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pmc.ncbi.nlm.nih.gov/articles/PMC11307418/
F1 ÅÖºû¤Æ©w¸q¬° LSM < 7 kPa
F2 ÅÖºû¤Æ©w¸q¬° 7 kPA ≤ LSM < 8.7 kPa
F3 ÅÖºû¤Æ©w¸q¬° 8.7 kPA ≤ LSM < 10.3 kPa
F4 ÅÖºû¤Æ©w¸q¬° 10.3 kPA ≤ LSM < 13.6 kPa

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·|­û:ROGER588910148151µoªí®É¶¡:2023/7/26 ¤W¤È 11:17:20²Ä3321½g¦^À³
SNP-612 achieves the primary endpoint of an improvement in ALT after 12-weeks treatment in the mITT population
1.F0/1 (kpa<7), n=12 Sig. 0.037
2.F2/3 (7≤kpa<10.3), n=14 Sig.0.016
3.F4 (kpa≥10.3), n=9 Sig. 0.021
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SNP-6 Mitigates MASH in Mice Model GSP Back to normal !!
ATP Sufficient -> normal Galactokinase activity
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2025.10.1-²Ä9©¡¯×ªÕ¨xª¢ÃĪ«¶}µo°ª®p·|www.sinewpharma.com/Upload/download/9th%20MASH%2020251001.pdf

Galactose is metabolized in the liver into glucose-1-phosphate, which then produces ATP,
not glucose, making it suitable for use in patients with DM

GSP Increases with Ultrasound-graded Steatosis in MASLD
GSP Tracks Steatosis Severity by CT in MASLD
GSP Levels Correlate with Fibrosis Severity


Mechanisms Underlying Impaired Galactose Clearance in MASH
1. Normal Blood Flow
2. Intact Hepatocytes
3. ATP Sufficient -> normal Galactokinase activity
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11:45 am One Drop, One Answer: Galactose Single Point for Tracking Liver Health in MASH
Time: 11:45 am
day: Conference Day 1
Details:
A simple, rapid, and quantitative method for assessing liver function
A POC quantitative non-invasive test for MASH: Insights from animal and clinical trials
Exploring a safe, simple, and highly sensitive quantitative liver function test


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CYP2E1 level may be important in FGF21 expression
CYP2E1 level may be important in FGF21 expression

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www.litigationandtrial.com/files/2011/12/2009-4429b1-02-FDA.pdf
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´£¨Ñ¤@¬q2005¦~ Dr.Woodcock(«ôµn¤W¥ô«áªºFDA¥N²z§½ªø)¦b°ê·|³Æ¸ßªºµª´_ www.govinfo.gov/content/pkg/CHRG-109shrg20047/html/CHRG-109shrg20047.htm
...But in general, in my professional opinion, it is very important to have people involved in decisionmaking who actually treat patients with that condition, because if you
only look at risk we would not have any drugs. It would not be sensible to have any drugs because they all cause harm. Even acetaminophen very common drug, over-the-counter, number one cause of drug-induced liver failure in the United States. If you took that fact in isolation what you would say is that should not be on the market. So you have to have the benefit side right in front of you when you are evaluating the safety problems of drugs.

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2017. 7.20 William M. Lee
Public Health: Acetaminophen (APAP) Hepatotoxicity¡XIsn¡¦t It Time for APAP to Go Away?
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www.ncbi.nlm.nih.gov/pmc/articles/PMC5696016/
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ã÷®Ø William M. Lee ³o½g¤å:www.journal-of-hepatology.eu/article/S0168-8278(17)32148-7/fulltext (³oºØ·s«¬ÂíµhÃĪº¦^³ø±N¬O¥¨¤jªº!)¥H¯÷ªí´­Æg¹|!
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