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MK 8669
Known as:
MK-8669
, MK8669
National Institutes of Health
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Related topics
Related topics
2 relations
AP-23573
Broader (1)
ridaforolimus
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Safety/efficacy of MK-8669 (ridaforolimus) plus MK-2206 (AKT inhibitor) in patients with advanced breast cancer with low RAS signature and PTEN deficient prostate cancer.
Shilpa Gupta
,
P. Munster
,
+6 authors
S. Piha-Paul
2014
Corpus ID: 59301145
2509 Background: The PI3K/AKT/mTOR signaling pathway is aberrantly activated in a variety of cancers. The combination of…
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2013
2013
A phase I study of ridaforolimus in adult Chinese patients with advanced solid tumors
Lian Liu
,
Wen Zhang
,
+9 authors
Jin Li
Journal of Hematology & Oncology
2013
Corpus ID: 3143899
PurposeRidaforolimus (AP23573, MK-8669 or deforolimus) is an inhibitor of mammalian target of rapamycin (mTOR), an important…
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2012
2012
Analysis of the pharmacodynamic activity of the mTOR inhibitor ridaforolimus (AP23573, MK-8669) in a phase 1 clinical trial
L. Berk
,
M. Mita
,
+4 authors
V. Rivera
Cancer Chemotherapy and Pharmacology
2012
Corpus ID: 20568591
PurposeAs part of a phase 1 dose-escalation trial, the pharmacodynamic activity of the mammalian target of rapamycin (mTOR…
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2011
2011
The effect of hepatic insufficiency on the pharmacokinetics of ridaforolimus.
J. McCrea
,
M. Stroh
,
+8 authors
M. Iwamoto
Journal of Clinical Oncology
2011
Corpus ID: 28403895
e13001 Background: Ridaforolimus (RIDA) (AP23573; MK-8669), a unique rapamycin analog and a potent inhibitor of mTOR signaling…
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2010
2010
A multicenter, first-in-pediatrics phase I study of ridaforolimus (AP23573, MK-8669) in patients (pts) with refractory solid tumors.
L. Gore
,
T. Trippett
,
+7 authors
M. Nieder
2010
Corpus ID: 74695778
9531 Background: The mTOR inhibitor ridaforolimus (R) has shown antitumor activity in adults with sarcomas and other malignancies…
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2010
2010
Abstract PR3: Preclinical and molecular profiling data suggest LumB breast cancer as a potential indication for co-targeting IGF1R and mTOR with MK-0646 and MK-8669
Theresa Zhang
,
I. Feldman
,
+12 authors
J. Watters
2010
Corpus ID: 84961803
There has been increasing interest in developing cancer therapies targeting PI3K pathway nodes. However, inhibition of a single…
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Highly Cited
2008
Highly Cited
2008
Deforolimus trial 106- A Phase I trial evaluating 7 regimens of oral Deforolimus (AP23573, MK-8669)
M. Mita
,
C. Britten
,
+7 authors
A. Tolcher
2008
Corpus ID: 73931164
3509 Background: Deforolimus is a non-pro-drug rapamycin analog which specifically and potently inhibits mTOR. In Trial 202…
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2008
2008
Pharmacokinetics of oral deforolimus (AP23573, MK-8669)
G. Fetterly
,
M. Mita
,
+7 authors
A. Tolcher
2008
Corpus ID: 74005504
14555 Background: Deforolimus is a non-pro drug rapamycin analog which specifically inhibits mTOR. Intravenous deforolimus has…
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2008
2008
324 POSTER Synergistic activity of the mTOR inhibitor deforolimus (AP23573; MK-8669) and the anti-androgen bicalutamide in prostate cancer models
R. Squillace
,
David Miller
,
Scott D. Wardwell
,
Frank Y. Wang
,
T. Clackson
,
V. Rivera
2008
Corpus ID: 72011971
2008
2008
321 POSTER A phase I trial evaluating pharmacodynamics of deforolimus (AP23573, MK-8669) delivered orally on multiple dosing schedules
L. Berk
,
David Miller
,
+7 authors
V. Rivera
2008
Corpus ID: 72147286
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