patients which is literally a very small population. $MDGL has been working on same F4 trial with 700 patients
$VKTX Viking’s MASH candidate VK2809 Ph2 trial is completed back in Q2 2024, but no further progress has been reported by the company
$LLY Eli Lilly’s ‘tirzepatide’
Ph2 SYNERGY-NASH trial is completed back in Q2 2024, but no further updates have been provided by the company
Post Madrigal’s $MDGL Rezdiffra’s FDA approval back in March 2024, many companies are rethinking MASH strategy
$XBI #MASH #GLP1 #RareDisease
sentiment -0.44


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