Page last updated: 2024-11-05

thalidomide and B16 Melanoma

thalidomide has been researched along with B16 Melanoma in 5 studies

Thalidomide: A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppressive and anti-angiogenic activity. It inhibits release of TUMOR NECROSIS FACTOR-ALPHA from monocytes, and modulates other cytokine action.
thalidomide : A racemate comprising equimolar amounts of R- and S-thalidomide.
2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione : A dicarboximide that is isoindole-1,3(2H)-dione in which the hydrogen attached to the nitrogen is substituted by a 2,6-dioxopiperidin-3-yl group.

Research Excerpts

ExcerptRelevanceReference
" Since thalidomide exhibits low oral bioavailability due to limitations in solubility, inclusion complexation using sulfobutyl ether-7 beta-cyclodextrin was used to improve the delivery of thalidomide."1.35Molecular encapsulation of thalidomide with sulfobutyl ether-7 beta-cyclodextrin for immediate release property: enhanced in vivo antitumor and antiangiogenesis efficacy in mice. ( Juvekar, A; Kale, R; Saraf, M; Tayade, P, 2008)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Shah, JH1
Swartz, GM1
Papathanassiu, AE1
Treston, AM1
Fogler, WE1
Madsen, JW1
Green, SJ1
Fujiwara, Y1
Sun, Y1
Torphy, RJ1
He, J1
Yanaga, K1
Edil, BH1
Schulick, RD1
Zhu, Y1
Lu, L1
Payvandi, F1
Wu, L1
Zhang, LH1
Hariri, RJ1
Man, HW1
Chen, RS1
Muller, GW2
Hughes, CC1
Stirling, DI2
Schafer, PH1
Bartlett, JB1
Kale, R1
Tayade, P1
Saraf, M1
Juvekar, A1
Dredge, K1
Marriott, JB1
Todryk, SM1
Chen, R1
Dalgleish, AG1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Pilot Study of Lenalidomide Maintenance Therapy in Stage IIIB/IV Non-small Cell Lung Cancer After First-line Chemotherapy[NCT02018523]Phase 17 participants (Actual)Interventional2014-06-30Terminated (stopped due to Study did not enroll enough subjects to make a statistically sound conclusion.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

5 other studies available for thalidomide and B16 Melanoma

ArticleYear
Synthesis and enantiomeric separation of 2-phthalimidino-glutaric acid analogues: potent inhibitors of tumor metastasis.
    Journal of medicinal chemistry, 1999, Aug-12, Volume: 42, Issue:16

    Topics: Animals; Antineoplastic Agents; Drug Screening Assays, Antitumor; Glutarates; Indoles; Lung Neoplasm

1999
Pomalidomide Inhibits PD-L1 Induction to Promote Antitumor Immunity.
    Cancer research, 2018, 12-01, Volume: 78, Issue:23

    Topics: Animals; Antineoplastic Agents; B7-H1 Antigen; Cell Line, Tumor; Cytotoxicity, Immunologic; Gene Exp

2018
The anti-cancer drug lenalidomide inhibits angiogenesis and metastasis via multiple inhibitory effects on endothelial cell function in normoxic and hypoxic conditions.
    Microvascular research, 2009, Volume: 77, Issue:2

    Topics: Adherens Junctions; Angiogenesis Inhibitors; Animals; Antigens, CD; Antineoplastic Agents; Basic Hel

2009
Molecular encapsulation of thalidomide with sulfobutyl ether-7 beta-cyclodextrin for immediate release property: enhanced in vivo antitumor and antiangiogenesis efficacy in mice.
    Drug development and industrial pharmacy, 2008, Volume: 34, Issue:2

    Topics: Angiogenesis Inhibitors; Animals; beta-Cyclodextrins; Biological Availability; Calorimetry, Differen

2008
Protective antitumor immunity induced by a costimulatory thalidomide analog in conjunction with whole tumor cell vaccination is mediated by increased Th1-type immunity.
    Journal of immunology (Baltimore, Md. : 1950), 2002, May-15, Volume: 168, Issue:10

    Topics: Adjuvants, Immunologic; Animals; Antigens, CD; Antineoplastic Combined Chemotherapy Protocols; B7-1

2002