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Antineoplastic Agent Combination SM-88

Known as: SM-88 
An orally bioavailable, proprietary combination of four agents with potential antineoplastic activity. Although the four agents and their exact… 
National Institutes of Health

Papers overview

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2019
2019
200 Background: SM-88 (tyrosine derivative [Td], mTOR inhibitor, CYP3a4 inducer and oxidative stress catalyst) is a relatively… 
2019
2019
Abstract Background SM-88 (D,L-alpha-metyrosine; racemetyrosine [USAN]) is a relatively non-toxic, targeted therapy based on the… 
2019
2019
Background: A wide range of cancers, including pancreatic cancer, display altered expression of amino acid transporter LAT-1. LAT… 
2019
2019
e15714 Background: Refractory PDAC has no established therapy (JCO 37, 2019 supp 4; 226). SM-88 (D,L-alpha-metyrosine) is a novel… 
2019
2019
The novel drug SM-88 seems to be a promising therapy for previously treated patients with advanced pancreatic ductal… 
2019
2019
83 Background: Absolute PSA change is an imperfect surrogate of clinical benefit; CTCs and PSA doubling time (DT) may also be… 
2019
2019
79 Background: Treatment for rising PSA non-metastatic prostate cancer (nmPC) includes multifaceted hormone therapies (HT… 
2018
2018
457Background: SM-88 (tyrosine derivative, mTOR inhibitor, CYP3a4 inducer and oxidative stress catalyst) is a relatively non… 
Review
2018
Review
2018
e13100Background: SM-88 is a relatively non-toxic novel combination therapy (dysfunctional tyrosine, CYP3a4 inducer, mTOR… 
2018
2018
TPS4156Background: Treatment options for recurrent/refractory advanced pancreatic cancer (PC) include largely ineffective toxic…